US3483110A - Preparation of thin films of vanadium dioxide - Google Patents

Preparation of thin films of vanadium dioxide Download PDF

Info

Publication number
US3483110A
US3483110A US639902A US3483110DA US3483110A US 3483110 A US3483110 A US 3483110A US 639902 A US639902 A US 639902A US 3483110D A US3483110D A US 3483110DA US 3483110 A US3483110 A US 3483110A
Authority
US
United States
Prior art keywords
film
thin films
vanadium
cathode
films
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 - Lifetime
Application number
US639902A
Inventor
George A Rozgonyi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AT&T Corp
Original Assignee
Bell Telephone Laboratories Inc
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Bell Telephone Laboratories Inc filed Critical Bell Telephone Laboratories Inc
Application granted granted Critical
Publication of US3483110A publication Critical patent/US3483110A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/08Oxides
    • C23C14/083Oxides of refractory metals or yttrium
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/06Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material characterised by the coating material
    • C23C14/14Metallic material, boron or silicon
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/58After-treatment
    • C23C14/5806Thermal treatment
    • CCHEMISTRY; METALLURGY
    • C23COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
    • C23CCOATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; SURFACE TREATMENT OF METALLIC MATERIAL BY DIFFUSION INTO THE SURFACE, BY CHEMICAL CONVERSION OR SUBSTITUTION; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL
    • C23C14/00Coating by vacuum evaporation, by sputtering or by ion implantation of the coating forming material
    • C23C14/58After-treatment
    • C23C14/5846Reactive treatment
    • C23C14/5853Oxidation
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10NELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10N70/00Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
    • H10N70/011Manufacture or treatment of multistable switching devices
    • H10N70/021Formation of the switching material, e.g. layer deposition
    • H10N70/026Formation of the switching material, e.g. layer deposition by physical vapor deposition, e.g. sputtering
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10NELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10N70/00Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
    • H10N70/011Manufacture or treatment of multistable switching devices
    • H10N70/041Modification of the switching material, e.g. post-treatment, doping
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10NELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10N70/00Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
    • H10N70/20Multistable switching devices, e.g. memristors
    • H10N70/231Multistable switching devices, e.g. memristors based on solid-state phase change, e.g. between amorphous and crystalline phases, Ovshinsky effect
    • H10N70/235Multistable switching devices, e.g. memristors based on solid-state phase change, e.g. between amorphous and crystalline phases, Ovshinsky effect between different crystalline phases, e.g. cubic and hexagonal
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10NELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10N70/00Solid-state devices without a potential-jump barrier or surface barrier, and specially adapted for rectifying, amplifying, oscillating or switching
    • H10N70/801Constructional details of multistable switching devices
    • H10N70/881Switching materials
    • H10N70/883Oxides or nitrides
    • H10N70/8833Binary metal oxides, e.g. TaOx
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/118Oxide films
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S148/00Metal treatment
    • Y10S148/158Sputtering

