JPH05333579A - Electrophotographic sensitive body - Google Patents

Abstract

PURPOSE:To provide an electrophotographic sensitive body having. excellent sensitivity which is useful for a high-speed printer, high-speed digital copy machine, or high-speed facsimile, to provide an electrophotographic sensitive body showing little change in sensitivity against change in humidity, to provide an electrophotographic sensitive body having stable characteristics for repetition of use, and further, to provide an electrophotographic sensitive body having excellent production stability and little change in characteristics. CONSTITUTION:This electrophotographic sensitive body contains crystalline titanylphthalocyanine/vanadylphthalocyanine and polyalkylene glycol of 110-2000 mol.wt. by 0.1-500 pts.wt. to 100 pts.wt. of the titanylphthalocyanine/ vanadylphthalocyanine. The X-ray diffraction spectrum of the titanylphthalocyanine/vanadylphthalaocyanine for Cu-Kalpha ray has the max. peak at 27.2+ or -0.2 deg. Bragg angle 2theta.

Description

Detailed Description of the Invention

[0001]

FIELD OF THE INVENTION The present invention relates to an electrophotographic photoreceptor,
In particular, titanyl phthalocyanine having a specific crystal type is used as a photoconductive material, it is effective for a printer, a copying machine and the like, and is also suitable when an image is formed by using a semiconductor laser light and an LED light as an exposing means. Electrophotographic photoconductor.

[0002]

2. Description of the Related Art In recent years, photoconductive materials have been actively researched and applied to photoelectric conversion elements such as electrophotographic photoreceptors, solar cells and image sensors. Conventionally, inorganic materials are mainly used for these photoconductive materials. For example, in an electrophotographic photoreceptor, a photosensitive layer containing an inorganic photoconductive material such as selenium, zinc oxide, or cadmium sulfide as a main component is provided. Inorganic photoreceptors have been widely used.

However, such an inorganic photoconductor has not always been satisfactory in characteristics such as photosensitivity, thermal stability, moisture resistance and durability required for electrophotographic photoconductors for copying machines, printers and the like. For example, selenium is crystallized by heat, stains on fingerprints, etc., so that the characteristics as an electrophotographic photoreceptor are likely to deteriorate. Further, the electrophotographic photoreceptor using cadmium sulfide is inferior in moisture resistance and durability, and the electrophotographic photoreceptor using zinc oxide also has a problem in durability.

Further, in recent years, environmental problems have been particularly emphasized, but electrophotographic photoreceptors such as selenium and cadmium sulfide have a drawback in that they are severely restricted in production and handling in terms of toxicity.

In order to remedy the drawbacks of such inorganic photoconductive materials, various organic photoconductive materials have been attracting attention, and in recent years, attempts have been made to use them in the photosensitive layer of electrophotographic photoreceptors. Active research is being conducted. For example, Japanese Patent Publication No. 50-10496 discloses an organic photoreceptor having a photosensitive layer containing polyvinylcarbazole and trinitrofluorenone. However, this photoreceptor is not sufficient in sensitivity and durability. Therefore, a function-separated type electrophotographic photosensitive member has been developed in which different substances have different functions of carrier generation and carrier transport.

In such an electrophotographic photosensitive member, since a wide range of materials can be selected, it is easy to obtain arbitrary characteristics,
Therefore, it is expected that an organic photoreceptor having high sensitivity and high durability can be obtained.

Various organic compounds have been proposed as the carrier-generating substance and the carrier-transporting substance of such a function-separated type electrophotographic photosensitive member, but the carrier-generating substance is particularly important for controlling the basic characteristics of the photosensitive member. Has various functions. As the carrier generating substance, photoconductive substances such as polycyclic quinone compounds typified by dibromoanthanthrone, pyrylium compounds and eutectic complexes of pyrylium compounds, squarylium compounds, phthalocyanine compounds, and azo compounds have been put to practical use. It was

It is known that a titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal having a particular crystal form exhibits excellent properties. The performance of the titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal differs depending on the crystal type, but the crystal type having the maximum peak at 27.2 ± 0.2 ° of Bragg angle 2θ in Cu-Kα has high photon efficiency. The electrophotographic photosensitive member used as a carrier generating material is useful for designing high speed printers, high speed digital copiers, high speed facsimiles and the like.

