JPH0697443A - Manufacture of semiconductor device - Google Patents
Manufacture of semiconductor deviceInfo
- Publication number
- JPH0697443A JPH0697443A JP3198943A JP19894391A JPH0697443A JP H0697443 A JPH0697443 A JP H0697443A JP 3198943 A JP3198943 A JP 3198943A JP 19894391 A JP19894391 A JP 19894391A JP H0697443 A JPH0697443 A JP H0697443A
- Authority
- JP
- Japan
- Prior art keywords
- semiconductor layer
- gate electrode
- type semiconductor
- film
- gate
- 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.)
- Granted
Links
- 239000004065 semiconductor Substances 0.000 title claims abstract description 93
- 238000004519 manufacturing process Methods 0.000 title claims description 15
- 239000000758 substrate Substances 0.000 claims abstract description 37
- 238000010438 heat treatment Methods 0.000 claims abstract description 11
- 239000007790 solid phase Substances 0.000 claims abstract description 9
- 238000000034 method Methods 0.000 claims description 23
- 229910052782 aluminium Inorganic materials 0.000 claims description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 10
- 229920002120 photoresistant polymer Polymers 0.000 claims description 3
- 150000002500 ions Chemical class 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 claims description 2
- 230000003213 activating effect Effects 0.000 claims 1
- 238000007743 anodising Methods 0.000 claims 1
- 239000012535 impurity Substances 0.000 abstract description 14
- 239000012298 atmosphere Substances 0.000 abstract description 11
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 abstract description 9
- 229910052710 silicon Inorganic materials 0.000 abstract description 9
- 239000010703 silicon Substances 0.000 abstract description 9
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 abstract description 7
- 229910052698 phosphorus Inorganic materials 0.000 abstract description 7
- 239000011574 phosphorus Substances 0.000 abstract description 7
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 abstract description 6
- 229910052796 boron Inorganic materials 0.000 abstract description 6
- 238000000059 patterning Methods 0.000 abstract description 6
- 230000004913 activation Effects 0.000 abstract 1
- 239000010408 film Substances 0.000 description 74
- 239000010410 layer Substances 0.000 description 54
- 239000004973 liquid crystal related substance Substances 0.000 description 14
- 238000004544 sputter deposition Methods 0.000 description 13
- 239000010409 thin film Substances 0.000 description 13
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 7
- 229910052814 silicon oxide Inorganic materials 0.000 description 7
- 238000000137 annealing Methods 0.000 description 6
- 238000005268 plasma chemical vapour deposition Methods 0.000 description 6
- 239000011229 interlayer Substances 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229910052786 argon Inorganic materials 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 230000000903 blocking effect Effects 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 230000007423 decrease Effects 0.000 description 4
- PZPGRFITIJYNEJ-UHFFFAOYSA-N disilane Chemical compound [SiH3][SiH3] PZPGRFITIJYNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000007789 gas Substances 0.000 description 4
- 238000004518 low pressure chemical vapour deposition Methods 0.000 description 4
- 229910021421 monocrystalline silicon Inorganic materials 0.000 description 4
- 239000012808 vapor phase Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 238000002048 anodisation reaction Methods 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 239000004593 Epoxy Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004642 Polyimide Substances 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 2
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 230000000295 complement effect Effects 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- ZOCHARZZJNPSEU-UHFFFAOYSA-N diboron Chemical compound B#B ZOCHARZZJNPSEU-UHFFFAOYSA-N 0.000 description 2
- 230000005669 field effect Effects 0.000 description 2
- 238000005468 ion implantation Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229920001721 polyimide Polymers 0.000 description 2
- 235000002906 tartaric acid Nutrition 0.000 description 2
- 239000011975 tartaric acid Substances 0.000 description 2
- VEDJZFSRVVQBIL-UHFFFAOYSA-N trisilane Chemical compound [SiH3][SiH2][SiH3] VEDJZFSRVVQBIL-UHFFFAOYSA-N 0.000 description 2
- 238000007740 vapor deposition Methods 0.000 description 2
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241000283986 Lepus Species 0.000 description 1
- 239000004988 Nematic liquid crystal Substances 0.000 description 1
- 238000001069 Raman spectroscopy Methods 0.000 description 1
- FKNQFGJONOIPTF-UHFFFAOYSA-N Sodium cation Chemical compound [Na+] FKNQFGJONOIPTF-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 229910021417 amorphous silicon Inorganic materials 0.000 description 1
- 238000004873 anchoring Methods 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 230000002457 bidirectional effect Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 239000007772 electrode material Substances 0.000 description 1
- 229920006332 epoxy adhesive Polymers 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910021478 group 5 element Inorganic materials 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 238000007562 laser obscuration time method Methods 0.000 description 1
- 239000013081 microcrystal Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 150000002926 oxygen Chemical class 0.000 description 1
- SWELZOZIOHGSPA-UHFFFAOYSA-N palladium silver Chemical compound [Pd].[Ag] SWELZOZIOHGSPA-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 239000005361 soda-lime glass Substances 0.000 description 1
- 229910001415 sodium ion Inorganic materials 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Landscapes
- Metal-Oxide And Bipolar Metal-Oxide Semiconductor Integrated Circuits (AREA)
- Thin Film Transistor (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】相補型電界効果型トランジスタと
同様の動作を一つの素子で行える様な電気特性を持つ、
通称「変形スタックドゲート型半導体装置」と呼ばれて
いる半導体装置がある。この半導体装置は、液晶表示装
置等に用いた場合、明快な階調表示を得ることが出来、
自然画像に近い表示を得ることが出来る。本発明は、そ
の半導体装置の性能を向上させるための新しい作成方法
を提示するものである。[Industrial field of application] It has the electrical characteristics that one element can perform the same operation as a complementary field effect transistor.
There is a semiconductor device that is commonly called a “modified stacked gate semiconductor device”. When this semiconductor device is used in a liquid crystal display device or the like, clear gradation display can be obtained,
It is possible to obtain a display close to a natural image. The present invention presents a new fabrication method for improving the performance of the semiconductor device.
【0002】[0002]
【従来の技術】「変形スタックドゲート型半導体装置」
は、「SID’91」で公知になったように、その特性
は2つのゲート電極にかける信号の電位を変化させるこ
とによって、ソース・ドレイン間に双方向の電流電圧特
性を持たせることができる装置である。図2にその電流
電圧特性を示す。2. Description of the Related Art "Modified stacked gate semiconductor device"
As has been known in "SID'91", its characteristic is that bidirectional current-voltage characteristics can be provided between the source and drain by changing the potential of the signal applied to the two gate electrodes. It is a device. The current-voltage characteristics are shown in FIG.
