CA2051112C - Semiconductor device - Google Patents
Semiconductor deviceInfo
- Publication number
- CA2051112C CA2051112C CA002051112A CA2051112A CA2051112C CA 2051112 C CA2051112 C CA 2051112C CA 002051112 A CA002051112 A CA 002051112A CA 2051112 A CA2051112 A CA 2051112A CA 2051112 C CA2051112 C CA 2051112C
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- CA
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- Prior art keywords
- layer
- resistance
- voltage
- pulse
- contact
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 239000004065 semiconductor Substances 0.000 title description 7
- 229910021417 amorphous silicon Inorganic materials 0.000 claims description 34
- 229910052751 metal Inorganic materials 0.000 claims description 25
- 239000002184 metal Substances 0.000 claims description 25
- 238000000034 method Methods 0.000 claims description 22
- 239000000758 substrate Substances 0.000 claims description 15
- 238000000151 deposition Methods 0.000 claims description 9
- 229910052720 vanadium Inorganic materials 0.000 claims description 9
- 229910000676 Si alloy Inorganic materials 0.000 claims description 5
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- 229910052763 palladium Inorganic materials 0.000 claims description 5
- 238000013528 artificial neural network Methods 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 239000010410 layer Substances 0.000 description 47
- 239000011651 chromium Substances 0.000 description 17
- 239000000523 sample Substances 0.000 description 16
- 230000008859 change Effects 0.000 description 15
- 238000012360 testing method Methods 0.000 description 14
- 230000001965 increasing effect Effects 0.000 description 13
- 229910052710 silicon Inorganic materials 0.000 description 11
- 239000010703 silicon Substances 0.000 description 11
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 10
- 239000007789 gas Substances 0.000 description 9
- 229910052804 chromium Inorganic materials 0.000 description 7
- 238000002474 experimental method Methods 0.000 description 7
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 6
- 239000011521 glass Substances 0.000 description 6
- 230000008021 deposition Effects 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 4
- 238000005259 measurement Methods 0.000 description 3
- 229910000077 silane Inorganic materials 0.000 description 3
- 150000003376 silicon Chemical class 0.000 description 3
- 238000002207 thermal evaporation Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 230000006870 function Effects 0.000 description 2
- 239000012212 insulator Substances 0.000 description 2
- 238000001459 lithography Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000206 photolithography Methods 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 2
- 229910052721 tungsten Inorganic materials 0.000 description 2
- 239000010937 tungsten Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- 229910000577 Silicon-germanium Inorganic materials 0.000 description 1
- LEVVHYCKPQWKOP-UHFFFAOYSA-N [Si].[Ge] Chemical compound [Si].[Ge] LEVVHYCKPQWKOP-UHFFFAOYSA-N 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 238000001465 metallisation Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000000059 patterning Methods 0.000 description 1
- 229920002120 photoresistant polymer Polymers 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000004756 silanes Chemical group 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Classifications
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N70/00—Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
- H10N70/20—Multistable switching devices, e.g. memristors
- H10N70/25—Multistable switching devices, e.g. memristors based on bulk electronic defects, e.g. trapping of electrons
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N70/00—Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
- H10N70/011—Manufacture or treatment of multistable switching devices
- H10N70/021—Formation of the switching material, e.g. layer deposition
- H10N70/023—Formation of the switching material, e.g. layer deposition by chemical vapor deposition, e.g. MOCVD, ALD
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N70/00—Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
- H10N70/801—Constructional details of multistable switching devices
- H10N70/821—Device geometry
- H10N70/826—Device geometry adapted for essentially vertical current flow, e.g. sandwich or pillar type devices
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N—ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10N70/00—Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
- H10N70/801—Constructional details of multistable switching devices
- H10N70/881—Switching materials
- H10N70/884—Other compounds of groups 13-15, e.g. elemental or compound semiconductors
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S438/00—Semiconductor device manufacturing: process
- Y10S438/90—Bulk effect device making
Abstract
SUBSTITUTE
REMPLACEMENT
SECTION is not Present Cette Section est Absente
REMPLACEMENT
SECTION is not Present Cette Section est Absente
Description
20~1 112 ANAT.OGU33 MEMORY DEVICE
The present invention relates t:o novel analogue memory devices capable of being set and reset to a plurality of different conductance states.
Most semiconductor devices are used in binary digital systems in which the device is in one of two states (e.g. a high and low resistance) which can be used to present binary 0 and binary 1. Howevex there is increasing interest in devices which can be in more than two states.
Devices which can be set and reset into more than two conductance states (as opposed to the two states of digital devices) are potentially useful in structures known as neural networks which attempt to reproduce some of the arrangements of the human brain.
According to the present invention there is provided an analogue memory device capable of being set and reset into a resistance which is a measure of a voltage applied to it, and which device comprises~
(a) a first conducting layer;
(b) a single thin layer in direct electrical contact with layer (a);
(c) a metal top contact in electrical contact with layer (b), the metal being one of V, Co, Ni, Pd! Fe or Mn;
wherein layer (b) constitutes said resistance and it is located between layer (a) and layer (c), said layer (b) being formed of pure or doped amorphous silicon; pure or doped amorphous hydrogenated silicon or a hydrogenated silicon alloy and wherein layer (b~ had been subjected to a voltage sufficiently high to convert it into an analogue .,. . ~ .
memory device. -~
The nature of the first conducting layer is not critical as long as it is possible to grow the required , . ... . .
amoxphous silicon (a-Si) layer upon it. Examples of ~ -suitable materials are Cr or V. Examples of unsuitable : ~ --,. .. ,:
~b ; "..':.:
~:: . - : ,, 20~12 materials are gold (which diffuses into the a-Si layer and mercury (which is liquid). The first conducting layer need not extend on the whole area of the amorphous silicon overlying it. Reference to the amorphous silicon layer being above the first conducting layer do not carry any implication about the orientation of the device in use but are intended to indicate only that the silicon is deposited after the first conducting layer.
The amorphous silicon must be dopable i.e. it must be possible to increase its conductivity by incorporating elements having higher or lower valency than silicon. Some techniques of depositing amorphous silicon may give silicon containing high levels of defects which cannot be doped e.g. Argon sputtering of a Si target in the absence of hydrogen. However methods of making dopable amorphous silicon are well known to those skilled in the art. Thus low pressure pIasma decomposition of silanes (optionally in the presence of hydrogen or fluorine on to a heated substrate may be used).
The deposition of amorphous silicon is discussed in W. E. Spear and P. G. LeComber, Topics in Applied Physics, Vol 55, (The-Physics of Hydrogenated Amorphous Silicon I) 1934 pages 65-71.
The amorphous silicon is doped. The silicon may be doped to produce n-type conductivity by incorporating an element with a higher valency e.g. P, or may be doped to give p-type conductivity as a result of introducing element of lower valency e.g. B.
The amorphous silicon is, preferably, doped so as to have a conductivity in the bulk state of at least 10-6 (ohms cm)-1. The degxee of doping is more preferably such as to correspond to p' or n~-silicon e.g. to conductivities greater than 10-4 (oh~s cm) 1.
:
.:~ , , ::
B
The present invention relates t:o novel analogue memory devices capable of being set and reset to a plurality of different conductance states.
Most semiconductor devices are used in binary digital systems in which the device is in one of two states (e.g. a high and low resistance) which can be used to present binary 0 and binary 1. Howevex there is increasing interest in devices which can be in more than two states.
Devices which can be set and reset into more than two conductance states (as opposed to the two states of digital devices) are potentially useful in structures known as neural networks which attempt to reproduce some of the arrangements of the human brain.
