JPH0217021B2 - - Google Patents
Info
- Publication number
- JPH0217021B2 JPH0217021B2 JP15119183A JP15119183A JPH0217021B2 JP H0217021 B2 JPH0217021 B2 JP H0217021B2 JP 15119183 A JP15119183 A JP 15119183A JP 15119183 A JP15119183 A JP 15119183A JP H0217021 B2 JPH0217021 B2 JP H0217021B2
- Authority
- JP
- Japan
- Prior art keywords
- layer
- selenium
- tellurium
- less
- weight
- 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
Links
- 239000010410 layer Substances 0.000 claims description 27
- 239000011669 selenium Substances 0.000 claims description 24
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 21
- 229910052711 selenium Inorganic materials 0.000 claims description 16
- 229910052714 tellurium Inorganic materials 0.000 claims description 14
- 108091008695 photoreceptors Proteins 0.000 claims description 13
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 claims description 13
- 229910001370 Se alloy Inorganic materials 0.000 claims description 9
- 230000003647 oxidation Effects 0.000 claims description 4
- 238000007254 oxidation reaction Methods 0.000 claims description 4
- 239000000758 substrate Substances 0.000 claims description 4
- 239000002344 surface layer Substances 0.000 claims description 4
- 229910052785 arsenic Inorganic materials 0.000 claims description 3
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 230000014759 maintenance of location Effects 0.000 description 7
- 230000000052 comparative effect Effects 0.000 description 6
- 230000035945 sensitivity Effects 0.000 description 5
- 238000010586 diagram Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 239000004065 semiconductor Substances 0.000 description 3
- 229910001215 Te alloy Inorganic materials 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000001678 irradiating effect Effects 0.000 description 2
- 238000010030 laminating Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000005211 surface analysis Methods 0.000 description 2
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 2
- 101100494773 Caenorhabditis elegans ctl-2 gene Proteins 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000001941 electron spectroscopy Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 229910052732 germanium Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 238000000682 scanning probe acoustic microscopy Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 150000003497 tellurium Chemical class 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G5/00—Recording members for original recording by exposure, e.g. to light, to heat, to electrons; Manufacture thereof; Selection of materials therefor
- G03G5/02—Charge-receiving layers
- G03G5/04—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor
- G03G5/08—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being inorganic
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
Description
〔発明の属する技術分野〕
本発明はLEDあるいはHe−Neレーザまたは半
導体レーザなどを光源とする光プリンタのように
長波長光の光源に対して使用される電子写真用セ
レン感光体に関する。
〔従来技術とその問題点〕
長波長の光に対するセレン系の感光体として
は、導電性基体側から、純セレン系材料からなる
キヤリア輸送層(CTL)、テルル35重量%以上の
高濃度Te/Se材料からなるキヤリア発生層
(CGL)および純セレン系材料からなる電荷保持
に役立つ表面層(OCL)を順次積層した3層構