In order to form a photosensitive layer, a desired titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal is usually obtained by adding a binder polymer in an organic solvent, if necessary, and finely dispersing it using various dispersing devices. The dispersion is applied on a conductive substrate. In general, a compound having a crystal polymorph has a different crystal stability depending on environmental conditions, and thus a crystal state is often changed in a dispersion liquid under the influence of a solvent or a binder. In particular, titanyl phthalocyanine used in the present invention is used. Since the / vanadyl phthalocyanine mixed crystal has a very high photon efficiency, such a slight change in the crystalline state has an important influence on the photoreceptor characteristics. Therefore, it is important to suppress such changes in the dispersion liquid, and it is further important to ensure crystal stability in the photosensitive layer for a long period of time against environmental conditions and the like.

[0010]

SUMMARY OF THE INVENTION It is an object of the present invention to provide an electrophotographic photosensitive member which has excellent sensitivity characteristics and is useful for a high speed printer, a high speed digital copying machine or a high speed facsimile.

Another object of the present invention is to provide an electrophotographic photosensitive member having a small change in sensitivity characteristic with respect to humidity fluctuation.

Another object of the present invention is to provide an electrophotographic photosensitive member having stable characteristics upon repeated use.

A further object of the present invention is to obtain an electrophotographic photosensitive member which is excellent in production stability and has little characteristic fluctuation.

[0014]

The structure and effects of the present invention have been intensively studied in accordance with the above object of the present invention, and the stability of the specific crystal form of titanyl phthalocyanine / vanadyl phthalocyanine used in the present invention is remarkably improved by the presence of a specific substance. I found that That is, in an electrophotographic photosensitive member using a crystal type titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal having a maximum peak at 27.2 ± 0.2 ° of Bragg angle 2θ in an X-ray spectrum for Cu-Kα line as a carrier generating substance, 100 parts by weight of a titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal containing an alkyl diol compound having 3 to 12 carbon atoms in which two hydroxyl groups are bonded to carbon atoms having non-adjacent positions to each other in the same layer as the titanyl phthalocyanine / vanadyl phthalocyanine in the photosensitive layer. It is achieved by containing 0.1 to 1000 parts by weight with respect to.

The X-ray diffraction spectrum was measured under the following conditions, and the peak here is a protrusion having a sharp acute angle different from noise.

X-ray tube Cu voltage 40.0 KV current 100 mA start angle 6.0 deg. Stop angle 35.0 deg. Step angle 0.02 deg. Measurement time 0.50 sec. Various methods can be used for synthesizing the titanyl phthalocyanine used for preparing the mixed crystal of the present invention. Typically, it can be synthesized according to the following reaction formula (1) or (2).

[0017]

[Chemical 1]

In the formula, R _{1 to} R ₄ represent a leaving group.

Similarly to titanyl phthalocyanine, vanadyl phthalocyanine is prepared by using o-phthalonitrile, 1,3-diiminoisoindoline, vanadium pentoxide, and a vanadium reagent typified by vanadium acetylacetone in an inert solvent such as 1-chloronaphthalene. It can be obtained by reacting with.

To form a mixed crystal of titanyl phthalocyanine and vanadyl phthalocyanine obtained as described above,
For example, a method of dissolving titanyl phthalocyanine and vanadyl phthalocyanine of any crystalline form by ordinary acid paste treatment, and dissolving the sulfuric acid solution in water and collecting the precipitated crystals by filtration, or titanyl phthalocyanine of any crystalline form. And vanadyl phthalocyanine are mixed, and the mixture is pulverized by a mechanical force such as milling to obtain an amorphous crystal composed of titanyl phthalocyanine-vanadyl phthalocyanine. When amorphization is performed by acid paste treatment here, it is achieved under general conditions, and the weight ratio of concentrated sulfuric acid to phthalocyanine is not particularly limited, but it is 5 times to 200 times.
About twice is desirable. The amount of water used for draining the concentrated sulfuric acid is preferably about 5 to 100 times by weight. Furthermore, the temperature at which phthalocyanine is dissolved in concentrated sulfuric acid is 5
It is desirable that the water temperature is 0 ° C or higher and 50 ° C or lower.