【0003】この様な特性を有する装置は多種多様な使
用用途が考えられるが、特に液晶電気光学装置への応用
が有効と考えられる。従来液晶電気光学装置に用いられ
ている半導体装置は、図3の回路構成に示すようなnチ
ャネル型薄膜トランジスタが主であった。ここにnチャ
ネル型薄膜トランジスタまたはpチャネル型薄膜トラン
ジスタを用いた場合、OFF状態からON状態に移行
(画素電極にため込む電荷が増加する方向)する際には
nチャネル型薄膜トランジスタの順特性を利用できるた
めに、高速の動作が可能となっている。しかしながら、
ON状態からOFF状態へ移行(画素電極にため込む電
荷が減少する方向)する際には、nチャネル型薄膜トラ
ンジスタの逆特性となるために、動作の阻害が起きてい
た。A device having such characteristics can be used for various purposes, but it is considered to be particularly effective when applied to a liquid crystal electro-optical device. Conventionally, the semiconductor device used in the liquid crystal electro-optical device is mainly an n-channel thin film transistor as shown in the circuit configuration of FIG. When an n-channel thin film transistor or a p-channel thin film transistor is used here, the forward characteristics of the n-channel thin film transistor can be used when the state changes from the OFF state to the ON state (direction in which the charge accumulated in the pixel electrode increases). , High-speed operation is possible. However,
At the time of transition from the ON state to the OFF state (direction in which the charge accumulated in the pixel electrode decreases), the operation is hindered because the characteristics are opposite to those of the n-channel thin film transistor.
【0004】そこで、図4に示す「トランスファーゲー
ト型C/MOS薄膜トランジスタ」のように、nチャネ
ル型薄膜トランジスタとpチャネル型薄膜トランジスタ
を相補型に組み合わせて使用することで、ONからOF
F、OFFからONの両動作に対しても、電荷の移動が
早いために高速の動作を行うことが出来ることが公知と
なっており、液晶電気光学装置への応用に期待が寄せら
れている。Therefore, by using an n-channel type thin film transistor and a p-channel type thin film transistor in a complementary type, such as a "transfer gate type C / MOS thin film transistor" shown in FIG.
It is well known that high-speed operations can be performed even in both F, OFF to ON operations due to the fast movement of electric charges, and it is expected to be applied to a liquid crystal electro-optical device. .
【0005】このように、C/MOS装置を液晶電気光
学装置に用いた場合のメリットが多く言われているが、
実際のデバイスを考慮した場合、素子としてnチャネル
型薄膜トランジスタとpチャネル型薄膜トランジスタの
両方を各画素に設置することは、従来のnチャネル型薄
膜トランジスタのみの場合と比較して、倍の素子を設け
ることから歩留りの向上を考えた場合、画質の向上は望
めるものの製品化には逆行する考え方であった。具体的
に考えると640×400ドットの画素を有する液晶電
気光学装置を考えた場合、現在パネル単位で50%程度
ある歩留りが、素子を2倍にすることで、単純に計算し
ても25%以下になることは必至である。マスク数が増
加することで、さらに歩留りの低下となる要因が積算さ
れることは言うまでもない。As described above, there are many merits when the C / MOS device is used in a liquid crystal electro-optical device.
In consideration of an actual device, installing both an n-channel thin film transistor and a p-channel thin film transistor as an element in each pixel means providing twice as many elements as in the case of using a conventional n-channel thin film transistor alone. Therefore, when considering the improvement of yield, the idea was to improve the image quality, but it was against the idea of commercialization. Specifically, when considering a liquid crystal electro-optical device having pixels of 640 × 400 dots, the yield which is currently about 50% per panel is 25% even if simply calculated by doubling the elements. The following is inevitable. It goes without saying that as the number of masks increases, the factors that further reduce the yield are added up.
【0006】また、単に歩留りだけの問題ではなく、液
晶電気光学装置で重要なファクターである開口率の問題
がある。素子を1つ設けることで減少する開口率は約5
%程度と一般にいわれているが、C/MOSのように2
つの素子を作成した場合、それだけで10%以上の減少
になることは言うまでもない。そこで、素子数を減らし
ても同一の動作が出来るような素子が望まれていた。Further, not only the problem of yield, but also the problem of aperture ratio, which is an important factor in liquid crystal electro-optical devices. The aperture ratio reduced by providing one element is about 5
It is generally said to be about%, but it is 2 like C / MOS.
It is needless to say that when one element is produced, it is reduced by 10% or more. Therefore, an element that can perform the same operation even if the number of elements is reduced has been desired.
【0007】そこで、前記の「変形スタックドゲート型
半導体装置」がこれらの欠点を補い得る素子として提案
されるに至っている。Therefore, the above-mentioned "modified stacked gate type semiconductor device" has been proposed as an element capable of compensating for these drawbacks.
【0008】公知例に見る本素子の製造方法は、図5に
あるような工程を踏んでいる。The manufacturing method of the present element, which is seen in the publicly known example, includes steps as shown in FIG.
【0009】まずガラス等の透光性基板1上にプラズマ
CVDもしくは減圧CVD法を用いて、p型半導体膜と
n型半導体膜を積層させ、図5(A)に示すようにマス
クにて島状にパターニングし、p型半導体層2とn型半
導体層3を得る。その後、真性半導体膜を堆積させ、そ
れを次のマスクを用いてパターニング後、600℃の窒
素雰囲気中にて固相成長をさせ、アモルファス相から結
晶化をさせてチャネル領域となる多結晶真性半導体層4
とし、図5(B)を得る。その後減圧CVDまたはスパ
ッタ法を用いてゲート絶縁膜となるSiO2 膜を100
0Å、減圧CVD法等でメインゲート電極となるリンド
ープのSi層を2000Å堆積させ、次のマスクを用い
てパターニングし、ゲート絶縁膜5およびメインゲート
電極6を形成し図5(C)を得る。その後、減圧CVD
またはプラズマCVD法等を用いて層間絶縁膜7である
SiO2 膜を5000Å堆積後、Alを3000Å堆積
させ、次のマスクを用いてパターニングし図5(E)に
示すようにサブゲート電極8を得る、という方法であ
る。First, a p-type semiconductor film and an n-type semiconductor film are laminated on a transparent substrate 1 made of glass or the like by plasma CVD or low pressure CVD, and an island is formed by a mask as shown in FIG. 5 (A). Patterning to obtain a p-type semiconductor layer 2 and an n-type semiconductor layer 3. After that, an intrinsic semiconductor film is deposited, patterned using the following mask, and then solid phase growth is performed in a nitrogen atmosphere at 600 ° C. to crystallize from an amorphous phase to form a polycrystalline intrinsic semiconductor serving as a channel region. Layer 4
Then, FIG. 5B is obtained. After that, a SiO 2 film serving as a gate insulating film is formed to 100 by using low pressure CVD or sputtering.
A phosphorus-doped Si layer to be a main gate electrode is deposited to 2000 Å by a low pressure CVD method or the like, and patterned by using the following mask to form a gate insulating film 5 and a main gate electrode 6 to obtain FIG. 5C. After that, low pressure CVD
Alternatively, the SiO 2 film which is the interlayer insulating film 7 is deposited by 5000 Å using plasma CVD method or the like, and then Al is deposited by 3000 Å, and patterned by using the following mask to obtain the sub-gate electrode 8 as shown in FIG. 5 (E). , Is the method.
