US2588253A - Alloys and rectifiers made thereof - Google Patents

Alloys and rectifiers made thereof Download PDF

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US2588253A
US2588253A US135745A US13574549A US2588253A US 2588253 A US2588253 A US 2588253A US 135745 A US135745 A US 135745A US 13574549 A US13574549 A US 13574549A US 2588253 A US2588253 A US 2588253A
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alloys
germanium
alloy
contact
volts
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Lark-Horovitz Karl
Randall M Whaley
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Purdue Research Foundation
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Purdue Research Foundation
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Priority claimed from US604744A external-priority patent/US2514879A/en
Priority to GB19884/46A priority patent/GB636248A/en
Priority to FR941699D priority patent/FR941699A/en
Priority to US66946A priority patent/US2637770A/en
Priority to US135748A priority patent/US2801376A/en
Priority to US135745A priority patent/US2588253A/en
Priority to US135746A priority patent/US2615966A/en
Application filed by Purdue Research Foundation filed Critical Purdue Research Foundation
Priority to US135749A priority patent/US2745046A/en
Priority to US135747A priority patent/US2600997A/en
Priority to US136284A priority patent/US2691577A/en
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B41/00Obtaining germanium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22BPRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B11/00Obtaining noble metals
    • C22B11/10Obtaining noble metals by amalgamating
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01LSEMICONDUCTOR DEVICES NOT COVERED BY CLASS H10
    • H01L21/00Processes or apparatus adapted for the manufacture or treatment of semiconductor or solid state devices or of parts thereof
    • 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
    • Y10S420/00Alloys or metallic compositions
    • Y10S420/903Semiconductive

Definitions

  • sultant materials are not alloys in the common meaning of the word.
  • alloy of germanium means to include a union of two or more elements, one of which is germanium, and the other or others being metals, non-metals, or gases, and
  • the known contact rectiers i. e., rectiers comprising suitable metal electrodes,'and a semiconductor have at least one of the ⁇ following disadvantages:
  • germanium alloys of our present invention 13 claims. l C1. lis-366) megohinsi as measured at about 5 volts.
  • germanium alloys herein disclosed are all of the class of N-ty'pe semi-conductors, i. e., semiconductors which when made into contact type rectiers present a high resistance to current flow ⁇ across the rectifying contact when the semiconductor is positive and the contacting metal electrode or Whisker is negative, andy a lower resistance when the potential is reversed.
  • Peak back voZtage The voltage-current characteristics measured on rectifiers using the alloys of our invention show a voltage peak in 'the back or high resistance direction. This peak generally occurs within a range greater than 10 volts and approaching the order of 200 volts. It will also appear that all of these rectifiers using alloys of our invention exhibit a negative resistance region in the back direction for currents exceeding the current at the peak back voltage.
  • these rectiers have resistances ranging from the order of 10,000 ohms to several High resistancesare substantially maintained nearly to the peak back! voltage.
  • N-type semi-conductors of germanium may also be formed by allowing small amounts of, for example, phosphorous, arsenic, or antimony with germanium, but in rectiers using such semiconductors it has found that excessive currents pass at voltages greater than about 3 to 10 volts in the back direction which permanently injure the rectifying contact. It will be understood therefore that our present invention only relates to semi-conductors of the N-type which exhibit ⁇ high back voltage characteristics in excess of at least volts, and does not concern all N-type semi-conductors consisting of an alloy of germanium, as for example, the group last referred to.
  • Figure 1 shows the voltage-current characterfistic curves of several rectiflers using certain of the alloys of our invention, which curves are not to be taken as typical of given alloys but merely to represent the type of characteristic exhibited by such alloys in general.
  • amount of the added element alloyed with Figure 2 is a graph illustrating the electrical characteristics of rectiiiers using different types of surfaces on one alloy of our invention.
  • Figure 3 is a sectional View of a rectier, the semi-conductor of which comprises an alloy of our present invention.
  • Each alloy represented by the curves of Figure 1 is designated by a code number.
  • the latter part of each code denotes the amount in atomic percent of the particular element or elements added to germanium to produce that alloy. No atomic percentage figures for the addition of nitrogen to germanium are given since it is difcult to determine accurately the amount or number of nitrogen atoms alloyed with the germanium.
  • each alloy may usually be found with electrical characteristics which lie toward the upper limit of the ranges above set out. However, as will later be discussed in more detail, some of the alloys are of greater uniformity than others with respect to rectification characteristics.
  • Thegermaniumalloys of our invention may be prepared' inall cases exceptfcr the germanium- ⁇ nitrogen alloy, by melting pure germanium' with kthe desiredalloying element 'or combination of elements in either a high vacuum of the order of d10-51mm.. mercury fat about. 100.0 C. or in an atmosphere; of.' helium. Precautionf should be.
  • Alloying germanium with nitrogen may be ⁇ effected by melting the germanium in an atmosphere of nitrogen. which may be either puried nitrogen or nitrogen direct from a commercial cylinder.
  • the ger- Vmanium is melted in nitrogen at pressures ranging from about 2 mm. to '760 mm. Hg at altemperature of 1000 to 1050 C. Good results appear to be independent of pressure and melts prepared within the above range of pressures were all satisfactory.
  • the germanium successfully used ffori-.bese alloys had purity approaching and electrical resistivity greater than about one ohm cm.
  • the germanium which we have successfully alloyed with other elements to form the alloys listed in Tables I and II was prepared from GeOz obtained from the Eagle-'Eicher1 Lead Company of Joplin. Missouri. The oxide was reduced in an atmosphere of commercial hydrogen at temperatures of 650 to 700 C. over a period of three to four hours. The oxide reduced. in this manner leaves the germanium metal in the form of a gray-green powder which is then alloyed with another elementor elements in the described.
  • melts of germanium andl the added element or elements were held in the molten state long enough to allow mixing ofthe constituents, and. it1 has been found that about 5 to 15 minutes is sulcient for this purpose.
  • ingredients to form melts of. about ve to si-x grams each were used in proportions above setforth in detail.