Next, the crystal form used in the present invention can be obtained by treating the amorphous crystal with a specific organic solvent. Examples of the organic solvent used include a hydrocarbon solvent, an aromatic solvent, a halogen solvent, an alcohol, an ether solvent, an ester solvent, an organic acid, an organic amine, and a heterocyclic compound, but if necessary. An acid such as sulfonic acid or trichloroacetic acid may be added. On the other hand, as the state of the amorphous crystal, either a wet paste state containing water or a dry state containing no water can be used, which can be selected depending on the type of organic solvent to be treated and the purpose. .. Furthermore, in this solvent treatment, operations such as heating or milling treatment can be performed as necessary. Further, as shown in Synthesis Example 6, the crystal once converted into the crystal form of the present invention by these methods can be further subjected to a crystal treatment as necessary such as a treatment with the above-mentioned organic solvent. However, the crystal conversion method is not necessarily limited to such a method.

The alkyl diol compound used in combination with these titanyl phthalocyanine / vanadyl phthalocyanine mixed crystals has a carbon number of 3 to 12, and
The excellent effect of the present invention is obtained when the two hydroxyl groups are bonded to carbon atoms which are not adjacent to each other. Furthermore, the range of 3 to 8 carbon atoms is particularly preferable.

Specific examples of such compounds include 1,3-propanediol 1,4-butanediol, 1,3-butanediol 1,4-pentanediol, 1,5-pentanediol, 2,
4-pentanediol, 2,2-dimethyl-1,3-propanediol 1,5-hexanediol, 1,6-hexanediol, 2,
5-hexanediol, 2-methyl-2,4-pentanediol, 2-ethyl-2-methyl-1,3-propanediol 1,7-heptanediol, 2,2-diethyl-1,3-propanediol, 2,4-dimethyl-2,4-pentanediol, 2-
Methyl-2-propyl-1,3-propanediol 1,8-octanediol, 2,5-dimethyl-2,5-hexanediol, 2-ethyl-1,3-hexanediol, 2,2,4-
Trimethyl-1,3-pentanediol and the like can be mentioned.

These alkyl diol compounds are used in the range of 0.1 to 1000 parts by weight based on 100 parts by weight of the titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal. This is because if it is less than this range, the effect is insufficient, and if it is more than this range, the sensitivity characteristics of the photoreceptor are deteriorated.

In the electrophotographic photosensitive member of the present invention, other photoconductive substances may be used in combination with the above-mentioned phthalocyanine. Other photoconductive substances include titanyl phthalocyanines such as A, B, C, amorphous and AB mixed types which are different in crystal form from the titanyl phthalocyanines used in the present invention, other phthalocyanine compounds, naphthalocyanine compounds, and other porphyrins. Examples thereof include derivatives, azo compounds, polycyclic quinone compounds represented by dibromoanthanthrone, pyrylium compounds, eutectic complexes of pyrylium compounds, and squarylium compounds.

The electrophotographic photoreceptor of the present invention may be used in combination with a carrier transport material. As the carrier transporting substance, various ones can be used, but as a typical one, for example, a compound having a nitrogen-containing heterocyclic nucleus represented by oxazole, oxadiazole, thiazole, thiadiazole, imidazole or the like, and a condensed ring nucleus thereof, poly Arylalkane compounds, pyrazoline compounds, hydrazone compounds, triarylamine compounds, styryl compounds, polis (bis) styryl compounds, styryltriphenylamine compounds, β-phenylstyryltriphenylamine compounds, butadiene System compounds, hexatriene compounds, carbazole compounds, condensed polycyclic compounds and the like. Specific examples of these carrier-transporting substances include the carrier-transporting substances described in JP-A-61-107356, and the structures of particularly representative ones are shown below.

[0027]

[Chemical 2]

[0028]

[Chemical 3]

[0029]

[Chemical 4]

[0030]

[Chemical 5]

[0031]

[Chemical 6]

[0032]

[Chemical 7]

Various forms of the photoreceptor are known. The photoconductor of the present invention may take any of these forms, but it is desirable to use a laminated or dispersed function-separated photoconductor. In this case, normally, FIG.
The configuration is as shown in (6). In the layer structure shown in FIG. 1 (1), a carrier generation layer 2 is formed on a conductive support 1, a carrier transport layer 3 is laminated on the carrier generation layer 2, and a photosensitive layer 4 is formed. () Is a photosensitive layer 4'in which the carrier generating layer 2 and the carrier transporting layer 3 are reversed. In FIG. 3C, an intermediate layer 5 is provided between the photosensitive layer 4 having the layer structure of FIG. 1A and the conductive support 1. The layer structure of FIG. 5 (5) is formed by forming a photosensitive layer 4 ″ containing a carrier generating substance 6 and a carrier transporting substance 7, and FIG. 6 (6) shows such a photosensitive layer 4 ″ and a conductive support. The intermediate layer 5 is provided between the first and second layers. Figure 1 (1) to (6)
In the above constitution, a protective layer may be further provided on the outermost layer.

