JPS6122444B2 - - Google Patents
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- Publication number
- JPS6122444B2 JPS6122444B2 JP15103179A JP15103179A JPS6122444B2 JP S6122444 B2 JPS6122444 B2 JP S6122444B2 JP 15103179 A JP15103179 A JP 15103179A JP 15103179 A JP15103179 A JP 15103179A JP S6122444 B2 JPS6122444 B2 JP S6122444B2
- Authority
- JP
- Japan
- Prior art keywords
- sputtering
- gas
- film
- carbide
- resistor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
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- 238000004544 sputter deposition Methods 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 15
- 239000000463 material Substances 0.000 claims description 14
- 238000004519 manufacturing process Methods 0.000 claims description 13
- 239000011261 inert gas Substances 0.000 claims description 10
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 9
- 239000001301 oxygen Substances 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 229910010271 silicon carbide Inorganic materials 0.000 claims description 6
- HBMJWWWQQXIZIP-UHFFFAOYSA-N silicon carbide Chemical compound [Si+]#[C-] HBMJWWWQQXIZIP-UHFFFAOYSA-N 0.000 claims description 4
- 229910052580 B4C Inorganic materials 0.000 claims 1
- INAHAJYZKVIDIZ-UHFFFAOYSA-N boron carbide Chemical compound B12B3B4C32B41 INAHAJYZKVIDIZ-UHFFFAOYSA-N 0.000 claims 1
- 239000007789 gas Substances 0.000 description 28
- 239000010408 film Substances 0.000 description 24
- 239000000758 substrate Substances 0.000 description 10
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- 229910052786 argon Inorganic materials 0.000 description 6
- 238000005546 reactive sputtering Methods 0.000 description 6
- 239000013077 target material Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 238000007796 conventional method Methods 0.000 description 4
- 239000013078 crystal Substances 0.000 description 4
- 229910004298 SiO 2 Inorganic materials 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 238000012916 structural analysis Methods 0.000 description 3
- 239000010409 thin film Substances 0.000 description 3
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000035939 shock Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000003990 capacitor Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 238000000151 deposition Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000001247 metal acetylides Chemical class 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000004065 semiconductor Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 238000005478 sputtering type Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000013076 target substance Substances 0.000 description 1
- 150000003568 thioethers Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Landscapes
- Apparatuses And Processes For Manufacturing Resistors (AREA)
Description
本発明はスパツタリングにより炭化物抵抗材料
を薄膜化してなる抵抗体の製造方法に関するもの
である。
従来よりこの種スパツタリングは、種々の物質
たとえば導電体物質、誘電体物質、半導体物質な
どを薄膜化して、抵抗,コンデンサなど電子部品
を製造する一方法として利用されていることは衆
