US3828186A - Apparatus for intensifying radiation images - Google Patents
Apparatus for intensifying radiation images Download PDFInfo
- Publication number
- US3828186A US3828186A US00278894A US27889472A US3828186A US 3828186 A US3828186 A US 3828186A US 00278894 A US00278894 A US 00278894A US 27889472 A US27889472 A US 27889472A US 3828186 A US3828186 A US 3828186A
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- United States
- Prior art keywords
- layer
- radiation
- piezoelectric
- cesium fluoride
- lead zirconate
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- 230000005855 radiation Effects 0.000 title claims abstract description 51
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical group [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 claims abstract description 51
- HFGPZNIAWCZYJU-UHFFFAOYSA-N lead zirconate titanate Chemical group [O-2].[O-2].[O-2].[O-2].[O-2].[Ti+4].[Zr+4].[Pb+2] HFGPZNIAWCZYJU-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910052451 lead zirconate titanate Inorganic materials 0.000 claims abstract description 21
- 239000000758 substrate Substances 0.000 claims abstract description 21
- 238000004519 manufacturing process Methods 0.000 claims abstract description 18
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims abstract description 15
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 5
- -1 rare earth halide Chemical class 0.000 claims description 6
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 5
- 239000012535 impurity Substances 0.000 claims description 2
- 239000000463 material Substances 0.000 abstract description 22
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 abstract description 20
- 229910015900 BF3 Inorganic materials 0.000 abstract description 10
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract description 10
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 abstract description 10
- 229910052792 caesium Inorganic materials 0.000 abstract description 9
- TVFDJXOCXUVLDH-UHFFFAOYSA-N caesium atom Chemical compound [Cs] TVFDJXOCXUVLDH-UHFFFAOYSA-N 0.000 abstract description 9
- 239000000919 ceramic Substances 0.000 abstract description 9
- 238000001704 evaporation Methods 0.000 abstract description 9
- 230000008020 evaporation Effects 0.000 abstract description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 abstract description 6
- 238000001771 vacuum deposition Methods 0.000 abstract description 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract description 4
- 239000001301 oxygen Substances 0.000 abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 abstract description 4
- 229910052786 argon Inorganic materials 0.000 abstract description 3
- 230000000740 bleeding effect Effects 0.000 abstract description 2
- 238000005137 deposition process Methods 0.000 abstract description 2
- 239000002019 doping agent Substances 0.000 abstract description 2
- 239000010410 layer Substances 0.000 description 103
- QHGNHLZPVBIIPX-UHFFFAOYSA-N tin(ii) oxide Chemical compound [Sn]=O QHGNHLZPVBIIPX-UHFFFAOYSA-N 0.000 description 8
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 6
- 238000000151 deposition Methods 0.000 description 5
- 230000008021 deposition Effects 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- 238000007738 vacuum evaporation Methods 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 150000002894 organic compounds Chemical class 0.000 description 3
- 239000011241 protective layer Substances 0.000 description 3
- 238000005546 reactive sputtering Methods 0.000 description 3
- 230000004044 response Effects 0.000 description 3
- 239000010936 titanium Substances 0.000 description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000011651 chromium Substances 0.000 description 2
- 230000005684 electric field Effects 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 229910052719 titanium Inorganic materials 0.000 description 2
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical compound C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 description 1
- KKHFRAFPESRGGD-UHFFFAOYSA-N 1,3-dimethyl-7-[3-(n-methylanilino)propyl]purine-2,6-dione Chemical compound C1=NC=2N(C)C(=O)N(C)C(=O)C=2N1CCCN(C)C1=CC=CC=C1 KKHFRAFPESRGGD-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 101100204264 Arabidopsis thaliana STR4 gene Proteins 0.000 description 1
- JQUCWIWWWKZNCS-LESHARBVSA-N C(C1=CC=CC=C1)(=O)NC=1SC[C@H]2[C@@](N1)(CO[C@H](C2)C)C=2SC=C(N2)NC(=O)C2=NC=C(C=C2)OC(F)F Chemical compound C(C1=CC=CC=C1)(=O)NC=1SC[C@H]2[C@@](N1)(CO[C@H](C2)C)C=2SC=C(N2)NC(=O)C2=NC=C(C=C2)OC(F)F JQUCWIWWWKZNCS-LESHARBVSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 235000014676 Phragmites communis Nutrition 0.000 description 1
- 241000206607 Porphyra umbilicalis Species 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 1
- 101150076149 TROL gene Proteins 0.000 description 1
- 229910021626 Tin(II) chloride Inorganic materials 0.000 description 1
- 239000005083 Zinc sulfide Substances 0.000 description 1
- JRPBQTZRNDNNOP-UHFFFAOYSA-N barium titanate Chemical compound [Ba+2].[Ba+2].[O-][Ti]([O-])([O-])[O-] JRPBQTZRNDNNOP-UHFFFAOYSA-N 0.000 description 1
- 229910002113 barium titanate Inorganic materials 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052810 boron oxide Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 230000008878 coupling Effects 0.000 description 1
- 238000010168 coupling process Methods 0.000 description 1
- 238000005859 coupling reaction Methods 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- ZOIVSVWBENBHNT-UHFFFAOYSA-N dizinc;silicate Chemical compound [Zn+2].[Zn+2].[O-][Si]([O-])([O-])[O-] ZOIVSVWBENBHNT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005670 electromagnetic radiation Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 238000002594 fluoroscopy Methods 0.000 description 1
- 239000003574 free electron Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910000765 intermetallic Inorganic materials 0.000 description 1
- 230000007246 mechanism Effects 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
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 1
