JP2631413B2 - Selentellur photoconductor for electrophotography - Google Patents

Selentellur photoconductor for electrophotography

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Publication number
JP2631413B2
JP2631413B2 JP2137257A JP13725790A JP2631413B2 JP 2631413 B2 JP2631413 B2 JP 2631413B2 JP 2137257 A JP2137257 A JP 2137257A JP 13725790 A JP13725790 A JP 13725790A JP 2631413 B2 JP2631413 B2 JP 2631413B2
Authority
JP
Japan
Prior art keywords
tellurium
arsenic
photoreceptor
selenium
layer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP2137257A
Other languages
Japanese (ja)
Other versions
JPH0431869A (en
Inventor
要次 土橋
光広 吉留
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.)
Shindengen Electric Manufacturing Co Ltd
Yamanashi Electronics Co Ltd
Original Assignee
Shindengen Electric Manufacturing Co Ltd
Yamanashi Electronics 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 Shindengen Electric Manufacturing Co Ltd, Yamanashi Electronics Co Ltd filed Critical Shindengen Electric Manufacturing Co Ltd
Priority to JP2137257A priority Critical patent/JP2631413B2/en
Publication of JPH0431869A publication Critical patent/JPH0431869A/en
Application granted granted Critical
Publication of JP2631413B2 publication Critical patent/JP2631413B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Photoreceptors In Electrophotography (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は電子写真用セレンテルル感光体に関し、特に
その耐環境特性の向上に関するものである。
Description: TECHNICAL FIELD The present invention relates to a selentellurium photoreceptor for electrophotography, and more particularly to an improvement in its environmental resistance.

(従来技術とその問題点) 機能分離形セレンテルル感光体、例えば第1図に示す
ような導電性基体(1)上にセレン−テルル−塩素系か
らな電荷移動層(2)を形成し、更にその上にセレン−
テルルからなる電荷発生層(3)を形成してなるセレン
テルル感光体は、光感度にすぐれるため現在でも電子写
真装置に広く利用されている。
(Prior Art and Problems Thereof) A charge transfer layer (2) made of selenium-tellurium-chlorine is formed on a function-separated selenium telluride photoconductor, for example, a conductive substrate (1) as shown in FIG. Selenium on it
A selenium telluride photoreceptor formed with a tellurium charge generation layer (3) has excellent photosensitivity and is still widely used in electrophotographic devices even today.

しかしながらセレンテルル感光体は周知のように耐高
温性,耐高湿性など、いわゆる環境保存性において有機
感光体その他の感光体に比べ大きく劣る欠点をもつ。ま
た感光体表面に異物の付着、或いは接触があると、容易
にアモルファス状態から結晶状態に移行して、感光体と
しての特性を維持できなくなる欠点がある。
However, as is well known, the selentellur photoconductor has drawbacks in terms of so-called environmental preservation, such as high temperature resistance and high humidity resistance, which are significantly inferior to organic photoconductors and other photoconductors. Further, if foreign matter adheres or comes into contact with the surface of the photoreceptor, there is a disadvantage that the state easily transitions from the amorphous state to the crystalline state, and the characteristics of the photoreceptor cannot be maintained.

そこで上記の欠点の改善を図るため、第1図の電荷発
生層(3)または全層に亘ってヒ素を添加する試みがな
されているが、しかしこの方法では暗減衰の増大や残留
電位の上昇を招く。従ってヒ素添加濃度の制限、ヒ素添
加層の膜厚の制限等の考慮が必要になるため、充分な環
境保存性の向上効果を発揮できない。しかもヒ素を添加
しないセレンテルル感光体であっても、高温時(特に35
℃以上)において劣化して暗減衰を増大するため、前記
ヒ素の添加にもとづく更なる暗減衰の増大は、表面電位
の低下を著しく助長して電気的特性を悪化させることに
なる。
In order to improve the above drawbacks, attempts have been made to add arsenic to the charge generation layer (3) or to the whole layer in FIG. 1, but this method increases dark decay and increases residual potential. Invite. Therefore, it is necessary to consider the limitation of the arsenic addition concentration, the limitation of the thickness of the arsenic addition layer, and the like, and the effect of sufficiently improving the environmental preservation cannot be exhibited. In addition, even when the photoreceptor does not contain arsenic, even at high temperatures (especially 35
(° C. or more), which increases the dark decay, and further increase in the dark decay due to the addition of the arsenic significantly promotes a decrease in surface potential and deteriorates electrical characteristics.