In forming the photosensitive layer, it is effective to apply a solution in which the carrier-generating substance or the carrier-transporting substance is dissolved alone or together with a binder and additives. However, since the solubility of the carrier-generating substance is generally low, in such a case, the carrier-generating substance is dispersed by an ultrasonic disperser,
A method of applying a liquid in which fine particles are dispersed in an appropriate dispersion medium by using a dispersing device such as a ball mill, a sand mill, a homomixer is effective. In this case, the binder and additives are usually used by adding them to the dispersion liquid.

A wide variety of solvents or dispersion media can be used as the solvent or dispersion medium for forming the photosensitive layer. For example, butylamine, ethylenediamine, N, N-dimethylformamide, acetone, methyl ethyl ketone, methyl isopropyl ketone, methyl isobutyl ketone, cyclohexanone, 4-methoxy-4-methyl-2-pentanone, tetrahydrofuran, dioxane, ethyl acetate, butyl acetate,
Acetic acid-t-butyl, methyl cellosolve, ethyl cellosolve, butyl cellosolve, ethylene glycol dimethyl ether, toluene, xylene, acetophenone, chloroform, dichloromethane, dichloroethane, trichloroethane, methanol, ethanol, propanol, butanol and the like can be mentioned.

When a binder is used for forming the carrier generating layer or the carrier transporting layer, any binder can be selected, but a high molecular polymer having hydrophobicity and film forming ability is particularly desirable. Examples of such a polymer include the following,
It is not limited to these. Polycarbonate Polycarbonate Z resin Acrylic resin Methacrylic resin Polyvinyl chloride Polyvinylidene chloride Polystyrene Styrene-butadiene copolymer Polyvinyl acetate Polyvinyl formal Polyvinyl butyral Polyvinyl acetal Polyvinylcarbazole Styrene-alkyd resin Silicone resin Silicone-alkyd resin Silicone-butyral resin Polyester Polyurethane Polyamide Polyamide Epoxy Resin Phenolic resin Vinylidene chloride-acrylonitrile copolymer Vinyl chloride-Vinyl acetate copolymer Vinyl chloride-Vinyl acetate-Maleic anhydride copolymer The ratio of the carrier generating substance to the binder is preferably 10 to 600% by weight, and further 50 It is desirable to set it to 400% by weight. The ratio of carrier transport material to binder is
It is desirable to be 10 to 500% by weight. The thickness of the carrier generation layer is 0.01 to 20 μm, preferably 0.05 to 5 μm. The thickness of the carrier transport layer is 1 to 100 μm, more preferably 5 to 30 μm.

The above-mentioned photosensitive layer may contain an electron accepting substance for the purpose of improving sensitivity, reducing residual potential, or reducing fatigue during repeated use. Examples of such an electron accepting substance include succinic anhydride, maleic anhydride, dibromosuccinic anhydride, phthalic anhydride, tetrachlorophthalic anhydride, tetrabromophthalic anhydride, 3-nitrophthalic anhydride and 4-nitrophthalic anhydride. Acid, pyromellitic dianhydride, mellitic dianhydride, tetracyanoethylene, tetracyanoquinodimethane, o-dinitrobenzene, m-dinitrobenzene, 1,3,5-trinitrobenzene, p-nitrobenzonitrile, picryl chloride, Quinone chlorimide, chloranil, bromanil, dichlorodicyano-p-benzoquinone, anthraquinone, dinitroanthraquinone, 9-fluorenylidene malononitrile, polynitro-9-fluorenylidene malononitrile, picric acid, o-nitrobenzoic acid, p- Nitrobenzoic acid, 3,5-dinitrobenzoic acid, pentafluorobenzoic acid Acid, 5-nitro salicylic acid, 3,5-dinitrosalicylic acid, phthalic acid, mellitic acid, and larger compounds of other electron affinity. The addition ratio of the electron accepting substance is 0.0 with respect to 100 by weight of the carrier generating substance.
It is preferably 1 to 200, more preferably 0.1 to 100.