- 230000010287 polarization Effects 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 239000005297 pyrex Substances 0.000 description 1
- 150000002910 rare earth metals Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 229910001948 sodium oxide Inorganic materials 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 239000001119 stannous chloride Substances 0.000 description 1
- 235000011150 stannous chloride Nutrition 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21K—NON-ELECTRIC LIGHT SOURCES USING LUMINESCENCE; LIGHT SOURCES USING ELECTROCHEMILUMINESCENCE; LIGHT SOURCES USING CHARGES OF COMBUSTIBLE MATERIAL; LIGHT SOURCES USING SEMICONDUCTOR DEVICES AS LIGHT-GENERATING ELEMENTS; LIGHT SOURCES NOT OTHERWISE PROVIDED FOR
- F21K2/00—Non-electric light sources using luminescence; Light sources using electrochemiluminescence
-
- G—PHYSICS
- G21—NUCLEAR PHYSICS; NUCLEAR ENGINEERING
- G21K—TECHNIQUES FOR HANDLING PARTICLES OR IONISING RADIATION NOT OTHERWISE PROVIDED FOR; IRRADIATION DEVICES; GAMMA RAY OR X-RAY MICROSCOPES
- G21K4/00—Conversion screens for the conversion of the spatial distribution of X-rays or particle radiation into visible images, e.g. fluoroscopic screens
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01L—SEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
- H01L31/00—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof
- H01L31/12—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof structurally associated with, e.g. formed in or on a common substrate with, one or more electric light sources, e.g. electroluminescent light sources, and electrically or optically coupled thereto
- H01L31/14—Semiconductor devices sensitive to infrared radiation, light, electromagnetic radiation of shorter wavelength or corpuscular radiation and specially adapted either for the conversion of the energy of such radiation into electrical energy or for the control of electrical energy by such radiation; Processes or apparatus specially adapted for the manufacture or treatment thereof or of parts thereof; Details thereof structurally associated with, e.g. formed in or on a common substrate with, one or more electric light sources, e.g. electroluminescent light sources, and electrically or optically coupled thereto the light source or sources being controlled by the semiconductor device sensitive to radiation, e.g. image converters, image amplifiers or image storage devices
Definitions
- ABSTRACT A radiation-responsive layer preferably of cesium fluoride is bonded to an electrically-conductive radiationtranspa'rent layer of material which is also utilized as an electrode.
- a piezoelectric polarized ferroelectric ceramic layer preferably of lead zirconate titanate is bonded to the radiation-responsive layer.
- An output device such as a visible-light emitting phosphor is bonded along with a radiation-opaque electrical conductive layer, also used as an electrode, to the piezoelectric layer.
- a source of electrical potential is connected between the two electrodes to thereby apply an electrical potential across the piezoelectric layer and the radiation-sensitive layer.
- the cesium fluoride layer is formed by vacuum deposition from a metallic cesium source in a boron trifluoride atmosphere while bleeding in small amounts of boron trifluoride to maintain a substantially constant atmospheric level thereof during evaporation.
- the piezoelectric layer is formed by vacuum deposition of lead zirconate titantate in an atmosphere containing trimethylamine, dimethylamine, argon and oxygen upon a bonding coat deposited on the previously-deposited cesium fluoride layer while retaining the substrate heated. During the deposition process, the trimethylamine and dimethylamine are thermally cracked thereby to provide carbon as a dopant for the lead zirconate titanate layer.
- prior art apparatus providing results similar to those achieved by applicant are, constructed using high voltage vacuum tube circuits and technology.
- Some prior art devices have utilized electroluminescent apparatus of the kind comprising a layer of electroluminescent material and a layer of photoconductive material.
- the photoconductive material is arranged to control the value of voltage applied across the electroluminescent material proportional to the intensity of incident radiation lying within the particular bandwidth of radiation to which the device is sensitive.
- Such devices have been utilized singly or in tandem depending upon the particular application.
- a radiation-responsive layer excitable by incident radiation within a predetermined bandwidth is bonded to a ferroelectric ceramic layer which is properly polarized to provide piezoelectric characteristics.
- An output-signal-producing means is connected with the piezoelectric layer and provides an output signal responsive to incident radiation.
- the apparatus includes cesium fluoride as a raditionresponsive layer and carbon-doped lead zirconate titanate as the piezoelectric layer with a phosphor bonded thereto as the output-signal-producing means.
- An electrical potential is applied across the lead zirconate titanate and cesium fluoride layers.
- the cesium fluoride layer is provided by vacuum evaporating metallic cesium through a boron trifluoride atmosphere onto a heated substrate.
- the lead zirconate titanate layer is provided by vacuum deposition and reactive sputtering of lead zirconate titanate through a thermally decomposable organic compound atmosphere including oxygen to thereby epitaxially deposit carbon-doped lead zirconate titanate.
- FIG. 1 schematically illustrates a radiation imageintensifying apparatus constructed in accordance with the present invention
- FIG. 2 is a schematic illustration of apparatus which may be used in manufacture of the present invention.
- FIG. 3 is a schematic illustration, in cross-section, of an alternative embodiment of an article constructed in accordance with the present invention.
- FIG. 1 there is illustrated in greatly enlarged schematic form a radiation image-intensifying apparatus 10 constructed in accordance with the present invention.