Definitions

  • This invention relates to a process for making thin films of various vanadium oxides and to the products produced in accordance with the process.
  • vanadium oxides for example, vanadium dioxide (V0 and vanadium sesquioxide (V 0
  • V0 and V 0 vanadium dioxide
  • V 0 vanadium sesquioxide
  • these vanadium compounds are provided only as single crystals and not in the form of thin films for planar devices.
  • a fracture phenomenon often occurs causing a breakdown of the material, thus possibly imposing limits on the useful life of any device incorporating them.
  • the process involves the steps of sputtering a V 0 cathode in an inert atmosphere in the presence of a desired substrate to produce an amorphous film of a composition VO where x is greater than 1.5 but less than 2, and then either weakly oxidizing the film to end-product V0 or strongly oxidizing the film to V 0 and then reducing the V 0 so produced as a V 0 endproduct.
  • a vanadium cathode can be sputtered in an inert atmosphere in a similar manner to provide a r' evacuating the reaction chamber to 10* to l0 3,483,110 Patented Dec. 9, 1969 ice polycrystalline vanadium film which then is oxidized to V 0 and then reduced to V 0
  • the initial VO film is amorphous
  • the V0 V 0 and V 0 films produced in accordance with the inventive method are made polycrystalline during the 0xidative and/or reductive steps utilized.
  • the process of the invention can provide the vanadium oxides noted, VO V0 V 0 and V 0
  • thin films of V0 and V 03 are especially of interest because of their phase transition characteristic and resistance to recycling fracture.
  • the cylindrical cathode of either V 0 or V was 3 cm. in diameter and 3 cm. long.
  • the vacuum system used was an all metal, sputter-ion pumped station with a watercooled cylindrical reaction chamber 10 cm. in diameter and 15 cm. long.
  • the cathode-to-anode spacing was 2 to 3 cm., although other spacings would be acceptable.
  • the pressures used were of the order of 10a to 300 although these can be extended to 1000p. with satisfactory results.
  • Typical voltages to meet this requirement are from several hundred to a few thousand volts.
  • Substrate temperatures may vary from C. to 500 C. with the quality of the deposited film improving somewhat at the higher temperatures. Preferably, greater temperatures are not used in order to avoid damage to the film or substrate.
  • the cathode material that is sputtered can form a thin film on a variety of substrates; by way of example, films of -VO and V have been successfully deposited on single crystal sapphire, amorphous glass, Si N and Ta O The thicknesses of the films produced ranged from 200 to 6000 A.
  • Substrate tempertatures are not critical, and temperatures within 100 to 500 C. are convenient.
  • a cathode of V 0 a thin film of amorphous vanadium oxide is produced which has a composition VO where x is greater than 1.5 but less than 2. It is theorized that the V 0 results in V O +O and that an amount of oxygen associates with the V 0 to provide a stoichiometric composition for the film between V 0 and V0
  • the VO film can be converted either to V0 or V 0 or V 0 by suitable post-deposition treatment involving oxidation and/ or reduction in open tube furnaces.
  • the VO film is contacted with an oxidizing atmosphere of water vapor which is found not to strongly oxidize the film to an oxidation state higher than V0 Optimum results are obtained at a furnace temperature of 400-500 C. with contact maintained for about 4 hours. Other weak oxidants could also be employed to achieve a V0 composition.
  • V 0 is obtained with stronger oxidants, for instance by an oxygen-rich atmosphere.
  • a or greater O mixture proves excellent, at a furnace temperature optimally at 450550 C. for about 4 hours.
  • the amount of oxygen is not critical to obtaining the desired end product, but secondary factors such as the rate of reaction depend on the oxygen concentration. The greater the oxygen content the more rapid the oxidation.
  • the V 0 film produced is characteristically yellowish and polycrystalline.
  • V 0 is produced by sputtering a vanadium cathode to obtain a polycrystalline vanadium film that is typically black.
  • the same sputtering conditions as described for V 0 are applicable.
  • the same postdeposition treatment just described for producing V 0 from V0 is also operable on the vanadium film to It was not found possible to obtain V 0 films by direct treatment of VO or V films with oxidants alone. Apparently the tendency is for these lower states to reach a vanadium pentoxide equilibrium rather than an intermediate V O state.
  • V 0 is obtainable from a V 0 film, regardless of whether it is produced by sputtering with a cathode of V 0 or V, by contacting it with a reducing atmosphere, such as wet hydrogen that has been saturated with water vapor (room temperature), while in a furnace at about 500-600 C. for about 1 hour.
  • a reducing atmosphere such as wet hydrogen that has been saturated with water vapor (room temperature)
  • This reductive step takes considerably less time than the oxidative steps above described, indicating the relative ease with which the reduction step takes place (less active reductants would take longer).
  • FIG. 2 shows the resistivity vs. reciprocal temperature characteristics for the thin films of interest. The arrows indicate the direction of change.
  • V 0 Thin films of V 0 exhibit only the properties of a semiconductive material over the temperature range studied.
  • the V0 and V 0 films clearly show the phase transition from the semiconductor to the metal state which accompanies change in temperature through the transition temperature.
  • the V0 shows a narrow hysteresis at about 65 C., which compares very favorably with the transition temperature for single crystal V0 Films of V 0 exhibited an abrupt transition to the metal state at about 110 C., with a transition back to the semiconductor state at about 145 C.
  • the resistance of these films to fracture was checked by cycling the V0 samples from room temperature to about 100 C., and by dipping the V 0 samples in and out of liquid nitrogen.
  • the samples underwent repeated resistance changes of 10 ohms for V0 and 10 ohms for V 0 A point-by-point measurement after cycling did not reveal any change in performance.
  • a process for making a thin film vanadium oxide comprising the steps of sputtering with a cathode of a composition consisting essentially of V 0 onto a substrate heated to a temperature in the range from to 500 C., in an atmosphere consisting essentially of inert gas and up to 50 percent by volume oxygen at 10 to 1000 thus forming an amorphous film, and contacting said amorphous film with a weakly oxidizing atmosphere for a time sufiicient to form a polycrystalline V0 film.