造の感光体が知られている。しかしながら、例え
ば近年特に光プリンタの主流をなす半導体レーザ
プリンタ用に波長約800μmの近赤外光に対して
感度を持たせるべく、高濃度Te/Se層のTe濃度
を増大させた場合、電荷保持性を良好に保つこと
は上記の3層構造では困難であり、暗減衰の大き
い感光体になつてしまう。
〔発明の目的〕
本発明はこれに対し、半導体レーザ波長領域に
おいても充分な感度を有する高濃度Te/Se層を
CGLとして有しながら、その電荷保持能力が一
般のPPC複写機用セレン感光体と同等である電
子写真用セレン感光体を提供することを目的とす
る。
〔発明の要点〕
本発明による電子写真用感光体は、導電性基体
上に純セレンあるいは低濃度セレン合金よりなる
CTL、高濃なテルル・セレン合金よりなるCGL、
厚さ20Å以上のテルル酸化層と純セレンあるいは
セレン合金よりなるOCLが順次積層されてなる
ことにより上記の目的を達成する。
CTLとしては、膜厚30〜100μmで純セレンも
しくは7重量%以下のTe、7原子%以下のひ素
(As)あるいは10000ppm以下のハロゲン元素
(I,Cl)を含むセレン合金からなる層が用いら
れる。
CGLとしては、膜厚0.3〜2μmでCTL側界面で
25重量%以下、OCL側界面で35重量%以上のTe
を含み、その中に7原子%以下のAsを含んでも
よい高濃度Se/Te合金からなる層が用いられる。
テルル酸化層としては、CGLとOCLの間に存
在するTeの内、少なくともその50%が酸化して
いる層が有効である。
OCLは単層でも多層でもよく、純Seもしくは
13.5%以下の濃度のTe/Se合金よりなり、ある
いはGe,Sb,As,Zn,Sn等を7原子%以下を
含んでもよく、厚さは0.5〜5μmが有効である。
〔発明の実施例〕
本発明 1:
長さ340mm、直径120mmのアルミニウム素管上に
純セレンを60μmの厚さに真空蒸着した。この時
の素管温度を65℃に保つた。第1図に示すように
CTL2が形成された素管1を一旦真空ブレーク
して炉内から取り出した。次にこのドラム上にま
ず40重量%の高濃度Te/Se層3を0.6μmの厚さ
にフラツシユ蒸着した。所要時間は約10分、素管
温度40℃、蒸発源ボート温度450℃である。この
ようにしてCTLおよびCGLが形成されたドラム
を真空蒸着槽より取り出し、45℃の恒温器の中に
200時間放置した。これによりテルル酸化層4が
形成された。つづいて恒温器より取り出したドラ
ムにOCL5として純セレンを2μmの厚さにフラ
ツシユ蒸着した。この時のボート温度は420℃、
素管温度は40℃、所要時間は約15分であつた。
実施例 2:
実施例1における恒温器中での放置の代りに
1kWの紫外線灯下で約1時間紫外線照射を行つ
て第1図のテルル酸化層4を形成後、OCL5を
被着した。
比較例 1
実施例1、2における恒温器放置、紫外線照射
を除いたもので、その他は同じ工程でアルミニウ
ム素管上にCTL,CGLを積層ののち引きつづき
OCLを形成した。
比較例 2
比較例1と同様に恒温器放置、紫外線照射は行
わないが、CTL,CGL積層後一旦真空ブレーク
したのち約1時間を経て再び真空引きを行い、5
×10-5Torrにした後2μmの厚さに純セレンをフ
ラツシユ蒸着してOCLを形成した。
このようにして得た4種類の感光体試料につい
て次のような試験を行つた。
(1) ゼログラフイ特性試験
試料ドラムを16rpmの回転速度で回転しながら
コロナ帯電を行い、帯電後1/4回転した点で回転
を止め、その点における表面電位の1秒間の暗減
衰特性を測定し、電荷保持率を計算した。この後
再び試料ドラムの回転を行い、ドラムを止めて今
度は800nmの波長の単色光を照射しながら電位の
放電特性を測定し、感光体の感度に関連する半減
衰露光量を得た。得られた結果を第1表に示す。
[Technical Field to Which the Invention Pertains] The present invention relates to a selenium photoreceptor for electrophotography used for a long wavelength light source such as an optical printer that uses an LED, a He--Ne laser, or a semiconductor laser as a light source. [Prior art and its problems] As a selenium-based photoreceptor for long-wavelength light, from the conductive substrate side, there is a carrier transport layer (CTL) made of pure selenium-based material, a high-concentration Te/35% by weight tellurium or more, A photoreceptor having a three-layer structure is known, in which a carrier generation layer (CGL) made of a Se material and a surface layer (OCL) useful for charge retention made of a pure selenium-based material are sequentially laminated. However, for example, if the Te concentration of the high-concentration Te/Se layer is increased in order to make semiconductor laser printers, which have become the mainstream of optical printers in recent years, sensitive to near-infrared light with a wavelength of approximately 800 μm, charge retention It is difficult to maintain good properties with the above three-layer structure, resulting in a photoreceptor with large dark decay. [Object of the Invention] In order to solve this problem, the present invention provides a highly concentrated Te/Se layer that has sufficient sensitivity even in the semiconductor laser wavelength region.