According to the present invention there is provided an analogue memory device capable of being set and reset into a resistance which is a measure of a voltage applied to it, and which device comprises~
(a) a first conducting layer;
(b) a single thin layer in direct electrical contact with layer (a);
(c) a metal top contact in electrical contact with layer (b), the metal being one of V, Co, Ni, Pd! Fe or Mn;
wherein layer (b) constitutes said resistance and it is located between layer (a) and layer (c), said layer (b) being formed of pure or doped amorphous silicon; pure or doped amorphous hydrogenated silicon or a hydrogenated silicon alloy and wherein layer (b~ had been subjected to a voltage sufficiently high to convert it into an analogue .,. . ~ .
memory device. -~
The nature of the first conducting layer is not critical as long as it is possible to grow the required , . ... . .
amoxphous silicon (a-Si) layer upon it. Examples of ~ -suitable materials are Cr or V. Examples of unsuitable : ~ --,. .. ,:
~b ; "..':.:
~:: . - : ,, 20~12 materials are gold (which diffuses into the a-Si layer and mercury (which is liquid). The first conducting layer need not extend on the whole area of the amorphous silicon overlying it. Reference to the amorphous silicon layer being above the first conducting layer do not carry any implication about the orientation of the device in use but are intended to indicate only that the silicon is deposited after the first conducting layer.
The amorphous silicon must be dopable i.e. it must be possible to increase its conductivity by incorporating elements having higher or lower valency than silicon. Some techniques of depositing amorphous silicon may give silicon containing high levels of defects which cannot be doped e.g. Argon sputtering of a Si target in the absence of hydrogen. However methods of making dopable amorphous silicon are well known to those skilled in the art. Thus low pressure pIasma decomposition of silanes (optionally in the presence of hydrogen or fluorine on to a heated substrate may be used).
The deposition of amorphous silicon is discussed in W. E. Spear and P. G. LeComber, Topics in Applied Physics, Vol 55, (The-Physics of Hydrogenated Amorphous Silicon I) 1934 pages 65-71.
The amorphous silicon is doped. The silicon may be doped to produce n-type conductivity by incorporating an element with a higher valency e.g. P, or may be doped to give p-type conductivity as a result of introducing element of lower valency e.g. B.
The amorphous silicon is, preferably, doped so as to have a conductivity in the bulk state of at least 10-6 (ohms cm)-1. The degxee of doping is more preferably such as to correspond to p' or n~-silicon e.g. to conductivities greater than 10-4 (oh~s cm) 1.
:
.:~ , , ::
B
2 ~ 2 Methods of producing doped amorphous silicon are well known to those skilled in the art. The silicon is preferably p~ silicon.
The thickness of the doped amorphous silicon is 5preferably in the range 200 Angstrom to 0.35 micrometres (20 to 350 nm). The amorphous silicon ]Layer may be pure hydrogenated amorphous silicon (apart from any doping) or may be a hydrogenated silicon alloy, e.g. a silicon germanium alloy.
10The dopable silicon or silicon alloy may contain fluorine.
The identity of the top contact is important in obtaining analogue memory properties. In the production of semiconductor devices semiconductor layer~ are often 15deposited on a conducting substrate and a metal layer is deposited in a final step after the semiconductor layers have been deposited. This metal layer is the top contact of the device. The metal layer may, of course, be covered by encapsulating layers or by an additional metal layer 20which is used to obtain better contact with the metal layer in direct contact with the silicon. It is common in the semiconductor industry to stack devices one above the other in integrated circuits. It may be possible to stack other semiconducting and conducting layers above the device of 25the present invention to form other devices within a single integrated circuit.
Preferably the top contact metal is V, Co, Ni or Pd.
The metal may be deposited for example by thermal 30evaporation or by sputtering.
The thickness of the metal is not believed to be critical. Those skilled in the art will understand that the normal requirements for producing metal contacts will imply certain limits~ Thus there may be problems of :.- .: . . , ''' " "''': .
~- :
2 ~ 2 electrical continuity if the layer is too thin and there may be problems of mechanical strain if the layer is too thick. The thickness of the layer may for example be 50 Angstrom (5 nm) to 50 micrometres, pre~erably lO0 Angstroms (10 nm) to l micrometre, more preferably 20 nm to 50 nm.
The device is a two terminal device. It is preferably in the form of a layer of amorphous silicon of a single conductivity type deposited on a conductive substrate as bottom contact. The nature of the bottom contact is not believed to be critical. Thus the bottom contact may be Cr even though Cr does not give usePul analogue memory properties when used as a top contact.
The top contact is preferably in contact only with a relatively small area oP the amorphous silicon layer for each device, as this allows large numbers of devices to be fabricated in a small area, so giving compact integrated circuits. A typical contact has an area of 10-6 cm2. This can be readily achieved by the well-known process of photolithography.
A step of applying a voltage across the device to ~ -change the electrical characteristics is re~uired~ Such -permanent electrical modification of semiconductor devices ~ -is often known as "forming" to those skilled in the art. -~ -The device as initially produced, before being subjected to the "forming" step has a relatively high resistance. Thus the resistance may be of the order of 109 ohms.
For the prePerred device containing only silicon of a single conductivity type reference to Porward on backward bias are meaningless and in principle it does not matter whether the top contact is positive or negative in relation to the bottom contact during the forming process.
Preferably, however, the top contact is positive in relation to the bottom contact during the forming process.
-; ' , ; : .
2 ~ 2 The forming step is preferably divided into two stages, a "soft" forming step and a "hard" ~orming step.
The "hard" forming step is a step which converts the a-Si structure into a device having the desired analogue memory properties. It is possible to "hard" form the device in a single step by applying a voltage which is sufficiently large to convert the structure to a memory device having a resistance less than the full OFF state. However, as indicated above, it is preferred to carry out a "soft"
forming step initially. This involves applying a voltage which is sufficiently high (for example 13-14 volts3 to permanently change the characteristics of the device and to reduce its resistance (for example, by two orders of magnitude) without transforming it to a device having analogue mPmory properties. The final "hard" forming step may be carried out by applying a further, slightly higher voltage (for example the order of 1 to 2 volts above the soft-forming voltage). Thus the initial "soft" forming events can be used to judge the voltage required for hard forming, resulting in a more controlled process. After "hard" forming the resistance of the analogue memory device will be lower than that of the "so~t" formed structure ~for example an order of magnitude or more lower). It will then be below the maximum resistance (the fully OFF stage) to which it can be reset in use.
The magnitude of the forming voltage depends on the thickness of the amorphous silicon layer. It is preferably in the range 6 to 16 volts.
It is necessary to control the energy applied to the structure, as excessive energy can produce damage which prevents a satisfactory device being produced. The energy ; can be controlled by placing a resistance in circuit and by using short voltage pulses. Example of pulse lengths which may be used are 50 ns to ~ microsecond.
:
~ ~ . "' ~ .
2~1112 The devices of the present invention can be set and xeset to a resistance which is a measure of an applied voltage. By "set" we mean that the device will retain this resistance even when the voltage which caused it to take this resistance has been removed. By "reset" we mean that the resistance can be changad to a new set value and is not permanently fixed in the original set value. The devices of the present invention are thus distinguished from threshold devices which only retain a given stage as long as a holding voltage is applied to them. They are different fr~m the known binary memory devices in which the resistance may depend on the applied voltage but all voltages below a certain value correspond to one resistance and all voltages above another value correspond to another resistance. The devices of the present invention do not show analogue memory properties over the whole range of voltages which can be applied to them. It will bP
appreciated that a device which shows analogue memory properties over a voltage rang~ of say 10 millivolts is not in practice a useful device. It is preferred therefore to select metal contacts which give analogue memory properties over a voltage range of at least 0O5V, and preferably over at least one V, more preferably over more than 2V.
The device after "forming" will normally be in a resistance state between the ON and OFF states. By applying a positive voltage pulse of sufficient voltage to the top contact, the device can be set into its highest (or OFF) resistance state. It can then be placed in a lower resistance state by making the bottom contact positive with respect to the top contact. If the voltage is sufficiently high the devicP will be switched to its minimum resistance (the fully ON state). Lesser voltages, providing they are within the appropriate voltage range will switch the device -. -~ B
~ .
