JPS6341861B2 - - Google Patents
Info
- Publication number
- JPS6341861B2 JPS6341861B2 JP16602683A JP16602683A JPS6341861B2 JP S6341861 B2 JPS6341861 B2 JP S6341861B2 JP 16602683 A JP16602683 A JP 16602683A JP 16602683 A JP16602683 A JP 16602683A JP S6341861 B2 JPS6341861 B2 JP S6341861B2
- Authority
- JP
- Japan
- Prior art keywords
- glass
- semiconductor
- coating
- present
- powder
- 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
Links
- 239000011521 glass Substances 0.000 claims description 31
- 239000004065 semiconductor Substances 0.000 claims description 21
- 239000011248 coating agent Substances 0.000 claims description 17
- 238000000576 coating method Methods 0.000 claims description 17
- 239000000843 powder Substances 0.000 claims description 11
- 229910052844 willemite Inorganic materials 0.000 claims description 5
- 229910004298 SiO 2 Inorganic materials 0.000 claims description 3
- 238000007789 sealing Methods 0.000 description 7
- 230000015556 catabolic process Effects 0.000 description 6
- 229910052710 silicon Inorganic materials 0.000 description 6
- 239000010703 silicon Substances 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 230000000903 blocking effect Effects 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- 229910015902 Bi 2 O 3 Inorganic materials 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910007472 ZnO—B2O3—SiO2 Inorganic materials 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 239000005394 sealing glass Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C03—GLASS; MINERAL OR SLAG WOOL
- C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
- C03C8/00—Enamels; Glazes; Fusion seal compositions being frit compositions having non-frit additions
- C03C8/24—Fusion seal compositions being frit compositions having non-frit additions, i.e. for use as seals between dissimilar materials, e.g. glass and metal; Glass solders
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Glass Compositions (AREA)
- Structures Or Materials For Encapsulating Or Coating Semiconductor Devices Or Solid State Devices (AREA)
- Formation Of Insulating Films (AREA)
Description
本発明は、半導体被覆用ガラス、特に電極を含
めてP―N接合部を有するシリコンダイオード等
の半導体素子全体を厚いガラス層で被覆する。所
謂モールド型半導体を製造するために好適な封着
用ガラス組成物に関する。
半導体被覆用ガラスに要求される特性として
は、封着後のガラスの熱膨張係数が半導体素子の
シリコン及び電極材料であるモリブデンまたはタ
ングステンの金属に整合すること、高温ではシリ
コン等の半導体素子の特性が劣化する恐れがある
ため封着温度が750℃以下であること、封置後の
半導体の電気的特性が優れ信頼性が高いこと等が
ある。
本発明の目的は、上記半導体被覆用ガラスに要
求される諸特性中、封着後の半導体の電気的特
性、具体的には高い逆耐電圧を有し、且つ逆方向
洩れ電流の極めて小さい、所謂ハードブレークダ
ウン(hard breakdown)の波形を示し、しかも
ブロツキング特性に優れた半導体被覆用ガラスを
提供することである。尚、ハードブレークダウン
に対して逆耐電圧が低く、逆方向洩れ電流の大き
い場合には、所謂ソフトブレークダウン(soft
breakdown)の波形を示し、半導体の信頼性に
欠けることになる。
本発明者は、ZnO―B2O3―SiO2―PbO系のガ
ラス粉末にウイレマイト粉末を粉末を所定量添加
することにより、前記目的に合致する半導体被覆
用ガラスが得られることを見出した。
本発明の被覆用ガラスは、主成分の割合が重量
%で、ZnO45〜75、B2O315〜35、SiO22〜20、
PbO0.5〜10からなるガラス粉末に、ウイレマイ
ト粉末を0.01〜20.0重量%添加してなる組成物で
ある。
本発明の被覆用ガラスにおいて、ガラス粉末の
各成分の範囲を上記のように限定したのは次のと
おりである。
ZnOが45%以下のときは熱膨張係数が大きくな
り過ぎ、75%以上になるとガラスが失透し易くな
る。
B2O3が15%以下になるとガラスが失透し易く
なり、35%以上になると均質なガラスが得られな
くなると共に、熱膨張係数が大きくなり過ぎる。
SiO2が2%以下になるとガラスが失透し易く
なり、15%以上になると均質なガラスが得にくく
なる。
PbOが0.5%以下になるとガラスの流動性が悪
くなり、充分な封着が得られず、が10%以上にな
ると熱膨張係数が大きくなり過ぎる。このガラス
粉末には、上記成分以外に、CeO2、Sb2O3、
Al2O3、Nb2O5、Bi2O3等を少量含有してもよい。
本発明の半導体被覆用ガラスは、上記説明のガ
ラス粉末に対して無機耐火物の添加剤、所謂「フ
イラー」として、ウイレマイト(2ZnO・SiO2)
粉末を重量比で0.01〜20.0%混合して成る。この
フイラーの添加によりガラスが結晶化し、初期の
半導体の表面電荷密度(初期NFB)を適当な値
に変化させると同時に、ガラス中の可動イオンを
不動化させることができる。これにより逆耐電圧
が高く逆方向洩れ電流の極めて小さい半導体装置
を得られる。このウイレマイト粉末のフイラーは
0.01%以上の含有で前記効果が発揮されるが、20
%以上含有するときは結晶化が促進されすぎて流
動性が低下し、半導体素子に対する塗れが悪くな
り気密封着が得られがたくなる。
下表は、本発明の半導体被覆用ガラスに係る実
施例の試料で、下段にはその熱膨張係数及び被覆
封着温度を示す。