  • the. melts werel allowed to solidify and cool which was accomplished either by immediately removing heat or by controlled cooling apparatus. In. certain. cases the uniformity of the melt is affected by the manner in ⁇ which it. 1s cooled.
  • Pure GeOz was reduced in hydrogen at atmospheric pressure for about three hours at 650 to 7009 C.
  • Six grams of pure germanium powder so obtained were then placed in a porcelain crucible together with small flakes of pure tin amounting to 25 milligrams or about 0.8 atomic percent of tin.
  • the Crucible and contents were then placed inside a graphite cylinder used as a heater in the high frequency field of an induction furnace, and lowered in a vertical quartz tube which was then evacuated and maintained at a pressure of about 10-5 mm. mercury. Power was then applied to the external coil of the induction furnace to melt the germanium and hold it molten for about minutes. The melt was then allowed to cool by merely turning off the power to the coil. the alloy, and were soldered with soft-solder to a suitable metal electrode to produce a very low resistance non-rectifying Contact with one face of the wafer.
  • the exposed face was then ground with 600 mesh alumina andetched for 2 minutes with an etching solution consisting essentially of HNO3, HF, Cu(NOa)2 and water in proportions to be later described herein.
  • etching solution consisting essentially of HNO3, HF, Cu(NOa)2 and water in proportions to be later described herein.
  • the surfaces of these alloys are usually ground flat and then etched in a manner to be described in detail.
  • the etching of the alloy surfaces is not essential 'sincel for example, by breaking open a melt, 4points may be found which exhibit lthe aforementioned electrical rectifying characteristics.
  • Such broken surfaces presentgeometrically irregular faces which introduce some difficulty in assembly of the rectiers.
  • grinding the alloy surface flat and etching it appears to be the most feasible manner of producing the rectiers in the commercial practicing of our invention.
  • Germanium containing above about 0.1 percent tin usually shows tin separated out, both at internal grain boundaries and on the outer surfaces.. In some melts containing tin in excess of 0.1 atomic percent, ductile layers of this tin-rich'material were frequently observed, particularly in the lower regions of the melt. In this connection we wish to observe that in making the germanium-tin alloys it is desirable in producing the melt that the boat or crucible in which the elements are ⁇ contained be gradually removed from the hot .furnace region. This will produce more uniform Thereafter wafers were cut from .8 tin merely segregated. At 17 atomic percent addition of tin, the entire melt was interlaced with tin-rich veins which had metallic low re sistance ohmic conductivity.
  • Whiskers made of the following metals have been'tried and only very slight deviations were noted over a large number of points of contact with the alloys of our invention: Mn, Pt," Ta, Ni, Fe, Zn, Mo, W, Au, Cu. Ag, Zr, Pt-Ir, and Pt-Ru. It appears'therefore, that choice vof a Whisker material may be determined on the basis of requirements other than the peak back volta-ge on rectiers using the alloys. 'hesc electrodes or whiskers may have contact with the surfaces vof the alloys as formed upon solidication, or on surfacesexposed by breaking the melt.. As mentioned above, however, it is desirable to grind and etch the surface.
  • the melts which usually were of pellet form 5 to 10 millimeters thick, may be cut into thin plates or slabs and a surface thereof ground with a suitable abrasive
  • the abrasive used is not critical in that it has been found that other abrasives such as CrzOs, MgO, VazOs, SnOz, ZnO and 4-O paper are equally satisfactory.
  • This may then be followed by a-further 4 parts by volume hydrofluoric acid (48%l reagent) 4 parts by volume distilled water 2 parts by volume concentrated nitric acid,
  • Such a solution will satisfactorily etch the surface of the plates or slabs in about 1 to 2 minutes at room temperature ⁇ and may be applied with either a swab or by immersing the surface in the solution.
  • This etching is not particularly critical but care should be taken not to unduly extend the etching since then a high polish is produced which may impair the performance of the alloy.
  • a solution consisting approximately of 1 gram stannyl chloride in 5G cc. of H2O may be used as an electrolytic bath for etching the alloy surfaces. Immersing the alloy as the anode in this soution will result in satisfactory etching within about 11/2 minutes at about 21/2 volts applied.
  • An alternative modification of an electrolytic etching solution may comprise 5 parts concentrated HNO3 and 50 parts H2O by volume. Using the alloy as the anode for about 11/2 minutes at 1 to 2 volts will result in a satisfactory etch.
  • FIG. 2 illustrates the effect of etching of one of the alloys of our invention.
  • the alloy selected to illustrate the effect of etching is identifed as melt 24 P-OU136-.25Sn. This melt as appears from the aforesaid designation consti- ⁇ tutes .25 atomic percent tin.
  • the curve identified by reference numeral l illustrates the electrical characteristic of the germanium-tin alloy above identified in which the surface was ground with 600 A1203 but not etched.
  • the curve indicated by the reference numeral 2 illustrates the electrical characteristics which were obtained on a freshly broken surface of an alloy of the above composition but which surface has not been etched.
  • Curve member 3 illustrates the electrical characteristic of a surface ground with 600 A1203 and then etched in accordance with the manner first described.
  • the curve indicated by the reference numeral 4 illustrates electrical characteristics of another point on the alloy after etching as described in connection with curve 3, the curves 3 and 4 representing the best and poorest performances, re spectively, of the ⁇ particular germanium-tin alloy above identified, after etching. It is ⁇ to be observed that in this graph the voltage scale in the forward direction isA there expanded by a factor of l as compared to the voltage scale indicating the high back voltage characteristics of the alloys of our invention. As indicated, the currents are given in milliamperes.
  • Table III shows the permanent effects of suchpower treatment upOn a few typical rectifiers using alloys of our invention and prepared as described. It will be seen from the table that the most signicant effect of the power treatment is the increase in the back resistance as measured at about 4.5 volts. This resistance is increased by factors ranging from about 10 to 50 times the values measured before treatment. Relatively minor increases of 10 to 20 percent are effected on the peak back voltage. Forward currents at one volt are in general decreased by amounts ranging from lO-to percent.