2~112 to an intermediate resistance which is related to the voltage applied.
An alternative method of setting the device is to apply a sufficient voltage to switch the "formed" device back to the fully ON state. It may then be switched to a lower resistance intermediate between the fully OFF and the full ON states, by the application of a positive voltage to the top contact.
The switching in the "formed" analogue memory device is preferably carried out with short voltage pulses for example pulses of length in the range 10 ns to 500 nsec. -~
The invention will now be described with reference to the accompanying drawings in which:
Figure 1 is a plan view (not to scale) of a memory element in accordance with the present invention;
Figure 2 is a diagrammatic representation of a -circuit used in testing a memory element made in accordance with the invention;
Figure 3 is a graphical representation of the change in resistance during the forming process: -Figures 4 and 5 are graphical representation of the change in resistance of a formed device with changing ERASE voltage;
Figures 6 and 7 are graphical representations of the variation of resistance with number of constant voltage ERASE and WRITE pulses applied to a device according to the invention, the constant ERASE pulse being of a greater magnitude in Figure 7 than in Figure 6; :
30 ~ Figure 8 is a graphical representation of the change in resistance of a device according to the invention -as WRITE Pulses of increasing magnitude are applied to it, Figure 9 is a graphical representation of the change in resistance of a device according to the invention ' . :, , ': ': .
2 ~ 1 2 alternatively subjected to an ERASE pulse of constant magnitude and a WRITE Pulse of increasing magnitude;
Figure 10 is a graphical representation of the change in resistance of a device according to the invention initially in its ON stage and subjected to ERASE pulses of increasing magnitude;
Figure 11 is a graphical representation of the change in re istance of a device according to the invention which is initially in its ON stage and which is alternatively subjected to ERASE pulses of varying magnitude and WRITE Pulses of constant magnitude;
Figure 12 is a graphical representation of the change in resistance of a device according to the invention which is initially in the OFF state and which is subjected to WRITE Pulses which increase in magnitude;
Figure 13 is a graphical representation of the change in resistance of a device according to the invention subjected to alternatively WRITE and ~RASE Pulsest with the ERASE Pulse held constant and the WRITE Pulse increasing in magnitude;
Figure 14 is a graphical representation of the change in resistance of a device not according to the present invention which is initially in a high resistance state and which is subjected to voltage pulses of increasing magnitude, showing the rapid transition from a very high resistance state to a high resistance staLe when a critical voltage threshold is exceeded;
Figure 15 is a graphical representation of the ~; change in resistance of a device not according to the invention which is initially in an ON state and is subjected to ERASE voltage pulses o~ increasing magnitude;
and Figure 16 is a graphical representation of the change in resistance of a device not according to the ::
.:
2051~12 g invention which is initially in the OFF state and which is subjected to WRITE Pulses of increasing magnitude.
It should be noted that in a digital device a WRITE pulse can be considered as one which sets the device to a state corresponding to either binary 0 or I while an ERASE pulse can be considered as a pulse whish always resets the device to a~ oppo ite state (binary 1 or 0). In the present specification a WRITE pulse is a pulse which tends to reduce the resistance of the devic~ and an ERASE
pulse is a pulse which tends to increase it. Thus a STORE
Pulse which stores analogue information in the device about the magnitude of the voltage applied to it may be a WRITE
or an ERASE pulse. A RESET Pulse which turns the device fully ON or OFF may thus be a WRITE or ERASE pulse provided it is of sufficient magnitude to change the device to the fully ON or OFF state. -Example 1 A structure comprising a glass substrate, chromium ~irst conducting layer, a layer of hydrogenated amorphous silicon doped with diborane, (B2H6), 1 and a top contact layer was fabricated as follows: ~ -The glass structure was "Corning 7059" glass ("Corning" is a trade mark) of thickness about 0.75 mm and length and width 45 mm and 20 mm respectively. A chromium layer of thickness about 150 nm was deposited on this substrate by standard thermal evaporation of chromium granules from an electrically heated tungsten ~ilament in vacuum and subsequently patterned by conventional photolithography.
The amorphous silicon was deposited on this substrate in a single layer by the radio frequency glow discharge decomposition o~ a mixture of SiH4 and about 104 ppm of B2H6, obtained by admitting silane gas and a gas mlxture of 5% diborane in hydrogen to the vacuum system via -~
., .,.: .' 2~1112 flow controllers. The glass substrate was mounted on a substrate holder contained within a vacuum pumped glass tube enclosure and heated to 310C (via a heater element contained within the substrate holder) at a vacuum of less than 10-6 torr. Nitrogen gas was then admitted to the system to raiss th~ vacuum to 0.1 torr and a gas plasma discharge induced (as defined below~ Eor a period of 4 minutes (power input 8~). The discharge was then extinguished, the Nz flow stopped and the system pumped below 10-6 torr. The silane/diborane/hydrogen gases were then admitted to the chamber, flow conditions being set to achieve both silane/diborane ratio and a constant gas pressure of 0.1 torr, resulting from the balance of incoming gas flow and outgoing pumped gas. A gas plasma discharge was then induced using a radio frequency generator running at 40MHz and capacitively coupled to the gas via the substrate holder and two external secondary electrodes 6cm away from the substrate. Power input from -the generator was 8 watts corresponding to a power density of 2OmW/cm2 at the substrate. The RF discharge was -~
maintained for 5.5 minutes and then extinguished. The resulting sample was cooled under vacuum and removed from the deposition system. The a-Si film resulting from this was measured to be 900 Angstrom thick +50 Angstrom (90 nm ~5 nm). The level o~ conductivity due to the B2H6 doping was measured to be between lo-3 and 10-2 (ohms.cm)-1 in separate experiments using the same deposition conditions, corresponding to pta-Si H. -The amorphous silicon layer was then patterned using conventional lithography into a number o~ discrete elements o~ dimensions 900 x 500 micrometres, overlying regions of the chromium first conducting layer. An insulator layer was then provided over all but a very small area of the amorphous silicon, (itself overlying the first :: :
~05~112 conducting layer), in order to define the area to be contacted by the final metal. This was done using a 1.2 micrometres thick insulator of photoresist (Shipley ~` Microposit Sl818) which was patterned, baked and cured at 200DC to d~lineate the device area of Io-6 cm2.
A top contact of vanadium was deposited over the device by the thermal evaporation of vanadium foil from an electrically heated tungsten filament in vacuum, to a -thickness of 60 nm. This was patterned using conventional lithography techniques to provide individual contacts to each of the previously defined a-Si elements; this patterning also provided probing pads of the vanadium to -~
one side of the devices, isolated from both chromium first layer and the a-Si layer except in the previously-defined contact area. Figure 1 shows a plan view of the device made by this technique. -The finished sample was designated 779/l. The electrical characteristics of an individual element on this sample were measured as follows.
2Q The element was contacted using two electrical probe needles contacting the top and bottom metallisations.
These probes were connected to a switching network, such that with the switch in either one of two positions one probe was connected to the pulse generator and the other probe was connected to one side of a resistor (Rs) and the input to an oscilloscope, the other side of the resistor being connected to earth. With the switch in the opposite position, these connections were reversed. The circuit is shown in Figure 2. Hence, application of a voltage pulse to the device, using the pulse generator, induced a current in both the device and resistor ~, thereby inducing a voltage proportional to this current at the oscilloscope ~;; input. Measurement o~ this voltage allowed calculation of -~ the device resistance. It will be appreciated that the 1: ;~` ~ . -'~ r.~
2~1112 value of Rs needs to be sufficiently low to permit most of the applied voltage to appear across the device, yet large enough to give a detectable signal on the oscilloscope.