知である。最も基本的な特性は、抵抗体材料(物
質)で決定され目的に応じた種々の物質がターゲ
ツト材に選ばれる。また抵抗体を形成するプロセ
スも膜質,抵抗値,付着量,比抵抗などの特性を
決定する重要な役割を持つている。スパツタリン
グで、スパツタガス圧、基板温度、高周波電力、
スパツタ時間およびガス雰囲気はスパツタ時の各
種パラメータ中最も重要である。スパツタリング
は、イオン化したガス分子が電界により加速され
ターゲツト電極に衝突することによりターゲツト
分子が放出される現像であり、使用されるガス雰
囲気は通常10-2〜10-3Torrのアルゴンガスであ
る。基板温度は良い密着性を得るために通常、適
当な温度に加熱保持される。基板表面の水や有機
物を除去するに要する温度(たとえば100℃以
上)、基板と膜の膨脹係数が近い温度範囲、さら
に膜質の粒子の成長度合にあつた温度、化合物の
分解のない温度などが考慮され選ばれる。高周波
電力は直接、単位時間当りの付着量に比列的に寄
与するので大きいにこしたことはないが、ある程
度以上になるとスパツタに寄与するイオンのエネ
ルギーは飽和するため通常1〜5KWである。ス
パツタ時間は、得ようとする膜厚に応じた範囲で
決定される。ガス雰囲気は通常、前述の高純度ア
ルゴンガスが用いられる。これはターゲツトに用
いる物質と同じ生成膜物質を得るため、不活性な
雰囲気を必要とするからである。通常このように
してスパツタ室壁面よりの蒸発ガス、残留ガスな
どをも極力抑制し、特に活性ガスなどは不純物質
として避けられてきた。
例えばスパツタリングで活性硅素の抵抗体を得
る場合、従来の方法ではターゲツト材に炭化硅素
の焼結体を用い、基板温度700℃、高周波電力
2.0KW、スパツタガス圧×10-5Torr、ガス雰囲
気99.9999%アルゴンガスでスパツタ時間7Hrsを
おこなつていた。これはサーミスタ特性(温度に
対して負の抵抗係数))を有した薄膜抵抗体を得
るための例であるが、この方法では比抵抗が大き
く、さらにサーミスタの基本特性、すなわち抵抗
値、B定数のコントロールも非常に困難であつ
た。また抵抗値の減少もスパツタ時間7Hrsあた
りから鈍化し、より小さい抵抗値を得ることは難
しかつた。さらに素子(図面参照)の形状は電極
間面積と膜の比抵抗との関係で決定されることか
ら、比抵抗の大きい場合、実用的抵抗値範囲(例
えば50℃の温度条件で1〜500KΩ)内で、小型
化した素子を得ることは難しかつた。同様に抵抗
器などへ用いる場合、従来の方法では抵抗値の小
さなものを得ようとすると、スパツタ時間が非常
に長くかかるという難点があつた。このため材
料、エネルギーなどを多く費やすのでコストが高
くつくという欠点を誘発していた。
また従来法では、他方に反応性スパツタリン
グ、あるいは化学的スパツタリングと呼ばれる方
法がある。今まで述べてきたのは普通のスパツタ
リングで反応を抑制する目的であつたが、反応性
スパツタリングのさいの反応性ガスの効果を積極
的に利用して、反応性気体の雰囲気中でスパツタ
リングを行ない、酸化物、硫化物、炭化物などの
薄膜を生成する。これは反応を目的とした活性ガ
スが用いられるが、多くの場合に不活性ガスをも
混合しておこなわれる。
例えば特に大きな面積のターゲツトを必要とす
る場合、バルクと同じものを得るのが困難な物質
たとえば金属酸化物は、金属ターゲツトを酸素分
圧の存在下で反応性スパツタしてつくられる。
Ta2O5生成膜を得る場合、Taターゲツトを用
い(Ar+O2)のガス雰囲気でスパツタリングされ
る。他にはMnO2生成膜(MnターゲツトinAr+
O2)、SiN4生成膜(Si inAr+N2)、SiO生成膜
(Si inAr+O2)などがある。
このようにターゲツト物質と異なつた組成を有
す生成膜を得る場合は、反応を目的とした活性ガ
スが使用される。
しかし反応性スパツタ法では、スパツタ後の生
成膜に酸化膜あるいは窒化膜などを生生成せしめ
るもので通常のスパツタ法とは異なる。
例えば上述のSiO2生成膜の場合、Siターゲツト
で酸素をアルゴンに対し60〜100vo%近く混合
しスパツタリングすることによつて形成され、そ
の体積抵抗率は1014Ω―cm以上であり、バルク
SiO2に近い値を有している。
つまり後述する本発明の方法は、ターゲツト材
料と同組成の生成膜を得るもので、反応性スパツ
タ法と異なり、通常のスパツタ法に属するもので
ある。すなわち炭化硅素ターゲツトを用いた場
合、本発明で得た生成膜は、反射電子線回析、X
―線回析でB―SiCの等軸結晶構造を確認した。
さらに、この生成膜の比抵抗は10KΩ―cm以下
のオーダーであり、構造解析などの点からも
SiO2の存在はなく反応を抑制した普通のスパツ
タ法であることは明白である。
以上述べたように、反応性スパツタ法以外の普
通のスパツタ法に属す炭化物抵抗材料のスパツタ
リングで微量の活性ガスを使用したという報告は
ない。
本発明は不活性ガス中に微量の空気もしくは酸
素を添加して、炭化物抵抗材料をスパツタリング
することを特徴とした炭化物膜抵抗体の製造方法
である。
すなわち本発明は、上述のように新規な炭化物
膜抵抗体の製造方法で、前述の如き従来欠点を解
消する製造方法を提供するものである。
以下、本発明の実施例について詳細に説明す
る。
実施例 1
素子の構成は図―1からなり、抵抗体を形成す
る電気絶縁性基板には、純度96%アルミナ基板1t
=O.65mmを用いた。次に抵抗体が形成される面
には電極2に導電性のAu―Ptペーストのパター
ンが形成されている。この電極パターンは幾何的
に構成される幅O.25mmの2本の電極と、その間
に相対向する同形の1本の電極が構成され、隣接
する距離はO.45mmで各々電極間の面積は1.35mm2か
らなる。このようにして構成された面上に抵抗3
の形成をおこなう。
次に上記基板をテストピースとして以下のスパ
ツタの実験に使用した。
装置は2極スパツタ装置(スパツタ真空室:
350φ×250hm/m)を使用し、スパツタの設定条
件は高周波電力2.0KW、スパツタ時間7.OHrs、
基板温度700℃、スパツタ圧は×10-2Torrに固定
した。
スパツタ真空は予め×10-6Torrまで真空排気
がおこなわれ、次に不活性ガス中の空気もしくは
酸素が>0〜10Vo%の範囲内で×10-4Torrま
で不活性ガスが一定量導入される。
抵抗体材料には炭化硅素を選びターゲツトにそ
の焼結体を使用した。不活性ガスは99.9999%Ar
ガス、空気は混合比を変えて一定量導入し、圧力
×10-2Torrでスパツタをおこなつた。この結果
を表―1(抵抗値は全て25℃の温度条件下で測定
した)のNo.2〜8に示す。No.1は従来の方法で
Arガスだけの雰囲気でおこなつたものである。
またNo.2〜8と同じ方法で純度99.999%の酸素