  • the power treatment can be effected with the use of either valternating or It has been demonstrated above that the ⁇ high back voltage, high back resistance, and good forward conductance properties disclosed are inherent in the germanium alloys of our invention. Modifications of surface treatments or power treatments as described above will, however, vary the magnitude of these properties Within ⁇ certain general limits. For example, on a given alloy surface, variations in surface treatment and power treatment may be expected to vary the average peak back voltage by a factor of about.2, the average forward current by a factor of about 2, and the average back resistance by factors up to 50. It will be noted that the back resistance is the property most sensitive to variations in treatment, particularly to power treatment.
  • FIG. 3 of the drawings We have shown one type of ⁇ rectifier in which our invention may be embodied.
  • a Wafer 5 which may be of any of the germanium alloys above disclosed is mounted to have a low resistance non-reetifying contact With a metal electrode member 5.
  • An electrode or Whisker l is connected at one end to an electrode supporting member 8 with the end of the Whisker in contact with the surface of the germanium alloy Wafer 5.
  • the standard 9 provides for mounting of the members supporting the wafer 5 and electrode or Whisker l in insulated relation.
  • the rectifier contemplated by our invention may be of various forms, the only critical constructional feature being that the germanium alloy Wafer comprising the semiconductor, and the Whisker for contacting the surface of the Wafer being arranged and supported so that one end of the Whisker engages the semi-conductor surface. It is understood that suitable leads areconnected to the wafer or semi-conductor and to the Whisker or metal electrode so that the device may have application in any desired circuit for use in the ⁇ recti' 1.
  • An electrical device comprising a semi-conductor, a counter electrode having substantially point contact with said semi-conductor and a second electrode having an area of contact with said semi-conductor which is large compared to that of the counter electrode, said semi-conductor consisting of germanium of the order of 99% purity in combination With at least one ofv the elements from the group consisting of cop' per and silver, said device having a peak back voltage in the range in excess of l0 volts andV approaching the order of 200 volts.
  • An electrical device comprising an alloy formed of a mixture of germanium having a purity of the order of 99% and copper in an amount of between 0.19 and 2.0 atomic percent, and a pair of electrode elements in contact With said formed alloy, one of said electrode elements having substantially point contact with said alloy and the second of said electrodes having an area of contact which is large compared to that of the point contact electrode.
  • An electrical device comprising an alloy" formed of a mixture of germanium having a4 purity of the order of 99% and silver in an amount of between 0.5 and 0.66 atomic percent," ⁇ and a pair of electrode elements in contact Withsaid formed alloy, one of said electrode elements having substantially point contact With said alloy and the second of said electrodes having an area of contact which is large compared to that:
  • the method of claim 4 including the ad' ditional steps of grinding the severed wafers and then etching the ground surfaces to provide optimum contact points for said contactingelectrode members. 6. The method of claim 4 including, in addition, the step of etching a surface of a Wafer cut from the ingot before applying a contact electrode.
  • the method of claim 4 including, in addition, the step of etching a surface of a Wafer cut from the ingot in a solution made up of approximately 4 parts by volume of hydrofluoric acid (48% reagent), 4 parts by volume of distilled Water, 2 parts by volume of concentrated nitric acid, and 200 milligrams Cu(NO3)zto each 10 cc. of solution for a time period in the general range of between 1 and 2 minutes. 4
  • the method of claim 8 including, in addition, regulating the supplied current in the forward direction through the cut wafer and limiting the current value to the range between 200 and 800 milliamperes applied in pulses of between 1A; to 1 second in length.
  • the method of claim 9 including, in addition, the steps of connecting the formed device in series with a current limiting resistance and a secondary of a transformer of alternating electric currents controlling the peak current in the forward direction to the order of between 300 and 1000 milliamperes so that the voltage across the device and limiting resistance is of the order of between 7 and 60 volts and the limiting resistance is oi the order of 10 to 40 ohms and regulating the period of application of the alternating current to intervals varying between 1A; and 1 second in time duration.
  • the method of claim 4 including electrolyticall;7 etching one of said wafers as an anode in a solution in the proportions of approximately 1 gram stannyl chloride to 50 cc. water for about 11/2 minutes at about 21/2 volts.
  • the method of claim 4 including electrolytically etching one of said wafers as an anode in a solution in the proportions of approximately 5 parts concentrated nitric acid to 50 parts water by volume for about 11/2 minutes at about 1 to 2 volts.
  • An electrical device comprising a semiconductor, a counter electrode having substantially point contact with said semi-conductor and a second electrode having an area of contact with said semi-conductor which is large compared to that of the counter electrode, said semi-conductor consisting of germanium of the order of 99% purity in combination with at least one of the elements from the class consisting of copper and silver, said rectifier having a peak back voltage in the range in excess of 10 volts and approaching the order of 200 volts, the back resistance of said device being in the order of between 10,000 ohms to several megohms at about 5 volts and the forward current being in the range of between 5and 40 milliarnperes at one volt in the low resistance direction of current ow through the device.

Description

K.' LARKHoRovlTz ET A1. 2,588,253
ALLoYs AND RECTIFIERS MADE THEREOF March- 4, 1952 originai Filed July 15,' 1945 2 Sl-IEETS--ShEET Mardi 4, 1952 K. LARK-HoRovlTz E-r AL 2,588,253
ALLoys AND RECTIFIERS MADE THEREOF Original Filed Jllly 13, 1945 2 SHEETS--SHEET 2 Patented Mar. 4, 1952 UNITED STATES PATENT OFFICE Indiana Original application July 1-3, 1945, Serial Noi` 604,744. Divided and this application DecemberV 29, 1949, Serial No. 135,745
sultant materials are not alloys in the common meaning of the word. However, for purposes of the present disclosure, it is to be understood that the word alloy of germanium as used herein, means to include a union of two or more elements, one of which is germanium, and the other or others being metals, non-metals, or gases, and
the combination of which exhibits electrical properties such as are found in metals and semiconductors.
The known contact rectiers, i. e., rectiers comprising suitable metal electrodes,'and a semiconductor have at least one of the `following disadvantages:
1. Inability to withstand in continuous use voltages in the back or high resistance direction greater than about volts without permanent injury to the rectifier.