(発明の目的) 本発明はヒ素の添加によっても表面電位の低下の少な
い、感光体の実現を目的としてなされたものである。
(Object of the Invention) The present invention has been made for the purpose of realizing a photoreceptor in which a decrease in surface potential is small even by addition of arsenic.

(問題点を解決するための本発明の手段) 機能分離型感光体においては、導電性基体から電荷発
生層に電荷の注入が行われて表面電位が変化し、しかも
この注入量はヒ素の添加量によって変化する。従って何
等かの手段により上記のような導電性基体からの電荷の
注入を制御できればヒ素の添加にもとづく表面電位の低
下を制限することができる。本発明は以上から着想され
たものであって、本発明の特徴とするところは次の点に
ある。即ち、第2図に示すように導電性基体(1)上に
樹脂絶縁層(4)を形成すると共に、その材質膜厚など
の選定により、導電性基体(1)から電荷発生層(3)
への電荷の注入量を制限するようにして、ヒ素の添加に
もとづく電気的特性への影響による表面電位の低下を制
限するようにしたことを特徴とするものである。
(Means of the Present Invention for Solving the Problems) In the function-separated type photoreceptor, charge is injected from the conductive substrate to the charge generation layer to change the surface potential. Varies by amount. Therefore, if the injection of charges from the conductive substrate as described above can be controlled by some means, it is possible to limit the decrease in the surface potential due to the addition of arsenic. The present invention has been conceived from the above, and the features of the present invention are as follows. That is, as shown in FIG. 2, a resin insulating layer (4) is formed on a conductive substrate (1), and the charge generation layer (3) is converted from the conductive substrate (1) by selecting the material thickness and the like.
It is characterized in that the amount of electric charge injected into the substrate is limited, so that the decrease in surface potential due to the influence on the electrical characteristics due to the addition of arsenic is limited.

このようにすれば、高温時の劣化にもとづく暗減衰の
増大による、表面電位の顕著な低下に更に加わるヒ素の
添加による表面電位の低下は制限される。従って、電気
的特性,環境保存性共にすぐれたセレンテルル感光体を
得ることが可能になる。
In this way, the decrease in surface potential due to the addition of arsenic in addition to the significant decrease in surface potential due to an increase in dark decay due to deterioration at high temperatures is limited. Therefore, it is possible to obtain a selentellur photoconductor excellent in both electrical characteristics and environmental preservation.

以下に実施例によって本発明を具体的に説明する。 Hereinafter, the present invention will be described specifically with reference to Examples.

(実施例) ベンゼンに溶解したPVK(ポリビニールカルバゾー
ル)を第2図の樹脂絶縁層(4)の形成材として用い
て、アルミニウム製導電性基体(1)上膜厚0.01,0.1,
0.5,1.0μmの樹脂絶縁層(4)を形成し、この上にセ
レン−テルル−塩素(テルル4%、塩素30ppm)からな
る電荷移動層(2)とセレン−テルル−ヒ素(テルル12
%,ヒ素1%)からなる電荷発生層(3)を順次積層し
た1〜4の評価サンプルを試作した。またこれと同時に
ヒ素の添加があっても樹脂絶縁層(4)のない(膜厚
0)比較例1と、無樹脂絶縁層であって、セレン−テル
ル−塩素(テルル4%,塩素30ppm)からなる電荷移動
層(2)と、セレン−テルル(テルル12%)からなる電
荷発生層(3)を備えた、ヒ素の添加のない比較例2を
試作した。
(Example) PVK (polyvinyl carbazole) dissolved in benzene was used as a material for forming the resin insulating layer (4) in FIG.
A resin insulating layer (4) of 0.5 and 1.0 μm is formed, and a charge transfer layer (2) made of selenium-tellurium-chlorine (tellurium 4%, chlorine 30 ppm) and selenium-tellurium-arsenic (tellurium 12) are formed thereon.
% And 1% of arsenic), and evaluation samples 1 to 4 in which charge generation layers (3) each composed of layers were sequentially laminated were produced. At the same time, even if arsenic was added, Comparative Example 1 having no resin insulating layer (4) (thickness: 0) and a resin-free insulating layer, comprising selenium-tellurium-chlorine (tellurium 4%, chlorine 30 ppm) Comparative Example 2 having no charge of arsenic, provided with a charge transfer layer (2) made of and a charge generation layer (3) made of selenium-tellurium (tellurium 12%).

