JPS63142356A - Electrophotographic sensitive body - Google Patents
Electrophotographic sensitive bodyInfo
- Publication number
- JPS63142356A JPS63142356A JP28915286A JP28915286A JPS63142356A JP S63142356 A JPS63142356 A JP S63142356A JP 28915286 A JP28915286 A JP 28915286A JP 28915286 A JP28915286 A JP 28915286A JP S63142356 A JPS63142356 A JP S63142356A
- Authority
- JP
- Japan
- Prior art keywords
- sensitivity
- wavelength region
- dried
- solution
- dispersion
- 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
Links
- 238000010521 absorption reaction Methods 0.000 claims abstract description 6
- 108091008695 photoreceptors Proteins 0.000 claims description 15
- 239000000126 substance Substances 0.000 claims description 8
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract description 9
- 239000007788 liquid Substances 0.000 abstract description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract description 8
- 230000035945 sensitivity Effects 0.000 abstract description 8
- 239000006185 dispersion Substances 0.000 abstract description 5
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 abstract description 4
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 abstract description 4
- 229920000515 polycarbonate Polymers 0.000 abstract description 3
- 239000004417 polycarbonate Substances 0.000 abstract description 3
- 229920006267 polyester film Polymers 0.000 abstract description 3
- YGBCLRRWZQSURU-UHFFFAOYSA-N 4-[(diphenylhydrazinylidene)methyl]-n,n-diethylaniline Chemical compound C1=CC(N(CC)CC)=CC=C1C=NN(C=1C=CC=CC=1)C1=CC=CC=C1 YGBCLRRWZQSURU-UHFFFAOYSA-N 0.000 abstract description 2
- NRCMAYZCPIVABH-UHFFFAOYSA-N Quinacridone Chemical compound N1C2=CC=CC=C2C(=O)C2=C1C=C1C(=O)C3=CC=CC=C3NC1=C2 NRCMAYZCPIVABH-UHFFFAOYSA-N 0.000 abstract description 2
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 0.000 abstract description 2
- 229920005989 resin Polymers 0.000 abstract description 2
- 239000011347 resin Substances 0.000 abstract description 2
- -1 acryl Chemical group 0.000 abstract 1
- 229910052755 nonmetal Inorganic materials 0.000 abstract 1
- 230000003595 spectral effect Effects 0.000 description 6
- 239000000975 dye Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 206010034972 Photosensitivity reaction Diseases 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 230000036211 photosensitivity Effects 0.000 description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 229910052711 selenium Inorganic materials 0.000 description 2
- 239000011669 selenium Substances 0.000 description 2
- 206010034960 Photophobia Diseases 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical class [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 208000013469 light sensitivity Diseases 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002964 rayon Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 150000003452 sulfinic acid derivatives Chemical class 0.000 description 1
- 229910052714 tellurium Inorganic materials 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 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
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0622—Heterocyclic compounds
- G03G5/0644—Heterocyclic compounds containing two or more hetero rings
- G03G5/0646—Heterocyclic compounds containing two or more hetero rings in the same ring system
- G03G5/0653—Heterocyclic compounds containing two or more hetero rings in the same ring system containing five relevant rings
-
- 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
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
-
- 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
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0601—Acyclic or carbocyclic compounds
- G03G5/0612—Acyclic or carbocyclic compounds containing nitrogen
- G03G5/0616—Hydrazines; Hydrazones
-
- 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
- G03G5/06—Photoconductive layers; Charge-generation layers or charge-transporting layers; Additives therefor; Binders therefor characterised by the photoconductive material being organic
- G03G5/0664—Dyes
- G03G5/0696—Phthalocyanines
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Photoreceptors In Electrophotography (AREA)
Abstract
Description
【発明の詳細な説明】
〔素業上の利用分野〕
本発明け、お）むね４００？Ｌ？７Ｌ””−ら８００ｒ
Ｌｍの広域にわたって極めて高い一様な感度を有する電
子写真感光体だ関する。[Detailed Description of the Invention] [Field of Industrial Application] The present invention costs 400 yen? L? 7L""-etc.800r
The present invention relates to an electrophotographic photoreceptor having extremely high uniform sensitivity over a wide range of Lm.
