JPH03155625A - Manufacture of plasma cvd film - Google Patents

Manufacture of plasma cvd film

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Publication number
JPH03155625A
JPH03155625A JP29552689A JP29552689A JPH03155625A JP H03155625 A JPH03155625 A JP H03155625A JP 29552689 A JP29552689 A JP 29552689A JP 29552689 A JP29552689 A JP 29552689A JP H03155625 A JPH03155625 A JP H03155625A
Authority
JP
Japan
Prior art keywords
reaction gas
pressure
gas
main reaction
plasma cvd
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.)
Pending
Application number
JP29552689A
Other languages
Japanese (ja)
Inventor
Hiroshi Yamamoto
宏 山本
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Seiko Epson Corp
Original Assignee
Seiko Epson Corp
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Seiko Epson Corp filed Critical Seiko Epson Corp
Priority to JP29552689A priority Critical patent/JPH03155625A/en
Publication of JPH03155625A publication Critical patent/JPH03155625A/en
Pending legal-status Critical Current

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  • Formation Of Insulating Films (AREA)

Abstract

PURPOSE:To decompose main reaction gas before RF is applied, and to form a film containing constant composition with high reproducibility without forming a lump of a deposit by previously feeding side reaction gas at the time of forming a plasma CVD film to stabilize pressure, gas flow rate, and then stabilizing the flow rate, pressure of the main reaction gas. CONSTITUTION:A semiconductor substrate 37 formed with semiconductor elements such as a transistor, a resistor, etc., and aluminum wirings is conveyed into a vacuum vessel 34 in which insulated electrodes 32, 33 are disposed in parallel. After the vessel is once evacuated in vacuum, nitrous oxide gas of side reaction gas is fed, a discharge system is controlled to stabilize its pressure. After it is stabilized, monosilane (SiH4) of main reaction gas is fed, its pressure is controlled, stabilized, held, and a high frequency (RF) is applied. After desired time is elapsed, the RF is stopped, the gas is simultaneously stopped, and the pressure is reduced.

Description

【発明の詳細な説明】[Detailed description of the invention]

[産業上の利用分野1 本発明は、プラズマCV D l!の製造方法に関する
ものである。 [従来の技術] 従来のプラズマCVD酸化シリコン膜の製造方法は、例
えば第3図に示すように表面を絶縁した電極32及び3
3を平行に配置し、一定温度に保たれた真空容器34内
にCVD膜を堆積する基板37等を搬送する。続いて、
容器内を真空に引いた後、主反応ガスであるモノシラン
と副反応ガスである亜酸化窒素を流す。ガスの容量と圧
力が設定値に達した後(第2図中のt22)、前記電極
に高周波(RF)を印加しくtas)、一定時間保持し
酸化シリコン膿を気相成長した後、高周波(RF)を停
止する(t□)。容器内のガスを真空弓きすることによ
って排出した後、真空容器を大気圧に戻し、基板37を
搬出する。 〔発明が解決しようとする課題〕 しかしながら、従来技術では、主反応ガスと副反応ガス
を同時に流し出し始めているが、第2図のグラフに示す
ように流量制御系の反応速度の差によってガス比が一定
とならない、特にモノシランガスの流量が多くなると、
場合によっては、RFの印加前にSiの組成比の多い膜
や比較的大きな堆積物の塊を形成する。また、圧力が設
定値に到達し、高周波(RF)の印加開始後も、最適な
混合比とはならず、目的とする膜質とは異なった膜が形
成されたりする。この膜は、膜質がポーラス気味で、絶
縁膜として使用した場合、電流リークの原因となること
がある。また、耐湿性の点や、下地との密着性の点でし
ばしば問題となっている。 しかるに本発明は、かかる課題を解決するものであり、
その目的とするところは、形成開始時にパーティクルの
発生がなく、膜質の安定したプラズマCVD膜を提供す
ることである。 〔課題を解決するための手段〕 本発明によるプラズマCVD膜の製造方法は、(1)a
)副反応ガスである。亜酸化窒素ガスを流し、ガス流量
を設定値に制御する工程と、b)圧力を設定値に制御す
る工程と、 C)主反応ガスであるモノシランを流し、ガス流量を設
定値に制御する工程と、 d)圧力を設定値に制御する工程と、 e)一定時間保持する工程と、 f)高周波(RF)印加する工程を上記順序で実行する
。 (2)請求項1記載の主反応ガスがモノシランで、副反
応ガスがアンモニアである。 (3)請求項1記載の主反応ガスがTEOS[S l 
(OCa Hs ) 4)で、副反応ガスが酸素である
ことを特徴とする。
[Industrial Application Field 1 The present invention is applicable to plasma CVD l! The present invention relates to a manufacturing method. [Prior Art] A conventional method for manufacturing a silicon oxide film by plasma CVD includes, for example, electrodes 32 and 3 whose surfaces are insulated, as shown in FIG.
3 are arranged in parallel, and a substrate 37 on which a CVD film is to be deposited is transported into a vacuum container 34 maintained at a constant temperature. continue,
After the inside of the container is evacuated, monosilane, which is the main reaction gas, and nitrous oxide, which is a side reaction gas, are flowed. After the gas volume and pressure reach the set values (t22 in Figure 2), high frequency (RF) is applied to the electrode and held for a certain period of time to grow silicon oxide pus in the vapor phase. RF) is stopped (t□). After the gas in the container is exhausted by vacuum evacuation, the vacuum container is returned to atmospheric pressure and the substrate 37 is carried out. [Problem to be Solved by the Invention] However, in the prior art, the main reaction gas and the side reaction gas start flowing out at the same time, but as shown in the graph of Figure 2, the gas ratio changes due to the difference in reaction speed of the flow rate control system. is not constant, especially when the flow rate of monosilane gas increases.
In some cases, a film with a high composition ratio of Si or a relatively large mass of deposits is formed before RF application. Further, even after the pressure reaches the set value and the application of radio frequency (RF) is started, the optimum mixing ratio is not achieved, and a film having a different film quality than the intended one may be formed. This film has a slightly porous quality and may cause current leakage when used as an insulating film. Moreover, there are often problems in terms of moisture resistance and adhesion to the base. However, the present invention solves these problems,
The purpose is to provide a plasma CVD film that does not generate particles at the start of formation and has stable film quality. [Means for Solving the Problems] The method for manufacturing a plasma CVD film according to the present invention includes (1) a.
) is a side reaction gas. A step of flowing nitrous oxide gas and controlling the gas flow rate to the set value; b) A step of controlling the pressure to the set value; C) A step of flowing monosilane, which is the main reaction gas, and controlling the gas flow rate to the set value. and d) controlling the pressure to a set value; e) holding the pressure for a certain period of time; and f) applying radio frequency (RF). The steps are executed in the above order. (2) The main reaction gas according to claim 1 is monosilane, and the side reaction gas is ammonia. (3) The main reaction gas according to claim 1 is TEOS [S l
(OCa Hs) 4), characterized in that the side reaction gas is oxygen.

