JPS6148865A - Electrophotographic sensitive body - Google Patents

Electrophotographic sensitive body

Info

Publication number
JPS6148865A
JPS6148865A JP17124884A JP17124884A JPS6148865A JP S6148865 A JPS6148865 A JP S6148865A JP 17124884 A JP17124884 A JP 17124884A JP 17124884 A JP17124884 A JP 17124884A JP S6148865 A JPS6148865 A JP S6148865A
Authority
JP
Japan
Prior art keywords
layer
substrate
amorphous
photoconductive layer
siox
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
JP17124884A
Other languages
Japanese (ja)
Inventor
Toshihiko Yoshitomi
吉富 敏彦
Hiroshi Horiuchi
堀内 博視
Yoshiharu Sato
佳晴 佐藤
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.)
Mitsubishi Kasei Corp
Original Assignee
Mitsubishi Kasei 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 Mitsubishi Kasei Corp filed Critical Mitsubishi Kasei Corp
Priority to JP17124884A priority Critical patent/JPS6148865A/en
Publication of JPS6148865A publication Critical patent/JPS6148865A/en
Pending legal-status Critical Current

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Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03GELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
    • G03G5/00Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
    • G03G5/02Charge-receiving layers
    • G03G5/04Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
    • G03G5/08Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being inorganic

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  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Photoreceptors In Electrophotography (AREA)

Abstract

PURPOSE:To improve the electrostatic charge characteristic of an electrophotographic sensitive body having an amorphous photoconductive layer consisting essentially of silicon and/or germanium on a conductive substrate by providing an insulating amorphous silicon oxide (a-SiOx) layer between the substrate and the photoconductive layer. CONSTITUTION:The insulating amorphous silicon oxide (a-SiOx) layer is provided on the substrate, then the photoconductive layer contg. the amorphous silicon and or amorphous germanium is formed on said a-SiOx layer by glow discharge decomposition onto the substrate. The electrophotographic sensitive body obtd. in the above-mentioned manner has such characteristics as high electrostatic charging power (surface potential in the stage of corona charge), small dark attenuation, stabilized repetitive charge characteristics, the freedom of the exfoliation of the amorphous photoconductive layer from the substrate and the absence of the residual potential.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は電子写真感光体に関する。[Detailed description of the invention] (Industrial application field) The present invention relates to an electrophotographic photoreceptor.

(従来の技術) 従来を子写冥感九体の光導電層には、 ca’s。(Conventional technology) Conventionally, the photoconductive layer of the photoconductive layer is ca's.

ZnO等の微粉末を有機物中に分散塗布したもの。A product in which fine powder such as ZnO is dispersed and coated in an organic substance.

As −? Teを添加したアモルファスse、ポリビ
ニルカルバゾールやトリニトロフルオレン等の有機半導
体が使われてきた。しかしながら、 OdS。
As-? Organic semiconductors such as amorphous se added with Te, polyvinylcarbazole, and trinitrofluorene have been used. However, OdS.

ZnO等の樹脂分散系の材料は耐湿性に問題があjl、
7−v−ルア7ス8eは高温度下での結晶化や材料自身
の人体への毒性という問題をかかえておシ、有機中導体
材料は耐刷性1c難点がある。
Resin dispersion materials such as ZnO have problems with moisture resistance.
7-v-lua 7s 8e has the problems of crystallization under high temperatures and the toxicity of the material itself to the human body, and organic medium conductive materials have problems with printing durability of 1c.

(発明が別法しようとする問題点) 以上の問題・難点を改良することが可能な材料として最
近水素化アモルファスシリコン(以下ra−131:H
Jと込う)及び水素化アモルファスゲルマニウム(以下
、ra−Ge:HJと−う)が脚光をあびている。、感
光体としてのa−8i:H。
(Problems to be solved by the invention) Hydrogenated amorphous silicon (hereinafter referred to as RA-131: H
ra-Ge) and amorphous germanium hydride (hereinafter referred to as ra-Ge:HJ) are attracting attention. , a-8i:H as a photoreceptor.

a−G6;)l及びこれらの混合体a −5iGay 
: Eは。
a-G6;)l and mixtures thereof a-5iGay
: E is.

光感度、耐刷住処すぐれ2分光g度を制御でき。It has excellent light sensitivity and printing durability, and can control the spectral density.

毒性に問題がないとhう利点をそなえて−る。It has the advantage of not having any toxicity problems.

これらの利点を4Aえて−るa−81:H感光体等では
あるが、静電写真用に使用した時には帯11特性上問題
がある。
A-81:H photoreceptors and the like have these advantages by 4A, but when used for electrostatic photography, there are problems in the characteristics of the band 11.

すなわち、たとえばa−8i:HIIの暗所での比”抵
抗は/ Qa −/ (712Ω・備と、従来の感光体
材料と比較して小さな値を示す。その九めにa−ai:
H膜を導電性基板の上にそのまま堆積しただけでは、暗
所ででもコロナ帯電時の表面電位が低下し、繰返し帯電
特性も良好とけいえないという難点を有する(たとえば
1%開昭3?−/グ33にグ号公報1%開昭j / −
J、2にゲタ号公報参照)。
That is, for example, the specific resistance of a-8i:HII in the dark is /Qa -/ (712 Ω · , which is a small value compared to conventional photoreceptor materials.The ninth one is a-ai:
If the H film is simply deposited on a conductive substrate, the surface potential during corona charging will decrease even in the dark, and the repeated charging characteristics cannot be said to be good (for example, 1%). /G No. 33 Publication 1% Kaishoj / -
J, 2, see Geta Publication).

(問題点を解決するための手段) そこで1本発明者らは、かかる点を改良して帯電圧特性
の良好な電子写真感光体の開発を目的にして棟々検討し
た結果1本発明に到達した。
(Means for Solving the Problems) Therefore, the inventors of the present invention conducted thorough studies with the aim of improving these points and developing an electrophotographic photoreceptor with good charging voltage characteristics, and as a result, they arrived at the present invention. did.

すなわち1本発明の要旨は、導電性基版上にシリコン及
び/又はゲルマニウムを主成分とするアモルファス光導
を層を有する電子写真感光体において、基板と光導電層
との間に絶縁性アモルファス酸化ケイ素(a−6iOメ
) jfAを設けたことを特徴とする電子写真感光体に
ある。
In other words, the gist of the present invention is to provide an electrophotographic photoreceptor having an amorphous photoconductive layer mainly composed of silicon and/or germanium on a conductive substrate, in which an insulating amorphous silicon oxide layer is provided between the substrate and the photoconductive layer. (a-6iOme) An electrophotographic photosensitive member is provided with a jfA.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

まず1本発明に係る電子写真用感光体において、基板は
通常、金属よシ遅る。
First, in the electrophotographic photoreceptor according to the present invention, the substrate is usually slower than metal.

たとえば、金属としては、アルミニウム、銅。For example, metals include aluminum and copper.

鉄、ニッケル、タンタル、ステンレス鋼等(セラミック
ス、有機物よりなる支持体上にアルミニウム等の金属を
蒸着等によう付加したものも含む)が挙げられるが、こ
れらの金属上にシリコン、ゲルマニウム、ff−ff族
(Zn 8等)、 III−V族(GaAs等)、有機
半導体等の半導体を付加させたものも使用し得る。
Examples include iron, nickel, tantalum, stainless steel, etc. (including those in which metals such as aluminum are added by vapor deposition on a support made of ceramics or organic materials), but silicon, germanium, ff- Those to which semiconductors such as FF group (Zn 8, etc.), III-V group (GaAs, etc.), and organic semiconductors are added may also be used.

ついで1本発明に係る感光体におりては、上記の基板上
に絶縁性アモルファス酸化ケイ素(a−8107)層が
設けられる。
Next, in the photoreceptor according to the present invention, an insulating amorphous silicon oxide (a-8107) layer is provided on the above substrate.

すなわち、”mH2n+t (n≧/)及び/又はB 
i a Ktn + * (Xはハロゲン原子)と酸化
性ガスを用いたグロー放電、又は熱分解によシ形成され
る。グロー放電で使用される酸化性ガスとしてhm素s
  N2o、 No、 N02J 00100.10s
 、 又td希iスもしくは〜7等の不活性ガスで希釈
したこれらの酸化性ガスが用いられる、空気も用いられ
るが、好ましくは希ガスで希釈した酸素ガス(通常02
#度0,0/ 〜! Ovol、%)が用いられる。グ
ロー放電時の装置内の圧力は1通常0.0 j 〜j 
Torr程度から選ばれる。a−8iOxにおいて、X
は通常0./≦X≦コ、3の範囲からS tJ、” ;
h 、  a −S io、 層の膜厚は通常0.02
〜0.jμの範囲から選ばれる。
That is, “mH2n+t (n≧/) and/or B
It is formed by glow discharge using ia Ktn + * (X is a halogen atom) and an oxidizing gas, or by thermal decomposition. hm element as an oxidizing gas used in glow discharge
N2o, No, N02J 00100.10s
In addition, these oxidizing gases diluted with an inert gas such as td diluted gas or ~7 are used.Air is also used, but preferably oxygen gas diluted with a rare gas (usually 02
#degree0,0/~! Ovol, %) is used. The pressure inside the device during glow discharge is 1 usually 0.0 j ~ j
Selected from around Torr. In a-8iOx, X
is usually 0. /≦X≦ko, from the range of 3 S tJ,”;
The thickness of the h, a-Sio, layer is usually 0.02
~0. selected from the range of jμ.

ツイテ、こ(D a −5iOメ%上に、アモルファス
シlj ニア ン及(J/Jl;tアモルファスゲルマ
ニウムを含む光導電層が、基板上にグロー放電分解釦よ
シ形成される。通常、膜圧は/〜!θμm、好ましくは
70〜30μmである。
A photoconductive layer containing amorphous silicon and (J/Jl;t) amorphous germanium is formed on the substrate using a glow discharge decomposition button. The pressure is /~!θμm, preferably 70-30μm.

このグロー放電分解に際しては、たとえばアモルファス
シリコンを言む光2s電層の場合1通常SiH,,等の
51nH2,+2.5inX2.n42 (X :/’
 ロゲン原子)(n≧7)等を含有するガスを諷圧雰囲
気中で、@論法、直流バイアスをかけた又論法又は高周
波法によってSIH,ガスを分角71することにより行
なう。このグロー放電に際しては、目的に応じホウ素、
屋紮、硫黄、酸素等を辿常数シー〜v%程度ドーピング
することができる。
In the case of this glow discharge decomposition, for example, in the case of a photoelectric layer made of amorphous silicon, 51nH2, +2.5inX2. n42 (X:/'
The SIH method is carried out using a gas containing (n≧7), etc., in a superatmospheric pressure atmosphere, using a DC bias method, a direct current bias method, or a radio frequency method. For this glow discharge, depending on the purpose, boron,
It is possible to dope the material with carbon dioxide, sulfur, oxygen, etc., at a constant value of about 0.0% to 0.0%.

キャリアーガスとし、ぞは N2. He、’ Ar、
 N2ガス等の通常使用されるガスを使用すればよい。
As a carrier gas, use N2. He, 'Ar,
A commonly used gas such as N2 gas may be used.

また、基板温度は、2jθ〜3!θ℃の範囲から選択さ
れる。
Also, the substrate temperature is 2jθ~3! Selected from the range of θ°C.

上記光導電層の形成に際しては、 5iIll)1.。When forming the above photoconductive layer, 5iIll) 1. .

+2または51nx2n+2のガスの濃度として10%
以上(体積比)、″cL圧、2 o o v 〜i K
V 、  Na密度として0.0 / 〜2 mA/g
l、圧力(層成長期)としてθ、/〜j Torr程度
の範囲が採用される。
+2 or 10% as the concentration of 51nx2n+2 gas
or more (volume ratio), ``cL pressure, 2 o ov ~ i K
V, Na density: 0.0/~2 mA/g
l, and the pressure (layer growth phase) is in the range of about θ,/~j Torr.

本発明に係る感光体において、上記a’−8iOx層と
アモルファス光導電層の界面は、好適には。
In the photoreceptor according to the present invention, the interface between the a'-8iOx layer and the amorphous photoconductive layer is preferably as follows.

不連続的であるように構成される。この不連続的とは、
光導′電層中への酸素の混入を他力防止することを意味
し、&!作上は、a−8iOx層を形成後プラズマを停
止し、原料ガスを排気した後。
Constructed to be discontinuous. This discontinuity is
It means to prevent oxygen from entering the photoconductive layer, &! In the photo, after forming the a-8iOx layer, the plasma was stopped and the source gas was exhausted.

ついで1次のアモルファス光d!電層形成のための原料
ガスを尋人することKよって構成しうる。
Next, first-order amorphous light d! It can be constructed by adding raw material gas for forming an electric layer.

具体的には0/S1比の膜厚方向の変化率が。Specifically, the rate of change in the 0/S1 ratio in the film thickness direction.

a −810,層と光導電層との界面で膜厚/μm当シ
、/桁以上、好ましくはθ、/μm当シ/桁当止7変化
を生せしめるように構成される。
The structure is such that at the interface between the a-810 layer and the photoconductive layer, the film thickness changes by an order of magnitude per .mu.m or more, preferably by 7 orders of magnitude per .mu.m.

さらに1本発明に係る電子写真感光体は光導i!層上に
各釉の表面保a層を設けることができる。
Furthermore, the electrophotographic photoreceptor according to the present invention is a light guide i! A surface retaining layer of each glaze can be provided on the layer.

上記のようにして祐られる電子写真用感光体は、帯電能
(コロナ帯箪時の表面電位)が窩ぐ。
The electrophotographic photoreceptor that is heated as described above has a high charging ability (surface potential when the corona band is removed).

#減りも小はく、繰返し帯電4?I:性が安定化し、基
板からのアモルファス光導電層のはく離がなく、かつ、
残′ti1’を位がないという特徴を有する、(実施例
) 以下、実施例にょシ1本発明をさらに詳細に説明する。
# Repetitive charging 4 with little decrease? I: The properties are stabilized, there is no peeling of the amorphous photoconductive layer from the substrate, and
(Example) The present invention will be described in more detail in Example 1 below.

実施例中、ガス濃度にっbての「φ」、「泗」は容量に
よる、 実施例/ 真空容器中におかれたヒーター上にアルミニウム基板を
とシつけ、ロータリーポンプで粗排気した係・、油拡散
ポンプによp、 j X / 0−’ Torr以下の
真空中で温度300℃で3a分間加熱する。、1,1F
気をロータリーポンプに戻して、基板温度を3.20℃
にしテシラン(SiB、 ) ! 500M圧力を6.
6 Torrにする。基板に600 Hzの交流電圧(
数百V)を印加し、接地された電極との間にグロー放電
を生じさせ、絶縁性a−,:5xox層を!分+i:i
J堆積させた(膜厚的θ、/μm)(なお、O/Si原
子数比XのX線マイクロアナライザー(EPMA)分析
値は約2./であった)。
In the examples, "φ" and "泵" for gas concentration are based on the capacity. , heated with an oil diffusion pump at a temperature of 300° C. for 3 a minute in a vacuum of p, j X / 0−′ Torr or less. ,1,1F
Return the air to the rotary pump and lower the substrate temperature to 3.20℃
Nishi Teshiran (SiB, )! 500M pressure 6.
Set to 6 Torr. A 600 Hz AC voltage (
Several hundred V) is applied to generate a glow discharge between the grounded electrode and the insulating a-,:5xox layer! minute+i:i
J was deposited (film thickness θ, /μm) (the X-ray microanalyzer (EPMA) analysis value of the O/Si atomic ratio X was about 2./μm).

つぎに反応ガスf 3iH4j o 500M、 B、
H6/2(2(,270pIn) x、g So(:t
M (B211,7BLH,−4t09%)、NHs 
/ ”θ(/ % ) 48 C! OM (NHs 
/ S 1H4= 0 、J %)−02/He (2
%)  0,6500M (o2/sia、=Q、θダ
%)に切り!!li!え、圧力/、/ Torr 、基
板温度J’、2(7℃で!!分分間ダグロー放電せ膜厚
的Zμmの光導電層を形成させた。
Next, the reaction gas f 3iH4j o 500M, B,
H6/2(2(,270pIn) x, g So(:t
M (B211,7BLH, -4t09%), NHs
/”θ(/%) 48 C!OM (NHs
/S1H4=0,J%)-02/He (2
%) Cut to 0,6500M (o2/sia, = Q, θ da%)! ! li! A photoconductive layer having a film thickness of Z μm was formed by douglow discharge for 3 minutes at a pressure of /, / Torr and a substrate temperature of J′, 2 (7° C.).

得られた感光体について感光体評価機(F、X’A)に
よシ帯電能と暗減衰率を測定した(コロナ電圧+乙KV
 )。
The charging ability and dark decay rate of the obtained photoconductor were measured using a photoconductor evaluation machine (F, X'A) (corona voltage + KV
).

蛍知1能30.j V/μm1暗減衰率≦、7チ/弐で
あった。
Fire intelligence 1 ability 30. j V/μm1 dark decay rate ≦, 7 chi/2.

比較例1 夾M flj /においてa−sIox層を設けないほ
かは、同様にグロー放電させて感光体を得た。
Comparative Example 1 A photoreceptor was obtained by glow discharge in the same manner, except that no a-sIox layer was provided in M flj /.

i 71V能/76θV/μm、暗減哀率20.0%/
鯉であった。
i 71V power/76θV/μm, darkening rate 20.0%/
It was a carp.

実施例λ Ai基板上に1次の条件で絶縁性a−8inx層及び光
導電層a−8i : H層よシなる感光体(膜厚j、9
μn1 )を得た。
Example λ A photoreceptor (thickness j, 9
μn1) was obtained.

Oa −5inxJ@ N20/S iH,流量比!=弘1Eli毛=3SCO
M圧  力 θ、9 j ’I’Orr 基板温度 32!℃ グロー放電分解(AO!00Hz)9分膜  厚 0.
コ!μm 0a−8i:HM SiH,20SC0M B2H6/1(、(/2jppm) 7 SOCM (
B2H,/biH,= &1−91Xn)圧  力 /
、、2 Torr 基板温度 323℃ グロー放電時間 100分 コロナ電圧+4 KV 、光量!ルックスでIFA繰り
返し帯電特性を測定し、結果を8g1図忙示した。
Oa -5inxJ@N20/S iH, flow rate ratio! = Hiro 1 Eli hair = 3 SCO
M pressure θ, 9 j 'I'Orr substrate temperature 32! ℃ Glow discharge decomposition (AO!00Hz) 9 minutes film thickness 0.
Ko! μm 0a-8i: HM SiH, 20SC0M B2H6/1(, (/2jppm) 7 SOCM (
B2H, /biH, = &1-91Xn) Pressure /
,,2 Torr Substrate temperature 323℃ Glow discharge time 100 minutes Corona voltage +4 KV, Light intensity! IFA repeated charging characteristics were measured using Lux, and the results are shown in Figure 8g1.

なお、残留電位は10V以下で、繰返しによっても増加
はみられなかった。
Note that the residual potential was 10 V or less, and no increase was observed even after repeated testing.

比較例λ a−Si隅層を設けないで次の条件で光導電層をグロー
放電により成膜し、感光体(膜厚30、/μfrL)を
得た。
Comparative Example λ A photoconductive layer was formed by glow discharge under the following conditions without providing an a-Si corner layer to obtain a photoreceptor (thickness: 30/μfrL).

反応ガス組成:実施例2と同一 圧  力 0.9Torr 基板温度 3コ!℃ グロー放電時間 600分 コロナ電圧+jKV(初期帯電圧を実施例の感光体のそ
れと一致させるため忙+r xvを採用)、光量!ルッ
クスでEPA繰返し特性を測定し、結果を第1図に示し
た。
Reaction gas composition: Same as Example 2 Pressure 0.9 Torr Substrate temperature 3 pieces! °C Glow discharge time 600 minutes Corona voltage + jKV (use +r xv was adopted to match the initial charging voltage with that of the photoreceptor in the example), light intensity! The EPA repeatability was measured using Lux, and the results are shown in Figure 1.

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

第1図は1本発明の実施例コ及び比較例λで得られた感
光体の繰シ返し帯電特性を示す。横軸は繰返し数、縦軸
は表面電位(v)を示す。○は実施例コ、・は比較例−
についての値を示す。 晃 1 図 繰惺し数
FIG. 1 shows the repeated charging characteristics of the photoreceptors obtained in Example 1 of the present invention and Comparative Example λ. The horizontal axis shows the number of repetitions, and the vertical axis shows the surface potential (v). ○: Example, ・: Comparative example
indicates the value for Akira 1 Figure repeating number

Claims (1)

【特許請求の範囲】[Claims] (1)導電性基板上にシリコン及び/又はゲルマニウム
を主成分とするアモルファス光導電層を有する電子写真
感光体において、基板と光導電層との間に絶縁性アモル
ファス酸化ケイ素(a−SiO_x)層を設けたことを
特徴とする電子写真感光体。
(1) In an electrophotographic photoreceptor having an amorphous photoconductive layer mainly composed of silicon and/or germanium on a conductive substrate, an insulating amorphous silicon oxide (a-SiO_x) layer is provided between the substrate and the photoconductive layer. An electrophotographic photoreceptor characterized by being provided with.
JP17124884A 1984-08-17 1984-08-17 Electrophotographic sensitive body Pending JPS6148865A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17124884A JPS6148865A (en) 1984-08-17 1984-08-17 Electrophotographic sensitive body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17124884A JPS6148865A (en) 1984-08-17 1984-08-17 Electrophotographic sensitive body

Publications (1)

Publication Number Publication Date
JPS6148865A true JPS6148865A (en) 1986-03-10

Family

ID=15919794

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17124884A Pending JPS6148865A (en) 1984-08-17 1984-08-17 Electrophotographic sensitive body

Country Status (1)

Country Link
JP (1) JPS6148865A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4906542A (en) * 1987-04-23 1990-03-06 Canon Kabushiki Kaisha Light receiving member having a multilayered light receiving layer composed of a lower layer made of aluminum-containing inorganic material and an upper layer made of non-single-crystal silicon material
US4906543A (en) * 1987-04-24 1990-03-06 Canon Kabushiki Kaisha Light receiving member having a multilayered light receiving layer composed of a lower layer made of aluminum-containing inorganic material and an upper layer made of non-single-crystal silicon material

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4906542A (en) * 1987-04-23 1990-03-06 Canon Kabushiki Kaisha Light receiving member having a multilayered light receiving layer composed of a lower layer made of aluminum-containing inorganic material and an upper layer made of non-single-crystal silicon material
US4981766A (en) * 1987-04-23 1991-01-01 Canon Kabushiki Kaisha Light receiving member having a multilayered light receiving layer composed of a lower layer made of aluminum-containing inorganic material and an upper layer made of a non-single-crystal silicon material
US4906543A (en) * 1987-04-24 1990-03-06 Canon Kabushiki Kaisha Light receiving member having a multilayered light receiving layer composed of a lower layer made of aluminum-containing inorganic material and an upper layer made of non-single-crystal silicon material

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