Typically, Rs values of from 1 M ohms (for forming and initial informed measurement) and 100 ohms (for switching measurement) were used.
In order t~ measure device resistance, a low voltage of 0.5V was output from the pulse generator as continuous DC level; pulses for forming and switching were superimposed on this. Initially, the resistance Q~ the element as made above was measured to be greater than 108 ohms. The element was then subjected to a procedure in which its electrical properties were modified by the application of voltage pulses. A succession oP 250 nsec.
voltage pulses of progressively increasing voltage were applied across the a-Si film, with top (V) contact being at positive potential with respect to the first (Cr) contact.
After each pulse the element resistance was determined as described above. Figure 3 curve~ 1 shows the device resistant against previous voltage pulse as successive pulses are applied. (Note that the device resistance is stable until a further voltage pulse is applied and never `-returns to its original value once modified). At a voltage -of between 13.5 and 14 volts, the resistance fell abruptly to a value of 7 x 105 ohms, within the expected switching range of this element. It was then possible to obtain an even lower resistance in the device using far smaller negative voltage pulses (3.4 V, 100 nsec), testifyiny to the permanent and dramatic change in device properties of the formed element were then studied.
Example l(a) A positive pulse (100 nsec, 3.4 V) was first applied to the element first contact (cr), resulting in an ON state of 2x103 ohms; (this is d~fined as a WRITE pulse).
. ; .
: -. ' t ~ c 2~51112 An opposite polarity pulse, positive to the top contact (V), (defined as an ERASE pulse), was then applied at successively higher voltages and the element resistance determined after each. The results of this test are shown in Figure 4. It can be seen that at a threshold voltage of about 1.6n V, the element resistance is gradually increased with each successively higher voltage until, at about 3.0 V, a final resistance state of about 4xlO5 ohms is achieved.
It should be noted that all the states attained were non-volatile and stablel i.e. in the absence of any attempt to switch the element (e.g. with zero bias or when disconnected), it retained the conductivity state it had last been set to.
Example l(b) In order to ~ully demonstrate the voltaye programmability of the device an alternative method of use was tested. In this positive, 100 nsec WRITE pulse of 3.4 V was applied to the element first or bottom contact (Cr) to set the element to its low resistance state and the resistance measured (2x103 ohms); a positive, 100 nsec ERASE
Pulse of, initially 1.2 V was then applied to the element top contact (V) and the device resistance remeasured. This procedure was repeated with the ERASE pulse being increased by 0.05 V on each successive occasion. The results of this test are shown in Figure 5: as expected, the application of the WRITE Pulse resulted in a constant resistance value whilst increasing ERASE Pulse amplitude gave rise to a range of resistance values between 2 x 103 ohms and 4 x 105 ohms. This demonstrates that, between the upper and lower switching thresholds, the element resistance is primarily a function of applied voltage pulse, not of the number of pulses applied as might be deduced from Figure ~. Thus the element can controllably be set on an intermediate resistance between an upper and lower bound. The 2051~1 2 reproducibility of the switching to these intermediate resistance states was tested by repeatedly applying fixed ERASE and WRITE Pulses of 100 nsec, 3.4 V and ERASE Pulses of loo nsec 2.1 V and 100 nsec 2.4 V are shown in Figures 6 and 7 respectively. Over the duration of the test, the application of fixed pulses results in constant resistance values. (The scatter in the value after ERASE is to be expected due to small fluctuations in the value of applied voltage from the equipment; it is because of its that a wide voltage threshold range is desirable, in order to provide as many usable intermediate states as possible.) Example lfc) A further method of using the element was teated.
The element was first set to its high resistivity state (8xlO5 ohms) using an ERA5E pulse of ~3.4 V, 100 nsec (applied to top contact ~V)). A series o~ WRITE Pulses of 100 nsec duration were then applied to the element, starting at 1.2 V and incrementing each successive pulse of 0.05 V up to 3.3 V. The element resistance was ~easured ~-a~ter each pulse and the results are shown in Figure 8. As before, intermediate resistance states are obtained for WRITE pulses between a lower threshold voltage and upper threshold voltage (of ~bout 1.6 V and 2.7 V respectively), -though there is far more scatter in the curve than for the case of incremental ERASE (Figure 4).
~ ;
A further test was made in which a constant ERASE
pulse of 3.4 V, lOO nsec was applied to the element to reset it to its highest resistance state, followed by a -WRITE Pulse of lOO nsec, voltage being incremented by 0.05 V ~rom 1.2 V to 3.4 V on successive repeats. Resistance was measured after each pulse and the results are shown in Figure 9; as was ths case for constant WRITE, incremental ERASE (Figure 5), the intermediate resistance states are ;~ ~ ''` . ''. :.
.
. .
~ .
-2~1112 seen to be primarily a function of previously applied voltage pulse.
Example ?
A sample was made as in Example 1, but with a first metal layer of 50 nm vanadium deposited by thermal evaporation as defined in Example 1. a-Si deposition was done simultaneously with Example 1 and the finished sample ~V-p~-V) designated 779/2.
An element of this sample was tested as in Example 1. Initially a series of 250 nsec positive voltage pulses were applied to the top contact, each successive pulse being of higher voltage than the last; element resistance was measured after each pulse. The test was stopped once the "forming" event was seen to take place (i.e. an abrupt change in resistance to 6 x 105 ohms). The results of this test are shown in curve 2 in Figure 3.
A further 4 experiments (~a)-(d~ defined ion Example 1) were then applied to the element to determine the dependence of the element resistance on previously applied voltage pulse.
Figure 10 shows the results of experiment (a), (in which after initial WRITE Pulse (100 nsec, 3.4 V to bottom contact), a sequence of 100 nsec ERASE pulses are applied from 1.2 V to 3.2 V in 0.05 V steps)0 Figure 11 shows the results of an experiment (b) (a sequence of alternating 3.4 V, lO0 nsec WRITE Pulses, each followed by an incremented 100 nsec ERAS~ pulse from experiment).
Figure 12 shows the results from experiment (c) (initial ERASE pulse of 3.4 kV, 100 n~ec, followed by incrementally increasing WRI~E pulses of 100 nsec, 1.2 V to 3.4 V in 0.05 V steps).
~; Figure 13 shows the result from experiment (d) (alternative 3.4 V, 100 nsec ERASE Pulses followed by 100 ~ ~ ~;p T
20511~2 nsec WRITE Pulses, incremented from 1.2 V to 3.4 V in 0.05 V steps).
These tests show that the V-p~-V sample behaves similarly to the V-p'-Cr sample of Example 1; most importantly, there is no indication that replacing the first Cr metal layer with V induces further (opposite polarity~ switching in the structure.
comparative Test A
A sample was made as in Example 1, but with a final (top) metal layer of about 50 nm Cr, deposited as for the first bottom metal layer. a-Si deposition was done simultaneously with Example 1 and the finished sample (Cr-p~-Cr) designated 779/3.
An element of this sample was tested as in Example 1. Initially a series of 250 nsec positive voltage pulses were applied to the top contact, each successive pulse being higher than the last, until the "forming" event took place. The results of this test are shown in Figure 14; note that resistance changes take place over a much narrower voltage range than in the corresponding test on Examples 1 and 2 (Figure 3).
After "forming", the element was tested using method (a) and method (c) previously defined to determine the presence of intermediate resistance states.
Figure 15 shows the results for method (a).
Figure 16 shows the results for method (c). Note that although similar resistance limits are seen in this element to those of Examples 1 and 2, (i.e. from 2 x 103 ohms to 3.5 x 105), and some intermediate states do exist, - . .
the voltage range over which these intermediate states can be obtained is far narrower than the range of Examples 1 and 2, (i.e. circa 0.15-0.2 kV compared with circa 2.2 V).
