JPS61156134A - Electrophotographic sensitive body - Google Patents
Electrophotographic sensitive bodyInfo
- Publication number
- JPS61156134A JPS61156134A JP27441984A JP27441984A JPS61156134A JP S61156134 A JPS61156134 A JP S61156134A JP 27441984 A JP27441984 A JP 27441984A JP 27441984 A JP27441984 A JP 27441984A JP S61156134 A JPS61156134 A JP S61156134A
- Authority
- JP
- Japan
- Prior art keywords
- oxygen
- added
- arsenic
- selenium
- 000ppm
- 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
Links
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
- G03G5/082—Photoconductive 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
- G03G5/08207—Selenium-based
Landscapes
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
本発明において用いられるセレンとしては4N〜5Nの
従来品グレードのものも用いることが可能と思われるが
、最近はより高純度品(6N)の製造も為されており、
本発明においてもそうした高純度(6N)のものを使用
することが好ましい。[Detailed Description of the Invention] As the selenium used in the present invention, it seems possible to use conventional grade selenium of 4N to 5N, but recently a higher purity product (6N) has also been produced. ,
In the present invention, it is preferable to use such a high purity (6N) material.
高純度セレンの方が不純物トラップが少なく、残留電位
が小さい。例えば従来品のセレンは47Vの残留電位を
示すのに対し、6N純度の高純度セレンの残留電位は2
8Vである。High-purity selenium has fewer impurity traps and a lower residual potential. For example, conventional selenium exhibits a residual potential of 47V, whereas high-purity selenium with 6N purity has a residual potential of 2.
It is 8V.
本発明においては、1〜1000 ppm酸素が残留電
位低減目的に添加される。酸素添加量は、セレンの純度
に依存するが、はば10■の残留電位を与えるよう選択
される。1000 ppmを越えて酸素を添加しても効
果は実質上飽和する。また、酸素を1000 ppmを
越えて添加すると蒸着時に突沸が起りやすくなり、蒸着
膜に欠陥が生じる。In the present invention, 1 to 1000 ppm of oxygen is added for the purpose of reducing residual potential. The amount of oxygen added depends on the purity of the selenium, but is selected to give a residual potential of about 10 μm. Even if oxygen is added in excess of 1000 ppm, the effect is substantially saturated. Furthermore, if oxygen is added in excess of 1000 ppm, bumping is likely to occur during vapor deposition, causing defects in the vapor deposited film.
砒素は主に暗減衰特性の悪化を防止するために酸素tに
応じて添加され、上記酸素量範囲に対して10〜10.
000 ppmの範囲で添加されうる。上記範囲の酸素
と砒素が協作用して、暗減衰特性を良好に保ったまま残
留電位を減少させることができる。好ましい範囲は砒素
100〜10. OOOppm及び酸素10〜t、 0
00 ppmである。Arsenic is added depending on the oxygen t mainly to prevent deterioration of dark decay characteristics, and is added in an amount of 10 to 10.
000 ppm. Oxygen and arsenic in the above range cooperate to reduce the residual potential while maintaining good dark decay characteristics. The preferred range is arsenic 100-10. OOOppm and oxygen 10~t, 0
00 ppm.
酸素は5ea2またはSe −5eOz から作った
母合金の形で或いは酸素バブリングによって添加され、
これは塩素添加の場合に較べて取扱い上何ら支障がない
。砒素は、純砒素或いはSe −As合金或いはAS
2 Se s の形で添加される。Oxygen is added in the form of a master alloy made from 5ea2 or Se-5eOz or by oxygen bubbling;
This poses no problem in handling compared to the case of adding chlorine. Arsenic is pure arsenic, Se-As alloy or AS
It is added in the form of 2 Se s .
こうして得られる蒸着源としてのセレン−砒素−酸素感
光材料をドラム導電性基板上に真空蒸着することによっ
て電子写真用感光体が得られる。An electrophotographic photoreceptor is obtained by vacuum evaporating the thus obtained selenium-arsenic-oxygen photosensitive material as a deposition source onto a drum conductive substrate.
感光体としては、前述の通り単層型及び積層型のものが
実用化されている。後者の場合、本発明感光材料は感光
層の形成に使用される。As mentioned above, single-layer type and laminated type photoreceptors have been put into practical use. In the latter case, the photosensitive material of the present invention is used to form a photosensitive layer.
真空蒸着の条件は%に限定されるものでなく、通常実施
されている条件で十分である。蒸着源温度250〜35
0℃、基板温度55〜75℃、真空度I O−5〜10
−’ Torr 、 蒸着時間60〜131)分の範
囲で適宜の条件を選択して実施しうる。基板としては、
アルミニウム、鋼等の金属或いは金属化された紙或いは
プラスチック等が用いられる。The conditions for vacuum deposition are not limited to %, and commonly used conditions are sufficient. Vapor deposition source temperature 250-35
0℃, substrate temperature 55~75℃, degree of vacuum IO-5~10
-' Torr and deposition time of 60 to 131) minutes by selecting appropriate conditions. As a substrate,
Metals such as aluminum and steel, metallized paper, or plastics are used.
発明の効果
セレンに砒素と酸素を同時添加することにより、砒素と
塩素の同時添加に少くとも匹敵する効果が得られる。酸
素の添加は塩素の添加に較べて取扱い上容易であり、生
産技術上のメリットは非常に大きい。Effects of the Invention By simultaneously adding arsenic and oxygen to selenium, effects at least comparable to the simultaneous addition of arsenic and chlorine can be obtained. Addition of oxygen is easier to handle than addition of chlorine, and has great advantages in terms of production technology.