【0010】[0010]
【発明が解決しようとする課題】上記の様なプロセスを
用いた場合、図5(B)のようにパターニング後固相成
長をさせると、高温雰囲気中にp型半導体層またはn型
半導体層の不純物であるリンまたはボロンが拡散し、そ
れらがチャネル領域となる真性半導体層4に混入、拡散
する危険がある。そうした場合、高性能なチャネルを形
成することができず、液晶電気光学装置用の駆動素子に
必要なOFF抵抗を十分に上げることが出来ないばかり
か、電界効果移動度を極端に落とす結果となる。また、
図5(D)にある層間絶縁膜7は立体交差配線のショー
トを防ぐ為に厚くなるため、サブゲートに加える電圧を
大きくしないと、十分に電界がかけられない結果となっ
ている。In the case of using the above process, if solid phase growth is performed after patterning as shown in FIG. 5B, the p-type semiconductor layer or the n-type semiconductor layer is formed in a high temperature atmosphere. There is a risk that phosphorus or boron, which is an impurity, diffuses and mixes and diffuses into the intrinsic semiconductor layer 4 that serves as a channel region. In such a case, a high-performance channel cannot be formed, the OFF resistance required for the drive element for the liquid crystal electro-optical device cannot be sufficiently increased, and the field effect mobility is extremely lowered. . Also,
The interlayer insulating film 7 shown in FIG. 5D is thick in order to prevent short-circuiting of the three-dimensional cross wiring, so that a sufficient electric field cannot be applied unless the voltage applied to the sub-gate is increased.
【0011】[0011]
【問題を解決するための手段】そこで本発明者らは次の
様な工程を踏むことにより上記の問題の解決を図った。
すなわち、透光性基板上にp型半導体層とn型半導体層
を積層した2つの積層部と、前記2つの積層部に接して
設けられた真性半導体層を形成した後、ゲート絶縁膜と
なる層、たとえば酸化珪素膜を前記透光性基板上の半導
体層の表面を全て覆うように形成して、その後熱アニー
ルを行って真性半導体層を固相成長させて多結晶化をお
こなう。このようにすることで、熱処理中にn型半導体
層またはp型半導体層の不純物であるリンまたはボロン
が高温雰囲気中に拡散せず、そのような不純物がチャネ
ル領域に混入、拡散する危険を防ぐことが出来、閾値の
シフトと移動度の低下を防止できる。[Means for Solving the Problems] Therefore, the present inventors have attempted to solve the above problems by taking the following steps.
That is, after forming two stacked parts in which a p-type semiconductor layer and an n-type semiconductor layer are stacked and an intrinsic semiconductor layer provided in contact with the two stacked parts on a transparent substrate, a gate insulating film is formed. A layer, for example, a silicon oxide film is formed so as to cover the entire surface of the semiconductor layer on the transparent substrate, and then thermal annealing is performed to solid-phase grow the intrinsic semiconductor layer for polycrystallization. By doing so, phosphorus or boron, which is an impurity of the n-type semiconductor layer or the p-type semiconductor layer, does not diffuse into the high temperature atmosphere during the heat treatment, and the risk that such an impurity mixes into the channel region and diffuses is prevented. It is possible to prevent the shift of the threshold value and the decrease of the mobility.
【0012】その後ゲート絶縁膜を成膜、パターニング
し、ゲート絶縁膜上に第一のゲート電極をアルミニウム
で形成し、陽極酸化を行うことで第一のゲート電極表面
を絶縁化し、その後第二のゲート電極を第一のゲート電
極に隣接してゲート絶縁膜上に形成する。After that, a gate insulating film is formed and patterned, a first gate electrode is formed of aluminum on the gate insulating film, and anodization is performed to insulate the surface of the first gate electrode, and then the second gate electrode is formed. A gate electrode is formed on the gate insulating film adjacent to the first gate electrode.
【0013】以上の様な工程を経ることで真性半導体層
の固相成長時の不純物の混入を防ぐことができ、また2
つのゲート電極が同一ゲート絶縁膜上に形成されること
で、第2のゲート電極に加える電圧を小さくできた。Through the above steps, it is possible to prevent impurities from being mixed during solid phase growth of the intrinsic semiconductor layer.
By forming the two gate electrodes on the same gate insulating film, the voltage applied to the second gate electrode can be reduced.
【0014】以上の工程の一応用例として以下の様な作
製方法を考案した。The following manufacturing method was devised as an application example of the above process.
【0015】まず図1(A)に示すように透光性基板1
0上にマスクを用いてパターニングされたp型半導体層
11を形成する。その後、真性半導体膜12を形成し、
その上にネガ型レジストを塗布し、基板裏面より紫外光
をあて、図1(B)に示すようにp型半導体層11を下
地に有しない部分のレジスト13を感光および現像させ
る。First, as shown in FIG. 1A, the transparent substrate 1
A patterned p-type semiconductor layer 11 is formed on the substrate 0 using a mask. Then, the intrinsic semiconductor film 12 is formed,
A negative resist is applied thereon, and ultraviolet light is applied from the back surface of the substrate to expose and develop the resist 13 in a portion not having the p-type semiconductor layer 11 as a base as shown in FIG.
【0016】次に図1(C)に示すように、前記レジス
ト13をマスクとして前記真性半導体膜12のうちのp
型半導体層11上の部分のn型半導体化のためにリン等
の5族元素のイオンを打ち込み、n型半導体層14を形
成する。Next, as shown in FIG. 1C, p of the intrinsic semiconductor film 12 is formed using the resist 13 as a mask.
Ions of a Group 5 element such as phosphorus are implanted to form an n-type semiconductor layer 14 on the type semiconductor layer 11 to form an n-type semiconductor layer 14.
【0017】次にレジスト13を除去し、ゲート絶縁膜
15となる酸化膜を、基板上に形成したp型半導体層1
1とn型半導体層14を含めた前記真性半導体膜12の
全表面のを覆うように形成し、次にn型半導体層14の
活性化と真性半導体膜12の残りの部分の固相成長を行
うための熱処理を行い、その後パターニングすることで
図1(D)に示すように真性半導体膜12の残りの部分
はチャネル領域である多結晶半導体層16となる。この
ようにすることで、熱処理中にn型半導体層またはp型
半導体層の不純物であるリンまたはボロンが高温雰囲気
中に拡散せず、そのような不純物がチャネル領域に混
入、拡散する危険を防ぐことが出来、閾値のシフトと移
動度の低下を防止できる。Next, the resist 13 is removed, and an oxide film to be the gate insulating film 15 is formed on the substrate to form the p-type semiconductor layer 1.