【実 施 例】【Example】

以下本発明の実施例における工程を、第1図に示すグラ
フに基づいて詳細に説明する。 まず、トランジスタや抵抗等の半導体素子及びアルミニ
ウム配線の形成された半導体基板37を約400℃に保
たれ、絶縁された電極32.33が平行に配置された真
空容器34内に搬送する。 この容器内を一旦真空に引いた後、副反応ガスである亜
酸化窒素ガスを約1500secM流し、排気系を制御
して圧力を約5Torrに安定させる(t+s)−安定
した後、主反応ガスであるモノシラン(SiH,)を約
11003CC流し、圧力を再度5Torrに制御し、
安定させ(t+s)、5秒間保持した後(t+i) 、
  13.56MHz、500Wの高周波(RF)をε
印加する。所望の時間経過した後(t+i)、RFを停
止すると同時にガスを停止し、圧力を下げる。 副反応ガスのガス流量と圧力を、安定させた後、主反応
ガスを導入することによって、主反応ガスがRF印加前
に分解して、堆積物の塊が形成されることがなくなった
。また、圧力安定後に一定時間保持したことによって反
応ガスの分圧が毎回同じとなり、組成の一定した膜を再
現性良く形成すること、が可能となった。 ここでは、モノシラン−亜酸化窒素系の酸化シリコン膜
について説明したが、TEOS−酸素系の酸化シリコン
膜、および、モノシラン−アンモニア系の窒化シリコン
膜等にも同様の結果が得られた。また、2種類の反応ガ
スからなるCVD膜の形成のみならず、31類以上の反
応ガスによるCVDJliの製造方法としても同様に適
用できた。 [発明の効果] 以上の如く本発明によれば、プラズマCVD膜の形成時
に、副反応ガスを先に流しで圧力、ガス流量を安定させ
た後、主反応ガスの流量と圧力を安定させることによっ
て、主反応ガスがRF印加前に分解して、堆積物の塊が
形成されることがなく、組成の一定した膜を再現性良く
形成することが可能となり、耐湿性や膜のリーク電流の
点で問題がなくなる。
Hereinafter, steps in an embodiment of the present invention will be explained in detail based on the graph shown in FIG. First, a semiconductor substrate 37 on which semiconductor elements such as transistors and resistors and aluminum wiring are formed is transported into a vacuum container 34 maintained at about 400° C. and in which insulated electrodes 32 and 33 are arranged in parallel. Once the inside of this container is evacuated, nitrous oxide gas, which is a side reaction gas, is flowed for about 1500 secM, and the exhaust system is controlled to stabilize the pressure at about 5 Torr (t+s) - After stabilizing, the main reaction gas is A certain monosilane (SiH,) was flowed at about 11003 CC, and the pressure was controlled to 5 Torr again.
After stabilizing (t+s) and holding for 5 seconds (t+i),
13.56MHz, 500W radio frequency (RF)
Apply. After the desired time has elapsed (t+i), the RF is stopped, the gas is simultaneously stopped, and the pressure is lowered. By introducing the main reaction gas after stabilizing the gas flow rate and pressure of the side reaction gas, the main reaction gas was no longer decomposed before RF application and no deposit lumps were formed. Furthermore, by holding the pressure for a certain period of time after the pressure stabilized, the partial pressure of the reaction gas remained the same every time, making it possible to form a film with a constant composition with good reproducibility. Although a monosilane-nitrous oxide-based silicon oxide film has been described here, similar results were obtained with a TEOS-oxygen-based silicon oxide film, a monosilane-ammonia-based silicon nitride film, and the like. In addition, the present invention could be applied not only to the formation of a CVD film using two types of reactive gases, but also as a method for producing CVDJli using reactive gases of 31 or more types. [Effects of the Invention] As described above, according to the present invention, when forming a plasma CVD film, the side reaction gas is first flowed to stabilize the pressure and gas flow rate, and then the flow rate and pressure of the main reaction gas are stabilized. This prevents the main reaction gas from decomposing before RF application and forming deposits, making it possible to form a film with a constant composition with good reproducibility, improving moisture resistance and reducing film leakage current. There will be no problem at all.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図(a)〜(C)は、本発明の一実施例によるプラ
ズマCVD膿形成時のRF出力、主反応ガス及び副反応
ガスの流量、圧力を示すグラフである。 第2図(a)〜(C)は、従来のプラズマCVD111
m形成時のRF出力、主反応ガス及び副反応ガスの流量
、圧力を示すグラフである。 第3図は、プラズマCVD膜の形成装置の概略断面図で
ある。 1 2 3 4 5 6 7 8 ・RF発振器 ・上部電極 ・下部電極 ・真空容器 ・ガス入口 ・ガス出口 ・基板 ・絶縁物 箪:L 回
FIGS. 1A to 1C are graphs showing RF output, flow rates of main reaction gas and side reaction gas, and pressure during plasma CVD pus formation according to an embodiment of the present invention. Figures 2 (a) to (C) show conventional plasma CVD 111.
FIG. 2 is a graph showing the RF output, the flow rate of the main reaction gas and the side reaction gas, and the pressure during the formation of m. FIG. 3 is a schematic cross-sectional view of a plasma CVD film forming apparatus. 1 2 3 4 5 6 7 8 ・RF oscillator, upper electrode, lower electrode, vacuum container, gas inlet, gas outlet, substrate, insulator cabinet: L times