- the apparatus of FIG. 1 shall in general be described for the case where the radiation of interestis visible light radiation. It is to be understood however that the apparatus is equally useful with other types of electro-magnetic radiation such as X-rays, ultraviolet radiation, or infrared radiation.
- image intensification is used herein, such is not intended to imply that the apparatus is only useful for reproducing intelligible images.
- the apparatus might be used as a radiation detector or amplifier where no particular image, as that term is normally used, is involved.
- the apparatus 10 includes a transparent substrate 12 which, when visible light is the radiation of concern, may be glass.
- a transparent substrate 12 which, when visible light is the radiation of concern, may be glass.
- the preferred glass is that identified as Pyrex which has a constituency of percent silicon dioxide, 4 percent sodium oxide, 13 percent boron oxide, 2 percent aluminum oxide and 1 percent other oxides.
- the substrate 12 is cleaned and etched as is well known to the art to thereby expose a fresh surface upon which further layers may be deposited and to assure tenacious adhesion thereof.
- a layer 14 of material which is electrically condu ctive but also transparent to the radiation is deposited upon the cleaned surface of the substrate 12.
- Various such materials are known to the art such for example as aluminum, titanium, chromium, and stannous oxide.
- a layer of stannous oxide approximately 1,000 angstroms in thickness is preferred.
- the stannous oxide layer may be deposited by any means known to the art, such for example as by spraying a 5 percent stannous chloride water solution onto the substrate 12, which has been heated to approximately 500 C. If one desires to have a greater selectivity as to bandwidth of the apparatus, then the layer 14 may be chosen for that purpose; for example, chromium may be utilized for the layer 14 and thereby effect a transparency for radiation falling within the infrared bandwidth.
- a radiation-responsive layer 16 is then deposited upon the transparent layer 14.
- the radiationresponsive layer 16 must have the characteristic of doning electrons in response to incident radiation.
- doning it is intended to mean a release of kinetic energy and may take the form of free electrons which are emitted from the layer 16 but may also include a variation in surface charge density or a mechanical change of form.
- the layer 16 may include various of the photosensitive rare earth halides but in accordance with the preferred embodiment of the present invention, the layer 16 is cesium fluoride.
- the cesium fluoride layer is deposited by vacuum evaporation onto the heated combination of the substrate 12 and the layer 14.
- the substrate 12 with the layer 14- properly adhered thereto is placed in a vacuum chamber such as a bell jar 30 (FIG. 2).
- a source of metallic cesium is placed in a boat 32 or similar holder.
- the vacuum pump 38 is utilized to provide a vacuum internally of the bell jar 30 which as is well known in the art should be at least 2 X 10 millimeters of mercury.
- a heater 34 is energized to heat the substrate 12 to a temperature between 150 200 C.
- the atmosphere source and control means 40 is energized to provide an atmosphere internally of the bell jar 30 of a minumum of .07 mole percent to a maximum of 1 mole percent with apreferred approximately l/ 10 mole percent of boron trifluoride from the source 42 thereof in gaseous form.
- Heat is then applied as indicated by the arrows 36 to the boat 32 containing the metallic cesium thereby causing the same to evaporate.
- the atoms thereof travel through the boron trifluoride atmosphere and a substantial percentage of the metallic cesium reacts with the boron trifluoride thereby forming cesium fluoride which is deposited upon and adheres to the stannous oxide layer 14 previously deposited.
- the evaporation is continued for a time sufficient to form a layer of cesium fluoride approximately 800 angstroms in thickness upon the layer 14.
- the atmosphere source and control means 40 is utilized to continuously bleed boron trifluoride into the interior of the bell jar 30 thereby maintaining the desired content thereof as the atmosphere.
- the atmosphere is not saturated and thus it is believed that some metallic cesium in elemental form (that is, not combined with fluoride) may be deposited as an integral part of the layer 16.
- a protective coating or layer 18 must be provided thereover to preclude external contamination of the cesium fluoride.
- Such protective layer may include various known elements but preferably in accordance with the present invention is a layer of silicon monoxide which may be deposited by vacuum evaporation as is well known in the art.
- the layer of silicon monoxide should be maintained relatively thin and in accordance with the present invention is approximatelySOO angstroms in thickness.
- a bonding coat 20 is then deposited upon the protective layer 18 and may include any material which will provide adequate adhesion of the additional layers to be further deposited upon the cesium flouride layer 16.
- the bonding coat 20 in accordance with the present invention preferably includes three separate layers of metal. The first of these is titanium which is deposited directly upon the silicon monoxide layer 18 and which is then followed by a layer of aluminum and a layer of gold. These layers may be deposited by vacuum evaporation as is well known to the art and it is believed they intermix during the evaporation steps to form an intermetallic compound.
- a layer 22 of piezoelectric material is epitaxially deposited.
- the epitaxially deposited piezoelectric layer 22 is a monocrystalline material such as a ferroelectric ceramic which has been polarized.
- Ferroelectric ceramics of this type are well known to the art and include for example lead zirconate, barium titanate, lead metaniobate and lead zirconate titanate.
- a layer 22 is formed of lead zirconate titanate which has been carbon-doped.
- the carbon-doped lead zirconate titanate layer 22 is applied to the bonding coat 20 by vacuum evaporation and reactive sputtering. Such occurs by placing in the container or boat 32 lead zirconate titanate in powder form along with the substrate 12 with the various layers previously deposited thereon.