Description

Dec. 9, 1969 e. A. ROZGONYI PREPARATION OF THIN FILMS OF VANADIUM DIOXIDE Filed May 19, 1967 FIG.
CA THODE COMPOSITION AMORPHOUS FILM RESULT ,OF SPUTTER/NG WEAK OX/DA T/VEK/ S 7' E P STRONG 0x104 T/VE f STEP AMORPHOUS F [LM POLYCRKSTALL/NE F lLM POLYCRVSTALL/NE F/LM POLYCRYSIALL/NE FIG. 2
lNVENZ'OR G. A. ROZGONW IVEV United States Patent 3,483,110 PREPARATION OF THIN FILMS OF VANADIUM DIOXIDE George A. Rozgonyi, Irvington, N.J., assiguor to Bell Telephone Laboratories, Incorporated, Murray Hill, N.J., a corporation of New York Filed May 19, 1967, Ser. No. 639,902 Int. Cl. C23c 15/00 US. Cl. 204-192 3 Claims ABSTRACT OF THE DISCLOSURE A method has been found for making thin films of V0 that possess the essential metal-semiconductor phase transition exhibited by the single crystal forms, and that do not suffer deterioration under repeated cycling through the transition. The process involves the steps of sputtering with a V cathode to produce a film which is then oxidized to the desired oxidation state.
This invention relates to a process for making thin films of various vanadium oxides and to the products produced in accordance with the process.
BACKGROUND OF THE INVENTION Recent interest has been shown in several materials which are able to undergo a metal-semiconductor phase transition at a characteristic temperature. Accompanying the transition are abrupt and substantial changes in various properties of the material, such as changes in its electrical resistance, light reflectance, etc. Devices which make use of these changes have been devised. Exemplary of those devices which take advantage of the abrupt change in resistance are switching devices as described in US. 3,149,298, issued to E. T. Handelman. Other devices, such as optical modulators and display devices, utilize the change in reflectance that occurs as the material passes through its transition temperature to modulate or alter some characteristic of impinging light.
Among the materials which possess such a phase transition characteristic are various vanadium oxides, for example, vanadium dioxide (V0 and vanadium sesquioxide (V 0 It is important that these materials be in a form that is compatible with the modern planar device technology that is revolutionizing the electronics field. At present, however, these vanadium compounds are provided only as single crystals and not in the form of thin films for planar devices. Moreover, when single crystals of some phase transition materials are repeatedly cycled through the transition temperature, a fracture phenomenon often occurs causing a breakdown of the material, thus possibly imposing limits on the useful life of any device incorporating them.
SUMMARY OF THE INVENTION In accordance with the present invention a method has been found for making thin films of V0 and V 0 that possess the essential phase transition property exhibited by the single crystal forms, and that do not suffer deterioration under repeated cycling through the transition temperature.
In one form, the process involves the steps of sputtering a V 0 cathode in an inert atmosphere in the presence of a desired substrate to produce an amorphous film of a composition VO where x is greater than 1.5 but less than 2, and then either weakly oxidizing the film to end-product V0 or strongly oxidizing the film to V 0 and then reducing the V 0 so produced as a V 0 endproduct.
Alternatively, a vanadium cathode can be sputtered in an inert atmosphere in a similar manner to provide a r' evacuating the reaction chamber to 10* to l0 3,483,110 Patented Dec. 9, 1969 ice polycrystalline vanadium film which then is oxidized to V 0 and then reduced to V 0 Although the initial VO film is amorphous, the V0 V 0 and V 0 films produced in accordance with the inventive method are made polycrystalline during the 0xidative and/or reductive steps utilized.
DESCRIPTION OF DRAWING DETAILED DESCRIPTION As indicated by the flowsheet description of FIG. 1, the process of the invention can provide the vanadium oxides noted, VO V0 V 0 and V 0 Of course, thin films of V0 and V 03 are especially of interest because of their phase transition characteristic and resistance to recycling fracture.
Conventional cathodic sputtering apparatus may be used in carrying out the invention. By way of example only. the following briefly sets forth the system used.
The cylindrical cathode of either V 0 or V was 3 cm. in diameter and 3 cm. long. The vacuum system used was an all metal, sputter-ion pumped station with a watercooled cylindrical reaction chamber 10 cm. in diameter and 15 cm. long. The cathode-to-anode spacing was 2 to 3 cm., although other spacings would be acceptable. The pressures used were of the order of 10a to 300 although these can be extended to 1000p. with satisfactory results.
The effect of pressure on the sputtering operation is well known in the art. Increasing the pressure results in greater deposition rates due to the large number of bombarding ions present. However, at high pressures (relative to a perfect vacuum), the current flow obtained reaches undesirable limits. The lowest tolerable pressure is that which results in the smallest deposition rate that is economically acceptable. Operating pressures were established by torr and backfilling with argon or other inert gas or mixtures thereof to reach the desired operating pressure. The cathode density should be adjusted to within the range 0.1 to 10 ma./cm. the lower limit providing an adequate deposition rate, and the higher limit establishing a practical maximum to avoid short cathode life. Typical voltages to meet this requirement are from several hundred to a few thousand volts. Substrate temperatures may vary from C. to 500 C. with the quality of the deposited film improving somewhat at the higher temperatures. Preferably, greater temperatures are not used in order to avoid damage to the film or substrate.