The present invention covers glass for semiconductor coating, and in particular covers the entire semiconductor device, such as a silicon diode having a PN junction, including electrodes, with a thick glass layer. The present invention relates to a sealing glass composition suitable for producing a so-called molded semiconductor. The properties required of glass for semiconductor coating include that the coefficient of thermal expansion of the glass after sealing matches the silicon of the semiconductor element and the metal of molybdenum or tungsten that is the electrode material, and that the characteristics of semiconductor elements such as silicon at high temperatures are required. The sealing temperature must be 750°C or lower to avoid the risk of deterioration, and the semiconductor after sealing must have excellent electrical characteristics and high reliability. The object of the present invention is to have the electrical properties of the semiconductor after sealing among the various properties required of the glass for semiconductor coating, specifically, to have high reverse withstand voltage and extremely low reverse leakage current. It is an object of the present invention to provide a glass for semiconductor coating that exhibits a so-called hard breakdown waveform and has excellent blocking characteristics. In addition, when the reverse withstand voltage is lower than hard breakdown and the reverse leakage current is large, so-called soft breakdown occurs.
breakdown), resulting in a lack of semiconductor reliability. The present inventors have discovered that by adding a predetermined amount of willemite powder to a ZnO--B 2 O 3 --SiO 2 --PbO-based glass powder, a glass for semiconductor coating that meets the above objective can be obtained. The coating glass of the present invention has the main components in weight% of ZnO45 to 75, B2O3 15 to 35, SiO2 2 to 20,
This composition is made by adding 0.01 to 20.0% by weight of willemite powder to glass powder consisting of 0.5 to 10 PbO. In the coating glass of the present invention, the range of each component of the glass powder is limited as described above. When ZnO is less than 45%, the thermal expansion coefficient becomes too large, and when it is more than 75%, the glass tends to devitrify. When B 2 O 3 is less than 15%, the glass tends to devitrify, and when it is more than 35%, homogeneous glass cannot be obtained and the coefficient of thermal expansion becomes too large. When SiO 2 is less than 2%, the glass tends to devitrify, and when it is more than 15%, it becomes difficult to obtain a homogeneous glass. When PbO is less than 0.5%, the fluidity of the glass deteriorates and sufficient sealing cannot be obtained, and when PbO is more than 10%, the coefficient of thermal expansion becomes too large. In addition to the above components, this glass powder also contains CeO 2 , Sb 2 O 3 ,
It may contain a small amount of Al 2 O 3 , Nb 2 O 5 , Bi 2 O 3 or the like. The glass for semiconductor coating of the present invention contains willemite (2ZnO.SiO 2 ) as an inorganic refractory additive, a so-called "filler", to the glass powder described above.
It is made by mixing powders in a weight ratio of 0.01 to 20.0%. The addition of this filler causes the glass to crystallize, changing the initial semiconductor surface charge density (initial NFB) to an appropriate value, and at the same time making it possible to immobilize mobile ions in the glass. This makes it possible to obtain a semiconductor device with high reverse withstand voltage and extremely low reverse leakage current. This willemite powder filler is
The above effect is exhibited when the content is 0.01% or more, but 20
When the content exceeds %, crystallization is promoted too much, fluidity is reduced, the coating on the semiconductor element becomes poor, and it becomes difficult to obtain airtight sealing. The table below shows samples of Examples of the glass for semiconductor coating of the present invention, and the lower row shows the thermal expansion coefficient and coating sealing temperature.