をNo.5と同じ混合比でスパツタをおこなつたのが
No.9である。さらに不活性ガスを純度99.99%Xe
ガスとし活性ガスを空気としてNo.5と同じ方法で
スパツタをおこなつたのがNo.10である。
これより明らかなようにAr,Xe不活性ガス中
へ微量の空気乃び酸素を添加することにより、抵
抗値が非常に小さく得られることが判る。
次に表―1のNo.1〜10のサンプルについて高温
放置試験350℃中.1000Hrs放置、耐熱衝撃性試
験RT、15分〜350℃.15分サイクルを3000サイク
ルおこなつた後、抵抗変化率は両者とも±6%以
内で表―1のNo.1と全く変わりなかつた。
また、No.2〜No.10の抵抗体膜は構造解析の結果
B―SiCでNo.1と同じ結晶構造であつた。膜厚も
No.1〜No.10では7μm±7%の範囲内で殆んど差
はなかつた。
The present invention relates to a method for manufacturing a resistor made by thinning a carbide resistive material by sputtering. It is well known that this type of sputtering has been used as a method for manufacturing electronic components such as resistors and capacitors by forming thin films of various materials such as conductive materials, dielectric materials, and semiconductor materials. The most basic characteristics are determined by the resistor material (substance), and various materials are selected as the target material depending on the purpose. The process of forming a resistor also plays an important role in determining characteristics such as film quality, resistance value, amount of adhesion, and specific resistance. In sputtering, sputtering gas pressure, substrate temperature, high frequency power,
Sputtering time and gas atmosphere are the most important among the various parameters during sputtering. Sputtering is a development in which ionized gas molecules are accelerated by an electric field and collide with a target electrode to release target molecules, and the gas atmosphere used is usually argon gas at 10 -2 to 10 -3 Torr. The substrate temperature is usually maintained at an appropriate temperature in order to obtain good adhesion. The temperature required to remove water and organic matter from the substrate surface (for example, 100℃ or higher), the temperature range where the expansion coefficients of the substrate and film are similar, the temperature that is suitable for the growth rate of film-like particles, and the temperature that does not decompose the compound, etc. considered and selected. The high frequency power directly and proportionally contributes to the amount of deposition per unit time, so it is not a big deal, but once it reaches a certain point, the energy of the ions that contribute to spatter becomes saturated, so it is usually 1 to 5 KW. The sputtering time is determined within a range depending on the desired film thickness. The above-mentioned high-purity argon gas is usually used as the gas atmosphere. This is because an inert atmosphere is required to obtain the same produced film material as the target material. Usually, in this way, evaporative gases and residual gases from the sputtering chamber walls are suppressed as much as possible, and in particular, active gases are avoided as impurities. For example, when obtaining an active silicon resistor by sputtering, the conventional method uses a sintered body of silicon carbide as the target material, a substrate temperature of 700°C, and high-frequency power.