The cathode material that is sputtered can form a thin film on a variety of substrates; by way of example, films of -VO and V have been successfully deposited on single crystal sapphire, amorphous glass, Si N and Ta O The thicknesses of the films produced ranged from 200 to 6000 A.
Substrate tempertatures are not critical, and temperatures within 100 to 500 C. are convenient. With a cathode of V 0 a thin film of amorphous vanadium oxide is produced which has a composition VO where x is greater than 1.5 but less than 2. It is theorized that the V 0 results in V O +O and that an amount of oxygen associates with the V 0 to provide a stoichiometric composition for the film between V 0 and V0 The VO film can be converted either to V0 or V 0 or V 0 by suitable post-deposition treatment involving oxidation and/ or reduction in open tube furnaces.
The just-described effect of oxygen on the stoichiometry of the film is, of course, more extensive when large amounts of oxygen are present during sputtering. It is found that if oxygen is present in an amount greater than about 50 percent (by volume), the VO composition noted is not reproducibly deposited. Accordingly, some precaution is taken to minimize this effect. Spectral grade inert gas is preferred, as is a procedure which bleeds gas from the sputtering chamber, from time to time, to remove oxygen produced during sputtering. In addition, baking the chamber at a few hundred degrees centigrade prior to backfilling with inert gas removes various impurities from the chamber walls that could possibly introduce unwanted gaseous species into the system.
If V is desired, the VO film is contacted with an oxidizing atmosphere of water vapor which is found not to strongly oxidize the film to an oxidation state higher than V0 Optimum results are obtained at a furnace temperature of 400-500 C. with contact maintained for about 4 hours. Other weak oxidants could also be employed to achieve a V0 composition.
On the other hand, V 0 is obtained with stronger oxidants, for instance by an oxygen-rich atmosphere. For this purpose a or greater O mixture proves excellent, at a furnace temperature optimally at 450550 C. for about 4 hours. The amount of oxygen is not critical to obtaining the desired end product, but secondary factors such as the rate of reaction depend on the oxygen concentration. The greater the oxygen content the more rapid the oxidation. The V 0 film produced is characteristically yellowish and polycrystalline.
Alternatively, V 0 is produced by sputtering a vanadium cathode to obtain a polycrystalline vanadium film that is typically black. The same sputtering conditions as described for V 0 are applicable. The same postdeposition treatment just described for producing V 0 from V0 is also operable on the vanadium film to It was not found possible to obtain V 0 films by direct treatment of VO or V films with oxidants alone. Apparently the tendency is for these lower states to reach a vanadium pentoxide equilibrium rather than an intermediate V O state. However, V 0 is obtainable from a V 0 film, regardless of whether it is produced by sputtering with a cathode of V 0 or V, by contacting it with a reducing atmosphere, such as wet hydrogen that has been saturated with water vapor (room temperature), while in a furnace at about 500-600 C. for about 1 hour. This reductive step takes considerably less time than the oxidative steps above described, indicating the relative ease with which the reduction step takes place (less active reductants would take longer). It was not possible, however, to reduce V 0 to the intermediate V0 FIG. 2 shows the resistivity vs. reciprocal temperature characteristics for the thin films of interest. The arrows indicate the direction of change.
Thin films of V 0 exhibit only the properties of a semiconductive material over the temperature range studied. The V0 and V 0 films, however, clearly show the phase transition from the semiconductor to the metal state which accompanies change in temperature through the transition temperature. The V0 shows a narrow hysteresis at about 65 C., which compares very favorably with the transition temperature for single crystal V0 Films of V 0 exhibited an abrupt transition to the metal state at about 110 C., with a transition back to the semiconductor state at about 145 C.
The resistance of these films to fracture was checked by cycling the V0 samples from room temperature to about 100 C., and by dipping the V 0 samples in and out of liquid nitrogen. The samples underwent repeated resistance changes of 10 ohms for V0 and 10 ohms for V 0 A point-by-point measurement after cycling did not reveal any change in performance.
The invention has been described with reference to particular embodiments and examples thereof, but it is intended that variations therefrom which basically rely on the teachings of the invention are to be considered as within the scope of the description and the appended claims.
What is claimed is:
1. A process for making a thin film vanadium oxide comprising the steps of sputtering with a cathode of a composition consisting essentially of V 0 onto a substrate heated to a temperature in the range from to 500 C., in an atmosphere consisting essentially of inert gas and up to 50 percent by volume oxygen at 10 to 1000 thus forming an amorphous film, and contacting said amorphous film with a weakly oxidizing atmosphere for a time sufiicient to form a polycrystalline V0 film.
2. The process of claim 1 wherein said amorphous film is contacted with water vapor at 400 to 500 C.
3. The polycrystalline V0 film produced in accordance with the process of claim 1.
References Cited UNITED STATES PATENTS 2,917,442 12/1959 Hanlet 204l92 3,294,669 12/1966 Theuerer 204298 OTHER REFERENCES Holland: Vacuum Deposition of Thin Films, Chapman & Hall Ltd., London, 1963, pp. 450-455.
ROBERT K. MIHALEK, Primary Examiner US. Cl. X.R.
US639902A 1967-05-19 1967-05-19 Preparation of thin films of vanadium dioxide Expired - Lifetime US3483110A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US63990267A 1967-05-19 1967-05-19