2. Inability to pass sufficient current in the forward direction for satisfactory operation of associated apparatus..
3. Low back resistance prohibiting use of the rectifier in high impedance circuits, that is, circuits over about 100,000 ohms.
` 4. Seriously decreased efficiency in rectifying at frequencies greater than about l to 5 megacycles.
5. Capacity too high to allow efficient operation at frequencies greater than about 5 megacycles. Y
Due to the aforesaid deficiencies/of these kio'wn contact rectiers, the art turned to widespread use of vacuum tube diodes for rectifying alternat ing currents. However, vacuum tube diodes, While overcoming certain of the aforementioned disadvantages of the known contact rectiers, in turn have the following disadvantages:
l`. Inter-electrode capacities which are seriously objectionable at high frequencies.
2. Low forward direction conductance.
3. Requirement of power for heating a cathode.
4. Require a large amount of spaceas com# `pared to a contact rectifier.
The germanium alloys of our present invention 13 claims. l C1. lis-366) megohinsi as measured at about 5 volts.
order approaching 200 volts.
2. Low forward resistances, for example, 30 to 100 ohms at one volt.
3.- High back resistances, at about 4 volts ranging from about 10,000l ohms to several megohms.
4. May be used with frequencies up to megacycles and will still rectify at 3,000 megacycles.
5. Provide rectifiers of low capacity of about 0.5 micro micro farads` 6; Less than 50%' decrease in peak back voltage when ambient temperature increases from 23 C. to C.
7 Do not require power for heating a cathode; and
8. Do not require more space than about that needed for a common one-half watt carbon resistor.`
The germanium alloys herein disclosed are all of the class of N-ty'pe semi-conductors, i. e., semiconductors which when made into contact type rectiers present a high resistance to current flow `across the rectifying contact when the semiconductor is positive and the contacting metal electrode or Whisker is negative, andy a lower resistance when the potential is reversed.
rI-he various germanium alloys of our invention will be described and compared according to the properties they exhibit when made into contact type rectiiiers. Specific electrical properties here'- after referred to4 are:`
Peak back voZtage.-The voltage-current characteristics measured on rectifiers using the alloys of our invention show a voltage peak in 'the back or high resistance direction. This peak generally occurs within a range greater than 10 volts and approaching the order of 200 volts. It will also appear that all of these rectifiers using alloys of our invention exhibit a negative resistance region in the back direction for currents exceeding the current at the peak back voltage.
Back resistance-In the back or high resistance direction these rectiers have resistances ranging from the order of 10,000 ohms to several High resistancesare substantially maintained nearly to the peak back! voltage.
Forwrd conductance-The currents passed at one volt in the forward o1' low resistance direc- Copper and silver of column I of the periodic table;
Magnesium, calcium, zinc, strontium, cadmium, or barium of column II of the periodic table; Titanium, tin, or lead, of column IV of the periodic table;
Nitrogen, vanadium, columbium, tantalum, or
bismuth of column V of the periodic table; Chromium or uranium of column VI of the periodic table. Cobalt, nickel, or palladium of column VIII of the periodic table.
N-type semi-conductors of germanium may also be formed by allowing small amounts of, for example, phosphorous, arsenic, or antimony with germanium, but in rectiers using such semiconductors it has found that excessive currents pass at voltages greater than about 3 to 10 volts in the back direction which permanently injure the rectifying contact. It will be understood therefore that our present invention only relates to semi-conductors of the N-type which exhibit `high back voltage characteristics in excess of at least volts, and does not concern all N-type semi-conductors consisting of an alloy of germanium, as for example, the group last referred to.
Other features and advantages of our invention will appear from the detail description.
Now, in order to acquaint those skilled'in the 'art with the manner of making alloys in accordance with our invention, and the utilization thereof as rectiers of electricity, we shall describe in connection with the accompanying drawings and Athe tables following hereafter certain of the processes used in making the alloys which lie within our invention.
In the drawings: Figure 1 shows the voltage-current characterfistic curves of several rectiflers using certain of the alloys of our invention, which curves are not to be taken as typical of given alloys but merely to represent the type of characteristic exhibited by such alloys in general.
kgeneral procedure to be described later. amount of the added element alloyed with Figure 2 is a graph illustrating the electrical characteristics of rectiiiers using different types of surfaces on one alloy of our invention.
Figure 3 is a sectional View of a rectier, the semi-conductor of which comprises an alloy of our present invention.
Each alloy represented by the curves of Figure 1 is designated by a code number. The latter part of each code denotes the amount in atomic percent of the particular element or elements added to germanium to produce that alloy. No atomic percentage figures for the addition of nitrogen to germanium are given since it is difcult to determine accurately the amount or number of nitrogen atoms alloyed with the germanium.
In the following Table I there are set forth minimum, average, and maximum values of peak back voltage and forward current obtained on rectifying contacts using certain germanium alloys which we have made in accordance with the The germanium is set forth for each melt in atomic percent, i. e., the proportionate number of atoms in percent of the elements added to the total number of the atoms of germanium and added elements present. For purposes of adequately setting forth and claiming our invention, these additions to germanium are to be understood as being included in the term group A used hereinafter. Substantially all melts in which the addition consisted of a single element made to date in accordance with our invention are contained in Table I. It will be observed from that table that a large number of melts with certain added elements were prepared and it will be understood that the results given are the average results of all of the melts in each instance. It is -to be understood, however, that the spread or range of values given in connection with each of the elements added to germanium might not be true for any particular melt of such addition agent. Characteristics for rectifying contacts on any given alloy will lie somewhere within the range given. Further, all points on any given alloy listed in Table I and Table I'I, referred to hereinafter, will not exhibit the same electrical characteristics. Points may be found on each of the alloys disclosed at which the peak back voltages, back resistances, or forward currents lie in the lower regions of the ranges given above for these values. Also on the same surface of each alloy other points of contact may usually be found with electrical characteristics which lie toward the upper limit of the ranges above set out. However, as will later be discussed in more detail, some of the alloys are of greater uniformity than others with respect to rectification characteristics.