- the bell jar is evacuated as above referred to after which the atmosphere source and control means 40 is activated to provide an atmosphere within the bell jar of a thermally decomposable organic compound 44 in an oxidizing atmosphere.
- any thermally decomposable organic compound which upon cracking provides carbon but will not contaminate the lead zirconate titanate may be used, in accordance with the present invention, the following atmosphere is preferred: 50 percent molar composition trimethylamine, 50 percent molar composition dimethylamine, 10 percent molar composition of argon as a diluent, and 2-5 percent molar composition oxygen.
- the substrate 12 is heated to between 200 and 300 C after which heat is applied as indicated by the arrows 36 to evaporate the lead zirconate titanate.
- a source of potential 31 is connected through an appropriate resistor 33 in such manner as to utilize the container 32 of lead zirconate titanate as the cathode and the substrate 12 as the anode.
- the magnitude of the source is controlled so as to maintain a substantially constant current flow between 10 milliamps and 200 milliamps depending upon the parameters of the system such as vacuum, cooling, time and the like.
- the parameters of the system such as vacuum, cooling, time and the like.
- a layer 24 of electrically-conductive and radiation-opaque material is deposited.
- the purpose of this material is to provide an electrode and also to preclude feedback of light which will be emitted by the phosphor layer 26 when deposited and as will be discussed more fully hereinafter.
- Various materials may be utilized but in accordance with the present invention, a layer consisting of titanium and platinum black co-deposited has been found preferable.
- leads are attached to the layer 14 and the layer 24 and the polarizing field applied as above referred to.
- an output-signal-producing layer such as a lightemitting phosphor 26 is deposited.
- a lightemitting phosphor 26 Any of the known phosphors which emit radiant energy when excited such as by application of energy thereto through friction, electron bombardment, application of an electric field or the like may be used.
- Such phosphors include for example zinc orthosilicate and zinc sulfide which may be activated with copper or silver.
- the phosphor layer 26 is silver-activated zinc sulfide.
- the layer 26 may be applied by any of the known techniques such as evaporating, sputtering or settling out of a dilute potassium silicate solution.
- a source 28 of driving potential is connected through the leads, as illustrated, to the electrically conductive layers 14 and 24, which operate as electrodes to apply an electrical potential across the piezoelectric layer 22 and the radiation-responsive layer 16.
- the application of an electrical potential to the piezoelectric material causes it to expand along one axis and contract along another axis.
- the piezoelectric material also produces opposite charges on opposed surfaces of the material when the material is stressed by application thereto of external forces whether created by mechanical or electrical means.
- the driving source provides excellent output at a magnitude of approximately volts and may vary in frequency from a few hertz to approximately l5 kilohertz.
- the apparatus constructed as above described has been found to provide an image intensifier with a gain of approximately 6,000.
- FIG. 3 Devices employing a plurality of elements as shown in FIG. 1 but cascaded may also be utilized in accordance with the present invention.
- Such a structure is illustrated in FIG. 3, and includes substrates 50, 52 and 54 upon which there has been deposited layers of material as above described and as illustrated generally as a single layer 56, 58, and 60, respectively, upon each of the substrates.
- a layer of optical coupling compound 62 and 64 is utilized to secure each of the devices together and provide good transmission of radiation therethrough.
- Sources of driving potential 66, 68 and 70 are connected in the manner above described, one respectively to each of the devices.
- the radiation 80 entering from the left as shown in FIG. 3 provides an output from the phosphor layer 56 which output is transmitted to the substrate 52 with like result and also the output thereof through substrate 54 with like result. Thereby, an increased gain is provided by cascading the gains of each of the devices in the manner shown in FIG. 3.
- Apparatus constructed as above described with reference to either FIG. 1 or FIG. 3 is very rugged and small in size.
- well known solid-state circuits may be used to provide the driving voltage and no particular protection is required as compared to the prior art where high voltages were used.
- the apparatus constructed in accordance with the invention may be used to provide image intensification for binoculars, underwater use, medical use for fluoroscopy as well as many additional uses as will be recognized by those skilled in the art.
- An article of manufacture comprising:
- C. phosphor means connected with said piezoelectric layer and responsive to vibration thereof for producing emitted radiation
- D. means for applying an electrical potential across said piezoelectric layer for establishing vibrations therein, and said radiation-responsive layer, whereby, upon said radiationresponsive emissive layer being excited by incident radiation, energy is transferred therefrom through said piezoelectric layer to said phosphor means to intensify the image of said incident radiation.
- An article of manufacture comprising:
- C. a carbon-doped lead zirconate titanate piezoelectric layer bonded to said cesium fluoride layer; D. a phosphor bonded to said piezoelectric layer;
- E. means for applying a varying electrical potential across said cesium fluoride and piezoelectric layers whereby upon said cesium fluoride layer being excited by incident radiation, energy is transferred therefrom through said piezoelectric layer to said phosphor to intensify the image of said incident radiation.