そしてこれらの感光体を通常の電子写真装置に装着し
て、残留電位,表面電位の低下量などの各種の電気特性
の測定と100枚の画像試験を実施したところ第1表の結
果を得た。
These photoreceptors were mounted on a normal electrophotographic apparatus, and various electric characteristics such as residual potential and surface potential reduction were measured and an image test of 100 sheets was performed. The results shown in Table 1 were obtained. .

第1表から明らかなように樹脂絶縁層を設けた感光体
は比較例2に示した通常のセレンテルル感光体に比べて
若干残留電位の上昇は見られるが、例えばサンプルNo.3
と比較例2とを対比して明ら かなように膜厚を選定することにより、表面電位の低下
量を少なくできる。
As is clear from Table 1, the residual potential of the photoreceptor provided with the resin insulating layer is slightly higher than that of the normal selentelluric photoreceptor shown in Comparative Example 2, but for example, Sample No. 3
And Comparative Example 2 By appropriately selecting the film thickness, the decrease in the surface potential can be reduced.

また100枚の画像試験後、50℃,60%RHの環境において
放置試験を実施したところ、ヒ素の添加のない比較例品
2は表面が白濁し、感光特性も失われていたが、ヒ素を
添加した評価サンプル1〜4および比較例1は外観、電
気特性共に変化しないことが明らかにされた。
After 100 image tests, a standing test was performed in an environment of 50 ° C. and 60% RH. As a result, the surface of the comparative example 2 without arsenic was clouded and the photosensitive characteristics were lost. It was clarified that the added evaluation samples 1 to 4 and Comparative Example 1 did not change in both appearance and electrical characteristics.

また電荷移動層をセレン−テルル−塩素とし、そのテ
ルル濃度を2〜8%、塩素濃度を10〜100ppm、電荷発生
層をセレン−テルル−ヒ素とし、そのテルル濃度を5〜
20%,ヒ素濃度を0.1〜5%とした感光体に本発明を適
用した場合についても、実用上所要の電気的特性を得な
がら耐環境特性を向上できることが確かめられた。
The charge transfer layer is selenium-tellurium-chlorine, the tellurium concentration is 2 to 8%, the chlorine concentration is 10 to 100 ppm, the charge generation layer is selenium-tellurium-arsenic, and the tellurium concentration is 5 to 5%.
Even when the present invention was applied to a photoreceptor having an arsenic concentration of 20% and an arsenic concentration of 0.1% to 5%, it was confirmed that environmental resistance could be improved while obtaining practically required electrical characteristics.

また樹脂絶縁層(2)の材料として、以上のPVKの他
にPC(ポリカーボネート)を用いた場合について実験し
たが、同等の結果が得られた。
An experiment was performed using PC (polycarbonate) in addition to the above PVK as the material of the resin insulating layer (2), and equivalent results were obtained.

(発明の効果) 以上から明らかなように本発明によれば、ヒ素の添加
による耐環境特性の向上を、感光体として要求される電
気的特性をほぼ維持しながら行うことができるすぐれた
効果を得られるもので、複写機等の電子写真装置の市場
での実用性は極めて高い。
(Effects of the Invention) As is clear from the above, according to the present invention, an excellent effect that environmental resistance characteristics can be improved by adding arsenic while substantially maintaining the electrical characteristics required for a photoreceptor is obtained. As a result, the utility of the electrophotographic apparatus such as a copying machine in the market is extremely high.