Publications (1)

Publication Number Publication Date
US3483110A true US3483110A (en) 1969-12-09

Family

ID=24566045

Family Applications (1)

Application Number Title Priority Date Filing Date
US639902A Expired - Lifetime US3483110A (en) 1967-05-19 1967-05-19 Preparation of thin films of vanadium dioxide

Country Status (3)

Country Link
US (1) US3483110A (en)
BE (1) BE715161A (en)
FR (1) FR1565917A (en)

Cited By (37)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3620715A (en) * 1969-07-24 1971-11-16 Us Interior Steel scrap oxidation acceleration by surface impregnation techniques
US3648124A (en) * 1970-06-10 1972-03-07 Ibm Gated metal-semiconductor transition device
US3660155A (en) * 1970-04-15 1972-05-02 Us Navy Method for preparing solid films
US3688160A (en) * 1971-03-25 1972-08-29 Matsushita Electric Ind Co Ltd Thin film non-rectifying negative resistance device
US3886578A (en) * 1973-02-26 1975-05-27 Multi State Devices Ltd Low ohmic resistance platinum contacts for vanadium oxide thin film devices
US3899407A (en) * 1973-08-01 1975-08-12 Multi State Devices Ltd Method of producing thin film devices of doped vanadium oxide material
US3916432A (en) * 1974-05-17 1975-10-28 Us Energy Superconductive microstrip exhibiting negative differential resistivity
US4315905A (en) * 1980-06-30 1982-02-16 The United States Of America As Represented By The Secretary Of The Navy Process for producing an electronically conductive oxidizer material
US4393095A (en) * 1982-02-01 1983-07-12 Ppg Industries, Inc. Chemical vapor deposition of vanadium oxide coatings
FR2520727A1 (en) * 1982-02-01 1983-08-05 Ppg Industries Inc PROCESS FOR FORMING VANADIUM OXIDE COATINGS ON GLASS SUPPORTS AND PRODUCTS OBTAINED
US4400412A (en) * 1982-02-01 1983-08-23 Ppg Industries, Inc. Thermochromic vanadium oxide coated glass
US4401690A (en) * 1982-02-01 1983-08-30 Ppg Industries, Inc. Thermochromic vanadium oxide with depressed switching temperature
WO1992016959A1 (en) * 1991-03-25 1992-10-01 Commonwealth Scientific And Industrial Research Organisation Arc source macroparticle filter
US5330855A (en) * 1991-09-23 1994-07-19 The United States Of America, As Represented By The Secretary Of Commerce Planar epitaxial films of SnO2
US5387481A (en) * 1990-07-19 1995-02-07 Westinghouse Electric Corporation Method of preparing a switchable shield
US5419890A (en) * 1994-01-19 1995-05-30 Valence Technology, Inc. Use of organic solvents in the synthesis of V6 O13+x [0<x≦2]
US5482697A (en) * 1994-01-19 1996-01-09 Valence Technology, Inc. Method of making V6 O13+x [0<X≦2.0]
US5825046A (en) * 1996-10-28 1998-10-20 Energy Conversion Devices, Inc. Composite memory material comprising a mixture of phase-change memory material and dielectric material
WO1999004441A1 (en) * 1997-07-21 1999-01-28 Nanogram Corporation Vanadium oxide particles and batteries with electroactive nanoparticles
US5952125A (en) * 1997-07-21 1999-09-14 Nanogram Corporation Batteries with electroactive nanoparticles
US5989514A (en) * 1997-07-21 1999-11-23 Nanogram Corporation Processing of vanadium oxide particles with heat
US6106798A (en) * 1997-07-21 2000-08-22 Nanogram Corporation Vanadium oxide nanoparticles
US6225007B1 (en) 1999-02-05 2001-05-01 Nanogram Corporation Medal vanadium oxide particles
US6391494B2 (en) 1999-05-13 2002-05-21 Nanogram Corporation Metal vanadium oxide particles
US6503646B1 (en) 2000-08-28 2003-01-07 Nanogram Corporation High rate batteries
US20040005472A1 (en) * 2000-05-23 2004-01-08 Saint-Gobain Glass France Glazing coated with at least one layer having thermochromic properties
US20040121195A1 (en) * 2002-07-22 2004-06-24 Ghantous Dania I. High capacity and high rate batteries
WO2005028390A1 (en) * 2003-09-13 2005-03-31 Schott Ag Method for producing substrates comprising temperature-resistant protective coatings
EP1560008A1 (en) * 2004-01-29 2005-08-03 Korea Institute of Science and Technology Oxide thin film for bolometer and infrared detector using the oxide thin film
JP2005239516A (en) * 2004-02-27 2005-09-08 Japan Science & Technology Agency Vanadium oxide and recording material using the same
US7214446B1 (en) 1997-07-21 2007-05-08 Nanogram Corporation Batteries with electroactive nanoparticles
US20090253369A1 (en) * 2006-09-08 2009-10-08 Mpb Communications Inc. Variable emittance thermochromic material and satellite system
US9952096B2 (en) 2012-06-05 2018-04-24 President And Fellows Of Harvard College Ultra-thin optical coatings and devices and methods of using ultra-thin optical coatings
US20180212145A1 (en) * 2017-01-26 2018-07-26 Hrl Laboratories, Llc Low-voltage threshold switch devices with current-controlled negative differential resistance based on electroformed vanadium oxide layer
US10541274B2 (en) 2017-01-26 2020-01-21 Hrl Laboratories, Llc Scalable, stackable, and BEOL-process compatible integrated neuron circuit
US10600961B2 (en) * 2017-07-27 2020-03-24 Hrl Laboratories, Llc Scalable and low-voltage electroforming-free nanoscale vanadium dioxide threshold switch devices and relaxation oscillators with current controlled negative differential resistance
US11861488B1 (en) 2017-06-09 2024-01-02 Hrl Laboratories, Llc Scalable excitatory and inhibitory neuron circuitry based on vanadium dioxide relaxation oscillators