Further, in the above-mentioned photosensitive layer, storability, durability,
For the purpose of improving the resistance to environment, a deterioration inhibitor such as an antioxidant or a light stabilizer can be contained. Examples of compounds used for such purpose include chromanol derivatives such as tocopherol and etherified or esterified compounds thereof, polyarylalkane compounds,
Hydroquinone derivatives and mono- and dietherified compounds thereof, benzophenone derivatives, benzotriazole derivatives, thioether compounds, phosphonic acid esters, phosphorous acid esters, phenylenediamine derivatives, phenol compounds, hindered phenol compounds, linear amine compounds,
Cyclic amine compounds and hindered amine compounds are effective. Specific examples of particularly effective compounds include "IRGANOX
"1010", "IRGANOX 565" (manufactured by Ciba Geigy), "Sumilyzer BHT", "Sumilyzer MDP" (manufactured by Sumitomo Chemical Co., Ltd.), and other hindered phenolic compounds "Sanol LS-2626",
Examples thereof include hindered amine compounds such as "Sanol LS-622LD" (manufactured by Sankyo Co., Ltd.).

As the binder used for the intermediate layer, the protective layer and the like, those mentioned above for the carrier generating layer and the carrier transporting layer can be used. In addition to them, nylon resin, ethylene-vinyl acetate copolymer, Ethylene resins such as ethylene-vinyl acetate-maleic anhydride copolymer and ethylene-vinyl acetate-methacrylic acid copolymer, polyvinyl alcohol, and cellulose derivatives are effective.
Further, a curable binder utilizing heat curing or chemical curing of melamine, epoxy, isocyanate or the like can be used.

As the conductive support, a metal plate or a metal drum is used, and a conductive polymer, a conductive compound such as indium oxide, or a thin layer of a metal such as aluminum or palladium is applied, vapor-deposited, laminated or the like. Accordingly, a material provided on a substrate such as paper or plastic film can be used.

[0041]

【Example】

Example 1 1 part by weight of powder of a titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal having the X-ray diffraction spectrum of FIG.
100 parts by weight of methyl ethyl ketone and 0.4 parts by weight of 1,4-butanediol were added and dispersed using a sand mill.
After a part of the obtained dispersion liquid was evaporated to dryness, the X-ray diffraction spectrum was measured and it was as shown in FIG. On the other hand, a 0.3 μm-thick undercoating layer made of polyamide resin “CM-8000” (manufactured by Toray Industries, Inc.) was formed on a polyester base on which aluminum was vapor-deposited by a wire bar coating method, and then the obtained dispersion was coated with a wire bar. A carrier generation layer having a thickness of 0.3 μm was obtained. Next, 1 part by weight of carrier-transporting substance (10), 1.5 parts by weight of polycarbonate resin "Iupilon Z-200" (manufactured by Mitsubishi Gas Chemical Co., Inc.) and a small amount of silicone oil "KF-54" (manufactured by Shin-Etsu Chemical Co., Ltd.) 1,2- A solution dissolved in 8 parts by weight of dichloroethane was blade-coated to form a carrier transport layer having a thickness of 20 μm. The photoreceptor thus obtained is referred to as Sample 1.

Examples 2 to 4 Example 1 was repeated except that 1,3-butanediol, 1,3-propanediol and 1,5-pentanediol were used in place of 1,4-butanediol in Example 1. Similarly, a photoconductor of the present invention was obtained. This will be referred to as Samples 2 to 4. The X-ray diffraction spectrum measured after dispersion was the same as in Example 1, and no change in the crystalline state was observed.

Comparative Example (1) A comparative photoconductor was obtained in the same manner as in Example 1 except that 1,4-butanediol was removed. This is designated as Comparative Sample (1). Further, an X-ray diffraction spectrum measured by evaporating and drying a part of the obtained dispersion liquid is shown in FIG.

It can be seen that the crystal state is changed.