TABLE I Additions to germanium [In atomic per cent] Forward Current at Y Peak glltsgotage one von D. C.'(Mi11i Addition and percentages amperes) Min. Ave. Max. Min. Ave. Max.
Ba: .40. .50 15 50 125 7 13 19 Bit 1.0. .20, 1.25, .70. .28, .20, .31, 2.0, 2.3, 2.3, .023, .20.
Cd: .90, .30 20 50 105 8 l2 16 Ca2 2.0. 1.35, .80, .50, .50, .28 80,
so, .80, so, .80--. I 25 75 15o 5 f25 TABLE If-Continued Additions to germanium-Continued Forward Current at Peak lglfts'g 01mg@ one vou D. o. (M1111- Addition and percentages amperes) Mn Ave. Max Min Ave. Max.
Cr: 15 25 5 `15 25 c5: --.1..- 201 30 35 1 101 15 20- cb: .20, .43, .0451-- -1. -15 25 40 5 15 40 `on: .50,2.o0;.42, .19, 54,. 15 40 75 1 5 40 l1 h:3.,. ,1. .0s,. 25 70 135 1 15` `25 iM :a.o,.3.0-
U 50 115 2` `1 0 e 20 1.25, .10, .5o1.0,41.0,1.0,1;0, 20 1 50 90 7 15 30 N2: solidified-111 N1 ati pressures nim. Hg. 20 80 160 7 l0 2,5 Pd: .50, .50- 30 e 65 110 5 1 5 `25 Y; 25 40 so 7 10 20 .40 o' 25 75 15o 2 15 30 Tr. 10 30 7o e 3 7 15 U: 09, .09A 2o 25 50 2 5 20 .v:1.0,.15. 1o i 25 05 10 25 40 z11`:.50,'.30 25 5o 100 5 12 l 20 ythe alloys set forth in this 'table arealso to be includedin the term group A above referred "to forpurp'oses of claiming our present invention. The peak back voltages andthe forward currents at one volt of rectiers made of these alloys are also set forth inthis'table.
TABLE II Melts of moreA than one addition to germanium In atomicper cent] Peak Bock Voltage. Fglgarou Oil/121%? Aadditions and (Volts) amprres);
Percentages 1 1 1 .Y 1
Min Ave Max. Min. Ave.1 Max.
,111,120 .20 1 25` 50 8 15 25 gcu, .70 Sn 25 40 150 15 20K1 `30 .210'11, 55 Sn 15 50' 30 1'5` 22 50 .21 011,1.98 Sn- 15 1 .40 65 `115y 30. 60 .30.011,30511 50 70 1 110 5 v 14 20 .'80 sr, .3o Sn- 50 70 100 5 15 35 .sc Ni, .50 Se. .551 75; V100 i 9 30 30 .50 Pd, .80 Sr. 35 65 90 s 15 1 25 :501111, .80 Sr... 35 50 95 5 12` 20 .50 Ni, .10 Si.-- 39 50 95 -8 15 1 25 .50 Ni, .30 Mg 50 75 12 20 40 .5oNi.30`Cu 451 75 10 l20 35 .50 Ni, .50 Sr. 40 50 9 12 14 .50 Ni, .50 Sr. 15 25 35 10 `15 20 .50Ni,1.00 Sr 69 1 `90 160 ,10. 15 f 25 1.00 09,1.00 Sr. l10 30 50 13 20` 25 .30 Mg, .5051..- 10` 30 45 10 20 40 11. Ni,.`.50,sr.- 30 65 100 7 10 1s 1. 20 100 165 5 13 19 1 15 90 100 6 10 i 15 1l `30 70 110 15 20 25 1, 151 50 90 1 1 9 19 1 75 140 2. 7. 9 15' 40 75 3 5 7 7o 100 1.75: s -15 24 Thegermaniumalloys of our invention may be prepared' inall cases exceptfcr the germanium- `nitrogen alloy, by melting pure germanium' with kthe desiredalloying element 'or combination of elements in either a high vacuum of the order of d10-51mm.. mercury fat about. 100.0 C. or in an atmosphere; of.' helium. Precautionf should be. taken to prevent the accidental introduction of unknown and perhaps detrimental impurities into the melt from sources such as the crucible or boat in which the ingredients are disposed for melting, the furnace itself, or lsome .material volatilized in the furnace. Alloying germanium with nitrogen may be` effected by melting the germanium in an atmosphere of nitrogen. which may be either puried nitrogen or nitrogen direct from a commercial cylinder. The ger- Vmanium is melted in nitrogen at pressures ranging from about 2 mm. to '760 mm. Hg at altemperature of 1000 to 1050 C. Good results appear to be independent of pressure and melts prepared within the above range of pressures were all satisfactory.
The germanium successfully used ffori-.bese alloys had purity approaching and electrical resistivity greater than about one ohm cm. The germanium which we have successfully alloyed with other elements to form the alloys listed in Tables I and II was prepared from GeOz obtained from the Eagle-'Eicher1 Lead Company of Joplin. Missouri. The oxide was reduced in an atmosphere of commercial hydrogen at temperatures of 650 to 700 C. over a period of three to four hours. The oxide reduced. in this manner leaves the germanium metal in the form of a gray-green powder which is then alloyed with another elementor elements in the described.
The aforesaid melts of germanium andl the added element or elements were held in the molten state long enough to allow mixing ofthe constituents, and. it1 has been found that about 5 to 15 minutes is sulcient for this purpose. Usually ingredients to form melts of. about ve to si-x grams each were used in proportions above setforth in detail. After the constituents had been allowed to mix, the. melts werel allowed to solidify and cool which was accomplished either by immediately removing heat or by controlled cooling apparatus. In. certain. cases the uniformity of the melt is affected by the manner in `which it. 1s cooled. These variations will'be discussed later.1
manner and proportions1 A specific melt in accordance with our invention was prepared as follows:
Pure GeOz was reduced in hydrogen at atmospheric pressure for about three hours at 650 to 7009 C. Six grams of pure germanium powder so obtained were then placed in a porcelain crucible together with small flakes of pure tin amounting to 25 milligrams or about 0.8 atomic percent of tin.