従来、積層型電子写真感光体の電荷発生１勿質（以下、
ＣＧ Ｍと略す）としてｖｉ、有機第一アＳン類に可溶
なモノマゾ染料・ジスマゾ染料・スフフィン酸誘導体染
料（ｌｒｆ開昭５２−５５６４３号）、キノシアニン顔
料（特開昭５３−４２８３０号）、銅フタロシアニン顔
料（特開昭５１−１１７６３号）等の有機物ｈ１多数提
示され、また、テルルヒ素アモルファスセレン（特開昭
５０−１５１３７号）、アモルファスセレン（特開昭５
２−７５３９２号）等の無機物も提示されている。一方
近年、近赤外光（波長７５０ｎｍ以上）に感度を有する
ＣＧＭとして、Ｘ型無金属７タロシアニンや１色素増感
した有機物が多数提案されている。Conventionally, charge generation in a laminated electrophotographic photoreceptor (hereinafter referred to as
(abbreviated as CGM), vi, monomaso dyes, dismazo dyes, and sulfinic acid derivative dyes soluble in organic monosulfur compounds (lrf 1985-55643), quinocyanine pigments (Japanese Patent Laid-Open No. 53-42830) , copper phthalocyanine pigment (JP-A-51-11763), and tellurium arsenide amorphous selenium (JP-A-50-15137), amorphous selenium (JP-A-50-15137), etc.
Inorganic substances such as No. 2-75392) have also been proposed. On the other hand, in recent years, many X-type metal-free 7-thalocyanines and single-dye sensitized organic substances have been proposed as CGMs sensitive to near-infrared light (wavelengths of 750 nm or more).
しかしこれらＯＧＭは、ある特定の波長域の光にしか高
い感度を示さず、つまり、光源の光の大部分はキャリア
発生に寄与しないこととなり、効率ｈＳ悪いとい５欠点
を有する。あるいは、ＣＧＭの吸収波長域の波長を有す
る光源を利用しないといけないといへ欠点も有する。However, these OGMs exhibit high sensitivity only to light in a specific wavelength range, that is, most of the light from the light source does not contribute to carrier generation, and has five drawbacks such as poor hS efficiency. Another disadvantage is that a light source having a wavelength in the CGM absorption wavelength range must be used.
そこで、本発明は上記の問題点を解決するものであって
、その目的とするところは、おおむね４００７１７ＦＬ
から８００？Ｌ？ＦＬ の広域にわたって極めて高い一
様な感電を有するＣＧＬを構成要素とする電子写真感光
体を提供するところにある。Therefore, the present invention is intended to solve the above problems, and its purpose is to
From 800? L? An object of the present invention is to provide an electrophotographic photoreceptor including a CGL as a component which has an extremely high uniform electric shock over a wide range of FL.
未発明の電子写真感光体は、ｃ Ｇ Ｌ ｂ；吸収波長
の具なるＺｆｆ類以上の有鳴光導電性物質を含有するこ
とを特徴とする。The uninvented electrophotographic photoreceptor is characterized in that it contains a photoconductive substance with a photoconductive signal having an absorption wavelength equal to or higher than that of the Zff class.
以下（Ｃ本発明について、実施例にもとづいて詳細：ｆ
Ｃ説明する。なお、Ｃ！ＧＭ−ＯＧＭの組合せ、ＣＴＭ
、バインダ樹脂、溶剤等は本実施例に限定されない。Below (CDetails of the present invention based on examples: f
C.Explain. In addition, C! GM-OGM combination, CTM
, binder resin, solvent, etc. are not limited to those in this example.
′ｊ！識例１
５５０ｎｍから８ＱＱｎｍまで感光波長を有する大型年
金＜７タロシアニン（犬日本インキ）２ｊ、ポリビニル
ブチラール（Ｓ−ＬＥＯ−ＢＭ−８−噴水化学）２ｇ、
テトラヒドロフラン６０．９を混合し、ボールミル？（
て６時間分散した液をＡ液とする。'j! Case 1 Large pension <7 talocyanin (Inu Nippon Ink) 2j, polyvinyl butyral (S-LEO-BM-8-Fountain Chemical) 2g, with photosensitive wavelengths from 550nm to 8QQnm,
Mix 60.9% of tetrahydrofuran and ball mill? (
The solution dispersed for 6 hours is called Solution A.