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- Engineering & Computer Science (AREA)
- Electromagnetism (AREA)
- General Engineering & Computer Science (AREA)
- Condensed Matter Physics & Semiconductors (AREA)
- General Physics & Mathematics (AREA)
- Computer Hardware Design (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Power Engineering (AREA)
- High Energy & Nuclear Physics (AREA)
- Conversion Of X-Rays Into Visible Images (AREA)
Abstract
A radiation-responsive layer preferably of cesium fluoride is bonded to an electrically-conductive radiation-transparent layer of material which is also utilized as an electrode. A piezoelectric polarized ferroelectric ceramic layer preferably of lead zirconate titanate is bonded to the radiation-responsive layer. An output device such as a visible-light emitting phosphor is bonded along with a radiation-opaque electrical conductive layer, also used as an electrode, to the piezoelectric layer. A source of electrical potential is connected between the two electrodes to thereby apply an electrical potential across the piezoelectric layer and the radiation-sensitive layer. In the manufacture of the apparatus, the cesium fluoride layer is formed by vacuum deposition from a metallic cesium source in a boron trifluoride atmosphere while bleeding in small amounts of boron trifluoride to maintain a substantially constant atmospheric level thereof during evaporation. The piezoelectric layer is formed by vacuum deposition of lead zirconate titantate in an atmosphere containing trimethylamine, dimethylamine, argon and oxygen upon a bonding coat deposited on the previouslydeposited cesium fluoride layer while retaining the substrate heated. During the deposition process, the trimethylamine and dimethylamine are thermally cracked thereby to provide carbon as a dopant for the lead zirconate titanate layer.
Description
United States Patent Grolitzer [111 3,828,186 5 Aug. 6,1974
[ APPARATUS FOR INTENSIFYING RADIATION IMAGES [75] Inventor: Arthur J. Grolitzer, Tarzana, Calif.
[73] Assignee: Vocon, Inc., Los Angeles, Calif.
[22] Filed: Aug. 9, 1972 [21] Appl. No.: 278,894
[52] US. Cl. 250/213 R, 313/108 A [51] Int. Cl. H0lj 31/50 [58] Field of Search 250/213 R, 213 VT, 211 R,
250/211 .1, 83.3 R, 83.3 H; 313/108 R, 108
[56] References Cited UNITED STATES PATENTS 2,816,236 12/1957 Rosen 313/108 A 2,905,830 9/1959 Kazan 250/213 2,989,636 6/1961 Lieb 250/213 3,054,900 9/1962 Orthurber.... 250/213 3,112,404 11/1963 Reed 250/213 3,154,720 10/1964 Cooperman 313/108 B 3,293,441 12/1966 Kazan 250/213 3,300,645 l/l967 Winslow 250/213 3,315,080 4/1967 Kohashi 250/213 3,356,850 12/1967 Fleming-William 250/213 3,446,974 5/1969 Seiwatz 310/81 Primary Examiner-James W. Lawrence Assistant Examiner-D. C. Nelms Attorney, Agent, or Firm-Nilsson, Robbins, Bissell, Dalgarn & Berliner pyospuoz 26 [57] ABSTRACT A radiation-responsive layer preferably of cesium fluoride is bonded to an electrically-conductive radiationtranspa'rent layer of material which is also utilized as an electrode. A piezoelectric polarized ferroelectric ceramic layer preferably of lead zirconate titanate is bonded to the radiation-responsive layer. An output device such as a visible-light emitting phosphor is bonded along with a radiation-opaque electrical conductive layer, also used as an electrode, to the piezoelectric layer. A source of electrical potential is connected between the two electrodes to thereby apply an electrical potential across the piezoelectric layer and the radiation-sensitive layer.
In the manufacture of the apparatus, the cesium fluoride layer is formed by vacuum deposition from a metallic cesium source in a boron trifluoride atmosphere while bleeding in small amounts of boron trifluoride to maintain a substantially constant atmospheric level thereof during evaporation. The piezoelectric layer is formed by vacuum deposition of lead zirconate titantate in an atmosphere containing trimethylamine, dimethylamine, argon and oxygen upon a bonding coat deposited on the previously-deposited cesium fluoride layer while retaining the substrate heated. During the deposition process, the trimethylamine and dimethylamine are thermally cracked thereby to provide carbon as a dopant for the lead zirconate titanate layer.
8 Claims, 3 Drawing Figures LAVER 24 P/EZOE L E CTR/C LA? YER 22 PROT'CT/VE LAYER /8 RAD/,4 r/o/v- TRANSPARENT LEC77?/CALLP- GOA/00C r/vs m HE/Q /4 PAIENTED PHOSPHO/Q 26 P/EZOELECTR/C LAYER 2a BOND/N6 COAT 2O PRO7'5CT/VE LAYER /8 LAYER /4 40 HER E AND co/v. TROL MEANS IOTA/'05P SOURCE Vncc/c/M PUMP BACKGROUND OF THE INVENTION 1. Field of the Invention This invention relates generally to solid-state devices and more particularly to such devices adapted for intensification of incident radiation images.
2. Description of the Prior Art It has long been desirable to enhance images which are relatively weak and difficult to detect by means of intensification thereof. Such would be helpful in the visible light portion of the radiation spectrum particularly during low ambient light conditions. There have been various prior art attempts to construct such apparatus which, although operationally successful, have met with various problems. Some of these problems are extremely limited bandwidth of transmitted radiation, large size of the resulting apparatus, the extremely high voltages (kilovolts) required to obtain satisfactory operation of the apparatus, sensitivity of the apparatus to vibrations, to temperature and to external magnetic fields.
For the most part, prior art apparatus providing results similar to those achieved by applicant are, constructed using high voltage vacuum tube circuits and technology. Some prior art devices have utilized electroluminescent apparatus of the kind comprising a layer of electroluminescent material and a layer of photoconductive material. The photoconductive material is arranged to control the value of voltage applied across the electroluminescent material proportional to the intensity of incident radiation lying within the particular bandwidth of radiation to which the device is sensitive. Such devices have been utilized singly or in tandem depending upon the particular application.