This makes it extremely difficult to obtain reliable programming of the intermedlate states and the element lS
B
only suitable for digital use, (i.e. from the 2 x 103 ohms state to the 3.5 x 105 ohms state), and is correspondingly classified as a digital device.
Examples 3-8 and comparative Tests A number of samples were made essentially as for Example 1, (i.e. glass Cr first conducting layer, circa 900 Angstrom a-Si:H doped with H2H6), but a number of different top contact metal films were deposited in place of the V
film of Example 1. Each sample was then tested as in ~ -Example 1 and the range of switching voltages over which intermediate states could be obtained was determined.
Devices were accordingly classified as digital ~switching range 0.5 V) or analogue ~switching range 0.5 V); preferred analogue devices were defined as those exhibiting a switching range of 2.0 V or more. Table 1 lists the results of this test. -.:
B `::
2051~12 TAaLE 1 Swvey of p+ -switching with different top metals all the bottom contacts ars chromium.
T.E. = thormal evaporation of top metal.
S = sputterad top metal.
i_xampie Metal Switchlng Switching Comments or top Method Type Range test contact B Cr T.E. Digital ~0.5 V Intermadiate states oxist 3 v T.E. Analogue ~ 2.0V Preferrrd 2 0 4 Fe T.E. Analogue 0.5 - 1.0 V
Nl T.E. Analogue 2.0 V Preferred C Au T.E. No swltchlng - -D Cu T.E. No swltchln9 - - .; .
6 Co T.E. Analogue > 2.0V Prefsrred 3 0 E Ti T.E. Unstable ~ - ~
F Mo S Unstable - - .
7 Pd S Analogue 2.0 V Preferred G W S Dlgltal 8 Mn - Analogua 0.5 -1.0 V
H Ag - Digital ~0.5V No intermediate states obtalned Ai - No swUching .. -.
.
, - :
The thickness of the doped amorphous silicon is 5preferably in the range 200 Angstrom to 0.35 micrometres (20 to 350 nm). The amorphous silicon ]Layer may be pure hydrogenated amorphous silicon (apart from any doping) or may be a hydrogenated silicon alloy, e.g. a silicon germanium alloy.
10The dopable silicon or silicon alloy may contain fluorine.
The identity of the top contact is important in obtaining analogue memory properties. In the production of semiconductor devices semiconductor layer~ are often 15deposited on a conducting substrate and a metal layer is deposited in a final step after the semiconductor layers have been deposited. This metal layer is the top contact of the device. The metal layer may, of course, be covered by encapsulating layers or by an additional metal layer 20which is used to obtain better contact with the metal layer in direct contact with the silicon. It is common in the semiconductor industry to stack devices one above the other in integrated circuits. It may be possible to stack other semiconducting and conducting layers above the device of 25the present invention to form other devices within a single integrated circuit.
Preferably the top contact metal is V, Co, Ni or Pd.
The metal may be deposited for example by thermal 30evaporation or by sputtering.
The thickness of the metal is not believed to be critical. Those skilled in the art will understand that the normal requirements for producing metal contacts will imply certain limits~ Thus there may be problems of :.- .: . . , ''' " "''': .
~- :
2 ~ 2 electrical continuity if the layer is too thin and there may be problems of mechanical strain if the layer is too thick. The thickness of the layer may for example be 50 Angstrom (5 nm) to 50 micrometres, pre~erably lO0 Angstroms (10 nm) to l micrometre, more preferably 20 nm to 50 nm.
The device is a two terminal device. It is preferably in the form of a layer of amorphous silicon of a single conductivity type deposited on a conductive substrate as bottom contact. The nature of the bottom contact is not believed to be critical. Thus the bottom contact may be Cr even though Cr does not give usePul analogue memory properties when used as a top contact.
The top contact is preferably in contact only with a relatively small area oP the amorphous silicon layer for each device, as this allows large numbers of devices to be fabricated in a small area, so giving compact integrated circuits. A typical contact has an area of 10-6 cm2. This can be readily achieved by the well-known process of photolithography.
A step of applying a voltage across the device to ~ -change the electrical characteristics is re~uired~ Such -permanent electrical modification of semiconductor devices ~ -is often known as "forming" to those skilled in the art. -~ -The device as initially produced, before being subjected to the "forming" step has a relatively high resistance. Thus the resistance may be of the order of 109 ohms.
For the prePerred device containing only silicon of a single conductivity type reference to Porward on backward bias are meaningless and in principle it does not matter whether the top contact is positive or negative in relation to the bottom contact during the forming process.
Preferably, however, the top contact is positive in relation to the bottom contact during the forming process.
-; ' , ; : .
2 ~ 2 The forming step is preferably divided into two stages, a "soft" forming step and a "hard" ~orming step.
The "hard" forming step is a step which converts the a-Si structure into a device having the desired analogue memory properties. It is possible to "hard" form the device in a single step by applying a voltage which is sufficiently large to convert the structure to a memory device having a resistance less than the full OFF state. However, as indicated above, it is preferred to carry out a "soft"
forming step initially. This involves applying a voltage which is sufficiently high (for example 13-14 volts3 to permanently change the characteristics of the device and to reduce its resistance (for example, by two orders of magnitude) without transforming it to a device having analogue mPmory properties. The final "hard" forming step may be carried out by applying a further, slightly higher voltage (for example the order of 1 to 2 volts above the soft-forming voltage). Thus the initial "soft" forming events can be used to judge the voltage required for hard forming, resulting in a more controlled process. After "hard" forming the resistance of the analogue memory device will be lower than that of the "so~t" formed structure ~for example an order of magnitude or more lower). It will then be below the maximum resistance (the fully OFF stage) to which it can be reset in use.
The magnitude of the forming voltage depends on the thickness of the amorphous silicon layer. It is preferably in the range 6 to 16 volts.
It is necessary to control the energy applied to the structure, as excessive energy can produce damage which prevents a satisfactory device being produced. The energy ; can be controlled by placing a resistance in circuit and by using short voltage pulses. Example of pulse lengths which may be used are 50 ns to ~ microsecond.
:
~ ~ . "' ~ .
2~1112 The devices of the present invention can be set and xeset to a resistance which is a measure of an applied voltage. By "set" we mean that the device will retain this resistance even when the voltage which caused it to take this resistance has been removed. By "reset" we mean that the resistance can be changad to a new set value and is not permanently fixed in the original set value. The devices of the present invention are thus distinguished from threshold devices which only retain a given stage as long as a holding voltage is applied to them. They are different fr~m the known binary memory devices in which the resistance may depend on the applied voltage but all voltages below a certain value correspond to one resistance and all voltages above another value correspond to another resistance. The devices of the present invention do not show analogue memory properties over the whole range of voltages which can be applied to them. It will bP
appreciated that a device which shows analogue memory properties over a voltage rang~ of say 10 millivolts is not in practice a useful device. It is preferred therefore to select metal contacts which give analogue memory properties over a voltage range of at least 0O5V, and preferably over at least one V, more preferably over more than 2V.
The device after "forming" will normally be in a resistance state between the ON and OFF states. By applying a positive voltage pulse of sufficient voltage to the top contact, the device can be set into its highest (or OFF) resistance state. It can then be placed in a lower resistance state by making the bottom contact positive with respect to the top contact. If the voltage is sufficiently high the devicP will be switched to its minimum resistance (the fully ON state). Lesser voltages, providing they are within the appropriate voltage range will switch the device -. -~ B
~ .
2~112 to an intermediate resistance which is related to the voltage applied.
An alternative method of setting the device is to apply a sufficient voltage to switch the "formed" device back to the fully ON state. It may then be switched to a lower resistance intermediate between the fully OFF and the full ON states, by the application of a positive voltage to the top contact.