Ａ２０ｎｍから６００ｎｍまで感光波長を有するそナク
リドン（Ｒｕｂｉｃｒｏｎ７Ｒｅｄｕ５０ｔ３ Ｆ、
ｓ東洋曹達工業）２Ｉ、アクリル（アクリベット、三菱
レーヨン）２１、トルエン６０Ｉを混合し、ボールミル
にて１２蒔間分散した液をＢ液とする。Ｐ−ジエチルア
ミノベンツアルデヒドジフェニルヒドラゾン（ＣＴＣ−
２３６阿南香料）５ｇ、ポリカーボネート（Ｎ０ＶＡＲ
Ｅ乙口三菱化成）５Ｉ、テトラヒドロ７ラン１００ ！
１に溶解した液をＣ液とする。A Sonacridone (Rubicron7Redu50t3F,
Toyo Soda Kogyo) 2I, acrylic (Acrivet, Mitsubishi Rayon) 21, and toluene 60I were mixed and dispersed in a ball mill for 12 minutes, and the solution was designated as Solution B. P-diethylaminobenzaldehyde diphenylhydrazone (CTC-
236 Anan fragrance) 5g, polycarbonate (N0VAR
E Otsuguchi Mitsubishi Kasei) 5I, Tetrahydro 7 Run 100!
The solution dissolved in 1 is called Solution C.
工ＴＯｆｆ表面に蒸着し之ポリエステルフィルム（ハイ
ビーム１００ Ｌ −ＢＫＯ２東し）上に、Ａ液を塗工
、温風乾燥し、その上からＢ液を塗工、温風乾燥し、２
層からなる厚み０．５μｍ（各層の厚み０．２５μｍ）
のＯＧＬを形成した。さらに、その上にＯＴＬとして、
Ｃ液を塗工、温風乾燥し念、、ｃＴＬの膜厚け１８μｍ
とした。Coat liquid A on the polyester film (high beam 100 L-BKO2 east side) vapor-deposited on the surface of the TOff and dry with warm air, then apply liquid B on top of that and dry with warm air.
Thickness of 0.5 μm consisting of layers (thickness of each layer 0.25 μm)
OGL was formed. Furthermore, as an OTL,
Coat liquid C, dry with warm air, and make cTL film thickness 18 μm.
And so.
このようにして形成した電子写Ｊｌｃ感光体について、
静電複写紙試験装置ＥＩＰ−４２８型（川口電気製作所
）を用いて電子写真特性を組１定した。測定は一５ＫＶ
のコロナ帯電を５秒間行ない、タングステンランプによ
り光照射して半減露光量Ｅ３Ａを調べさちに、干渉フィ
ルターによりモノクロ化し次光（光の半値巾〜７πｍ）
を照射して分光特性を調べｆｃ、白色光による電子写真
特性及び感光波長を第１表に、分光特性を第１図に示す
。縦軸は感♂（Ｆ、％）１（ｃ！ｎ２／μＪ）、横軸は
光の波長（諧）である。Regarding the electrophotographic JLC photoconductor formed in this way,
The electrophotographic properties were determined using an electrostatic copying paper tester model EIP-428 (Kawaguchi Denki Seisakusho). Measurement is -5KV
After corona charging for 5 seconds, irradiate with light using a tungsten lamp to check the half-decreased exposure amount E3A, and then convert it into monochrome using an interference filter.
The spectral characteristics were investigated by irradiating fc with white light, and the electrophotographic characteristics and photosensitive wavelength are shown in Table 1, and the spectral characteristics are shown in FIG. The vertical axis is the sensitivity (F, %) 1 (c!n2/μJ), and the horizontal axis is the wavelength (tone) of light.
グラフより、４２０〜８［］Ｑ７１？７Ｌまでパンクロ
な光感度を有する電子写真感光体ｈ″−できていること
がわかる。From the graph, it can be seen that the electrophotographic photoreceptor h''- has a panchromatic photosensitivity of 420~8[]Q71~7L.
実施例２゜
Ｘ型無金属フタロシアニン２ｇ、キナクリドン２ｇ、ポ
リビニルブチラール３１．ポリエステル（パイロン２０
０ 東洋紡）１ｇ、テトラヒドロフラン１００ｇを混
合し、ボールミルにて１２時間分散した液をＤ液とする
。Example 2゜Type X metal-free phthalocyanine 2g, quinacridone 2g, polyvinyl butyral 31. Polyester (pylon 20
0 (Toyobo) and 100 g of tetrahydrofuran were mixed and dispersed in a ball mill for 12 hours, and the resulting solution was designated as Solution D.