The sputtering time was 7 hours at 2.0KW, sputtering gas pressure x 10 -5 Torr, and a gas atmosphere of 99.9999% argon gas. This is an example of obtaining a thin film resistor with thermistor characteristics (negative resistance coefficient with respect to temperature). It was also very difficult to control. Furthermore, the decrease in resistance value slowed down from around 7 hours of sputtering time, and it was difficult to obtain a smaller resistance value. Furthermore, since the shape of the element (see drawing) is determined by the relationship between the area between the electrodes and the specific resistance of the film, if the specific resistance is large, the practical resistance value range (for example, 1 to 500KΩ at a temperature of 50℃) However, it has been difficult to obtain miniaturized devices. Similarly, when used in resistors and the like, conventional methods have the disadvantage that sputtering takes a very long time when attempting to obtain a product with a small resistance value. For this reason, a large amount of materials, energy, etc. are used, leading to the disadvantage of high costs. Another conventional method is called reactive sputtering or chemical sputtering. The purpose of what has been described so far has been to suppress the reaction with ordinary sputtering, but the effect of reactive gas during reactive sputtering is actively utilized to perform sputtering in an atmosphere of reactive gas. , produce thin films of oxides, sulfides, carbides, etc. Although an active gas is used for the purpose of the reaction, in many cases an inert gas is also mixed. For example, when particularly large area targets are required, materials that are difficult to obtain in bulk, such as metal oxides, are produced by reactive sputtering of metal targets in the presence of partial pressures of oxygen. When obtaining a Ta 2 O 5 film, sputtering is performed using a Ta target in an (Ar+O 2 ) gas atmosphere. In addition, MnO 2 production film (Mn target inAr +
O 2 ), SiN 4 production film (Si inAr+N 2 ), SiO production film (Si inAr+O 2 ), etc. In order to obtain a produced film having a composition different from that of the target substance in this way, an active gas for the purpose of reaction is used. However, the reactive sputtering method is different from the normal sputtering method in that it produces an oxide film or a nitride film on the film produced after sputtering. For example, in the case of the above-mentioned SiO 2 production film, it is formed by sputtering a mixture of oxygen and argon at a ratio of 60 to 100 vol% using a Si target, and its volume resistivity is 10 14 Ω-cm or more.
It has a value close to SiO 2 . In other words, the method of the present invention, which will be described later, obtains a film having the same composition as the target material, and is different from the reactive sputtering method and belongs to the ordinary sputtering method. That is, when a silicon carbide target is used, the film obtained by the present invention can be measured by reflection electron beam diffraction,
-The equiaxed crystal structure of B-SiC was confirmed by line diffraction. Furthermore, the specific resistance of this produced film is on the order of 10KΩ-cm or less, which is also useful from the point of view of structural analysis.
It is clear that this is a normal sputtering method in which SiO 2 is not present and the reaction is suppressed. As mentioned above, there is no report on the use of a trace amount of active gas in sputtering a carbide resistance material that belongs to an ordinary sputtering method other than the reactive sputtering method. The present invention is a method for manufacturing a carbide film resistor, characterized by sputtering a carbide resistor material by adding a small amount of air or oxygen to an inert gas. That is, the present invention is a novel method for manufacturing a carbide film resistor as described above, and provides a manufacturing method that eliminates the conventional drawbacks as described above. Examples of the present invention will be described in detail below. Example 1 The device configuration is shown in Figure 1. The electrically insulating substrate forming the resistor is a 1 ton alumina substrate with a purity of 96%.