The most pertinent prior art references known to applicant are US. Pat. Nos. 2,816,236; 2,951,168;
2,972,694; 3,058,002; 3,072,821; 3,121,824; 3,132,276; 3,154,720; 3,187,184; 3,268,755; 3,286,027; 3,356,850 and 3,501,638.
SUMMARY OF THE INVENTION A radiation-responsive layer excitable by incident radiation within a predetermined bandwidth is bonded to a ferroelectric ceramic layer which is properly polarized to provide piezoelectric characteristics. An output-signal-producing means is connected with the piezoelectric layer and provides an output signal responsive to incident radiation.
In a more specific aspect of the present invention, the apparatus includes cesium fluoride as a raditionresponsive layer and carbon-doped lead zirconate titanate as the piezoelectric layer with a phosphor bonded thereto as the output-signal-producing means. An electrical potential is applied across the lead zirconate titanate and cesium fluoride layers.
In accordance with the method of the present invention, the cesium fluoride layer is provided by vacuum evaporating metallic cesium through a boron trifluoride atmosphere onto a heated substrate. The lead zirconate titanate layer is provided by vacuum deposition and reactive sputtering of lead zirconate titanate through a thermally decomposable organic compound atmosphere including oxygen to thereby epitaxially deposit carbon-doped lead zirconate titanate.
BRIEF DESCRIPTION OF THE DRAWINGS FIG. 1 schematically illustrates a radiation imageintensifying apparatus constructed in accordance with the present invention;
FIG. 2 is a schematic illustration of apparatus which may be used in manufacture of the present invention; and,
FIG. 3 is a schematic illustration, in cross-section, of an alternative embodiment of an article constructed in accordance with the present invention.
DESCRIPTION OF THE PREFERRED. EMBODIMENT Referring now to FIG. 1, there is illustrated in greatly enlarged schematic form a radiation image-intensifying apparatus 10 constructed in accordance with the present invention. For the sake of a concrete illustration of its use, the apparatus of FIG. 1 shall in general be described for the case where the radiation of interestis visible light radiation. It is to be understood however that the apparatus is equally useful with other types of electro-magnetic radiation such as X-rays, ultraviolet radiation, or infrared radiation. Although the. term image intensification is used herein, such is not intended to imply that the apparatus is only useful for reproducing intelligible images. For example, the apparatus might be used as a radiation detector or amplifier where no particular image, as that term is normally used, is involved.
As shown in FIG. 1, the apparatus 10 includes a transparent substrate 12 which, when visible light is the radiation of concern, may be glass. Although various glasses are useful, the preferred glass is that identified as Pyrex which has a constituency of percent silicon dioxide, 4 percent sodium oxide, 13 percent boron oxide, 2 percent aluminum oxide and 1 percent other oxides. The substrate 12 is cleaned and etched as is well known to the art to thereby expose a fresh surface upon which further layers may be deposited and to assure tenacious adhesion thereof.
A layer 14 of material which is electrically condu ctive but also transparent to the radiation is deposited upon the cleaned surface of the substrate 12. Various such materials are known to the art such for example as aluminum, titanium, chromium, and stannous oxide. In accordance with the preferred embodiment of the present invention and for visible light, a layer of stannous oxide approximately 1,000 angstroms in thickness is preferred. The stannous oxide layer may be deposited by any means known to the art, such for example as by spraying a 5 percent stannous chloride water solution onto the substrate 12, which has been heated to approximately 500 C. If one desires to have a greater selectivity as to bandwidth of the apparatus, then the layer 14 may be chosen for that purpose; for example, chromium may be utilized for the layer 14 and thereby effect a transparency for radiation falling within the infrared bandwidth.
A radiation-responsive layer 16 is then deposited upon the transparent layer 14. The radiationresponsive layer 16 must have the characteristic of doning electrons in response to incident radiation. By the term doning it is intended to mean a release of kinetic energy and may take the form of free electrons which are emitted from the layer 16 but may also include a variation in surface charge density or a mechanical change of form. The layer 16 may include various of the photosensitive rare earth halides but in accordance with the preferred embodiment of the present invention, the layer 16 is cesium fluoride. The cesium fluoride layer is deposited by vacuum evaporation onto the heated combination of the substrate 12 and the layer 14.
To accomplish the foregoing deposition, the substrate 12 with the layer 14- properly adhered thereto is placed in a vacuum chamber such as a bell jar 30 (FIG. 2). A source of metallic cesium is placed in a boat 32 or similar holder. The vacuum pump 38 is utilized to provide a vacuum internally of the bell jar 30 which as is well known in the art should be at least 2 X 10 millimeters of mercury. Thereafter a heater 34 is energized to heat the substrate 12 to a temperature between 150 200 C. Thereafter, the atmosphere source and control means 40 is energized to provide an atmosphere internally of the bell jar 30 of a minumum of .07 mole percent to a maximum of 1 mole percent with apreferred approximately l/ 10 mole percent of boron trifluoride from the source 42 thereof in gaseous form. Heat is then applied as indicated by the arrows 36 to the boat 32 containing the metallic cesium thereby causing the same to evaporate. During evaporation of the metallic cesium the atoms thereof travel through the boron trifluoride atmosphere and a substantial percentage of the metallic cesium reacts with the boron trifluoride thereby forming cesium fluoride which is deposited upon and adheres to the stannous oxide layer 14 previously deposited. The evaporation is continued for a time sufficient to form a layer of cesium fluoride approximately 800 angstroms in thickness upon the layer 14. During the evaporation of the metallic cesium from the source 32, the atmosphere source and control means 40 is utilized to continuously bleed boron trifluoride into the interior of the bell jar 30 thereby maintaining the desired content thereof as the atmosphere. At the percentages of boron trifluoride provided in the bell jar 30, the atmosphere is not saturated and thus it is believed that some metallic cesium in elemental form (that is, not combined with fluoride) may be deposited as an integral part of the layer 16. By providing thus a layer of radiation-responsive material 16 consisting of a majority of a rare earth halide but with a rare earth metal inits elemental form, the response of the layer 16 to incident radiation is surprisingly increased.