1 and the n-type semiconductor layer 14 are formed so as to cover the entire surface of the intrinsic semiconductor film 12, and then the n-type semiconductor layer 14 is activated and the remaining portion of the intrinsic semiconductor film 12 is solid-phase grown. By performing heat treatment for this purpose and then patterning, the remaining portion of the intrinsic semiconductor film 12 becomes a polycrystalline semiconductor layer 16 which is a channel region, as shown in FIG. By doing so, phosphorus or boron, which is an impurity of the n-type semiconductor layer or the p-type semiconductor layer, does not diffuse into the high temperature atmosphere during the heat treatment, and the risk that such an impurity mixes into the channel region and diffuses is prevented. It is possible to prevent the shift of the threshold value and the decrease of the mobility.
【0018】図1(E)において、第一のゲート電極す
なわちメインゲート電極17をアルミニウムにて形成後
その表面を陽極酸化し、酸化層18を形成することで電
極表面を絶縁化する。無孔質の酸化アルミ膜を得るため
に、発明者らはエチレングリコールまたはプロピレング
リコール中で酒石酸を希釈してpH7.0±0.5の溶
液を用いた。その後ソース電極19、ドレイン電極20
を形成する。また電極材料により可能であればメインゲ
ート電極17と同時にソース電極19、ドレイン電極2
0を形成し、メインゲート電極と同様にその表面に陽極
酸化を施すことは有効である。In FIG. 1 (E), the first gate electrode, that is, the main gate electrode 17 is formed of aluminum, and then the surface thereof is anodized to form an oxide layer 18 to insulate the electrode surface. To obtain a non-porous aluminum oxide film, we used a solution of pH 7.0 ± 0.5 diluted with tartaric acid in ethylene glycol or propylene glycol. After that, the source electrode 19 and the drain electrode 20
To form. Also, if possible depending on the electrode material, the source electrode 19 and the drain electrode 2 at the same time as the main gate electrode 17.
It is effective to form 0 and subject the surface thereof to anodization similarly to the main gate electrode.
【0019】その後、図1(F)に示すように第二のゲ
ート電極すなわちサブゲート電極21をアルミニウムに
て形成する。この後、層間絶縁膜22を形成する。Then, as shown in FIG. 1F, a second gate electrode, that is, a sub-gate electrode 21 is formed of aluminum. After that, the interlayer insulating film 22 is formed.
【0020】メインゲート電極17表面に直接陽極酸化
法によって酸化膜18を設けたことで、メインゲート電
極17とサブゲート電極21を同一ゲート絶縁膜15上
に形成することができた。従って閾値を小さく出来ただ
けでなく、界面準位密度の低減も可能になった。By providing the oxide film 18 directly on the surface of the main gate electrode 17 by the anodic oxidation method, the main gate electrode 17 and the sub-gate electrode 21 can be formed on the same gate insulating film 15. Therefore, not only was the threshold value reduced, but also the interface state density could be reduced.
【0021】以下に実施例によって更に詳細な説明を加
える。Further detailed description will be given below with reference to examples.
【0022】[0022]
【実施例】本実施例では、対角1インチを有する液晶電
気光学装置を用いた、ビデオカメラ用ビューファインダ
ーを作製し、本発明を実施したので説明を加える。EXAMPLE In this example, a viewfinder for a video camera using a liquid crystal electro-optical device having a diagonal of 1 inch was manufactured and the present invention was carried out.
【0023】本実施例では、画素数が387×128の
構成にして、低温プロセスによる高移動度変形スタック
ドゲート素子を用いた素子を形成し、ビューファインダ
ーを構成した。本実施例で使用する液晶表示装置の基板
上のアクティブ素子の配置の様子を図6に示し図6のA
−A’断面を示す作製プロセスを図7に描く。In this embodiment, a viewfinder is constructed by forming a device having a high mobility modified stacked gate device by a low temperature process with a structure of 387 × 128 pixels. FIG. 6 shows the arrangement of the active elements on the substrate of the liquid crystal display device used in this embodiment.
The fabrication process showing the -A 'cross section is depicted in FIG.
【0024】図7(A)において、安価な、700℃以
下、例えば約600℃の熱処理に耐え得るガラス基板3
0上にマグネトロンRF(高周波) スパッタ法を用いて
ブロッキング層31としてのアモルファス酸化珪素膜を
1000〜3000Åの厚さに作製する。プロセス条件
は酸素100%雰囲気、成膜温度150℃、出力400
〜800W、圧力0.5Paとした。タ−ゲットに石英
または単結晶シリコンを用いた成膜速度は30〜100
Å/分であった。In FIG. 7A, an inexpensive glass substrate 3 that can withstand heat treatment at 700 ° C. or lower, for example, about 600 ° C.
An amorphous silicon oxide film as the blocking layer 31 is formed on the surface of the substrate 0 to a thickness of 1000 to 3000 Å by using a magnetron RF (radio frequency) sputtering method. Process conditions are 100% oxygen atmosphere, film forming temperature 150 ° C., output 400.
˜800 W and pressure 0.5 Pa. The deposition rate using quartz or single crystal silicon for the target is 30 to 100
It was Å / min.
【0025】この上にp型Si(シリコン)膜をLPC
VD(減圧気相)法、スパッタ法またはプラズマCVD
法により1000〜3000Å、ここでは2000Åの
厚さに形成した。減圧気相法で形成する場合、結晶化温
度よりも100〜200℃低い450〜550℃、例え
ば530℃でジシラン(Si2H6) またはトリシラン(Si
3H8) をCVD装置に供給して成膜した。不純物源ガス
としてジボラン(B2H6) をホストガスに対して0.5〜
3%混合した。反応炉内圧力は30〜300Paとし
た。成膜速度は50〜250Å/ 分であった。A p-type Si (silicon) film is formed on this by LPC.
VD (vacuum vapor phase) method, sputtering method or plasma CVD
It was formed to a thickness of 1000 to 3000 Å, here 2000 Å. When forming by a low pressure vapor phase method, disilane (Si 2 H 6 ) or trisilane (Si 2 H 6 ) is added at 450 to 550 ° C., which is 100 to 200 ° C. lower than the crystallization temperature, for example, 530 ° C.
3 H 8 ) was supplied to the CVD device to form a film. Diborane (B 2 H 6 ) as an impurity source gas is added to the host gas in an amount of 0.5 to
3% mixed. The pressure in the reaction furnace was 30 to 300 Pa. The film forming rate was 50 to 250 Å / min.
【0026】スパッタ法で行う場合、スパッタ前の背圧
を1×10-5Pa以下とし、p型単結晶シリコンをタ−ゲ
ットとして、アルゴンに水素を20〜80%混入した雰
囲気で行った。例えばアルゴン20%、水素80%とし
た。成膜温度は150℃、周波数は13.56MHz、
スパッタ出力は400〜800W、圧力は0.5Paで
あった。In the case of the sputtering method, the back pressure before sputtering was set to 1 × 10 -5 Pa or less, the p-type single crystal silicon was used as the target, and the atmosphere was mixed with 20% to 80% of hydrogen in argon. For example, argon is 20% and hydrogen is 80%. The film forming temperature is 150 ° C., the frequency is 13.56 MHz,
The sputter output was 400 to 800 W and the pressure was 0.5 Pa.