The switching in the "formed" analogue memory device is preferably carried out with short voltage pulses for example pulses of length in the range 10 ns to 500 nsec. -~
The invention will now be described with reference to the accompanying drawings in which:
Figure 1 is a plan view (not to scale) of a memory element in accordance with the present invention;
Figure 2 is a diagrammatic representation of a -circuit used in testing a memory element made in accordance with the invention;
Figure 3 is a graphical representation of the change in resistance during the forming process: -Figures 4 and 5 are graphical representation of the change in resistance of a formed device with changing ERASE voltage;
Figures 6 and 7 are graphical representations of the variation of resistance with number of constant voltage ERASE and WRITE pulses applied to a device according to the invention, the constant ERASE pulse being of a greater magnitude in Figure 7 than in Figure 6; :
30 ~ Figure 8 is a graphical representation of the change in resistance of a device according to the invention -as WRITE Pulses of increasing magnitude are applied to it, Figure 9 is a graphical representation of the change in resistance of a device according to the invention ' . :, , ': ': .
2 ~ 1 2 alternatively subjected to an ERASE pulse of constant magnitude and a WRITE Pulse of increasing magnitude;
Figure 10 is a graphical representation of the change in resistance of a device according to the invention initially in its ON stage and subjected to ERASE pulses of increasing magnitude;
Figure 11 is a graphical representation of the change in re istance of a device according to the invention which is initially in its ON stage and which is alternatively subjected to ERASE pulses of varying magnitude and WRITE Pulses of constant magnitude;
Figure 12 is a graphical representation of the change in resistance of a device according to the invention which is initially in the OFF state and which is subjected to WRITE Pulses which increase in magnitude;
Figure 13 is a graphical representation of the change in resistance of a device according to the invention subjected to alternatively WRITE and ~RASE Pulsest with the ERASE Pulse held constant and the WRITE Pulse increasing in magnitude;
Figure 14 is a graphical representation of the change in resistance of a device not according to the present invention which is initially in a high resistance state and which is subjected to voltage pulses of increasing magnitude, showing the rapid transition from a very high resistance state to a high resistance staLe when a critical voltage threshold is exceeded;
Figure 15 is a graphical representation of the ~; change in resistance of a device not according to the invention which is initially in an ON state and is subjected to ERASE voltage pulses o~ increasing magnitude;
and Figure 16 is a graphical representation of the change in resistance of a device not according to the ::
.:
2051~12 g invention which is initially in the OFF state and which is subjected to WRITE Pulses of increasing magnitude.
It should be noted that in a digital device a WRITE pulse can be considered as one which sets the device to a state corresponding to either binary 0 or I while an ERASE pulse can be considered as a pulse whish always resets the device to a~ oppo ite state (binary 1 or 0). In the present specification a WRITE pulse is a pulse which tends to reduce the resistance of the devic~ and an ERASE
pulse is a pulse which tends to increase it. Thus a STORE
Pulse which stores analogue information in the device about the magnitude of the voltage applied to it may be a WRITE
or an ERASE pulse. A RESET Pulse which turns the device fully ON or OFF may thus be a WRITE or ERASE pulse provided it is of sufficient magnitude to change the device to the fully ON or OFF state. -Example 1 A structure comprising a glass substrate, chromium ~irst conducting layer, a layer of hydrogenated amorphous silicon doped with diborane, (B2H6), 1 and a top contact layer was fabricated as follows: ~ -The glass structure was "Corning 7059" glass ("Corning" is a trade mark) of thickness about 0.75 mm and length and width 45 mm and 20 mm respectively. A chromium layer of thickness about 150 nm was deposited on this substrate by standard thermal evaporation of chromium granules from an electrically heated tungsten ~ilament in vacuum and subsequently patterned by conventional photolithography.
The amorphous silicon was deposited on this substrate in a single layer by the radio frequency glow discharge decomposition o~ a mixture of SiH4 and about 104 ppm of B2H6, obtained by admitting silane gas and a gas mlxture of 5% diborane in hydrogen to the vacuum system via -~
., .,.: .' 2~1112 flow controllers. The glass substrate was mounted on a substrate holder contained within a vacuum pumped glass tube enclosure and heated to 310C (via a heater element contained within the substrate holder) at a vacuum of less than 10-6 torr. Nitrogen gas was then admitted to the system to raiss th~ vacuum to 0.1 torr and a gas plasma discharge induced (as defined below~ Eor a period of 4 minutes (power input 8~). The discharge was then extinguished, the Nz flow stopped and the system pumped below 10-6 torr. The silane/diborane/hydrogen gases were then admitted to the chamber, flow conditions being set to achieve both silane/diborane ratio and a constant gas pressure of 0.1 torr, resulting from the balance of incoming gas flow and outgoing pumped gas. A gas plasma discharge was then induced using a radio frequency generator running at 40MHz and capacitively coupled to the gas via the substrate holder and two external secondary electrodes 6cm away from the substrate. Power input from -the generator was 8 watts corresponding to a power density of 2OmW/cm2 at the substrate. The RF discharge was -~
maintained for 5.5 minutes and then extinguished. The resulting sample was cooled under vacuum and removed from the deposition system. The a-Si film resulting from this was measured to be 900 Angstrom thick +50 Angstrom (90 nm ~5 nm). The level o~ conductivity due to the B2H6 doping was measured to be between lo-3 and 10-2 (ohms.cm)-1 in separate experiments using the same deposition conditions, corresponding to pta-Si H. -The amorphous silicon layer was then patterned using conventional lithography into a number o~ discrete elements o~ dimensions 900 x 500 micrometres, overlying regions of the chromium first conducting layer. An insulator layer was then provided over all but a very small area of the amorphous silicon, (itself overlying the first :: :
~05~112 conducting layer), in order to define the area to be contacted by the final metal. This was done using a 1.2 micrometres thick insulator of photoresist (Shipley ~` Microposit Sl818) which was patterned, baked and cured at 200DC to d~lineate the device area of Io-6 cm2.
A top contact of vanadium was deposited over the device by the thermal evaporation of vanadium foil from an electrically heated tungsten filament in vacuum, to a -thickness of 60 nm. This was patterned using conventional lithography techniques to provide individual contacts to each of the previously defined a-Si elements; this patterning also provided probing pads of the vanadium to -~
one side of the devices, isolated from both chromium first layer and the a-Si layer except in the previously-defined contact area. Figure 1 shows a plan view of the device made by this technique. -The finished sample was designated 779/l. The electrical characteristics of an individual element on this sample were measured as follows.
2Q The element was contacted using two electrical probe needles contacting the top and bottom metallisations.
These probes were connected to a switching network, such that with the switch in either one of two positions one probe was connected to the pulse generator and the other probe was connected to one side of a resistor (Rs) and the input to an oscilloscope, the other side of the resistor being connected to earth. With the switch in the opposite position, these connections were reversed. The circuit is shown in Figure 2. Hence, application of a voltage pulse to the device, using the pulse generator, induced a current in both the device and resistor ~, thereby inducing a voltage proportional to this current at the oscilloscope ~;; input. Measurement o~ this voltage allowed calculation of -~ the device resistance. It will be appreciated that the 1: ;~` ~ . -'~ r.~
2~1112 value of Rs needs to be sufficiently low to permit most of the applied voltage to appear across the device, yet large enough to give a detectable signal on the oscilloscope.
Typically, Rs values of from 1 M ohms (for forming and initial informed measurement) and 100 ohms (for switching measurement) were used.
In order t~ measure device resistance, a low voltage of 0.5V was output from the pulse generator as continuous DC level; pulses for forming and switching were superimposed on this. Initially, the resistance Q~ the element as made above was measured to be greater than 108 ohms. The element was then subjected to a procedure in which its electrical properties were modified by the application of voltage pulses. A succession oP 250 nsec.
voltage pulses of progressively increasing voltage were applied across the a-Si film, with top (V) contact being at positive potential with respect to the first (Cr) contact.