Immediately after deposition of the cesium fluoride layer 16, a protective coating or layer 18 must be provided thereover to preclude external contamination of the cesium fluoride. Such protective layer may include various known elements but preferably in accordance with the present invention is a layer of silicon monoxide which may be deposited by vacuum evaporation as is well known in the art. The layer of silicon monoxide should be maintained relatively thin and in accordance with the present invention is approximatelySOO angstroms in thickness.
A bonding coat 20 is then deposited upon the protective layer 18 and may include any material which will provide adequate adhesion of the additional layers to be further deposited upon the cesium flouride layer 16. The bonding coat 20 in accordance with the present invention preferably includes three separate layers of metal. The first of these is titanium which is deposited directly upon the silicon monoxide layer 18 and which is then followed by a layer of aluminum and a layer of gold. These layers may be deposited by vacuum evaporation as is well known to the art and it is believed they intermix during the evaporation steps to form an intermetallic compound.
After deposition of the bonding coat 20, a layer 22 of piezoelectric material is epitaxially deposited. The epitaxially deposited piezoelectric layer 22 is a monocrystalline material such as a ferroelectric ceramic which has been polarized. Ferroelectric ceramics of this type are well known to the art and include for example lead zirconate, barium titanate, lead metaniobate and lead zirconate titanate. In accordance with the present invention, a layer 22 is formed of lead zirconate titanate which has been carbon-doped. Once the ferroelectric ceramic has been deposited,it must be heated beyond its ferroelectric Curie temperature, and then a large unidirectional electric field is applied to the material and the material is allowed to cool to room temperature while the field remains applied. This process of polarizing a ferroelectric ceramic is well known to the art.
The carbon-doped lead zirconate titanate layer 22 is applied to the bonding coat 20 by vacuum evaporation and reactive sputtering. Such occurs by placing in the container or boat 32 lead zirconate titanate in powder form along with the substrate 12 with the various layers previously deposited thereon. The bell jar is evacuated as above referred to after which the atmosphere source and control means 40 is activated to provide an atmosphere within the bell jar of a thermally decomposable organic compound 44 in an oxidizing atmosphere. Although any thermally decomposable organic compound which upon cracking provides carbon but will not contaminate the lead zirconate titanate may be used, in accordance with the present invention, the following atmosphere is preferred: 50 percent molar composition trimethylamine, 50 percent molar composition dimethylamine, 10 percent molar composition of argon as a diluent, and 2-5 percent molar composition oxygen. Thereafter, the substrate 12 is heated to between 200 and 300 C after which heat is applied as indicated by the arrows 36 to evaporate the lead zirconate titanate. A source of potential 31 is connected through an appropriate resistor 33 in such manner as to utilize the container 32 of lead zirconate titanate as the cathode and the substrate 12 as the anode. The magnitude of the source is controlled so as to maintain a substantially constant current flow between 10 milliamps and 200 milliamps depending upon the parameters of the system such as vacuum, cooling, time and the like. By maintaining the conditions above set forth, there is obtained a combination of evaporation and reactive sputtering of the lead zirconate titanate. By providing the appropriate atmosphere and temperatures above referred to, the layer 22 is epitaxially formed upon the bonding coat 20.
After deposition of the layer 22, a layer 24 of electrically-conductive and radiation-opaque material is deposited. The purpose of this material is to provide an electrode and also to preclude feedback of light which will be emitted by the phosphor layer 26 when deposited and as will be discussed more fully hereinafter. Various materials may be utilized but in accordance with the present invention, a layer consisting of titanium and platinum black co-deposited has been found preferable. After deposition of the layer 24,
leads are attached to the layer 14 and the layer 24 and the polarizing field applied as above referred to.
After polarization of the ferroelectric ceramic layer 22, an output-signal-producing layer such as a lightemitting phosphor 26 is deposited. Any of the known phosphors which emit radiant energy when excited such as by application of energy thereto through friction, electron bombardment, application of an electric field or the like may be used. Such phosphors include for example zinc orthosilicate and zinc sulfide which may be activated with copper or silver. In accordance with the preferred embodiment of the present invention, the phosphor layer 26 is silver-activated zinc sulfide. The layer 26 may be applied by any of the known techniques such as evaporating, sputtering or settling out of a dilute potassium silicate solution.
Thereafter, a source 28 of driving potential is connected through the leads, as illustrated, to the electrically conductive layers 14 and 24, which operate as electrodes to apply an electrical potential across the piezoelectric layer 22 and the radiation-responsive layer 16. As is well known to the art, the application of an electrical potential to the piezoelectric material causes it to expand along one axis and contract along another axis. In addition thereto, the piezoelectric material also produces opposite charges on opposed surfaces of the material when the material is stressed by application thereto of external forces whether created by mechanical or electrical means.