It is an object of the present invention to provide a selenium photoreceptor for electrophotography, which has a charge retention ability equivalent to that of a general selenium photoreceptor for PPC copying machines, while being a CGL. [Summary of the Invention] The electrophotographic photoreceptor according to the present invention is made of pure selenium or a low concentration selenium alloy on a conductive substrate.
CTL, CGL made of highly concentrated tellurium-selenium alloy;
The above object is achieved by sequentially laminating a tellurium oxide layer with a thickness of 20 Å or more and an OCL made of pure selenium or a selenium alloy. As the CTL, a layer of pure selenium or a selenium alloy containing 7% by weight or less of Te, 7 atomic% or less of arsenic (As), or 10,000ppm or less of halogen elements (I, Cl) is used as the CTL. . As a CGL, the film thickness is 0.3 to 2 μm and the CTL side interface is
Te less than 25% by weight, more than 35% by weight at the OCL side interface
A layer is used that is made of a high concentration Se/Te alloy which may contain 7 atomic % or less of As. As the tellurium oxide layer, a layer in which at least 50% of Te existing between CGL and OCL is oxidized is effective. OCL may be single layer or multilayer, and may be pure Se or
It is made of a Te/Se alloy with a concentration of 13.5% or less, or may contain Ge, Sb, As, Zn, Sn, etc. in an amount of 7 atomic % or less, and a thickness of 0.5 to 5 μm is effective. [Embodiments of the Invention] Invention 1: Pure selenium was vacuum-deposited to a thickness of 60 μm on an aluminum tube with a length of 340 mm and a diameter of 120 mm. At this time, the temperature of the raw tube was maintained at 65°C. As shown in Figure 1
The raw tube 1 on which the CTL 2 was formed was once vacuum-broken and taken out from the furnace. Next, a high concentration Te/Se layer 3 of 40% by weight was first flash-deposited on this drum to a thickness of 0.6 μm. The time required is approximately 10 minutes, the temperature of the raw tube is 40℃, and the temperature of the evaporation source boat is 450℃. The drum with CTL and CGL formed in this way was taken out of the vacuum deposition tank and placed in a constant temperature chamber at 45℃.
I left it for 200 hours. As a result, a tellurium oxide layer 4 was formed. Next, pure selenium was flash-deposited as OCL5 to a thickness of 2 μm on the drum taken out from the thermostat. The boat temperature at this time was 420℃.
The temperature of the raw tube was 40°C, and the time required was about 15 minutes. Example 2: Instead of leaving in a thermostat in Example 1
After UV irradiation was performed for about 1 hour under a 1kW UV lamp to form the tellurium oxide layer 4 shown in FIG. 1, OCL 5 was deposited. Comparative Example 1 This is the same process as in Examples 1 and 2, except for leaving it in a constant temperature chamber and irradiating it with ultraviolet rays.CTL and CGL were laminated on an aluminum tube and then continued.
OCL was formed. Comparative Example 2 As in Comparative Example 1, the product was left in a constant temperature oven and no UV irradiation was performed, but after laminating CTL and CGL, the vacuum was broken and then vacuumed again after about 1 hour.
After setting the temperature to ×10 −5 Torr, pure selenium was flash-deposited to a thickness of 2 μm to form an OCL. The following tests were conducted on the four types of photoreceptor samples thus obtained. (1) Xerographic characteristics test The sample drum was corona charged while rotating at a rotation speed of 16 rpm, and after 1/4 rotation after being charged, the rotation was stopped and the dark decay characteristics of the surface potential at that point for 1 second were measured. , charge retention was calculated. After this, the sample drum was rotated again, the drum was stopped, and the potential discharge characteristics were measured while irradiating monochromatic light with a wavelength of 800 nm to obtain a half-attenuation exposure dose related to the sensitivity of the photoreceptor. The results obtained are shown in Table 1.