ＩＴＯを表面に蒸着したポリエスルフィルム上ＩｃＤ液
を塗工ｔ７、温風乾燥させ、厚み０．４μｍのＣＧＬを
形成した。さらにＣ液をＣＴＬとして塗工。The IcD solution was coated on the polyester film on which ITO was vapor-deposited at t7, and dried with warm air to form a CGL with a thickness of 0.4 μm. Furthermore, apply C liquid as CTL.
乾燥させ、１８μｍの模を形成した。It was dried to form a pattern of 18 μm.
この電子写真感光体について、実施例１と同様の評価を
行なった。白色光による電子写真特性及び感光波長を第
１表に示す。分光特性は、実施例１とほぼ同様に４２０
ｎｍから８００ｎｍにわたってノ＜・ノクロな光感度を
もった。This electrophotographic photoreceptor was evaluated in the same manner as in Example 1. Table 1 shows the electrophotographic properties and sensitive wavelengths using white light. The spectral characteristics are almost the same as in Example 1.
It had excellent photosensitivity over the wavelength range of 800 nm to 800 nm.
実施例３゜
５００ｎｍから８５０ｎｍに感光波長を有するアルミク
Ｏｈフタσシアニン１ｐ、４００ｎｍから６００ｎｍ
に感光波長を有するテトラメチル） ＋１フエノジオ
千斗ジン（東洋曹達工業）２Ｆ、フヱノキシ樹１ｆｆｆ
（ＳＴＸ−０７東都化成）０５ｇ、ポリビニルブチラー
ル（Ｓ ＬＥＣ−ＢＭ−８，ｗ積木化学）０５１、ポ
リカーボネート（Ｎ０ＶＡＲＫＸ 三菱化成）２ｇ、
メチルエチルケトン／トルエン（＝１／１ ）８０ｇに
混合し、ボールミルにて１８時間分散した液をＢ液とす
る。Example 3 Aluminum Oh lid σ cyanine 1p with photosensitive wavelength from 500 nm to 850 nm, 400 nm to 600 nm
(Tetramethyl having a photosensitive wavelength)
(STX-07 Toto Kasei) 05g, polyvinyl butyral (S LEC-BM-8, w Building Chemical) 051, polycarbonate (N0VARKX Mitsubishi Chemical) 2g,
The solution was mixed with 80 g of methyl ethyl ketone/toluene (=1/1) and dispersed in a ball mill for 18 hours, and the solution was designated as Solution B.
この分散液Ｅ液をＯＧＬとして塗工し、乾燥させ０．５
μｍの厚さとし、その土足、実施例１と同様（てＣＴＬ
％−塗工した。This dispersion liquid E was applied as OGL and dried to give a 0.5
The thickness was 1 μm, and the shoes were the same as in Example 1 (CTL
%-Coated.
この電子写真感光体疋ついて実施例１と同様に評価した
結果を第１表に示す。また、分光特性はＡＯＯｎｍから
８５０ｎｍにわたってパンクロな光感度をも っ ｌ
ヒ 。This electrophotographic photoreceptor was evaluated in the same manner as in Example 1, and the results are shown in Table 1. In addition, the spectral characteristics have panchromatic photosensitivity from AOOnm to 850nm.
Hi.
比較例 液Ａを工ＴＯ蒸着フィルム上に０４μｍ塗工し。Comparative example Coat liquid A to a thickness of 04 μm on the TO vapor-deposited film.
さらに、液Ｃを１８μｍ塗工し、比較用電子写真感光体
を形成し之。Furthermore, 18 μm of liquid C was applied to form an electrophotographic photoreceptor for comparison.
この比較用電子写真感光体について、実施例１と同様に
して評価しｔ結果を第２図、第１表に示す。This comparative electrophotographic photoreceptor was evaluated in the same manner as in Example 1, and the results are shown in FIG. 2 and Table 1.
第 １ 表
〔発明の効果〕
以上述べ念ように１本発明だよれば、ＣＧＬとして吸収
波長域の異なる２種類以上の有機光導電性物質を含有す
ることによって、ｂ、ｔ、−むね４ＱＯｎｍからＢＯＱ
ｎｍの広域にわたって極めて高い一様な感変な有する電
子写真感光体を形成できる。Table 1 [Effects of the Invention] As mentioned above, according to the present invention, by containing two or more types of organic photoconductive substances with different absorption wavelength ranges as a CGL, it is possible to obtain a photoconductivity from b, t, -4Q Onm. BOQ
An electrophotographic photoreceptor having extremely high uniform sensitivity over a wide range of nm can be formed.