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

第1図は従来の感光体の説明図、第2図は本発明の感光
体の説明図である。 (1)……導電性基体、(2)……電荷移動層、 (3)……電荷発生層、(4)……樹脂絶縁層。
FIG. 1 is an explanatory view of a conventional photoreceptor, and FIG. 2 is an explanatory view of a photoreceptor of the present invention. (1) ... conductive substrate, (2) ... charge transfer layer, (3) ... charge generation layer, (4) ... resin insulation layer.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭60−250357(JP,A) 特開 昭61−204637(JP,A) 特開 昭61−20046(JP,A) 特開 昭61−273550(JP,A) 特開 昭61−52651(JP,A) 特開 昭62−49357(JP,A) ──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-60-250357 (JP, A) JP-A-61-204637 (JP, A) JP-A-61-20046 (JP, A) JP-A 61-204 273550 (JP, A) JP-A-61-52651 (JP, A) JP-A-62-49357 (JP, A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】導電性基体上に電荷移動層と電荷発生層を
順次積層した電子写真用セレンテルル感光体において、 前記導電性基体と電荷移動層との間に樹脂絶縁層を設け
ると共にその膜厚を0.05〜0.5μmとし、 前記電荷移動層をセレン−テルル−塩素として、そのテ
ルル濃度を2〜8%、塩素濃度10〜100ppmとし、 前記電荷発生層をセレン−テルル−ヒ素として、そのテ
ルル濃度を5〜20%、ヒ素濃度を0.1〜5%としたこと
を特徴とする電子写真用セレンテルル感光体。
1. An electrophotographic selentellurium photoreceptor having a charge transfer layer and a charge generation layer sequentially laminated on a conductive substrate, wherein a resin insulating layer is provided between the conductive substrate and the charge transfer layer, and the film thickness is provided. The charge transfer layer is selenium-tellurium-chlorine, the tellurium concentration is 2-8%, the chlorine concentration is 10-100 ppm, and the charge generation layer is selenium-tellurium-arsenic, and the tellurium concentration is Is 5 to 20% and the arsenic concentration is 0.1 to 5%.
JP2137257A 1990-05-29 1990-05-29 Selentellur photoconductor for electrophotography Expired - Fee Related JP2631413B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2137257A JP2631413B2 (en) 1990-05-29 1990-05-29 Selentellur photoconductor for electrophotography

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2137257A JP2631413B2 (en) 1990-05-29 1990-05-29 Selentellur photoconductor for electrophotography

Publications (2)

Publication Number Publication Date
JPH0431869A JPH0431869A (en) 1992-02-04
JP2631413B2 true JP2631413B2 (en) 1997-07-16

Family

ID=15194439

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2137257A Expired - Fee Related JP2631413B2 (en) 1990-05-29 1990-05-29 Selentellur photoconductor for electrophotography

Country Status (1)

Country Link
JP (1) JP2631413B2 (en)

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60250357A (en) * 1984-05-26 1985-12-11 Konishiroku Photo Ind Co Ltd Electrophotographic sensitive body
JPS6120046A (en) * 1984-07-09 1986-01-28 Fuji Electric Co Ltd Photosensitive body for electrophotography
JPS6152651A (en) * 1984-08-23 1986-03-15 Fuji Electric Co Ltd Selenium photosensitive body for electrophotography
US4609605A (en) * 1985-03-04 1986-09-02 Xerox Corporation Multi-layered imaging member comprising selenium and tellurium
DE3518999C2 (en) * 1985-05-25 1987-05-14 Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt Electrophotographic recording material
JPS6249357A (en) * 1985-08-29 1987-03-04 Ricoh Co Ltd Electrophotographic sensitive body

Also Published As

Publication number Publication date
JPH0431869A (en) 1992-02-04

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