After each pulse the element resistance was determined as described above. Figure 3 curve~ 1 shows the device resistant against previous voltage pulse as successive pulses are applied. (Note that the device resistance is stable until a further voltage pulse is applied and never `-returns to its original value once modified). At a voltage -of between 13.5 and 14 volts, the resistance fell abruptly to a value of 7 x 105 ohms, within the expected switching range of this element. It was then possible to obtain an even lower resistance in the device using far smaller negative voltage pulses (3.4 V, 100 nsec), testifyiny to the permanent and dramatic change in device properties of the formed element were then studied.
Example l(a) A positive pulse (100 nsec, 3.4 V) was first applied to the element first contact (cr), resulting in an ON state of 2x103 ohms; (this is d~fined as a WRITE pulse).
. ; .
: -. ' t ~ c 2~51112 An opposite polarity pulse, positive to the top contact (V), (defined as an ERASE pulse), was then applied at successively higher voltages and the element resistance determined after each. The results of this test are shown in Figure 4. It can be seen that at a threshold voltage of about 1.6n V, the element resistance is gradually increased with each successively higher voltage until, at about 3.0 V, a final resistance state of about 4xlO5 ohms is achieved.
It should be noted that all the states attained were non-volatile and stablel i.e. in the absence of any attempt to switch the element (e.g. with zero bias or when disconnected), it retained the conductivity state it had last been set to.
Example l(b) In order to ~ully demonstrate the voltaye programmability of the device an alternative method of use was tested. In this positive, 100 nsec WRITE pulse of 3.4 V was applied to the element first or bottom contact (Cr) to set the element to its low resistance state and the resistance measured (2x103 ohms); a positive, 100 nsec ERASE
Pulse of, initially 1.2 V was then applied to the element top contact (V) and the device resistance remeasured. This procedure was repeated with the ERASE pulse being increased by 0.05 V on each successive occasion. The results of this test are shown in Figure 5: as expected, the application of the WRITE Pulse resulted in a constant resistance value whilst increasing ERASE Pulse amplitude gave rise to a range of resistance values between 2 x 103 ohms and 4 x 105 ohms. This demonstrates that, between the upper and lower switching thresholds, the element resistance is primarily a function of applied voltage pulse, not of the number of pulses applied as might be deduced from Figure ~. Thus the element can controllably be set on an intermediate resistance between an upper and lower bound. The 2051~1 2 reproducibility of the switching to these intermediate resistance states was tested by repeatedly applying fixed ERASE and WRITE Pulses of 100 nsec, 3.4 V and ERASE Pulses of loo nsec 2.1 V and 100 nsec 2.4 V are shown in Figures 6 and 7 respectively. Over the duration of the test, the application of fixed pulses results in constant resistance values. (The scatter in the value after ERASE is to be expected due to small fluctuations in the value of applied voltage from the equipment; it is because of its that a wide voltage threshold range is desirable, in order to provide as many usable intermediate states as possible.) Example lfc) A further method of using the element was teated.
The element was first set to its high resistivity state (8xlO5 ohms) using an ERA5E pulse of ~3.4 V, 100 nsec (applied to top contact ~V)). A series o~ WRITE Pulses of 100 nsec duration were then applied to the element, starting at 1.2 V and incrementing each successive pulse of 0.05 V up to 3.3 V. The element resistance was ~easured ~-a~ter each pulse and the results are shown in Figure 8. As before, intermediate resistance states are obtained for WRITE pulses between a lower threshold voltage and upper threshold voltage (of ~bout 1.6 V and 2.7 V respectively), -though there is far more scatter in the curve than for the case of incremental ERASE (Figure 4).
~ ;
A further test was made in which a constant ERASE
pulse of 3.4 V, lOO nsec was applied to the element to reset it to its highest resistance state, followed by a -WRITE Pulse of lOO nsec, voltage being incremented by 0.05 V ~rom 1.2 V to 3.4 V on successive repeats. Resistance was measured after each pulse and the results are shown in Figure 9; as was ths case for constant WRITE, incremental ERASE (Figure 5), the intermediate resistance states are ;~ ~ ''` . ''. :.
.
. .
~ .
-2~1112 seen to be primarily a function of previously applied voltage pulse.
Example ?
A sample was made as in Example 1, but with a first metal layer of 50 nm vanadium deposited by thermal evaporation as defined in Example 1. a-Si deposition was done simultaneously with Example 1 and the finished sample ~V-p~-V) designated 779/2.
An element of this sample was tested as in Example 1. Initially a series of 250 nsec positive voltage pulses were applied to the top contact, each successive pulse being of higher voltage than the last; element resistance was measured after each pulse. The test was stopped once the "forming" event was seen to take place (i.e. an abrupt change in resistance to 6 x 105 ohms). The results of this test are shown in curve 2 in Figure 3.
A further 4 experiments (~a)-(d~ defined ion Example 1) were then applied to the element to determine the dependence of the element resistance on previously applied voltage pulse.
Figure 10 shows the results of experiment (a), (in which after initial WRITE Pulse (100 nsec, 3.4 V to bottom contact), a sequence of 100 nsec ERASE pulses are applied from 1.2 V to 3.2 V in 0.05 V steps)0 Figure 11 shows the results of an experiment (b) (a sequence of alternating 3.4 V, lO0 nsec WRITE Pulses, each followed by an incremented 100 nsec ERAS~ pulse from experiment).
Figure 12 shows the results from experiment (c) (initial ERASE pulse of 3.4 kV, 100 n~ec, followed by incrementally increasing WRI~E pulses of 100 nsec, 1.2 V to 3.4 V in 0.05 V steps).
~; Figure 13 shows the result from experiment (d) (alternative 3.4 V, 100 nsec ERASE Pulses followed by 100 ~ ~ ~;p T
20511~2 nsec WRITE Pulses, incremented from 1.2 V to 3.4 V in 0.05 V steps).
These tests show that the V-p~-V sample behaves similarly to the V-p'-Cr sample of Example 1; most importantly, there is no indication that replacing the first Cr metal layer with V induces further (opposite polarity~ switching in the structure.
comparative Test A
A sample was made as in Example 1, but with a final (top) metal layer of about 50 nm Cr, deposited as for the first bottom metal layer. a-Si deposition was done simultaneously with Example 1 and the finished sample (Cr-p~-Cr) designated 779/3.
An element of this sample was tested as in Example 1. Initially a series of 250 nsec positive voltage pulses were applied to the top contact, each successive pulse being higher than the last, until the "forming" event took place. The results of this test are shown in Figure 14; note that resistance changes take place over a much narrower voltage range than in the corresponding test on Examples 1 and 2 (Figure 3).
After "forming", the element was tested using method (a) and method (c) previously defined to determine the presence of intermediate resistance states.
Figure 15 shows the results for method (a).
Figure 16 shows the results for method (c). Note that although similar resistance limits are seen in this element to those of Examples 1 and 2, (i.e. from 2 x 103 ohms to 3.5 x 105), and some intermediate states do exist, - . .
the voltage range over which these intermediate states can be obtained is far narrower than the range of Examples 1 and 2, (i.e. circa 0.15-0.2 kV compared with circa 2.2 V).
This makes it extremely difficult to obtain reliable programming of the intermedlate states and the element lS
B
only suitable for digital use, (i.e. from the 2 x 103 ohms state to the 3.5 x 105 ohms state), and is correspondingly classified as a digital device.
Examples 3-8 and comparative Tests A number of samples were made essentially as for Example 1, (i.e. glass Cr first conducting layer, circa 900 Angstrom a-Si:H doped with H2H6), but a number of different top contact metal films were deposited in place of the V
film of Example 1. Each sample was then tested as in ~ -Example 1 and the range of switching voltages over which intermediate states could be obtained was determined.