【0027】プラズマCVD法により珪素膜を作製する
場合、温度は例えば300℃とし、モノシラン(SiH4)ま
たはジシラン(Si2H6) を用いた。不純物源ガスとしてジ
ボラン(B2H6) をホストガスに対して0.5〜3%混合
した。これらをPCVD装置内に導入し、13.56M
Hzの高周波電力を加えて成膜した。When a silicon film is formed by the plasma CVD method, the temperature is, for example, 300 ° C., and monosilane (SiH 4 ) or disilane (Si 2 H 6 ) is used. Diborane (B 2 H 6 ) as an impurity source gas was mixed with the host gas in an amount of 0.5 to 3%. Introducing these into the PCVD equipment, 13.56M
A high frequency power of Hz was applied to form a film.
【0028】前記p型Si膜を島状にパターニングし
て、p型半導体層であるp+ Si層32を形成した後、
この上に図7(B)に示すように真性Si膜33をLP
CVD(減圧気相)法、スパッタ法またはプラズマCV
D法により1000〜3000Å、ここでは2000Å
の厚さに形成した。減圧気相法で形成する場合、結晶化
温度よりも100〜200℃低い450〜550℃、例
えば530℃でジシラン(Si2H6) またはトリシラン(Si3
H8) をCVD装置に供給して成膜した。反応炉内圧力は
30〜300Paとした。成膜速度は50〜250Å/
分であった。スレッシュホ−ルド電圧(Vth)を任意に
制御するため、ホウ素をジボランを用いて1×1015〜1
×1018cm-3の濃度として成膜中に添加してもよい。After patterning the p-type Si film into an island shape to form a p + Si layer 32 which is a p-type semiconductor layer,
An intrinsic Si film 33 is formed on top of this by LP as shown in FIG.
CVD (Low Pressure Vapor Phase) method, Sputtering method or Plasma CV
1000-3000Å by method D, here 2000Å
Formed to a thickness of. When forming by a reduced pressure vapor phase method, disilane (Si 2 H 6 ) or trisilane (Si 3 ) is added at 450 to 550 ° C., which is lower than the crystallization temperature by 100 to 200 ° C., for example, at 530 ° C.
H 8 ) was supplied to the CVD device to form a film. The pressure in the reaction furnace was 30 to 300 Pa. Deposition rate is 50 ~ 250Å /
It was a minute. In order to arbitrarily control the threshold voltage (Vth), boron is used in an amount of 1 × 10 15 to 1 by using diborane.
It may be added as a concentration of × 10 18 cm -3 during film formation.
【0029】スパッタ法で行う場合、スパッタ前の背圧
を1×10-5Pa以下とし、単結晶シリコンをタ−ゲット
として、アルゴンに水素を20〜80%混入した雰囲気
で行った。例えばアルゴン20%、水素80%とした。
成膜温度は150℃、周波数は13.56MHz、スパ
ッタ出力は400〜800W、圧力は0.5Paであっ
た。When the sputtering method is used, the back pressure before the sputtering is set to 1 × 10 -5 Pa or less, the single crystal silicon is used as the target, and the atmosphere is mixed with hydrogen of 20 to 80% in argon. For example, argon is 20% and hydrogen is 80%.
The film forming temperature was 150 ° C., the frequency was 13.56 MHz, the sputter output was 400 to 800 W, and the pressure was 0.5 Pa.
【0030】プラズマCVD法により珪素膜を作製する
場合、温度は例えば300℃とし、モノシラン(SiH4)ま
たはジシラン(Si2H6) を用いた。これらをPCVD装置
内に導入し、13.56MHzの高周波電力を加えて成
膜した。When the silicon film is formed by the plasma CVD method, the temperature is, for example, 300 ° C., and monosilane (SiH 4 ) or disilane (Si 2 H 6 ) is used. These were introduced into a PCVD apparatus, and high-frequency power of 13.56 MHz was applied to form a film.
【0031】これらの方法によって形成された被膜は、
酸素が5×1021cm-3以下であることが好ましい。この酸
素濃度が高いと、結晶化させにくく、熱アニ−ル温度を
高くまたは熱アニ−ル時間を長くしなければならない。
また少なすぎると、バックライトによりオフ状態のリ−
ク電流が増加してしまう。そのため4×1019〜4×1021
cm-3の範囲とした。水素は4×1020cm-3であり、珪素4
×1022cm-3として比較すると1原子%であった。The coatings formed by these methods are
It is preferable that oxygen is 5 × 10 21 cm −3 or less. If this oxygen concentration is high, it is difficult to crystallize and the thermal annealing temperature must be high or the thermal annealing time must be long.
If it is too small, the backlight will turn off the light.
The current will increase. Therefore 4 × 10 19 to 4 × 10 21
The range was cm -3 . Hydrogen is 4 × 10 20 cm -3 and silicon 4
When compared with x10 22 cm -3 , it was 1 atom%.
【0032】その後、表面にネガ型レジストを塗布し、
基板背面より紫外光を照射すると、p型半導体層を有す
る場所は紫外光を透過しないために、硬化せず現像の段
階で取り除かれ、レジスト34が残る。この様にして、
次の工程であるイオンうち込みに用いるマスクをセルフ
ァライン工程で作製することができるのである。After that, a negative resist is applied on the surface,
When ultraviolet rays are radiated from the back surface of the substrate, the portions having the p-type semiconductor layer do not transmit the ultraviolet rays, so that they are not cured and removed at the stage of development, and the resist 34 remains. In this way
The mask used for the next step of ion implantation can be manufactured in the self-aligning step.
【0033】図7(C)において、p+ Si層32上の
真性Si膜33に対しリン(P)を1〜5×1015cm-2
のド−ズ量でイオン注入法により添加することにより、
n+Si層を形成した。In FIG. 7C, phosphorus (P) is added to the intrinsic Si film 33 on the p + Si layer 32 at 1 to 5 × 10 15 cm -2.
By adding by the ion implantation method with a dose amount of
An n + Si layer was formed.
【0034】次にレジスト34を除去し、酸化珪素膜を
500〜2000Å例えば1000Åの厚さに形成し
た。これはブロッキング層31としての酸化珪素膜の作
製と同一条件とした。この成膜中に弗素を少量添加し、
ナトリウムイオンの固定化をさせてもよい。Next, the resist 34 was removed, and a silicon oxide film was formed to a thickness of 500 to 2000Å, for example 1000Å. This is the same condition as the production of the silicon oxide film as the blocking layer 31. Add a small amount of fluorine during this film formation,
You may fix sodium ion.