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2917442A (en) * 1955-12-30 1959-12-15 Electronique & Automatisme Sa Method of making electroluminescent layers
US3294669A (en) * 1963-07-22 1966-12-27 Bell Telephone Labor Inc Apparatus for sputtering in a highly purified gas atmosphere

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2917442A (en) * 1955-12-30 1959-12-15 Electronique & Automatisme Sa Method of making electroluminescent layers
US3294669A (en) * 1963-07-22 1966-12-27 Bell Telephone Labor Inc Apparatus for sputtering in a highly purified gas atmosphere

Cited By (56)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3620715A (en) * 1969-07-24 1971-11-16 Us Interior Steel scrap oxidation acceleration by surface impregnation techniques
US3660155A (en) * 1970-04-15 1972-05-02 Us Navy Method for preparing solid films
US3648124A (en) * 1970-06-10 1972-03-07 Ibm Gated metal-semiconductor transition device
US3688160A (en) * 1971-03-25 1972-08-29 Matsushita Electric Ind Co Ltd Thin film non-rectifying negative resistance device
US3886578A (en) * 1973-02-26 1975-05-27 Multi State Devices Ltd Low ohmic resistance platinum contacts for vanadium oxide thin film devices
US3899407A (en) * 1973-08-01 1975-08-12 Multi State Devices Ltd Method of producing thin film devices of doped vanadium oxide material
US3916432A (en) * 1974-05-17 1975-10-28 Us Energy Superconductive microstrip exhibiting negative differential resistivity
US4315905A (en) * 1980-06-30 1982-02-16 The United States Of America As Represented By The Secretary Of The Navy Process for producing an electronically conductive oxidizer material
US4400412A (en) * 1982-02-01 1983-08-23 Ppg Industries, Inc. Thermochromic vanadium oxide coated glass
JPS62256742A (en) * 1982-02-01 1987-11-09 ピ−ピ−ジ−・インダストリ−ズ・インコ−ポレ−テツド Chemical vapor deposition for vanadium oxide film
JPS58135154A (en) * 1982-02-01 1983-08-11 ピ−ピ−ジ−・インダストリ−ズ・インコ−ポレ−テツド Vanadium oxide coating method
DE3303154A1 (en) 1982-02-01 1983-08-11 PPG Industries, Inc., 15222 Pittsburgh, Pa. METHOD FOR CHEMICAL DEPOSITION OF VANADINOXIDE FILMS FROM THE STEAM PHASE AND OBJECTS COATED WITH VANADINOXIDE FILMS
US4393095A (en) * 1982-02-01 1983-07-12 Ppg Industries, Inc. Chemical vapor deposition of vanadium oxide coatings
US4401690A (en) * 1982-02-01 1983-08-30 Ppg Industries, Inc. Thermochromic vanadium oxide with depressed switching temperature
DE3347918A1 (en) * 1982-02-01 1985-05-15 Ppg Industries Inc
JPS6238313B2 (en) * 1982-02-01 1987-08-17 Ppg Industries Inc
JPS62256743A (en) * 1982-02-01 1987-11-09 ピ−ピ−ジ−・インダストリ−ズ・インコ−ポレ−テツド Manufacture of thermochromic window glass
FR2520727A1 (en) * 1982-02-01 1983-08-05 Ppg Industries Inc PROCESS FOR FORMING VANADIUM OXIDE COATINGS ON GLASS SUPPORTS AND PRODUCTS OBTAINED
US5387481A (en) * 1990-07-19 1995-02-07 Westinghouse Electric Corporation Method of preparing a switchable shield
WO1992016959A1 (en) * 1991-03-25 1992-10-01 Commonwealth Scientific And Industrial Research Organisation Arc source macroparticle filter
US5433836A (en) * 1991-03-25 1995-07-18 Commonwealth Scientific And Industrial Research Organization Arc source macroparticle filter
US5330855A (en) * 1991-09-23 1994-07-19 The United States Of America, As Represented By The Secretary Of Commerce Planar epitaxial films of SnO2
US5419890A (en) * 1994-01-19 1995-05-30 Valence Technology, Inc. Use of organic solvents in the synthesis of V6 O13+x [0<x≦2]
US5482697A (en) * 1994-01-19 1996-01-09 Valence Technology, Inc. Method of making V6 O13+x [0<X≦2.0]
US5825046A (en) * 1996-10-28 1998-10-20 Energy Conversion Devices, Inc. Composite memory material comprising a mixture of phase-change memory material and dielectric material
US6106798A (en) * 1997-07-21 2000-08-22 Nanogram Corporation Vanadium oxide nanoparticles
US5989514A (en) * 1997-07-21 1999-11-23 Nanogram Corporation Processing of vanadium oxide particles with heat