Devices were accordingly classified as digital ~switching range 0.5 V) or analogue ~switching range 0.5 V); preferred analogue devices were defined as those exhibiting a switching range of 2.0 V or more. Table 1 lists the results of this test. -.:
B `::
2051~12 TAaLE 1 Swvey of p+ -switching with different top metals all the bottom contacts ars chromium.
T.E. = thormal evaporation of top metal.
S = sputterad top metal.
i_xampie Metal Switchlng Switching Comments or top Method Type Range test contact B Cr T.E. Digital ~0.5 V Intermadiate states oxist 3 v T.E. Analogue ~ 2.0V Preferrrd 2 0 4 Fe T.E. Analogue 0.5 - 1.0 V
Nl T.E. Analogue 2.0 V Preferred C Au T.E. No swltchlng - -D Cu T.E. No swltchln9 - - .; .
6 Co T.E. Analogue > 2.0V Prefsrred 3 0 E Ti T.E. Unstable ~ - ~
F Mo S Unstable - - .
7 Pd S Analogue 2.0 V Preferred G W S Dlgltal 8 Mn - Analogua 0.5 -1.0 V
H Ag - Digital ~0.5V No intermediate states obtalned Ai - No swUching .. -.
.
, - :
Claims (6)
1. An analogue memory device capable of being set and reset into a resistance which is a measure of a voltage applied to it, and which device comprises:
(a) a first conducting layer;
(b) a single thin layer in direct electrical contact with layer (a);
(c) a metal top contact in electrical contact with layer (b), the metal being one of V, Co, Ni, Pd, Fe or Mn;
wherein layer (b) constitutes said resistance and it is located between layer (a) and layer (c), said layer (b) being formed of pure or doped amorphous silicon; pure or doped amorphous hydrogenated silicon or a hydrogenated silicon alloy and wherein layer (b) had been subjected to a voltage sufficiently high to convert it into an analogue memory device.
(a) a first conducting layer;
(b) a single thin layer in direct electrical contact with layer (a);
(c) a metal top contact in electrical contact with layer (b), the metal being one of V, Co, Ni, Pd, Fe or Mn;
wherein layer (b) constitutes said resistance and it is located between layer (a) and layer (c), said layer (b) being formed of pure or doped amorphous silicon; pure or doped amorphous hydrogenated silicon or a hydrogenated silicon alloy and wherein layer (b) had been subjected to a voltage sufficiently high to convert it into an analogue memory device.
2. A device according to claim 1, wherein layer (b) is formed of doped amorphous silicon.
3. A device according to claim 1, wherein the metal of the top contact is V, Co, Ni or Pd.
4. A method of making an analogue memory device capable of being set and reset into a resistance which is a measure of a voltage applied to it which method comprises:
(i) depositing a first conducting layer on an insulating substrate;
(ii) depositing a thin layer of pure or doped amorphous silicon; pure or doped amorphous hydrogenated silicon or a hydrogenated silicon alloy on the result of (i);
(iii) depositing a contact layer of V, Co, Ni, Pd, Fe or Mn on the result of (ii);
(iv) applying a first forming voltage to the device, said voltage being sufficient to permanently reduce the resistance of the device; and (v) applying a second voltage to further reduce the resistance of the element.
(i) depositing a first conducting layer on an insulating substrate;
(ii) depositing a thin layer of pure or doped amorphous silicon; pure or doped amorphous hydrogenated silicon or a hydrogenated silicon alloy on the result of (i);
(iii) depositing a contact layer of V, Co, Ni, Pd, Fe or Mn on the result of (ii);
(iv) applying a first forming voltage to the device, said voltage being sufficient to permanently reduce the resistance of the device; and (v) applying a second voltage to further reduce the resistance of the element.
5. A method according to claim 4, wherein the first forming voltage is 13-14 volts and the second forming voltage is 1-2 volts higher than the first forming voltage and layer (b) is 20-350 mm thick.
6. A neural network structure comprising a plurality of analogue memory devices wherein said neural network structure comprises an insulating substrate having deposited thereon a plurality of analogue memory devices each of which is as specified in claim 1, wherein each layer (a) is in contact with said insulating substrate.
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US (1) | US5360981A (en) |
EP (1) | EP0471737B1 (en) |
JP (1) | JPH0758813B2 (en) |
AT (1) | ATE115773T1 (en) |
AU (1) | AU628562B2 (en) |
CA (1) | CA2051112C (en) |
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US4115872A (en) * | 1977-05-31 | 1978-09-19 | Burroughs Corporation | Amorphous semiconductor memory device for employment in an electrically alterable read-only memory |
US4228524A (en) * | 1979-01-24 | 1980-10-14 | Harris Corporation | Multilevel sequence of erase pulses for amorphous memory devices |
FR2463508A1 (en) * | 1979-08-16 | 1981-02-20 | Anvar | Ohmic contact mfr. on hydrogenated amorphous silicon - using intermediate layer starved of hydrogen |
JPS57113296A (en) * | 1980-12-29 | 1982-07-14 | Seiko Epson Corp | Switching element |
JPS5933532B2 (en) * | 1981-04-03 | 1984-08-16 | スタンレー電気株式会社 | Method of forming amorphous silicon |
EP0095283A3 (en) * | 1982-05-15 | 1984-12-27 | The British Petroleum Company p.l.c. | Memory device |
US4665504A (en) * | 1982-11-26 | 1987-05-12 | The British Petroleum Company | Memory device containing electrically conducting substrate having deposited hereon a layer of amorphous or microcrystalline silicon-carbon alloy and a layer of amorphous or microcrystalline silicon-containing material |
GB8321254D0 (en) * | 1983-08-06 | 1983-09-07 | British Petroleum Co Plc | Memory devices |
GB8333033D0 (en) * | 1983-12-10 | 1984-01-18 | British Petroleum Co Plc | Memory device |
GB8400959D0 (en) * | 1984-01-13 | 1984-02-15 | British Petroleum Co Plc | Semiconductor device |
GB8816632D0 (en) * | 1988-07-13 | 1988-08-17 | Raychem Ltd | Electrical device |
-
1989
- 1989-05-11 GB GB898910854A patent/GB8910854D0/en active Pending
-
1990
- 1990-05-04 EP EP90907320A patent/EP0471737B1/en not_active Expired - Lifetime
- 1990-05-04 AT AT90907320T patent/ATE115773T1/en not_active IP Right Cessation
- 1990-05-04 CA CA002051112A patent/CA2051112C/en not_active Expired - Fee Related
- 1990-05-04 JP JP2506995A patent/JPH0758813B2/en not_active Expired - Fee Related
- 1990-05-04 DE DE69015177T patent/DE69015177T2/en not_active Expired - Fee Related
- 1990-05-04 AU AU55655/90A patent/AU628562B2/en not_active Ceased
- 1990-05-04 US US08/194,628 patent/US5360981A/en not_active Expired - Lifetime
- 1990-05-04 WO PCT/GB1990/000692 patent/WO1990013921A1/en active IP Right Grant
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1996
- 1996-07-25 HK HK138296A patent/HK138296A/en not_active IP Right Cessation
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EP0471737B1 (en) | 1994-12-14 |
JPH04504331A (en) | 1992-07-30 |
DE69015177T2 (en) | 1995-05-04 |
CA2051112A1 (en) | 1990-11-12 |
GB8910854D0 (en) | 1989-06-28 |
HK138296A (en) | 1996-08-02 |
EP0471737A1 (en) | 1992-02-26 |
ATE115773T1 (en) | 1994-12-15 |
JPH0758813B2 (en) | 1995-06-21 |
AU628562B2 (en) | 1992-09-17 |
AU5565590A (en) | 1990-11-29 |
DE69015177D1 (en) | 1995-01-26 |
WO1990013921A1 (en) | 1990-11-15 |
US5360981A (en) | 1994-11-01 |
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