【0035】酸化珪素膜を成膜した後、450〜700
℃の温度にて12〜70時間非酸化物雰囲気にて中温の
加熱処理、例えば水素雰囲気下にて600℃の温度で保
持した。真性Si膜33の下の基板表面にブロッキング
層31としてアモルファス構造の酸化珪素膜が形成され
ているため、この熱処理で特定の核が存在せず、全体が
均一に加熱アニ−ルされる。即ち、成膜時はアモルファ
ス構造を有し、また水素は単に混入しているのみであ
る。After forming the silicon oxide film, 450 to 700
The temperature was kept at a temperature of 600C for 12 to 70 hours at a temperature of 600C in a non-oxide atmosphere at a medium temperature, for example, in a hydrogen atmosphere. Since a silicon oxide film having an amorphous structure is formed as the blocking layer 31 on the surface of the substrate under the intrinsic Si film 33, no specific nucleus exists in this heat treatment, and the whole is uniformly annealed by heating. That is, it has an amorphous structure at the time of film formation, and hydrogen is simply mixed therein.
【0036】アニ−ルにより、真性Si膜33はアモル
ファス構造から秩序性の高い状態に移り、一部は結晶状
態を呈する。特にシリコンの成膜後の状態で比較的秩序
性の高い領域は特に結晶化をして結晶状態となろうとす
る。しかしこれらの領域間に存在する珪素により互いの
結合がなされるため、珪素同志は互いにひっぱりあう。
レ−ザラマン分光により測定すると単結晶の珪素のピ−
ク522cm-1より低周波側にシフトしたピ−クが観察さ
れる。それの見掛け上の粒径は半値巾から計算すると、
50〜500Åとマイクロクリスタルのようになってい
るが、実際はこの結晶性の高い領域は多数あってクラス
タ構造を有し、各クラスタ間は互いに珪素同志で結合
(アンカリング) がされたセミアモルファス構造の被膜
を形成させることができた。Due to the annealing, the intrinsic Si film 33 shifts from the amorphous structure to a highly ordered state, and a part thereof assumes a crystalline state. In particular, a region having a relatively high degree of ordering after the film formation of silicon tends to be crystallized and become a crystalline state. However, since silicon existing between these regions is bonded to each other, the silicon members pull each other.
The peak of single-crystal silicon measured by laser Raman spectroscopy
A peak shifted to a lower frequency side than 522 cm -1 is observed. When the apparent particle size of it is calculated from the half width,
Although it is a microcrystal with a thickness of 50 to 500Å, in reality there are many highly crystalline regions with a cluster structure, and each cluster is a semi-amorphous structure in which silicon is bonded to each other (anchoring). Was able to be formed.
【0037】結果として、被膜は実質的にグレインバウ
ンダリ(以下GBという)がないといってもよい状態を
呈する。キャリアは各クラスタ間をアンカリングされた
個所を通じ互いに容易に移動し得るため、いわゆるGBの
明確に存在する多結晶珪素よりも高いキャリア移動度と
なる。即ちホ−ル移動度(μh)=10〜200cm2/
VSec、電子移動度(μe )=15〜300cm2 /V
Secが得られる。As a result, the coating is in a state in which it may be said that there is substantially no grain boundary (hereinafter referred to as GB). Since the carriers can easily move between the clusters through the anchored portions, the carrier mobility is higher than that of polycrystalline silicon in which so-called GB is clearly present. That is, hole mobility (μh) = 10 to 200 cm 2 /
VSec, electron mobility (μe) = 15 to 300 cm 2 / V
Sec is obtained.
【0038】他方、上記の如き中温でのアニ−ルではな
く、900〜1200℃の高温アニ−ルにより被膜を多
結晶化してもよい。しかしながらその様にすると、核か
らの固相成長により被膜中の不純物の偏析がおきて、G
Bには酸素、炭素、窒素等の不純物が多くなり、結晶中
の移動度は大きいが、GBでのバリア(障壁)を作って
そこでのキャリアの移動を阻害してしまう。結果として
10cm2/Vsec以上の移動度がなかなか得られないのが実
情である。On the other hand, the coating may be polycrystallized by a high temperature anneal of 900 to 1200 ° C. instead of the medium temperature anneal as described above. However, in such a case, the solid phase growth from the nuclei causes the segregation of impurities in the coating film, resulting in G
Although B has a large amount of impurities such as oxygen, carbon, and nitrogen, and has a high mobility in the crystal, it creates a barrier in GB and hinders the movement of carriers there. As a result, it is difficult to obtain a mobility of 10 cm 2 / Vsec or more.
【0039】この様にして、多結晶真性Si層37がで
きた。この工程はn+ Si層35を活性化することも兼
ねている。この後前記酸化珪素膜をパターニングしてゲ
ート絶縁膜36とし、図7(D)を得る。In this way, the polycrystalline intrinsic Si layer 37 was formed. This step also serves to activate the n + Si layer 35. After that, the silicon oxide film is patterned to form a gate insulating film 36, and FIG. 7D is obtained.
【0040】その後、メインゲート電極38、ソース電
極40、ドレイン電極41およびリードとするために、
アルミニュームをスパッタ法または蒸着法によって、2
μmの厚みで成膜しパターニングを行なった。Then, in order to form the main gate electrode 38, the source electrode 40, the drain electrode 41 and the lead,
2 aluminum by sputtering or vapor deposition
A film having a thickness of μm was formed and patterned.
【0041】その後、燐酸をエチレングリコールで希釈
してpH5.0±0.5の溶液としその中に基板を浸し
た。メインゲート電極38、ソース電極40、ドレイン
電極41およびそれぞれの電極よりのびるリードに、+
25Vの電圧を供給して多孔質の酸化アルミニュームを
約1μm形成した。充分な洗浄の後、酒石酸をエチレン
グリコールで希釈して、pH7.0±0.5の溶液を作
り、その溶液中に基板を浸した。メインゲート電極3
8、ソース電極40、ドレイン電極41およびそれぞれ
の電極よりのびるリードに、+75Vの電圧を供給し
た。約30分後に前記多孔質の酸化アルミニュームの表
面を無孔質の酸化アルミニューム膜に変質させることが
出来、メインゲート電極38、ソース電極40、ドレイ
ン電極41およびリード上に無孔質で約1μmの酸化ア
ルミニューム膜39および42が得られ、図7(E)を
得た。After that, phosphoric acid was diluted with ethylene glycol to obtain a solution having a pH of 5.0 ± 0.5, and the substrate was dipped therein. + To the lead extending from the main gate electrode 38, the source electrode 40, the drain electrode 41 and the respective electrodes,
A voltage of 25 V was applied to form a porous aluminum oxide film of about 1 μm. After thorough washing, tartaric acid was diluted with ethylene glycol to make a solution having a pH of 7.0 ± 0.5, and the substrate was immersed in the solution. Main gate electrode 3
A voltage of +75 V was supplied to 8, the source electrode 40, the drain electrode 41, and the leads extending from the respective electrodes. After about 30 minutes, the surface of the porous aluminum oxide can be transformed into a non-porous aluminum oxide film, and the non-porous aluminum oxide film can be formed on the main gate electrode 38, the source electrode 40, the drain electrode 41 and the lead. Aluminum oxide films 39 and 42 of 1 μm were obtained, and FIG. 7E was obtained.