The Crucible and contents were then placed inside a graphite cylinder used as a heater in the high frequency field of an induction furnace, and lowered in a vertical quartz tube which was then evacuated and maintained at a pressure of about 10-5 mm. mercury. Power was then applied to the external coil of the induction furnace to melt the germanium and hold it molten for about minutes. The melt was then allowed to cool by merely turning off the power to the coil. the alloy, and were soldered with soft-solder to a suitable metal electrode to produce a very low resistance non-rectifying Contact with one face of the wafer. The exposed face was then ground with 600 mesh alumina andetched for 2 minutes with an etching solution consisting essentially of HNO3, HF, Cu(NOa)2 and water in proportions to be later described herein. These wafers were fthen assembled in suitable cartridges each provided with a conventional metal electrode or Whisker which was used to contact the alloy surface. Across the rectifying contact thus produced we obtain the electrical characteristics described above.
As mentioned in the above specic example, the surfaces of these alloys are usually ground flat and then etched in a manner to be described in detail. However, as hereinafter related, the etching of the alloy surfaces is not essential 'sincel for example, by breaking open a melt, 4points may be found which exhibit lthe aforementioned electrical rectifying characteristics. Such broken surfaces presentgeometrically irregular faces which introduce some difficulty in assembly of the rectiers. Thus, grinding the alloy surface flat and etching it appears to be the most feasible manner of producing the rectiers in the commercial practicing of our invention. Y
v From the above Table I itvwill be observed that the majority of experimental work conducted'in r the development of our invention has been with theY alloy lgermanium-tin. In connection with our experimental work with tin it has been found Athat above 0,1 atomic percent of tin content, the
amount of tin added is not critical. Germanium containing above about 0.1 percent tin usually shows tin separated out, both at internal grain boundaries and on the outer surfaces.. In some melts containing tin in excess of 0.1 atomic percent, ductile layers of this tin-rich'material were frequently observed, particularly in the lower regions of the melt. In this connection we wish to observe that in making the germanium-tin alloys it is desirable in producing the melt that the boat or crucible in which the elements are `contained be gradually removed from the hot .furnace region. This will produce more uniform Thereafter wafers were cut from .8 tin merely segregated. At 17 atomic percent addition of tin, the entire melt was interlaced with tin-rich veins which had metallic low re sistance ohmic conductivity.
With bismuth additions it is difficult to control the amount of bismuth actually remaining in the germanium during 'the Vmelting cycle. A considerable fraction of the bismuth volatilizes so that quantities added have little relation to the quantities actually remaining in the melt. However, the results indicated in Table Ifin .con-
' nection with bismuth were obtained by the 'adsuch as 600 mesh alumina (AlzOa).
dition of bismuth to the extent there indicated.
After the melts have. been made as above described they are suitable for use as rectiers of electricity by simply making contact with the surfaces of such alloys with suitable electrodes or whiskers. In most of our experimentalwork a 5 mil tungsten Whisker sharpenedelectrolytically with av tipdiameter of less than 0.'1 A. mil was used as one electrode or Whisker, the vother electrical contact usually being made by soldering the alloy to a suitable conductor. However, tests have shown that the peak back voltages of rectifiers made from the alloys of our invention are little affected by the metal of which the Whisker is made. Whiskers made of the following metals have been'tried and only very slight deviations were noted over a large number of points of contact with the alloys of our invention: Mn, Pt," Ta, Ni, Fe, Zn, Mo, W, Au, Cu. Ag, Zr, Pt-Ir, and Pt-Ru. It appears'therefore, that choice vof a Whisker material may be determined on the basis of requirements other than the peak back volta-ge on rectiers using the alloys. 'hesc electrodes or whiskers may have contact with the surfaces vof the alloys as formed upon solidication, or on surfacesexposed by breaking the melt.. As mentioned above, however, it is desirable to grind and etch the surface. Thus in one method of 'producing rectifiers using the alloys of. our invention, the melts, which usually were of pellet form 5 to 10 millimeters thick, may be cut into thin plates or slabs and a surface thereof ground with a suitable abrasive The abrasive used is not critical in that it has been found that other abrasives such as CrzOs, MgO, VazOs, SnOz, ZnO and 4-O paper are equally satisfactory. This may then be followed by a-further 4 parts by volume hydrofluoric acid (48%l reagent) 4 parts by volume distilled water 2 parts by volume concentrated nitric acid,
'200 milligrams Cu(NO3)2 to each 10 cc. of solution.
Such a solution will satisfactorily etch the surface of the plates or slabs in about 1 to 2 minutes at room temperature `and may be applied with either a swab or by immersing the surface in the solution. This etching is not particularly critical but care should be taken not to unduly extend the etching since then a high polish is produced which may impair the performance of the alloy.
We have also found that other types of etclies may be used effectively on the germaniumalloys of our invention in additionto the etching above described. Modied etching solutions andpro cedures are as follows:
A solution consisting approximately of 1 gram stannyl chloride in 5G cc. of H2O may be used as an electrolytic bath for etching the alloy surfaces. Immersing the alloy as the anode in this soution will result in satisfactory etching within about 11/2 minutes at about 21/2 volts applied. An alternative modification of an electrolytic etching solution may comprise 5 parts concentrated HNO3 and 50 parts H2O by volume. Using the alloy as the anode for about 11/2 minutes at 1 to 2 volts will result in a satisfactory etch.
Reference may now be had to Figure 2 of the drawings illustrating the effect of etching of one of the alloys of our invention. The alloy selected to illustrate the effect of etching is identifed as melt 24 P-OU136-.25Sn. This melt as appears from the aforesaid designation consti-` tutes .25 atomic percent tin. The curve identified by reference numeral l illustrates the electrical characteristic of the germanium-tin alloy above identified in which the surface was ground with 600 A1203 but not etched. The curve indicated by the reference numeral 2 illustrates the electrical characteristics which were obtained on a freshly broken surface of an alloy of the above composition but which surface has not been etched. Curve member 3 illustrates the electrical characteristic of a surface ground with 600 A1203 and then etched in accordance with the manner first described.