Claims (3)

【特許請求の範囲】[Claims] (1)a)副反応ガスである、亜酸化窒素ガスを流し、
ガス流量を設定値に制御する工程と、b)圧力を設定値
に制御する工程と、 c)主反応ガスであるモノシランを流し、ガス流量を設
定値に制御する工程と、 d)圧力を設定値に制御する工程と、 e)一定時間保持する工程と、 f)高周波(RF)印加する工程を上記順序で実行する
ことを特徴とするプラズマCVD膜の製造方法。
(1) a) Flowing nitrous oxide gas, which is a side reaction gas,
A step of controlling the gas flow rate to a set value; b) A step of controlling the pressure to a set value; c) A step of flowing monosilane, which is the main reaction gas, and controlling the gas flow rate to the set value; and d) Setting the pressure. A method for manufacturing a plasma CVD film, characterized in that the steps of: controlling the value to a constant value; e) holding it for a certain period of time; and f) applying radio frequency (RF) are performed in the above order.
(2)請求項1記載の主反応ガスがモノシランで、副反
応ガスがアンモニアであることを特徴とするプラズマC
VD膜の製造方法。
(2) The plasma C according to claim 1, wherein the main reaction gas is monosilane and the side reaction gas is ammonia.
A method for manufacturing a VD film.
(3)請求項1記載の主反応ガスがTEOS〔Si(O
C_2H_5)_4〕で、副反応ガスが酸素であること
を特徴とするプラズマCVD膜の製造方法。
(3) The main reaction gas according to claim 1 is TEOS [Si(O
C_2H_5)_4], a method for producing a plasma CVD film, characterized in that the side reaction gas is oxygen.
JP29552689A 1989-11-14 1989-11-14 Manufacture of plasma cvd film Pending JPH03155625A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29552689A JPH03155625A (en) 1989-11-14 1989-11-14 Manufacture of plasma cvd film

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29552689A JPH03155625A (en) 1989-11-14 1989-11-14 Manufacture of plasma cvd film

Publications (1)

Publication Number Publication Date
JPH03155625A true JPH03155625A (en) 1991-07-03

Family

ID=17821766

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29552689A Pending JPH03155625A (en) 1989-11-14 1989-11-14 Manufacture of plasma cvd film

Country Status (1)

Country Link
JP (1) JPH03155625A (en)

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JP2011054968A (en) * 2009-09-03 2011-03-17 Asm Japan Kk METHOD FOR FORMING CONFORMAL DIELECTRIC FILM HAVING Si-N COMBINATION BY PECVD
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