It has been found that the driving source provides excellent output at a magnitude of approximately volts and may vary in frequency from a few hertz to approximately l5 kilohertz. The apparatus constructed as above described has been found to provide an image intensifier with a gain of approximately 6,000.
Devices employing a plurality of elements as shown in FIG. 1 but cascaded may also be utilized in accordance with the present invention. Such a structure is illustrated in FIG. 3, and includes substrates 50, 52 and 54 upon which there has been deposited layers of material as above described and as illustrated generally as a single layer 56, 58, and 60, respectively, upon each of the substrates. Thus, radiation would enter from the left as viewed in FIG. 3 and as shown by the arrows 80. A layer of optical coupling compound 62 and 64 is utilized to secure each of the devices together and provide good transmission of radiation therethrough. Sources of driving potential 66, 68 and 70 are connected in the manner above described, one respectively to each of the devices. Thus, by utilizing an apparatus as constructed in FIG. 3, the radiation 80 entering from the left as shown in FIG. 3 provides an output from the phosphor layer 56 which output is transmitted to the substrate 52 with like result and also the output thereof through substrate 54 with like result. Thereby, an increased gain is provided by cascading the gains of each of the devices in the manner shown in FIG. 3.
Apparatus constructed as above described with reference to either FIG. 1 or FIG. 3 is very rugged and small in size. In view of the low voltages and non-critical frequencies for the power source, well known solid-state circuits may be used to provide the driving voltage and no particular protection is required as compared to the prior art where high voltages were used. Thus, the apparatus constructed in accordance with the invention may be used to provide image intensification for binoculars, underwater use, medical use for fluoroscopy as well as many additional uses as will be recognized by those skilled in the art.
The precise phenomena resulting in the excellent image intensification realized with apparatus when constructed in accordance with the present invention is not yet understood. It is thought that energy released by the radiation-responsive layers in response to incident radiation is coupled to the piezoelectric layers and enhances the vibration thereof. Such enhanced vibration imparts energy to the output-signal-producing layer such as the phosphors causing light to be emitted therefrom. The precise mechanism for the energy transfer is not known but is thought to be either electron emission or a physical deformation. In any event, highly surprising and unexpected results have been obtained when utilizing apparatus constructed as above described and illustrated.
What is claimed is:
1. An article of manufacture comprising:
A. a radiation-responsive emissive layer for doning electrons upon excitation by incident radiation; B. a piezoelectric polarized ferroelectric ceramic layer bonded to said radiation-responsive layer;
C. phosphor means connected with said piezoelectric layer and responsive to vibration thereof for producing emitted radiation; and,
D. means for applying an electrical potential across said piezoelectric layer for establishing vibrations therein, and said radiation-responsive layer, whereby, upon said radiationresponsive emissive layer being excited by incident radiation, energy is transferred therefrom through said piezoelectric layer to said phosphor means to intensify the image of said incident radiation.
2. An article of manufacture as defined in claim 1 wherein said piezoelectric layer is lead zirconate titanate.
3. An article of manufacture as defined in claim 2 wherein said piezoelectric layer includes carbon as an impurity.
4. An article of manufacture as defined in claim 3 wherein said piezoelectric layer is of mono-crystalline structure.
5. An article of manufacture as defined in claim 1 wherein said radiation-responsive layer is a rare earth halide.
6. An article of manufacture as defined in claim 5 wherein said radiation-responsive layer is cesium fluoride.
7. An article of manufacture comprising:
A. an optically-transparent substrate;
B. a cesium fluoride layer bonded to said substrate;
C. a carbon-doped lead zirconate titanate piezoelectric layer bonded to said cesium fluoride layer; D. a phosphor bonded to said piezoelectric layer; and
E. means for applying a varying electrical potential across said cesium fluoride and piezoelectric layers whereby upon said cesium fluoride layer being excited by incident radiation, energy is transferred therefrom through said piezoelectric layer to said phosphor to intensify the image of said incident radiation.
8. An article of manufacture as defined in claim 7 which further includes an optically-opaque means between said phosphor and said piezoelectric layers.
Claims (7)
- 2. An article of manufacture as defined in claim 1 wherein said piezoelectric layer is lead zirconate titanate.
- 3. An article of manufacture as defined in claim 2 wherein said piezoelectric layer includes carbon as an impurity.
- 4. An article of manufacture as defined in claim 3 wherein said piezoelectric layer is of mono-crystalline structure.
- 5. An article of manufacture as defined in claim 1 wherein said radiation-responsive layer is a rare earth halide.
- 6. An article of manufacture as defined in claim 5 wherein said radiation-responsive layer is cesium fluoride.
- 7. An article of manufacture comprising: A. an optically-transparent substrate; B. a cesium fluoride layer bonded to said substrate; C. a carbon-doped lead zirconate titanate piezoelectric layer bonded to said cesium fluoride layer; D. a phosphor bonded to said piezoelectric layer; and E. means for applying a varying electrical potential across said cesium fluoride and piezoelectric layers whereby upon said cesium fluoride layer being excited by incident radiation, energy is transferred therefrom through said piezoelectric layer to said phosphor to intensify the image of said incident radiation.
- 8. An article of manufacture as defined in claim 7 which further includes an optically-opaque means between said phosphor and said piezoelectric layers.
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US00278894A US3828186A (en) | 1972-08-09 | 1972-08-09 | Apparatus for intensifying radiation images |
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US00278894A US3828186A (en) | 1972-08-09 | 1972-08-09 | Apparatus for intensifying radiation images |
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