これＫよって、光のエネルＨ−ｈ′−有効にモヤ１フ
光感度が良くなった。さらに、この電子写真感光体げ、
光源にとら゛われることのない、つまり、レーザー用と
しても，白色光用としても使用可能であり，全く新しい
タイプの電子写貫感元体ｈ；実現で芦た。Due to this, the light energy H-h'-effectively improved the haze light sensitivity. Furthermore, this electrophotographic photoreceptor,
It is not dependent on the light source, that is, it can be used for both laser and white light, creating a completely new type of electronic photosensitive element.
第１図は、本発明の実施例１の電子写真感光体の分光特
性を示す図。
第２図は，比較例の電子写真感光体の分光特性を示す図
。
以 上
出頓入 セイコーエプソン株式会社
須玉（１ ４１１）
第１ｒｊｔＪ
貼イ、
齋２ｔ！１FIG. 1 is a diagram showing the spectral characteristics of the electrophotographic photoreceptor of Example 1 of the present invention. FIG. 2 is a diagram showing the spectral characteristics of an electrophotographic photoreceptor of a comparative example. Seiko Epson Corporation Sutama (1 411) 1st rjtJ pasted, sai 2t! 1
Claims (1)
と電荷輸送層（以下、ＣＴＬと略す）とからなる積層型
電子写真感光体において、ＣＧＬが吸収波長の異なる２
種類以上の有機光導電性物質を含有することを特徴とす
る電子写真感光体。A charge generation layer (hereinafter abbreviated as CGL) is provided on the conductive support.
In a laminated electrophotographic photoreceptor consisting of a CGL and a charge transport layer (hereinafter abbreviated as CTL), the CGL has two different absorption wavelengths.
An electrophotographic photoreceptor characterized by containing more than one type of organic photoconductive substance.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28915286A JPS63142356A (en) | 1986-12-04 | 1986-12-04 | Electrophotographic sensitive body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP28915286A JPS63142356A (en) | 1986-12-04 | 1986-12-04 | Electrophotographic sensitive body |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS63142356A true JPS63142356A (en) | 1988-06-14 |
Family
ID=17739435
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP28915286A Pending JPS63142356A (en) | 1986-12-04 | 1986-12-04 | Electrophotographic sensitive body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS63142356A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0345005A2 (en) * | 1988-05-31 | 1989-12-06 | Somar Corporation | Electrophotographic photosensitive element and method of preparing same |
| EP0402979A1 (en) * | 1989-06-16 | 1990-12-19 | Agfa-Gevaert N.V. | Electrophotographic recording material |
| JPH0566595A (en) * | 1991-02-01 | 1993-03-19 | Canon Inc | Electrophotographic sensitive body |
| US5312705A (en) * | 1990-07-27 | 1994-05-17 | Matsushita Electric Industrial Co., Ltd. | Photosensitive materials for electrophotography having a double-layer structure of a charge generation layer and a charge transport layer |
| US5328788A (en) * | 1990-07-26 | 1994-07-12 | Matsushita Electric Industrial Co., Ltd. | Organic photoconductive material for electrophotography and method for making the same |
-
1986
- 1986-12-04 JP JP28915286A patent/JPS63142356A/en active Pending
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0345005A2 (en) * | 1988-05-31 | 1989-12-06 | Somar Corporation | Electrophotographic photosensitive element and method of preparing same |
| EP0402979A1 (en) * | 1989-06-16 | 1990-12-19 | Agfa-Gevaert N.V. | Electrophotographic recording material |
| US5328788A (en) * | 1990-07-26 | 1994-07-12 | Matsushita Electric Industrial Co., Ltd. | Organic photoconductive material for electrophotography and method for making the same |
| US5312705A (en) * | 1990-07-27 | 1994-05-17 | Matsushita Electric Industrial Co., Ltd. | Photosensitive materials for electrophotography having a double-layer structure of a charge generation layer and a charge transport layer |
| JPH0566595A (en) * | 1991-02-01 | 1993-03-19 | Canon Inc | Electrophotographic sensitive body |
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