【表】
レーザ光に対する感度は半減衰露光量が2μJ/
cm2以下であればよいから、酸化層の形成は感度が
実用上支障ない範囲で電荷保持率を向上させるこ
とが第1表から分かる。しかし真空ブレークのみ
(比較例2)ではほとんど効果がない。
(2) 分析試験
実施例1、2、比較例1、2の試料ドラム作成
の際、予め表面にAl蒸着したシリコン板につい
て同時にCTL,CGL形成ならびに酸化処理を行
い、OCLのみを形成しないで分析試料として、
VG社製ESCALAB5による電子分光法による高
濃度Te/Se層の分析ならびにオージエ電子分光
法による表面近傍分析を行つた。得られた結果を
第2表に示す。[Table] Sensitivity to laser light is at half-attenuation exposure of 2μJ/
Table 1 shows that the formation of the oxide layer improves the charge retention within a range that does not impede the sensitivity in practical terms, since it is sufficient that the oxidation layer is not more than cm 2 . However, only the vacuum break (Comparative Example 2) has almost no effect. (2) Analytical test When preparing sample drums for Examples 1 and 2 and Comparative Examples 1 and 2, CTL and CGL formation and oxidation treatment were performed simultaneously on the silicon plate whose surface had been pre-evaporated with Al, and analysis was performed without forming only OCL. As a sample,
The high concentration Te/Se layer was analyzed using electron spectroscopy using VG's ESCALAB5, and near-surface analysis was performed using Auger electron spectroscopy. The results obtained are shown in Table 2.
本発明は純セレン系のCTL、高濃度Te/Seの
CGLならびに表面保護OCLからなるレーザ光の
ような長波長領域の光のための3層構造感光体に
おいて、CGLとOCLの界面に積極的酸化による
テルル酸化層を介在させることにより、長波長領
域光に対する充分な感度を有しながら極めて良好
な表面保持能力を備えさせるものである。
このテルル酸化層は、暗中でコロナ放電により
感光体表面を正に帯電した後にCGL内で発生す
るキヤリアのうちの電子が表面層へ注入するのを
阻止する働きをするものと推定され、その結果と
して電荷保持能力が向上する。
The present invention uses pure selenium-based CTL and high-concentration Te/Se.
In a three-layer structure photoreceptor for light in the long wavelength region such as laser light, which is made of CGL and surface-protected OCL, by interposing a tellurium oxide layer through active oxidation at the interface between CGL and OCL, it is possible to absorb light in the long wavelength region. It provides extremely good surface retention ability while having sufficient sensitivity to. This tellurium oxide layer is presumed to function to prevent electrons from among the carriers generated within the CGL from being injected into the surface layer after the surface of the photoreceptor is positively charged by corona discharge in the dark. As a result, the charge retention ability is improved.
第1図は本発明による感光体の構成の断面図、
第2図は比較例1の試料のオージエ表面近傍分析
結果を示す組成プロフアイル図、第3図は実施例
2の試料の同様な組成プロフアイル図、第4図は
光干渉試験の概念図、第5図は実施例1の試料で
得られた入射光波長変化の際の反射パターンであ
る。
1……導電性基体、2……CTL、3……CGL、
4……テルル酸化層、5……OCL。
FIG. 1 is a sectional view of the structure of a photoreceptor according to the present invention;
FIG. 2 is a composition profile diagram showing the results of near-Augier surface analysis of the sample of Comparative Example 1, FIG. 3 is a similar composition profile diagram of the sample of Example 2, and FIG. 4 is a conceptual diagram of the optical interference test. FIG. 5 shows a reflection pattern obtained with the sample of Example 1 when the wavelength of the incident light changes. 1... Conductive substrate, 2... CTL, 3... CGL,
4...tellurium oxide layer, 5...OCL.