【表】
半導体の初期特性としての逆耐電圧、逆洩れ電
流の特性評価は、シリコンダイオードのP―N接
合面に上表に掲げた本発明の被覆用ガラスを塗布
した後、乾燥させ、次いで封着した試料について
行つた。カーブトレーサーにて逆方向の波形を確
認したところ、本発明のガラスで被覆した前記ダ
イオード試料は、洩れ電流が1μA以下で、且つ
1700〜2000Vの設計耐圧に近い高電圧でハードブ
レークダウンの波形を示すものであつた。
半導体のブロツキング特性は、MOS構造体を
有するダイオードを作製し、これにBT処理を行
うことにより、高温バイアス下における電気的な
安定性を調べる方法により確認され得るが、本発
明者は、この方法により上表に掲げた本発明の被
覆用ガラス試料のブロツキング特性を評価した。
即ち、n型シリコン上に本発明の被覆用ガラス
を約5μの厚さに封着し、その上にアルミニユウ
ム電極を蒸着してMOS(metal―oxide―silicon)
構造体のダイオードを作製し、これにBT処理、
即ち200℃で400Vの電圧を2時間、アルミニウム
電極を+側として、且つまたは−側として夫々印
加する処理を行つた後、該MOS構造体の表面電
荷密度(NFB)の変化量、所謂△NFBを測定し
たところ0〜4×1011/cm2であつた。この結果
は、本発明の被覆用ガラスを用いた半導体が優れ
たブロツキング特性を有することを示ものであ
る。[Table] Characteristic evaluation of reverse withstand voltage and reverse leakage current as initial characteristics of semiconductors was performed by coating the coating glass of the present invention listed in the above table on the PN junction surface of a silicon diode, drying it, and then The tests were carried out on sealed samples. When the waveform in the opposite direction was confirmed using a curve tracer, it was found that the diode sample coated with the glass of the present invention had a leakage current of 1 μA or less, and
The waveform showed a hard breakdown at a high voltage close to the design breakdown voltage of 1700 to 2000V. The blocking characteristics of semiconductors can be confirmed by fabricating a diode with a MOS structure and performing BT processing on it to examine its electrical stability under high temperature bias. The blocking properties of the coating glass samples of the present invention listed in the above table were evaluated. That is, the coating glass of the present invention is sealed to a thickness of about 5μ on n-type silicon, and an aluminum electrode is deposited on it to form a MOS (metal-oxide-silicon).
Fabricate a diode structure, apply BT treatment to it,
That is, after applying a voltage of 400V at 200°C for 2 hours with the aluminum electrode on the + side and the aluminum electrode on the - side, the amount of change in the surface charge density (NFB) of the MOS structure, so-called △NFB When measured, it was 0 to 4×10 11 /cm 2 . This result shows that the semiconductor using the coating glass of the present invention has excellent blocking properties.
Claims (1)
35、SiO22〜20、PbO0.5〜10からなるガラス粉末
に、ウイレマイト粉末を0.01〜20.0重量%添加し
てなる半導体被覆用ガラス。1 The main components are ZnO45~75, B2O313 ~
35. Glass for semiconductor coating made by adding 0.01 to 20.0% by weight of willemite powder to glass powder consisting of 2 to 20 SiO 2 and 0.5 to 10 PbO.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16602683A JPS6060944A (en) | 1983-09-08 | 1983-09-08 | Glass for coating semiconductor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP16602683A JPS6060944A (en) | 1983-09-08 | 1983-09-08 | Glass for coating semiconductor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6060944A JPS6060944A (en) | 1985-04-08 |
| JPS6341861B2 true JPS6341861B2 (en) | 1988-08-19 |
Family
ID=15823556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP16602683A Granted JPS6060944A (en) | 1983-09-08 | 1983-09-08 | Glass for coating semiconductor |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6060944A (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0337412B1 (en) * | 1988-04-15 | 1995-07-05 | E.I. Du Pont De Nemours And Company | Encapsulant composition |
| KR101169049B1 (en) * | 2005-06-30 | 2012-07-26 | 엘지디스플레이 주식회사 | Thin film transistor device for liquid crystal display and method for fabricating the same |
| CN110642519B (en) * | 2019-09-25 | 2022-06-14 | 湖南利德电子浆料股份有限公司 | Encapsulation slurry for aluminum nitride substrate and preparation method and application thereof |
| JPWO2024253095A1 (en) * | 2023-06-08 | 2024-12-12 |
-
1983
- 1983-09-08 JP JP16602683A patent/JPS6060944A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6060944A (en) | 1985-04-08 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |