JPS5922052A - Electrophotographic receptor - Google Patents

Electrophotographic receptor

Info

Publication number
JPS5922052A
JPS5922052A JP13112482A JP13112482A JPS5922052A JP S5922052 A JPS5922052 A JP S5922052A JP 13112482 A JP13112482 A JP 13112482A JP 13112482 A JP13112482 A JP 13112482A JP S5922052 A JPS5922052 A JP S5922052A
Authority
JP
Japan
Prior art keywords
layer
oxygen
gas
amorphous silicon
silicon hydride
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
Application number
JP13112482A
Other languages
Japanese (ja)
Other versions
JPH052985B2 (en
Inventor
Yukio Suzuki
幸夫 鈴木
Genichi Adachi
元一 安達
Hideji Yoshizawa
吉沢 秀二
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.)
Toshiba Corp
Original Assignee
Toshiba Corp
Tokyo Shibaura Electric Co Ltd
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 Toshiba Corp, Tokyo Shibaura Electric Co Ltd filed Critical Toshiba Corp
Priority to JP13112482A priority Critical patent/JPS5922052A/en
Publication of JPS5922052A publication Critical patent/JPS5922052A/en
Publication of JPH052985B2 publication Critical patent/JPH052985B2/ja
Granted legal-status Critical Current

Links

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
    • G03G5/082Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being inorganic and not being incorporated in a bonding material, e.g. vacuum deposited
    • G03G5/08214Silicon-based
    • G03G5/08278Depositing methods
    • 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
    • G03G5/082Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being inorganic and not being incorporated in a bonding material, e.g. vacuum deposited
    • G03G5/08214Silicon-based
    • G03G5/08221Silicon-based comprising one or two silicon based layers

Abstract

PURPOSE:To obtain an electrophotographic receptor superior in photosensitivity, etc., by forming an amorphous silicon hydride layer contg. a specified amt. of oxygen as a charge transfer layer and an amorphous silicon hydride layer as a charge generating layer on a conductive substrate. CONSTITUTION:An amorphous silicon hydride layer contg. 0.1-40 atomic% O is formed as a charge transfer layer on the conductive substrate 1 by glow discharging in SiH4, Si2H6 or the like contg. 1.0-6.0vol% O2. Then, an amorphous silicon hydride layer is formed on it as a charge generating layer 3 by glow discharging in gaseous silane alone without adding O2. As a result, the obtained electrophotographic receptor is superior in charging characteristics and photosensitivity, and high in deposition speed during the formation of the layer 2.

Description

【発明の詳細な説明】 〔発明の技術分野〕 本発明は、電子写真感光体に関し、更に詳しくは、良好
な暗抵抗を有し、光感度特性が優れた電子写真感光体に
関する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field of the Invention] The present invention relates to an electrophotographic photoreceptor, and more particularly to an electrophotographic photoreceptor having good dark resistance and excellent photosensitivity characteristics.

〔発明の技術的背景とその問題点〕[Technical background of the invention and its problems]

従来、電子写真感光体に使用される感光材料としては、
例えば、アモルファスセレン(a−8e)、硫化カドミ
ウム(CdS)或いはセレン−テルル(Se−Te )
 等の無機材料や、ポIJ −N−ビニルカルバゾール
(PVCz)、トリニトロフルオレノン(TNF)等の
有機材料が知られている。しかしながら、これらの感光
材料を使用するにハ種々の問題点が残されている。即ち
、上記した感光材料の中で、無機材料は極めて毒性が強
いため、その製造に際しては人体に対する安全対策上の
特別な配lφ:fc’決するという問題点を有している
。又、無機材料を用いて、it’4造された電子写真感
光体は、熱安定性75h・飢って悪く、四に、感光体の
機械的強度が弱いという問題点を有しているため、シス
戸ムの・特性をある程度犠牲にして使用されているのが
実状である。
Conventionally, the photosensitive materials used in electrophotographic photoreceptors include:
For example, amorphous selenium (a-8e), cadmium sulfide (CdS), or selenium-tellurium (Se-Te)
Inorganic materials such as PVC-N-vinylcarbazole (PVCz) and trinitrofluorenone (TNF) are known. However, various problems remain when using these photosensitive materials. That is, among the above-mentioned photosensitive materials, inorganic materials are extremely toxic and therefore have the problem of requiring special precautions for human body safety when producing them. In addition, electrophotographic photoreceptors manufactured using inorganic materials have poor thermal stability of 75 hours, and fourth, the mechanical strength of the photoreceptor is weak. The reality is that it is used at the expense of some of the characteristics of the system.

又、上記したPVCzやTNF等の有機材料においては
、有機材料であるために熱安定性や耐摩耗性が不曳であ
り、従って製品寿命が4Hjいという間、′」点を有し
ている。
In addition, organic materials such as PVCz and TNF mentioned above have excellent thermal stability and abrasion resistance because they are organic materials, and therefore have a product life of 4 Hz. .

一方に卦いて、近年、高周波グロー改定分解法により成
膜されるアモルファス水素化ノリコン(以下、a −S
iHと称す。)7が、電子写真感光体の感光材料として
注目を集めている。このa−8iHは、上記した従来の
感光材料と比較して還境汚染性、耐熱性、耐摩耗性及び
光感間特性等の点(・(お・いて優れた性能を有してい
る。
On the other hand, in recent years, amorphous hydrogenated silicone (hereinafter referred to as a-S
It is called iH. )7 is attracting attention as a photosensitive material for electrophotographic photoreceptors. This a-8iH has excellent performance in terms of environmental contamination resistance, heat resistance, abrasion resistance, and photosensitive characteristics, as compared to the conventional photosensitive materials described above.

しかしなから、このa−8t)Iを使用した電子写真感
光体f、−12、+lij常のグロー・j:z t4分
解法を用いて′il+!潰した14合には、その暗抵抗
が最大Cも10I0Ω鑵以上の値を得られず、又、コロ
ナ帯電した用台にも所定の表面・電位が得られないとい
う間り1点を有している。fllEって、このa−8I
Hを使用した電子写真1叱光体は、未だ実用化されるに
it螢1]っていない。
However, using this a-8t)I electrophotographic photoreceptor f, -12, +lij using the usual glow j:z t4 decomposition method, 'il+! In the crushed 14 cases, the maximum dark resistance C could not be obtained with a value of more than 10I0Ω, and there was one point in between that the specified surface potential could not be obtained on the corona-charged table. ing. fllE is this a-8I
An electrophotographic scintillator using H has not yet been put into practical use.

このa−8IH感光体の暗抵抗を1011Ω1程度に向
上させるために、a−8iHにX・1してホウ素(H)
全20〜20′″Oppm程1> 、或いは酸素(0)
等を0.1〜30アトミック係程庶流加することが、例
えば、特開昭54−86341号公報、特開昭54−1
45539号公報十に開示されている。
In order to improve the dark resistance of this a-8IH photoreceptor to about 1011Ω1, boron (H) was added by adding X.1 to a-8iH.
Total 20~20'''Oppm 1>, or oxygen (0)
etc., with an atomic coefficient of 0.1 to 30 is described, for example, in Japanese Patent Application Laid-Open No. 54-86341 and Japanese Patent Application Laid-open No. 54-1.
It is disclosed in Publication No. 45539.

し゛・フシし、ホウ素添加によるa−8IHの暗抵抗の
向−ヒは極くわずかであり、大幅な改善にはならない。
However, the effect of boron addition on the dark resistance of a-8IH is extremely small and does not result in a significant improvement.

−力、B−8iI(に酸素を添加したものは、暗抵抗は
向上するものの、感光体の酸素含有曖が多くなると光;
音度特性が低下するという問題点を・)イしていl)。
- When oxygen is added to B-8iI, the dark resistance improves, but as the oxygen content of the photoreceptor increases, the light resistance increases
This eliminates the problem of reduced sound intensity characteristics.

又、酸素を含有するa−8iH感光体の光学吸収端(E
g Op t )け、a−8iH感光体のそれと比較し
て極端に犬へいだめに、長波長感光体としての機能が損
われるという問題点を有している。
Furthermore, the optical absorption edge (E
However, compared to that of the a-8iH photoreceptor, it has a problem in that its function as a long wavelength photoreceptor is significantly impaired.

更に、特開昭56−156834号公報には、電子写真
感光体に要求される約1013Ωα以上の1111抵抗
を得るだめには、a−SiHに酸示をドーピングすれば
効果的であることが開小されている。その中で、a−8
iHに対する酸素〔7)ドーピングlijは約10−′
乃至5 X I F2アトミック飴の範囲が2・、・適
であると記載されている。しかし、上記酸木ドーフ’ 
a−8ijl感光体は、良好々暗抵抗を力えるも 〕の
、その製造に際して堆積速度がJ′Y、jいために工業
的な生産には適していないという間’、11(’点を有
している。
Furthermore, Japanese Patent Application Laid-Open No. 56-156834 discloses that it is effective to dope a-SiH with an acid in order to obtain a 1111 resistance of about 1013 Ωα or more required for an electrophotographic photoreceptor. It has been small. Among them, a-8
Oxygen [7) doping lij for iH is about 10-'
It is stated that the range of 5 X I F2 atomic candy is suitable. However, the above acid tree Dofu'
Although the a-8ijl photoreceptor has good dark resistance, it is not suitable for industrial production because of the slow deposition rate during its manufacture. are doing.

〔発明の目的〕[Purpose of the invention]

本へへ明の目的は、上記した問題点を解消し、 s面電
位が得られる程度にまで篩い暗抵抗を有し、且つ、光感
度特性、特に((彼畏ijQ光!rケ性が1・とれた電
子写真感光体を提供することにある。
The purpose of this book is to solve the above-mentioned problems, to have a dark resistance that is high enough to obtain an s-plane potential, and to have light sensitivity characteristics, especially ( 1. To provide a high quality electrophotographic photoreceptor.

〔発明の概安〕[Summary of the invention]

本発明の電子写真感光体は、尋7M性支持基体と、該基
体上に設けられた、酸素を0.1〜40アトミツクチ含
有するアモルファス水素化シリコン層から成る電荷輸送
層及びアモルファス水素化シリコン)1すから成る電荷
発生層により+H(4成されることを特徴とするもので
ろる。
The electrophotographic photoreceptor of the present invention comprises a 7M supporting substrate and a charge transport layer comprising an amorphous silicon hydride layer provided on the substrate and containing 0.1 to 40 atoms of oxygen. It is characterized in that +H(4) is formed by the charge generation layer consisting of 1 and 1.

以下において、本発明を更に詳しく説明する。In the following, the invention will be explained in more detail.

本発明に係るアモルファス水素化シリコン層と、酸素ド
ープアモルファス水素化シリコン層(以下、a−8iT
I : 0層と称す。)とが積層されたべ子写真感光体
表面の断面図を図面に示す。
The amorphous hydrogenated silicon layer according to the present invention and the oxygen-doped amorphous hydrogenated silicon layer (hereinafter referred to as a-8iT
I: Referred to as 0 layer. ) is shown in the drawing.

図面において、導電性支持基体1」二に(rよ、酸、代
ドープアモルファス水素化シリコン層2及びアモルファ
ス水素化シリコン層3が積層されている。
In the drawings, a conductive support substrate 1 is laminated with an acid-doped amorphous hydrogenated silicon layer 2 and an amorphous hydrogenated silicon layer 3.

本発明に号、・いて支持基体上に形成されるa−8i)
(:0層は、電荷輸送層として機能する。該J・’Aは
、a−8i1丁に対する!1シ素のドーピング駄を増加
したことにより、堆積速度が著しく速く、コロナ電荷の
保持特開が優1%たものとなる。即ち、a−8iHと1
1ミに酸素が支持基体上に堆積するため、堆積速度は2
.0乃至6゜Oμ/I(程度にまで高速化し、暗抵抗も
帯電に必要とされる1 0”l’r至10140鍜程度
の値を有するa−8tl(: 0 治がイjlられるも
のである。かかるa−8iH: 0層の膜厚ば5μ乃至
1−00μであることが好ましく、1ぎに好−ましくは
10μ乃孕Iμである。又、酸素のドーピング)虹は、
0.1〜411アトミツク係であることが必′/′):
であり、好−ましくけ1.0〜20アトミツク係である
。酸素のドーピング量が0.1アトミツクチ未肖である
と、成1霞したa−8iH: 0層の暗抵抗が10′0
.0cm以下であり、一方、40アトミック%を、t<
4えると、f扛荷輸送時性が極端に低下する。
a-8i) formed on a supporting substrate according to the present invention;
(The :0 layer functions as a charge transport layer.The J・'A has an extremely high deposition rate due to the increased doping of !1 silicon to one a-8i, and retains the corona charge. is more than 1%. That is, a-8iH and 1
Since oxygen is deposited on the supporting substrate at 1 mm, the deposition rate is 2 mm.
.. The speed has been increased to 0 to 6゜Oμ/I (about 0 to 6゜Oμ/I), and the dark resistance has a value of about 10''l to 10140㎜, which is required for charging. The thickness of such a-8iH:0 layer is preferably 5μ to 1-00μ, most preferably 10μ to Iμ.Also, oxygen doping)
Must be in charge of 0.1~411 atoms):
, and preferably has a ratio of 1.0 to 20 atoms. When the oxygen doping amount is 0.1 atoms, the dark resistance of the a-8iH layer becomes 10'0.
.. 0 cm or less, while 40 atomic%, t<
4, the transportability of f-loaded cargo will be extremely reduced.

上記a−8IH: 0層上に積層されるa−8i[(J
li 3は、電荷発生層として機hi主する。該層はa
−8iH: 0層による長波長域の光感度の低下を補填
し、E1℃子僅真感光体の光感度特性をI・もめる。
Above a-8IH: a-8i[(J
li3 functions primarily as a charge generation layer. The layer is a
-8iH: Compensates for the decrease in photosensitivity in the long wavelength region due to the 0 layer, and improves the photosensitivity characteristics of the E1°C photoreceptor.

かかるa−8iH層の膜厚は0.1μ乃至10μである
ことが好1しく、更に好ましくは1μ乃至5μである。
The thickness of such a-8iH layer is preferably 0.1 μ to 10 μ, more preferably 1 μ to 5 μ.

本発明において使用される導電性支持基体it、特に限
定されないが、例えば、ガ゛ラスにステンレス、アルミ
ニウム或いはI T O(Indium Tinoxi
dθ)膜等を被覆したもの等が使用可能であり、その形
状ハ、フィルム、シート、ドラム、Rルト等のいずれで
あってよい。
The conductive support substrate used in the present invention is not particularly limited, but includes, for example, glass, stainless steel, aluminum, or ITO (Indium Tinoxy).
It is possible to use a material coated with a dθ) film, etc., and the shape thereof may be any of a film, a sheet, a drum, an R-rut, etc.

本発明の電子写真感光体は、例えば、次のようにして製
造することが可能である。
The electrophotographic photoreceptor of the present invention can be manufactured, for example, as follows.

即ち、a−8iH層及びa−8iHS 0層は、をれぞ
れ、化常の高周波グロー放電分解法により、シランガス
(SiH4)を分解して、或いは更に酸素を添+JFl
 l〜た5likガスを分解して、導電性支持基体上に
堆積ぜ(7め、+4’(膜さfLる。この時の基体温度
は50°C乃至300 cであることが好ましく、咀に
好ましくtrF: 100°C乃ij 250 ”Cで
ある。又、高1波電源としては、I MHz乃至50 
MHz  のラジオ波を使用「ることが好1しく、特に
13.56 MHzのものか好−ましい。そして、出力
密度はIOW乃至IKWを’+t 4it1間に印加し
てガス分解することが好ましい。
That is, the a-8iH layer and the a-8iHS 0 layer are formed by decomposing silane gas (SiH4) by a conventional high-frequency glow discharge decomposition method, or by adding oxygen + JFl.
The 5lik gas is decomposed and deposited on the conductive supporting substrate (7, +4'). Preferably trF: 100°C to 250"C. Also, as a high 1 wave power source, I MHz to 50"C.
It is preferable to use a radio wave of 13.56 MHz, particularly preferably one of 13.56 MHz.Then, it is preferable to apply a power density of IOW to IKW between '+t4it1 for gas decomposition. .

a−8iH: 0層を形成する場合に使用される原料ガ
スとしては、jyllえば、酸素ガスを含有せしめたシ
ランガス(Si&)、ソシランガス(Sid(a )等
が挙げられるが、酸素ガスを含有せしめたシランガスを
使用することが好ましい。シランガス中の酸素ガスの含
有脚は、a−8it(: 0層に0.1〜40アトミッ
ク係の酸素がドー ピングされるように適宜設定される
が、0.5〜12.0休情係であることが好ましく、更
に好ましくは1.0〜5.0休情係である。
A-8iH: Examples of the raw material gas used when forming the 0 layer include silane gas (Si&) containing oxygen gas, sosilane gas (Sid(a)), etc.; It is preferable to use a silane gas containing 0.1 to 40 atomic coefficients of oxygen in the silane gas. It is preferably .5 to 12.0 rest, more preferably 1.0 to 5.0 rest.

a−st、rI層を形成する場合には、−に記a−8I
H: 0層の形成において、C:y素ガスの供給を停止
するのみでよく、a−8iH: O層の1ト成に体重し
てa −S iII層の積層が可能である。
When forming a-st, rI layer, write a-8I in -
In the formation of the H:0 layer, it is only necessary to stop the supply of the C:y element gas, and it is possible to stack the a-S iII layer with one composition of the a-8iH:O layer.

グロー、放′イ分解法により141j脱されるa−8i
HU’?は、前述した直り、その暗抵抗が++、j大で
も10”Ω鋼に満たず、一般に、約101sΩ鑞腰上の
暗抵抗が必゛夕とされる電子写真感光体に適用するため
には、10−’〜5 X 10−2アトミック%程度酸
素をドーピングすればよいことが知られている。本発明
者−らは、a−8iHへの119素のドーピング骨を更
に増加して、0.1〜40アトミツク係とした場合に、
堆4、々速度が速く、優れたコロナ電荷の1層時特性を
何するa−8iH: 0層が得られることを見出した7
・しかし、上記a−8+H: 0層は、酸素のバ有縫が
極めて多いために、81−0結合が増加することになる
Glow, a-8i released from 141j by the free decomposition method
HU'? As mentioned above, its dark resistance is less than 10" Ω steel even at ++, and in general, in order to be applied to an electrophotographic photoreceptor that requires a dark resistance of about 101 s Ω or more. It is known that it is sufficient to dope oxygen by about 10-' to 5 x 10-2 atomic%.The present inventors further increased the doping bone of 119 elements to a-8iH to obtain 0. .1 to 40 atoms,
4. It was found that a-8iH: 0 layer can be obtained with a fast deposition speed and excellent corona charge characteristics in a single layer.7
-However, since the above a-8+H:0 layer has an extremely large number of oxygen barrings, the number of 81-0 bonds increases.

その結果、a−8iII : 0層の光学吸収端はa−
8iH層のそれよりも知波長にシフトし、長波長域にあ
−ける光感度が11(下することになる。このような欠
点を解消するために、本発明においては、堆積速度が速
く電荷保持性が優れたa−8iH: 0層を1−it荷
輸送層として使用すると共に、優れた光感度特性を有す
るa−8iH層を電荷発生層として積層せしめたもので
ある。
As a result, the optical absorption edge of the a-8iII: 0 layer is a-
The 8iH layer shifts to a wavelength that is lower than that of the iH layer, and the photosensitivity in the long wavelength region becomes 11 (lower). The a-8iH layer with excellent retention properties is used as a 1-it charge transport layer, and the a-8iH layer with excellent photosensitivity characteristics is laminated as a charge generation layer.

〔発明の効果〕〔Effect of the invention〕

本発明の構成から成る電子写真感光体は、a−8iH:
Oj−を重性輸送層として使用することにより、良好な
暗抵抗を有するものであり、又、a−8iH層を電荷発
生層として積層せしめることにより、優れた光感度特性
を有するものである。
The electrophotographic photoreceptor having the structure of the present invention includes a-8iH:
By using Oj- as a heavy transport layer, it has good dark resistance, and by stacking an a-8iH layer as a charge generation layer, it has excellent photosensitivity characteristics.

更に、その製造(で際しては、a−8iH: 0層中に
お・ける19素のドーピング量が多いために、堆積速度
が20乃至6.0μ/H程度と著しく増加し、速やかな
製造が”r fit:となる。
Furthermore, in its manufacture (in the case of a-8iH:0), due to the large amount of doping of 19 elements in the 0 layer, the deposition rate increases significantly to about 20 to 6.0 μ/H, and Manufacturing becomes "r fit:".

〔発明の実施例〕[Embodiments of the invention]

実施例1 平行平板方式の高周波グロー1夕・:主装置〜の一方の
′電極に、ITO膜が?jシ覆されているコーニング7
Q59(ダウコーニング慴)製)ガラス基板を段着した
Example 1 Parallel plate type high frequency glow for one night: ITO film on one electrode of the main device ~? Corning 7 overturned
Q59 (manufactured by Dow Corning) glass substrates were stacked.