実施例
Se −As −0合金を作製するため、日本砿業(株
)製高純度セレン(6N)と砒素(6N)及び二?lf
f化セレン(4N)をそれぞれ所定量秤取し、30踵外
径X22DlllI長さのパイレックスアンプル中に真
空封入した。これを揺動加熱炉中で10回/分の速さで
揺動させながら550℃において2時間溶製した。その
後、アンプルを粉砕して合金を取出した。Example To prepare a Se-As-0 alloy, high-purity selenium (6N), arsenic (6N), and Nippon Sogyo Co., Ltd. were used. lf
A predetermined amount of selenium fluoride (4N) was weighed out and vacuum-sealed into a Pyrex ampoule with a length of 30 heel outer diameter x 22Dllll. This was melted at 550° C. for 2 hours in a swinging heating furnace while swinging at a rate of 10 times/minute. Thereafter, the ampoule was crushed to remove the alloy.
このようにして作製した合金を抵抗加熱により55■×
55−の鏝面仕上げアルミニウム基板上に真空蒸着した
。蒸着条件は次の通りである。The alloy produced in this way was heated to 55cm×
It was vacuum deposited on a No. 55-finished aluminum substrate. The deposition conditions are as follows.
蒸発源温度 300°C
基板温度 70℃
真空度 2X10 Torr
蒸着時間 90分間
以上の条件によりアルミニウム基板上へ形成した蒸着膜
の厚さは、いずれも約50μmであった。Evaporation source temperature: 300° C. Substrate temperature: 70° C. Degree of vacuum: 2×10 Torr Vapor deposition time: The thickness of the deposited film formed on the aluminum substrate over 90 minutes was approximately 50 μm.
こうして得られた合金蒸着膜について静電試験装置を用
いて電子写真特性を測定した。測定条件は次の通りであ
る。The electrophotographic properties of the alloy vapor-deposited film thus obtained were measured using an electrostatic testing device. The measurement conditions are as follows.
コロナ放電電圧 5kV
光照射時間 2秒間
光 照 度 3000ルクス
繰返し数 200回
Asを2000 ppm一定とし、酸素を1 ppmか
ら1.000 ppmまで添加した結果を図面に示す。Corona discharge voltage: 5 kV Light irradiation time: 2 seconds Light Illuminance: 3000 lux Repetition number: 200 times As is kept constant at 2000 ppm, and the results of adding oxygen from 1 ppm to 1.000 ppm are shown in the drawing.
第1図において、曲線■は初期表面電位■。を示しそし
て曲線■は暗状態保持10秒後の電位V、。In Figure 1, the curve ■ is the initial surface potential ■. and the curve ■ is the potential V after 10 seconds of being kept in the dark state.
である。第2図は残留電位を示す。図面から、暗減衰特
性を劣化させることなく残留電位を減少させうろことが
わかる。It is. Figure 2 shows the residual potential. From the drawings, it can be seen that the residual potential can be reduced without deteriorating the dark decay characteristics.
第1図は砒素2000 ppm一定として酸素添加量と
表面電位の関係を示すグラフであり、そして第2図は同
じく酸素添加量と残留電位の関係を示すグラフである。
残蝙覧t(V)
表面1v−イカ= (V)FIG. 1 is a graph showing the relationship between the amount of oxygen added and the surface potential, assuming that arsenic is constant at 2000 ppm, and FIG. 2 is a graph showing the relationship between the amount of oxygen added and the residual potential. Residue list t (V) Surface 1v - Squid = (V)
Claims (1)
,000ppm酸素を添加したことを特徴とする電子写
真用感光材料。 2)セレンに10〜10,000ppm砒素及び1〜1
,000ppm酸素を添加した薄膜形成用材を用いて導
電性基板上に形成した薄膜感光層を具備する電子写真感
光体。 3)積層型電子写真感光体において、セレンに10〜1
0,000ppm砒素及び1〜1,000ppm酸素を
添加した薄膜形成用材を用いて導電性基板上に形成した
薄膜感光層を純セレンその他の感光層の上または下に一
層または複数層設けた電子写真感光体。[Claims] 1) Selenium with 10 to 10,000 ppm arsenic and 1 to 1
A photosensitive material for electrophotography, characterized in that ,000 ppm of oxygen is added. 2) Selenium with 10-10,000 ppm arsenic and 1-1
An electrophotographic photoreceptor comprising a thin film photosensitive layer formed on a conductive substrate using a thin film forming material to which ,000 ppm of oxygen is added. 3) In the laminated electrophotographic photoreceptor, selenium contains 10 to 1
Electrophotography in which a thin film photosensitive layer is formed on a conductive substrate using a thin film forming material to which 0,000 ppm arsenic and 1 to 1,000 ppm oxygen is added, and one or more layers are provided above or below a pure selenium or other photosensitive layer. Photoreceptor.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27441984A JPS61156134A (en) | 1984-12-28 | 1984-12-28 | Electrophotographic sensitive body |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP27441984A JPS61156134A (en) | 1984-12-28 | 1984-12-28 | Electrophotographic sensitive body |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS61156134A true JPS61156134A (en) | 1986-07-15 |
JPH0239787B2 JPH0239787B2 (en) | 1990-09-07 |
Family
ID=17541404
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP27441984A Granted JPS61156134A (en) | 1984-12-28 | 1984-12-28 | Electrophotographic sensitive body |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS61156134A (en) |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58123544A (en) * | 1982-01-19 | 1983-07-22 | Ricoh Co Ltd | Electrophotographic receptor |
-
1984
- 1984-12-28 JP JP27441984A patent/JPS61156134A/en active Granted
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS58123544A (en) * | 1982-01-19 | 1983-07-22 | Ricoh Co Ltd | Electrophotographic receptor |
Also Published As
Publication number | Publication date |
---|---|
JPH0239787B2 (en) | 1990-09-07 |
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