=O.65mm was used. Next, a pattern of conductive Au--Pt paste is formed on the electrode 2 on the surface where the resistor is to be formed. This electrode pattern consists of two geometrically constructed electrodes with a width of 0.25 mm, and one electrode of the same shape facing each other between them.The distance between adjacent electrodes is 0.45 mm, and the area between each electrode is Consists of 1.35mm2 . A resistor 3 is placed on the surface configured in this way.
formation. Next, the above substrate was used as a test piece in the following sputtering experiment. The device is a two-pole sputtering device (sputtering vacuum chamber:
350φ
The substrate temperature was fixed at 700°C and the sputtering pressure was fixed at ×10 -2 Torr. The spatsuta vacuum is preliminarily evacuated to ×10 -6 Torr, and then a constant amount of inert gas is introduced to ×10 -4 Torr with air or oxygen in the inert gas in the range of >0 to 10 Vo%. Ru. Silicon carbide was selected as the resistor material, and its sintered body was used as the target. Inert gas is 99.9999% Ar
A fixed amount of gas and air was introduced at different mixing ratios, and sputtering was performed at a pressure of ×10 -2 Torr. The results are shown in Nos. 2 to 8 of Table 1 (all resistance values were measured under a temperature condition of 25°C). No.1 is the conventional method
This was done in an atmosphere containing only Ar gas. Also, using the same method as Nos. 2 to 8, sputtering was performed with 99.999% pure oxygen at the same mixing ratio as No. 5.
It is No.9. Furthermore, the inert gas is 99.99% pure Xe
In No. 10, sputtering was performed in the same manner as in No. 5, using air as the active gas. As is clear from this, a very small resistance value can be obtained by adding a small amount of air or oxygen to the Ar or Xe inert gas. Next, samples Nos. 1 to 10 in Table 1 were subjected to a high temperature storage test at 350℃. Leave for 1000 hours, thermal shock resistance test RT, 15 minutes ~ 350℃. After 3,000 15-minute cycles, the resistance change rate was within ±6% for both, which was no different from No. 1 in Table 1. Further, as a result of structural analysis, the resistor films No. 2 to No. 10 were found to be B-SiC with the same crystal structure as No. 1. Film thickness too
No. 1 to No. 10 had almost no difference within the range of 7 μm±7%.
【表】【table】
【表】
実施例 2
ターゲツト材料にB4Cを選び、実施例1と同じ
方法でスパツタをおこなつた。ガス雰囲気も純度
99.9999%ArガスとしたのがNo.11Arガスをベース
に空気をNo.5と同じ割合で添加したのがNo.12,同
じく空気を純度99.999%酸素に置き換えたのがNo.
13である。さらにArガスを純度99.99%Xeガスと
してNo.5と同じ割合で空気を添加したのがNo.14で
ある。
これより明らかなように、実施例1と同様に活
性ガスの添加により、抵抗値が小さく得られるこ
とが判る。
次に表のNo.11〜14のサンプルについて実施例1
と同様に高温放置.耐熱衝撃性試験をおこなつた
が、抵抗変化率は両試験とも±10%の範囲内で表
―1のNo.11と変わりはなかつた。
またNo.12〜14の抵抗体膜は構造分解析上、菱面
体結晶構造で、No.11と同じ結晶構造であつた。膜
厚もNo.11〜14では7μm±7%の範囲内で殆んど
差はなかつた。
以上の結果から判るように、炭化物系材料をス
パツタする方法において、不活性ガス中へ微量の
空気もしくは酸素を添加することで抵抗値を非常
に小さく得られることが判る。このことは同抵抗
特性のものを得る場合、素子を非常に小型化でき
るということを意味している。さらにはこの添加
量に対しスパツタ時間も短時間で抵抗調整などコ
ントロールが簡単におこなえるとともに、スパツ
タ時間、消耗部材に掛るコストは削減され安価な
ものを得ることが出来た。またサーミスタ特性を
得る場合のB定数も抵抗値と殆んど同様の傾向に
あり、空気もしくは酸素添加の大きな効果があつ
た。[Table] Example 2 B 4 C was selected as the target material and sputtering was performed in the same manner as in Example 1. Purity of gas atmosphere
No. 12 uses 99.9999% Ar gas as a base, No. 12 uses Ar gas as a base and adds air at the same ratio as No. 5, and No. 1 uses 99.999% pure oxygen instead of air.