装置内を一旦、I X 10−6’l’orrtで排気
した凌、シラン(SIT−L)ガス及び酸素(07)ガ
スを樽入して、ガス圧を8 X 10−’Torrに調
゛)″とした。混合ガス中の酸素ガス含有附は、6.0
体積φとなるように浦。
Once the inside of the apparatus was evacuated at I x 10-6'l'orrt, silane (SIT-L) gas and oxygen (07) gas were put into barrels and the gas pressure was adjusted to 8 x 10-'Torr. )''.The oxygen gas content in the mixed gas is 6.0
Ura so that the volume is φ.

腿、計を用いて調整した。Adjustments were made using a thigh and scale.

ガラス基板温度を250 ’Cに加熱段゛・ぜした1な
、平行平板電極間に1.3.56 MITy、の高周波
を印jJIIすることによりグロー放電を惹き起こし、
5t)L及?′j:0、ガスを分角′rして基板上に酸
素を含有するアモルファス水素化シリコン層を形成した
。この時の堆積速度は5^/ secであり、約10μ
厚の′14元荷ψ:、)送層としでのa−8iH: 0
層を〒11だ。
A glow discharge was caused by applying a high frequency wave of 1.3.56 MITy between the parallel plate electrodes with the glass substrate temperature set to 250'C with a heating stage.
5t) L and? 'j: 0, and the gas was supplied at an angle of 'r' to form an amorphous hydrogenated silicon layer containing oxygen on the substrate. The deposition rate at this time was 5^/sec, and the thickness was about 10μ.
'14 original thickness ψ:,) a-8iH as feeding layer: 0
The layer is 〒11.

次いで、I”セ素ガスの供給を停止1−シ、シランガス
のみを供給して放電を続け、a−8iH: 0 !、Q
上(・ζ1賀素を含有しないアモルファス水素化シリコ
ン層を(、゛を層した。この時の堆r*4yはIA/s
eeであり、約2μ厚の電荷発生層としてのa−Fii
l[層を積層し、電子写真感光体を得た。
Next, stop the supply of the cerium gas, continue the discharge by supplying only the silane gas, and a-8iH: 0!, Q
An amorphous hydrogenated silicon layer (,゛) containing no element (・ζ1) was layered on the top.The deposition r*4y at this time was IA/s.
ee and a-Fii as a charge generation layer with a thickness of about 2μ
l [Layers were laminated to obtain an electrophotographic photoreceptor.

この1・1&光体について、マイナス6KVでコロナ帯
「(iさせたところ、550vの前面電位が観測された
。次いで、151uz、secの像露光を行なって静電
潜像を形成した後、磁気ブラシ現像法を用いてプラスド
ナーで現1′4!L、鉾通紙に転写したところ、コント
ラストが良好で鮮明な画像が得られた。
When this 1, 1 & light body was exposed to the corona zone (i) at -6 KV, a front potential of 550 V was observed.Next, image exposure of 151 uz, sec was performed to form an electrostatic latent image, and then magnetic When the image was transferred to 1'4!L paper using a brush development method using a positive donor, a clear image with good contrast was obtained.

実施例 実施例1で使用したものと同一の装置道を使用し、一方
の′ぺ極にアルミニウム基板(100順X100間×1
間)を設置f L、基体温度を200°Cに維持17た
Example Using the same equipment path as that used in Example 1, an aluminum substrate (100 order x 100 intervals x 1
The substrate temperature was maintained at 200°C.

この装置内に、酸素ガス含有叶全4.0体積係に調帯し
た7ラン/酸素の混合ガスを導入し、ガス圧を0−I 
Torrに1?11定した。ガス流址を50 SCCM
とし、平行平板電極間に13.56 M、EIzの高周
波を100W印加してグロー放電せしめた。この時の堆
積速度は4 A / seeで・りり、約12μplの
「・く素を含有するアモルファス水素化シリコントAが
I?g ++Zされた。
Into this device, a mixed gas of 7 runs/oxygen adjusted to a total volume ratio of 4.0 containing oxygen gas was introduced, and the gas pressure was adjusted to 0-I.
Torr was set at 1-11. 50 SCCM of gas flow
Then, a high frequency of 13.56 M and EIz of 100 W was applied between the parallel plate electrodes to cause glow discharge. The deposition rate at this time was 4 A/see, and about 12 μpl of amorphous hydrogenated silicon A containing hydrogen was deposited.