The curve indicated by the reference numeral 4 illustrates electrical characteristics of another point on the alloy after etching as described in connection with curve 3, the curves 3 and 4 representing the best and poorest performances, re spectively, of the` particular germanium-tin alloy above identified, after etching. It is` to be observed that in this graph the voltage scale in the forward direction isA there expanded by a factor of l as compared to the voltage scale indicating the high back voltage characteristics of the alloys of our invention. As indicated, the currents are given in milliamperes.
It will be observed from an examination of Figure 2 that the electrical characteristics of a rectifier using a broken surface exhibit high back voltages and forward conductances within the range of values obtained when using a ground and etched surface. However, such broken surfaces are shiny and geometrically irregular so that the Whisker tends to skid which is undesirable in assembling permanent rectifier units. From VFigure 2 it is apparent that the high back voltage and high back resistance properties are inherent in the alloys and that the etching is. effective for restoring such properties after grinding. Further, we have discovered that natural surfaces formed when solidifying the alloys in vacuum will, if not contaminated or otherwise affected by grinding, give high back voltages and high back resistances when mounted and tested 1n air.
For certain applications of these rectiers; itis desirable that they have back resistances exceeding one megohm atV about 5 volts. Using the procedure described above will occasionally produce such high back resistances. However, we have found that a substantial and permanent increase in the back resistance can be effected. by applying power overloads across the contact, for short direct current. By gradually increasing the voltage applied, and hence the current passed by the contact during successive pulses, an. optimum value can be found to produce the maximum back resistance for a given contact. For direct current treatment in the forward direction such optimum current values range from about 200 to 800 milliamperes. For alternating power treatment the optimum values of forward peak current range from about 300 milliamperes to 1000 milliamperes. One can apply such alternating current treatment simply by connecting the rectifier in series with a current limiting resistance and the secondary of. a transformer. Depending upon the size of this current limiting resistance, values of 10 to 40 ohms have been used, voltage pulses ran-ging from 7 to 60 volts across the rectifier and resistance serve to yield the maximum increase in back resistance.
Table III shows the permanent effects of suchpower treatment upOn a few typical rectifiers using alloys of our invention and prepared as described. It will be seen from the table that the most signicant effect of the power treatment is the increase in the back resistance as measured at about 4.5 volts. This resistance is increased by factors ranging from about 10 to 50 times the values measured before treatment. Relatively minor increases of 10 to 20 percent are effected on the peak back voltage. Forward currents at one volt are in general decreased by amounts ranging from lO-to percent.
TABLE III Effects of power treatment [Values before power treatment are followed in brackets by values after power treatment] Forward Cur- Back Resist- Alloy used in PtBack rent at one ance at 4 Rectifier (o lgf volt (millivolts v0 s amperes) (megohms) 24L.5()SD 75 (105) 9 (4. 5) .02 (3) 24L-.50SI1-.. 100 (140) 11 (6. 5) .30 (4) 24P-.25SI1- 95 (115) 13 25 (2.5) VAZZWVLSH (95) 6 6) .15 (8) 1221Vs-1.SD. 8 (8) .05 8) 24 (10) ..04 (7.5)
20 (17) .48 (15) 40 (10) .20 (4) 10 (8) .20 (1) 15 (10.5) .13 (2) 18 (1U) .10 (4) 4 (4) .40 10 (6) .20 (3) 10 (6. 1) 40 (7. 5) l5 (10) .20 (3) 14 (8) .38 (2.5) 30 (I6) .81 (3.9) 16 (10) 1.0 (7. 5)
intervals oftime, each of. length about 1A to l second or longer.` The power treatment can be effected with the use of either valternating or It has been demonstrated above that the` high back voltage, high back resistance, and good forward conductance properties disclosed are inherent in the germanium alloys of our invention. Modifications of surface treatments or power treatments as described above will, however, vary the magnitude of these properties Within` certain general limits. For example, on a given alloy surface, variations in surface treatment and power treatment may be expected to vary the average peak back voltage by a factor of about.2, the average forward current by a factor of about 2, and the average back resistance by factors up to 50. It will be noted that the back resistance is the property most sensitive to variations in treatment, particularly to power treatment.
The following Table IV summarizes, on the basis of all melts made inv experimental `worlc vconducted under our invention, the approximate l1 figures 'f the minimum, average) and maximum values of peak back voltage and forward current at one volt which might be expected on the germanium alloys consisting of the addition `of a single element.
TABLE IV l l Forward Current at Peak Back Voltage one Volt (mmi (Vous) am eres) Alloy P1 Min Ave Max Min. Ave Max It Will appear from the above table that the ranges of values for the better alloys appear to be quite similar. Differences enter in the manner in Which the Values, within the ranges indicated, are concentrated.: For example, the nitrogen alloys can usually be expected to have '70 to 90 percent of back peak voltages over` 60 volts. Values on tin melts are more uniformly spread Within the range of the limits given above. For the tin melts approximately 50% of the points on the surfaces thereof will have voltages above 60 volts. It appears that the pure germanium alloyed with tin or melted in an atmosphere of nitrogen represents the most advantageous alloy. Following them, alloys of pure germanium with calcium, strontium or nickel appear to be in order. It is to be understood, however, that one skilled in the art working Within the range of the alloys herein disclosed Will readily be able to produce alloys having high back voltage andresistance characteristics and good forward conductances.
In Figure 3 ofthe drawings We have shown one type of `rectifier in which our invention may be embodied. In the form of the device there shown a Wafer 5 which may be of any of the germanium alloys above disclosed is mounted to have a low resistance non-reetifying contact With a metal electrode member 5. An electrode or Whisker l is connected at one end to an electrode supporting member 8 with the end of the Whisker in contact with the surface of the germanium alloy Wafer 5. The standard 9 provides for mounting of the members supporting the wafer 5 and electrode or Whisker l in insulated relation. The rectifier contemplated by our invention may be of various forms, the only critical constructional feature being that the germanium alloy Wafer comprising the semiconductor, and the Whisker for contacting the surface of the Wafer being arranged and supported so that one end of the Whisker engages the semi-conductor surface. It is understood that suitable leads areconnected to the wafer or semi-conductor and to the Whisker or metal electrode so that the device may have application in any desired circuit for use in the `recti' 1. An electrical device comprising a semi-conductor, a counter electrode having substantially point contact with said semi-conductor and a second electrode having an area of contact with said semi-conductor which is large compared to that of the counter electrode, said semi-conductor consisting of germanium of the order of 99% purity in combination With at least one ofv the elements from the group consisting of cop' per and silver, said device having a peak back voltage in the range in excess of l0 volts andV approaching the order of 200 volts.