WO1999004441A1 (en) * 1997-07-21 1999-01-28 Nanogram Corporation Vanadium oxide particles and batteries with electroactive nanoparticles
US7214446B1 (en) 1997-07-21 2007-05-08 Nanogram Corporation Batteries with electroactive nanoparticles
US5952125A (en) * 1997-07-21 1999-09-14 Nanogram Corporation Batteries with electroactive nanoparticles
US7722787B2 (en) 1999-02-05 2010-05-25 Greatbatch Ltd. Metal vanadium oxide particles
US6225007B1 (en) 1999-02-05 2001-05-01 Nanogram Corporation Medal vanadium oxide particles
US6749966B2 (en) 1999-05-13 2004-06-15 Nanogram Devices Corporation Metal vanadium oxide particles
US6391494B2 (en) 1999-05-13 2002-05-21 Nanogram Corporation Metal vanadium oxide particles
US20040005472A1 (en) * 2000-05-23 2004-01-08 Saint-Gobain Glass France Glazing coated with at least one layer having thermochromic properties
US6872453B2 (en) * 2000-05-23 2005-03-29 Saint-Gobain Glass France Glazing coated with at least one layer having thermochromic properties
US20050147825A1 (en) * 2000-05-23 2005-07-07 Saint-Gobain Glass France Glazing coated with at least one layer having thermochromic properties
US7311976B2 (en) 2000-05-23 2007-12-25 Saint-Gobain Glass France Glazing coated with at least one layer having thermochromic properties
US20030077513A1 (en) * 2000-08-28 2003-04-24 Nanogram Corporation High rate batteries
US6503646B1 (en) 2000-08-28 2003-01-07 Nanogram Corporation High rate batteries
US20040121195A1 (en) * 2002-07-22 2004-06-24 Ghantous Dania I. High capacity and high rate batteries
US7198869B2 (en) 2002-07-22 2007-04-03 Greatbatch, Inc. High capacity and high rate batteries
WO2005028390A1 (en) * 2003-09-13 2005-03-31 Schott Ag Method for producing substrates comprising temperature-resistant protective coatings
EP1560008A1 (en) * 2004-01-29 2005-08-03 Korea Institute of Science and Technology Oxide thin film for bolometer and infrared detector using the oxide thin film
JP2005239516A (en) * 2004-02-27 2005-09-08 Japan Science & Technology Agency Vanadium oxide and recording material using the same
JP4526835B2 (en) * 2004-02-27 2010-08-18 独立行政法人科学技術振興機構 Vanadium oxide and recording material using the same
US20090253369A1 (en) * 2006-09-08 2009-10-08 Mpb Communications Inc. Variable emittance thermochromic material and satellite system
US7761053B2 (en) 2006-09-08 2010-07-20 Mpb Communications Inc. Variable emittance thermochromic material and satellite system
US20100247864A1 (en) * 2006-09-08 2010-09-30 Mpb Communications Inc. Variable emittance thermochromic material and satellite system
US9952096B2 (en) 2012-06-05 2018-04-24 President And Fellows Of Harvard College Ultra-thin optical coatings and devices and methods of using ultra-thin optical coatings
US20180212145A1 (en) * 2017-01-26 2018-07-26 Hrl Laboratories, Llc Low-voltage threshold switch devices with current-controlled negative differential resistance based on electroformed vanadium oxide layer
US10297751B2 (en) * 2017-01-26 2019-05-21 Hrl Laboratories, Llc Low-voltage threshold switch devices with current-controlled negative differential resistance based on electroformed vanadium oxide layer
US10541274B2 (en) 2017-01-26 2020-01-21 Hrl Laboratories, Llc Scalable, stackable, and BEOL-process compatible integrated neuron circuit
US10903277B2 (en) 2017-01-26 2021-01-26 Hrl Laboratories, Llc Scalable, stackable, and BEOL-process compatible integrated neuron circuit
US11861488B1 (en) 2017-06-09 2024-01-02 Hrl Laboratories, Llc Scalable excitatory and inhibitory neuron circuitry based on vanadium dioxide relaxation oscillators
US10600961B2 (en) * 2017-07-27 2020-03-24 Hrl Laboratories, Llc Scalable and low-voltage electroforming-free nanoscale vanadium dioxide threshold switch devices and relaxation oscillators with current controlled negative differential resistance