次いで、酸素ガスの供給を停止し、シランガスq)みを
供給してグローシ!ン市、を続げた。この時、アルミニ
ウム7隻叛ン晶度を250°Cに一ト昇させ、シランガ
ス圧を0.05 Torr  に変えた。この時の堆積
速度は1.2A/seeであり、杓3μ厚の酸素を):
(有しないアモルファス水素化シリコン層を積層して電
子写真感光体を11季た。
Next, the supply of oxygen gas is stopped, and only silane gas q) is supplied to perform Glossy! Nichi, continued. At this time, the aluminum crystallinity was raised to 250°C and the silane gas pressure was changed to 0.05 Torr. The deposition rate at this time was 1.2A/see, and a 3μ thick layer of oxygen was deposited):
(An electrophotographic photoreceptor was fabricated by laminating an amorphous hydrogenated silicon layer without any oxidation.)

この感光体について、グラス7I(Vでコロナ帯電させ
たところ、表i’jli電位+d、 700 Vであつ
プζ。次いで、201uxのハロケ9ンランプ光を照射
して、該感光体の半減露光時を測定1〜だところ、0.
51ux・8eeの高い光感度が得られ、実用性の高い
電子写真感光体であることが確認された。
When this photoreceptor was corona charged with a glass 7I (V), the surface potential +d was heated to 700 V.Next, the photoreceptor was irradiated with 201ux Haloke 9 lamp light, and when the photoreceptor was exposed to half light. When measured from 1 to 0.
A high photosensitivity of 51 ux and 8 ee was obtained, and it was confirmed that the electrophotographic photoreceptor was highly practical.

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

図面は、本゛・・へ明に係る電子写L(感光体の1新面
図である。 1・・・導電性支持基体、2・・・1唆索ド一ゾアモル
7アス水素化シリコン層、3・・・アモルファス水素化
シリコン層。
The drawings are a new view of an electrophotographic photoreceptor according to the present invention. , 3...Amorphous hydrogenated silicon layer.

Claims (1)

【特許請求の範囲】[Claims] 導電性支持基体と、該基体上に設けられた、酸素を0.
1〜40アトミツクチ含有するアモルファス水素化シリ
コン層から成る電荷輛送層及びアモルファス水素化シリ
コン層から成る電荷発生層により !’A成されること
を特徴とする’+1f;+1f;光写真
an electrically conductive supporting substrate; and an oxygen-containing substrate provided on the substrate.
Due to the charge transport layer consisting of an amorphous hydrogenated silicon layer containing 1 to 40 atoms and the charge generation layer consisting of an amorphous hydrogenated silicon layer! 'Characterized by being made'+1f;+1f;light photography
JP13112482A 1982-07-29 1982-07-29 Electrophotographic receptor Granted JPS5922052A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13112482A JPS5922052A (en) 1982-07-29 1982-07-29 Electrophotographic receptor

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13112482A JPS5922052A (en) 1982-07-29 1982-07-29 Electrophotographic receptor

Publications (2)

Publication Number Publication Date
JPS5922052A true JPS5922052A (en) 1984-02-04
JPH052985B2 JPH052985B2 (en) 1993-01-13

Family

ID=15050543

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13112482A Granted JPS5922052A (en) 1982-07-29 1982-07-29 Electrophotographic receptor

Country Status (1)

Country Link
JP (1) JPS5922052A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6198358A (en) * 1984-10-18 1986-05-16 ゼロツクス コーポレーシヨン Non-homogenous electrophotographic image forming member comprising amorphous silicon and silica

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57115554A (en) * 1981-01-08 1982-07-19 Canon Inc Photoconductive material

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS57115554A (en) * 1981-01-08 1982-07-19 Canon Inc Photoconductive material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6198358A (en) * 1984-10-18 1986-05-16 ゼロツクス コーポレーシヨン Non-homogenous electrophotographic image forming member comprising amorphous silicon and silica

Also Published As

Publication number Publication date
JPH052985B2 (en) 1993-01-13

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