Claims (1)
レンもしくは7重量%以下のテルル、7原子%以
下のひ素、あるいは10000ppm以下のハロゲン元
素を含むセレン合金よりなるキヤリア輸送層と、
膜厚0.3〜2μmで、キヤリヤ輸送層側界面で25重
量%以下、反対側界面で35重量%以上のテルルを
含むテルル・セレン合金よりなるキヤリア発生層
と、厚さ20Å以上であつてキヤリア発生層と表面
層の間に存在するテルルのうち、少なくともその
50%が酸化しているテルル酸化層と、膜厚0.5〜
5μmで純セレンないし13.5重量%以下のテルルを
含むセレン合金よりなる表面層とが順次積層され
てなることを特徴とする電子写真用セレン感光
体。1. On a conductive substrate, a carrier transport layer having a thickness of 30 to 100 μm and made of pure selenium or a selenium alloy containing 7% by weight or less of tellurium, 7% or less of arsenic, or 10,000ppm or less of a halogen element;
A carrier generation layer with a film thickness of 0.3 to 2 μm and made of a tellurium-selenium alloy containing tellurium of 25% by weight or less at the interface on the carrier transport layer side and 35% or more by weight at the opposite interface, and a carrier generation layer with a thickness of 20 Å or more and containing tellurium of 25% by weight or less at the interface on the opposite side. Of the tellurium present between the layer and the surface layer, at least
Tellurium oxide layer with 50% oxidation and film thickness 0.5~
A selenium photoreceptor for electrophotography, characterized in that a surface layer of pure selenium or a selenium alloy containing 13.5% by weight or less of tellurium is sequentially laminated with a thickness of 5 μm.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15119183A JPS6043662A (en) | 1983-08-19 | 1983-08-19 | Selenium photosensitive body for electrophotography |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15119183A JPS6043662A (en) | 1983-08-19 | 1983-08-19 | Selenium photosensitive body for electrophotography |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6043662A JPS6043662A (en) | 1985-03-08 |
JPH0217021B2 true JPH0217021B2 (en) | 1990-04-19 |
Family
ID=15513256
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15119183A Granted JPS6043662A (en) | 1983-08-19 | 1983-08-19 | Selenium photosensitive body for electrophotography |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS6043662A (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS61256353A (en) * | 1985-05-10 | 1986-11-13 | Fuji Electric Co Ltd | Electrophotographic selenium photosensitive body |
DE3518999C2 (en) * | 1985-05-25 | 1987-05-14 | Licentia Patent-Verwaltungs-Gmbh, 6000 Frankfurt | Electrophotographic recording material |
JPS61278858A (en) * | 1985-06-04 | 1986-12-09 | Fuji Electric Co Ltd | Selenium photosensitive body for electrophotography |
JPS6254269A (en) * | 1985-09-03 | 1987-03-09 | Fuji Electric Co Ltd | Electrophotographic sensitive body |
JPH01219753A (en) * | 1988-02-26 | 1989-09-01 | Fuji Electric Co Ltd | Electrophotographic selenic sensitive body |
-
1983
- 1983-08-19 JP JP15119183A patent/JPS6043662A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS6043662A (en) | 1985-03-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0163415B1 (en) | Substrate for light-receiving member and light-receiving member having the same | |
JPH0217021B2 (en) | ||
JPH0792611B2 (en) | Heterogeneous electrophotographic imaging member consisting of amorphous silicon and silicon oxide | |
FR2509063A1 (en) | MULTI-LAYER PHOTOCONDUCTIVE ASSEMBLY WITH INTERMEDIATE HETEROJUNCTION | |
JPS59181357A (en) | Photoconductive material | |
JPH0330853B2 (en) | ||
JPH0330854B2 (en) | ||
JPS636865B2 (en) | ||
EP0021751A1 (en) | Electrophotographic plate and a process for preparation of such a plate | |
JPS6354171B2 (en) | ||
JP2638185B2 (en) | Manufacturing method of photoreceptor for electrophotography | |
JP2599950B2 (en) | Photoconductor structure | |
JPH0216912B2 (en) | ||
Nesheva et al. | Electrophotographic photoreceptors including selenium-based multilayers | |
JPS5849954A (en) | Drum type electrophotographic receptor | |
JPS58223154A (en) | Electrophotographic receptor | |
JPS5944056A (en) | Photoreceptor | |
JPH0236938B2 (en) | ||
JPS59133550A (en) | Electrophotographic sensitive body | |
JPS62115459A (en) | Electrophotographic sensitive body | |
JPH0480388B2 (en) | ||
JPH0216913B2 (en) | ||
JPH0536785B2 (en) | ||
JPS62115458A (en) | Electrophotographic sensitive body | |
JPS60144752A (en) | Production of electrophotographic sensitive body |