【0042】その後サブゲート電極43およびリードと
して、アルミニュームをスパッタ法または蒸着法によっ
て、2μmの厚みで成膜しパターニングをおこなった。Thereafter, as the sub-gate electrode 43 and the lead, an aluminum film having a thickness of 2 μm was formed by sputtering or vapor deposition and patterned.
【0043】プラズマCVD法を用いて、この基板上に
層間絶縁膜44であるSiNX 膜を2μm成膜し、孔開
けパターニングの後に、透明導電膜であるITO(イン
ジュ−ム・スズ酸化膜)を1000Åスパッタ法にて成
膜後、パターニングを施して画素電極45を形成し、図
7(F)を得た。以上で第一の基板を得た。An interlayer insulating film 44 of SiN x film having a thickness of 2 μm is formed on this substrate by using the plasma CVD method, and after patterning holes, ITO (indium tin oxide film) which is a transparent conductive film is formed. Was deposited by a 1000Å sputtering method and then patterned to form a pixel electrode 45, to obtain FIG. 7 (F). Thus, the first substrate was obtained.
【0044】次に第二の基板として、青板ガラス上にス
パッタ法を用いて、酸化珪素膜を2000Å積層した基
板上に、カラーフィルターを形成してその上にスパッタ
法によりITOを形成した。このITOは室温〜150
℃で成膜し、200〜400℃の酸素または大気中のア
ニ−ルにより成就し、第二の基板とした。Next, as the second substrate, a color filter was formed on a substrate in which a silicon oxide film was laminated in 2000 liters on a soda lime glass by a sputtering method, and ITO was formed thereon by a sputtering method. This ITO is room temperature to 150
A film was formed at a temperature of ℃, and the second substrate was obtained by achieving oxygen at 200 to 400 ℃ or annealing in the air.
【0045】前記第一、第二の基板上に、オフセット法
を用いて、ポリイミド前駆体を印刷し、非酸化性雰囲気
たとえば窒素中にて350℃1時間焼成を行った。その
後、公知のラビング法を用いて、ポリイミド表面を改質
し、少なくとも初期において、液晶分子を一定方向に配
向させる手段を設けて第一および第二の基板とした。A polyimide precursor was printed on the first and second substrates by an offset method and baked at 350 ° C. for 1 hour in a non-oxidizing atmosphere such as nitrogen. After that, a known rubbing method was used to modify the surface of the polyimide, and at least in the initial stage, a means for orienting liquid crystal molecules in a certain direction was provided to obtain first and second substrates.
【0046】その後、前記第一の基板と第二の基板によ
って、ネマチック液晶組成物を挟持し、周囲をエポキシ
性接着剤にて固定した。基板上のリードはそのピッチが
46μmと微細なため、COG法を用いて接続をおこな
った。本実施例ではICチップ上に設けた金バンプをエ
ポキシ系の銀パラジウム樹脂で接続し、ICチップと基
板間を固着と封止を目的としたエポキシ変成アクリル樹
脂にて埋めて固定する方法を用いた。その後、外側に偏
光板を貼り、透過型の液晶表示装置を得た。After that, the nematic liquid crystal composition was sandwiched between the first substrate and the second substrate, and the periphery was fixed with an epoxy adhesive. Since the pitch of the leads on the substrate was as fine as 46 μm, the COG method was used for connection. In this embodiment, the gold bumps provided on the IC chip are connected by an epoxy-based silver-palladium resin, and the IC chip and the substrate are embedded and fixed by epoxy modified acrylic resin for the purpose of fixing and sealing. I was there. After that, a polarizing plate was attached to the outside to obtain a transmissive liquid crystal display device.
【0047】[0047]
【発明の効果】透光性基板上にp型半導体層とn型半導
体層を積層した2つの積層部と、前記2つの積層部に接
して設けられた真性半導体層を形成した後、前記透光性
基板上に形成した半導体層の表面を全て覆うように絶縁
膜を形成し、熱アニールを行って真性半導体層を固相成
長させて多結晶化をおこなうことで、熱処理中にn型半
導体層またはp型半導体層の不純物であるリンまたはボ
ロンが高温雰囲気中に拡散せず、そのような不純物がチ
ャネル領域に混入、拡散する危険を防ぐことが出来、閾
値のシフトと移動度の低下を防止できた。[Effects of the Invention] After forming two stacked parts in which a p-type semiconductor layer and an n-type semiconductor layer are stacked on a transparent substrate and an intrinsic semiconductor layer provided in contact with the two stacked parts, the transparent film is formed. An n-type semiconductor is formed during heat treatment by forming an insulating film so as to cover the entire surface of the semiconductor layer formed on the optical substrate and performing thermal annealing to solid-phase grow the intrinsic semiconductor layer to polycrystallize it. Phosphorus or boron, which is an impurity of the p-type semiconductor layer or the p-type semiconductor layer, does not diffuse into a high temperature atmosphere, and it is possible to prevent such impurities from being mixed in and diffused into the channel region, which may cause a shift in threshold and a decrease in mobility. I was able to prevent it.
【0048】また前記絶縁膜上に第一のゲート電極をア
ルミニウムで形成し、陽極酸化を行うことで前記電極表
面を絶縁化し、その後第二のゲート電極を前記第一のゲ
ート電極に隣接して前記ゲート絶縁膜上に形成する、す
なわち2つのゲート電極が同一ゲート絶縁膜上に形成さ
れることで、第二のゲート電極に加える電圧を小さくで
きた。それによって界面順位密度の低減も可能になっ
た。Further, the first gate electrode is formed of aluminum on the insulating film, and the electrode surface is insulated by performing anodization, and then the second gate electrode is adjacent to the first gate electrode. The voltage applied to the second gate electrode can be reduced by forming it on the gate insulating film, that is, by forming the two gate electrodes on the same gate insulating film. This also made it possible to reduce the interface rank density.
【0049】以上の如く、本願発明は工業上の発展に大
いに寄与するものと考える。As described above, the present invention is considered to greatly contribute to industrial development.
【図1】 本願発明における変形スタックドゲート型半
導体装置の構造とその作製工程FIG. 1 shows a structure of a modified stacked gate semiconductor device according to the present invention and a manufacturing process thereof.
【図2】 変形スタックドゲート型半導体装置の電流電
圧特性FIG. 2 is a current-voltage characteristic of a modified stacked gate semiconductor device.
【図3】 nチャネル型薄膜トランジスタを用いた液晶
電気光学装置における回路構成FIG. 3 is a circuit configuration of a liquid crystal electro-optical device using an n-channel thin film transistor.
【図4】 トランスファーゲート型C/MOS薄膜トラ
ンジスタを用いた液晶電気光学装置における回路構成。FIG. 4 is a circuit configuration of a liquid crystal electro-optical device using a transfer gate type C / MOS thin film transistor.
【図5】 公知例における変形スタックドゲート型半導
体装置の構造とその作製工程FIG. 5 is a structure of a modified stacked gate type semiconductor device in a known example and its manufacturing process.
【図6】 実施例における基板上のアクティブ素子の配
置FIG. 6 is a layout of active elements on a substrate according to an embodiment.