Comparative Examples (2) to (8) In Example 1, instead of 1,4-butanediol, 1-heptanol, 1-octanol, ethylene glycol, 1,2-butanediol, 1,2-hexanediol, Glycerin 1,
A comparative photoconductor was obtained in the same manner as in Example 1 except that 16-hexadecanediol was used. These are designated as comparative samples (2) to (8), respectively.

Comparative Example (9) A comparative photoconductor was obtained in the same manner as in Example 1 except that the amount of 1,4-butanediol was changed to 12 parts by weight. This is designated as Comparative Sample (9).

Comparative Example (10) A comparative photoconductor was obtained in the same manner as in Example 1 except that the amount of 1,4-butanediol was changed to 0.0005 parts by weight. This is designated as a comparative sample (10).

(Evaluation 1) The obtained sample was heated at 20 ° C. and 50%
Installed on a modified "Konica 9028" (made by Konica Corporation, using a semiconductor laser light source) under the environment of RH and grid voltage V _G
Was adjusted to -750 V, and the potential V _H of the unexposed portion and the potential V _L of the exposed portion at the time of light irradiation of 0.7 mW were measured. Then sample 1
After moving to 0 ℃, 20% RH environment and fully acclimatizing to the environment,
V _H and V _L were measured under the above conditions. Also, 10 ℃, 20RH
In this environment, V _H and V _L after repeated use of 10,000 prints were also measured.

(Evaluation 2) The sample was also 55 ° C. and 80% RH.
After being left for 1 week in the atmosphere of No. 2, the sample was mounted on "Konica 9028" in an environment of 20 ° C. and 50% RH, and V _H and V _L were measured.

The evaluation results are shown in Table 1. It can be seen that the alkyl diol of the present invention shows a remarkable effect in reducing fluctuations in humidity, changes in the characteristics of the photoreceptor due to repeated use, and stabilizing the dispersion liquid and the photoreceptor.

[0051]

[Table 1]

[0052]

According to the structure of the present invention, it is possible to obtain a photoconductor useful for high speed printers, digital copying machines, and facsimiles, which has little sensitivity to humidity variation and high durability.

[Brief description of drawings]

FIG. 1 is a sectional view of a photoconductor of the present invention.

FIG. 2 is an X-ray diffraction spectrum diagram of titanyl phthalocyanine / vanadyl phthalocyanine used in the present invention.

FIG. 3 Titanyl phthalocyanine / obtained in Example 1
The X-ray-diffraction spectrum figure of vanadyl phthalocyanine.

FIG. 4 is an X-ray diffraction spectrum diagram of the titanyl phthalocyanine / vanadyl phthalocyanine obtained in Comparative Example (1).

[Explanation of symbols]

 1 Conductive Support 2 Carrier Generation Layer 3 Carrier Transport Layer 4 Photosensitive Layer 5 Intermediate Layer 6 Carrier Generation Material 7 Carrier Transport Material

 ─────────────────────────────────────────────────── ─── Continuation of the front page (72) Inventor Akira Kinoshita 1st Sakura-cho, Hino-shi, Tokyo Konica Stock Company In-house (72) Inventor Kazumasa Watanabe 1st Sakura-cho, Hino-shi, Tokyo Konica Stock Company In-house (72) Invention Person Kiyoshi Tamaki 2970 Ishikawa-cho, Hachioji-shi, Tokyo Konica stock company (72) Inventor Yoshihide Fujimaki 2970 Ishikawa-cho, Hachioji-shi, Tokyo Konica stock company

Claims (2)

[Claims] 1. A titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal having a maximum peak at 27.2 ± 0.2 ° of Bragg angle 2θ in an X-ray diffraction spectrum for Cu-Kα rays, and two hydroxyl groups are in non-adjacent positions to each other. An electrophotographic photoreceptor comprising an alkyldiol compound having 3 to 12 carbon atoms bonded to a certain carbon atom in an amount of 0.1 to 1000 parts by weight based on 100 parts by weight of titanyl phthalocyanine. 2. A titanyl phthalocyanine / vanadyl phthalocyanine mixed crystal has a Bragg angle 2θ of 27.2 ± 0.2 ° and 24.1 ± 0.2 in an X-ray diffraction spectrum for Cu-Kα radiation.
The electrophotographic photosensitive member according to claim 1, which is a crystal having a peak at 90 °, 9.5 ± 0.2 °.