2. An electrical device comprising an alloy formed of a mixture of germanium having a purity of the order of 99% and copper in an amount of between 0.19 and 2.0 atomic percent, and a pair of electrode elements in contact With said formed alloy, one of said electrode elements having substantially point contact with said alloy and the second of said electrodes having an area of contact which is large compared to that of the point contact electrode.
3. An electrical device comprising an alloy" formed of a mixture of germanium having a4 purity of the order of 99% and silver in an amount of between 0.5 and 0.66 atomic percent,"` and a pair of electrode elements in contact Withsaid formed alloy, one of said electrode elements having substantially point contact With said alloy and the second of said electrodes having an area of contact which is large compared to that:
of the point contact electrode. v
4. The method of making an electrical devicel which comprises mixing germanium having a purity of the order of 99% With atleast one of the elements from the classrconsistingA of copper and silver, applying heat to the mixture toreduce the mixture to ,a uid state, maintaining the heat for a time period sufficiently long to permit mixing of the selected constituents, re-
moving the heat to permit solidiiication of theV mixture, cutting from the ingot formed upon mass solidication wafers to Which contact elec--4 trodes may be applied, and applying contact electrodes to said wafers.
5. The method of claim 4 including the ad' ditional steps of grinding the severed wafers and then etching the ground surfaces to provide optimum contact points for said contactingelectrode members. 6. The method of claim 4 including, in addition, the step of etching a surface of a Wafer cut from the ingot before applying a contact electrode.
'7. The method of claim 4 including, in addition, the step of etching a surface of a Wafer cut from the ingot in a solution made up of approximately 4 parts by volume of hydrofluoric acid (48% reagent), 4 parts by volume of distilled Water, 2 parts by volume of concentrated nitric acid, and 200 milligrams Cu(NO3)zto each 10 cc. of solution for a time period in the general range of between 1 and 2 minutes. 4
8. The method of claim 4 includingfsecuring one of said electrodes to one surface of a cut Wafer, locating a second substantially point contact electrode upon a diiferent surface-of the cut Wafer and in substantially point contact therewith, and then applying electric power between the electrodes and the wafer.
9. The method of claim 8 including, in addition, regulating the supplied current in the forward direction through the cut wafer and limiting the current value to the range between 200 and 800 milliamperes applied in pulses of between 1A; to 1 second in length.
10. The method of claim 9 including, in addition, the steps of connecting the formed device in series with a current limiting resistance and a secondary of a transformer of alternating electric currents controlling the peak current in the forward direction to the order of between 300 and 1000 milliamperes so that the voltage across the device and limiting resistance is of the order of between 7 and 60 volts and the limiting resistance is oi the order of 10 to 40 ohms and regulating the period of application of the alternating current to intervals varying between 1A; and 1 second in time duration.
11. The method of claim 4 including electrolyticall;7 etching one of said wafers as an anode in a solution in the proportions of approximately 1 gram stannyl chloride to 50 cc. water for about 11/2 minutes at about 21/2 volts.
12. The method of claim 4 including electrolytically etching one of said wafers as an anode in a solution in the proportions of approximately 5 parts concentrated nitric acid to 50 parts water by volume for about 11/2 minutes at about 1 to 2 volts.
13. An electrical device comprising a semiconductor, a counter electrode having substantially point contact with said semi-conductor and a second electrode having an area of contact with said semi-conductor which is large compared to that of the counter electrode, said semi-conductor consisting of germanium of the order of 99% purity in combination with at least one of the elements from the class consisting of copper and silver, said rectifier having a peak back voltage in the range in excess of 10 volts and approaching the order of 200 volts, the back resistance of said device being in the order of between 10,000 ohms to several megohms at about 5 volts and the forward current being in the range of between 5and 40 milliarnperes at one volt in the low resistance direction of current ow through the device.
KARL LARK-T-IGROVITZ. RANDALL M. WI-IALEY.
Name Date Woodyard Nov. 14, 1950 OTHER REFERENCES Briggs et al., J. Phys. Chem., vol. 33 (1929), pages 1085-1095.
Torrey and Whitmer, Crystal Rectiers (1948) 1st ed., pages 364, 365, and B14-316.
Number

Claims (1)

1. AN ELECTRICAL DEVICE COMPRISING A SEMI-CONDUCTOR, A COUNTER ELECTRODE HAVING SUBSTANTIALLY POINT CONTACT WITH SAID SEMI-CONDUCTOR AND A SECOND ELECTRODE HAVING AN AREA OF CONTACT WITH SAID SEMI-CONDUCTOR WHICH IS LARGE COMPARED TO THAT OF THE COUNTER ELECTRODE, SAID SEMI-CONDUCTOR CONSISTING OF GERMANIUM OF THE ORDER OF 99% PURITY IN COMBINATION WITH AT LEAST ONE OF
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US2776920A (en) * 1952-11-05 1957-01-08 Gen Electric Germanium-zinc alloy semi-conductors
US3545967A (en) * 1966-09-28 1970-12-08 Aerojet General Co Metal-semiconductor alloys for thin-film resistors
US3930870A (en) * 1973-12-28 1976-01-06 International Business Machines Corporation Silicon polishing solution preparation

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US2615966A (en) 1952-10-28
FR941699A (en) 1949-01-18
US2801376A (en) 1957-07-30
BE466591A (en)
GB636248A (en) 1950-04-26
US2600997A (en) 1952-06-17
US2745046A (en) 1956-05-08
US2691577A (en) 1954-10-12
US2637770A (en) 1953-05-05

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