【図7】 実施例における変形スタックドゲート型半導
体装置の構造とその作製工程7A and 7B are a structure of a modified stacked gate semiconductor device and a manufacturing process thereof in an example.
1,10 透光性基板 2,11 p型半導体層 3,14 n型半導体層 4,16 多結晶真性半導体層 5,15,36 ゲート絶縁膜 6,17,38 メインゲート電極 7,22,44 層間絶縁膜 8,21,43 サブゲート電極 12 真性半導体膜 13,34 レジスト 18 酸化層 19,40 ソース電極 20,41 ドレイン電極 30 ガラス基板 31 ブロッキング層 32 p+ Si層 33 真性Si層 35 n+ Si層 37 多結晶真性Si層 39,42 酸化アルミニューム層 45 画素電極1,10 Translucent Substrate 2,11 p-type Semiconductor Layer 3,14 n-type Semiconductor Layer 4,16 Polycrystalline Intrinsic Semiconductor Layer 5,15,36 Gate Insulating Film 6,17,38 Main Gate Electrode 7,22,44 Interlayer insulating film 8, 21, 43 Sub-gate electrode 12 Intrinsic semiconductor film 13, 34 Resist 18 Oxide layer 19, 40 Source electrode 20, 41 Drain electrode 30 Glass substrate 31 Blocking layer 32 p + Si layer 33 Intrinsic Si layer 35 n + Si Layer 37 Polycrystalline intrinsic Si layer 39, 42 Aluminum oxide layer 45 Pixel electrode
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.5 識別記号 庁内整理番号 FI 技術表示箇所 9056−4M H01L 29/78 311 Y (72)発明者 竹村 保彦 神奈川県厚木市長谷398番地 株式会社半 導体エネルギー研究所内─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 5 Identification number Internal reference number FI technical display location 9056-4M H01L 29/78 311 Y (72) Inventor Yasuhiko Takemura 398 Hase, Atsugi, Kanagawa Co., Ltd. Semiconductor Energy Laboratory
Claims (4)
層を積層した2つの積層部と、前記2つの積層部に接し
て設けられた真性半導体層を形成した後、前記透光性基
板上に形成した半導体層の表面を全て覆うように絶縁膜
を形成して、その後熱処理を行うことを特徴とする半導
体装置の作製方法。1. A transparent substrate, a p-type semiconductor layer and an n-type semiconductor layer are laminated on a translucent substrate, and an intrinsic semiconductor layer provided in contact with the two laminated parts is formed. A method for manufacturing a semiconductor device, comprising forming an insulating film so as to cover the entire surface of a semiconductor layer formed over an optical substrate and then performing heat treatment.
導体装置を作製するに際し、第一のゲート電極をアルミ
ニウムで形成した後、前記第一のゲート電極の表面に陽
極酸化を施すことで前記第一のゲート電極表面を絶縁化
し、その後第二のゲート電極を前記第一のゲート電極に
隣接して形成することを特徴とする半導体装置の作製方
法。2. When manufacturing an insulated gate semiconductor device having two gate electrodes, the first gate electrode is formed of aluminum, and then the surface of the first gate electrode is anodized to form the first gate electrode. A method for manufacturing a semiconductor device, comprising insulating the surface of one gate electrode and then forming a second gate electrode adjacent to the first gate electrode.
導体装置を作製するに際し、ゲート絶縁膜を形成し、前
記ゲート絶縁膜上に第一のゲート電極をアルミニウムで
形成した後、前記第一のゲート電極の表面に陽極酸化を
施すことで前記第一のゲート電極表面を絶縁化し、その
後第二のゲート電極を前記第一のゲート電極に隣接して
前記ゲート絶縁膜上に形成する事を特徴とする半導体装
置の作製方法。3. When manufacturing an insulated gate semiconductor device having two gate electrodes, a gate insulating film is formed, a first gate electrode is formed of aluminum on the gate insulating film, and then the first gate electrode is formed. The surface of the gate electrode is anodized to insulate the surface of the first gate electrode, and then a second gate electrode is formed adjacent to the first gate electrode on the gate insulating film. And a method for manufacturing a semiconductor device.
導体層を形成した後に真性半導体層を形成し、ネガ型レ
ジストを塗布後、基板裏面より紫外光をあて、p型半導
体層を下地に有しない部分のレジストを感光および現像
させる工程と、前記レジストをマスクとした前記真性半
導体層のn型半導体化のためのイオンを打ち込む工程
と、前記p型半導体層と前記真性半導体層と前記真性半
導体層のうちのn型化された部分の全表面を覆うように
絶縁膜を被覆後に、n型半導体層の活性化と真性半導体
部分の固相成長を行うための熱処理を行う工程と、第一
のゲート電極をアルミニウムにて形成後その表面を陽極
酸化する工程と、第二のゲート電極をアルミニウムにて
形成する工程とを少なくとも有することを特徴とする半
導体装置の作製方法。4. An intrinsic semiconductor layer is formed after forming a patterned p-type semiconductor layer on a light-transmissive substrate, a negative resist is applied, and then ultraviolet light is applied from the back surface of the substrate to form a base on the p-type semiconductor layer. Exposing and developing a portion of the resist not included in the above, implanting ions for making the intrinsic semiconductor layer into an n-type semiconductor using the resist as a mask, the p-type semiconductor layer, the intrinsic semiconductor layer, and the A step of performing a heat treatment for activating the n-type semiconductor layer and performing solid phase growth of the intrinsic semiconductor portion after covering the insulating film so as to cover the entire surface of the n-type portion of the intrinsic semiconductor layer; A method for manufacturing a semiconductor device, which comprises at least a step of forming a first gate electrode from aluminum and then anodizing its surface, and a step of forming a second gate electrode from aluminum.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3198943A JPH0817238B2 (en) | 1991-07-12 | 1991-07-12 | Method for manufacturing semiconductor device |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3198943A JPH0817238B2 (en) | 1991-07-12 | 1991-07-12 | Method for manufacturing semiconductor device |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH0697443A true JPH0697443A (en) | 1994-04-08 |
| JPH0817238B2 JPH0817238B2 (en) | 1996-02-21 |
Family
ID=16399548
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3198943A Expired - Fee Related JPH0817238B2 (en) | 1991-07-12 | 1991-07-12 | Method for manufacturing semiconductor device |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0817238B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008040478A (en) * | 2006-08-09 | 2008-02-21 | Samsung Sdi Co Ltd | Organic light emitting display |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58206121A (en) * | 1982-05-27 | 1983-12-01 | Toshiba Corp | Manufacture of thin-film semiconductor device |
-
1991
- 1991-07-12 JP JP3198943A patent/JPH0817238B2/en not_active Expired - Fee Related
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58206121A (en) * | 1982-05-27 | 1983-12-01 | Toshiba Corp | Manufacture of thin-film semiconductor device |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008040478A (en) * | 2006-08-09 | 2008-02-21 | Samsung Sdi Co Ltd | Organic light emitting display |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0817238B2 (en) | 1996-02-21 |
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