Also Published As

Publication number Publication date
FR1565917A (en) 1969-05-02
BE715161A (en) 1968-09-30

Similar Documents

Publication Publication Date Title
US3483110A (en) Preparation of thin films of vanadium dioxide
KR100649838B1 (en) Transparent conductive laminate and process of producing the same
Joseph et al. Ferroelectric behavior of Li-doped ZnO thin films on Si (100) by pulsed laser deposition
US4804640A (en) Method of forming silicon and aluminum containing dielectric film and semiconductor device including said film
US6897513B2 (en) Perovskite-type material forming methods, capacitor dielectric forming methods, and capacitor constructions
CA2136581C (en) Gallium oxide thin films
US4349425A (en) Transparent conductive films and methods of producing same
US3763026A (en) Method of making resistor thin films by reactive sputtering from a composite source
Theuerer et al. Getter sputtering for the preparation of thin films of superconducting elements and compounds
KR940004800A (en) Semiconductor memory device and manufacturing method thereof
US3627662A (en) Thin film transistor and method of fabrication thereof
Serikawa et al. Effect of N2 Ar mixing on the reactive sputtering characteristics of silicon
Lakshmi et al. The growth of highly resistive gallium nitride films
Duchene et al. RF and DC reactive sputtering for crystalline and amorphous VO2 thin film deposition
US3551312A (en) Vacuum evaporation deposition of group iii-a metal nitrides
US4151329A (en) Nb3 Ge Superconductive films
US3239368A (en) Method of preparing thin films on substrates by an electrical discharge
US3420763A (en) Cathodic sputtering of films of stoichiometric zinc oxide
US3491000A (en) Method of producing vanadium dioxide thin films
JPH1088332A (en) Sputtering target, transparent conductive coating and its production
US5610097A (en) Method for forming electrode on semiconductor
Ridge et al. Composition control in conducting oxide thin films
US3491433A (en) Method of making an insulated gate semiconductor device
US4214018A (en) Method for making adherent pinhole free aluminum films on pyroelectric and/or piezoelectric substrates
Gallego et al. Preparation and characterization of thin films of NbO2