It is 13. Furthermore, No. 14 is made by using Ar gas as 99.99% pure Xe gas and adding air in the same proportion as No. 5. As is clear from this, it can be seen that, as in Example 1, by adding the active gas, a small resistance value can be obtained. Next, Example 1 for samples No. 11 to 14 in the table
Similarly, leave it at high temperature. A thermal shock resistance test was conducted, and the resistance change rate was within ±10% in both tests, which was the same as No. 11 in Table 1. Moreover, the resistor films of Nos. 12 to 14 had a rhombohedral crystal structure according to structural analysis, which was the same crystal structure as No. 11. There was almost no difference in film thickness between Nos. 11 to 14 within the range of 7 μm±7%. As can be seen from the above results, in the method of sputtering carbide materials, it is possible to obtain a very low resistance value by adding a small amount of air or oxygen to the inert gas. This means that if the same resistance characteristics are obtained, the device can be made extremely compact. Furthermore, for this amount of addition, the sputtering time can be easily controlled such as resistance adjustment in a short time, and the sputtering time and the cost of consumable parts are reduced, making it possible to obtain an inexpensive product. Furthermore, the B constant when obtaining thermistor characteristics had almost the same tendency as the resistance value, indicating that the addition of air or oxygen had a large effect.
図は本発明の炭化物膜抵抗体の製造方法を用い
た素子の一実施例における斜視図である。
1…アルミナ基板、2…電極、3…抵抗体形成
部。
The figure is a perspective view of an embodiment of a device using the method for manufacturing a carbide film resistor of the present invention. DESCRIPTION OF SYMBOLS 1... Alumina substrate, 2... Electrode, 3... Resistor formation part.
Claims (1)
は酸素を添加して、炭化物抵抗材料をスパツタリ
ングすることを特徴とする炭化物膜抵抗体の製造
方法。 2 炭化物抵抗材料は炭化硅素、炭化硼素である
ことを特徴とする特許請求の範囲第1項記載の炭
化物膜抵抗体の製造方法。 3 空気もしくは酸素の量は、不活性ガスに対し
て少なくとも0〜10Vo%の範囲であることを
特徴とする特許請求の範囲第2項記載の炭化物膜
抵抗体の製造方法。[Claims] 1. A method for manufacturing a carbide film resistor, which comprises sputtering a carbide resistor material by adding a small amount of air or oxygen to at least an inert gas. 2. The method for manufacturing a carbide film resistor according to claim 1, wherein the carbide resistance material is silicon carbide or boron carbide. 3. The method for manufacturing a carbide film resistor according to claim 2, wherein the amount of air or oxygen is at least in the range of 0 to 10 Vo% based on the inert gas.
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15103179A JPS5673407A (en) | 1979-11-20 | 1979-11-20 | Method of manufacturing carbide film resistor |
| AU63093/80A AU524439B2 (en) | 1979-10-11 | 1980-10-09 | Sputtered thin film thermistor |
| GB8032616A GB2061002B (en) | 1979-10-11 | 1980-10-09 | Method for making a carbide thin film thermistor |
| US06/196,011 US4359372A (en) | 1979-10-11 | 1980-10-10 | Method for making a carbide thin film thermistor |
| CA000362125A CA1143865A (en) | 1979-10-11 | 1980-10-10 | Method for making a carbide thin film thermistor |
| DE3038375A DE3038375C2 (en) | 1979-10-11 | 1980-10-10 | Method of manufacturing an NTC thermistor with carbide resistor thin films |
| FR8022342A FR2467472A1 (en) | 1979-10-11 | 1980-10-13 | PROCESS FOR PRODUCING CARBIDE THIN FILM THERMISTOR |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15103179A JPS5673407A (en) | 1979-11-20 | 1979-11-20 | Method of manufacturing carbide film resistor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5673407A JPS5673407A (en) | 1981-06-18 |
| JPS6122444B2 true JPS6122444B2 (en) | 1986-05-31 |
Family
ID=15509781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15103179A Granted JPS5673407A (en) | 1979-10-11 | 1979-11-20 | Method of manufacturing carbide film resistor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5673407A (en) |
-
1979
- 1979-11-20 JP JP15103179A patent/JPS5673407A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5673407A (en) | 1981-06-18 |
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