Imaging system
AssigneeXerox Corporation
InventorsAnthony M. Horgan, Richard W. Radler, Jr.
Life of this patent
Estimating the term…
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AssigneeXerox Corporation
InventorsAnthony M. Horgan, Richard W. Radler, Jr.
Estimating the term…
An imaging member comprising a layer of particulate photoconductive material dispersed in an organic resinous binder, said photoconductive material comprising trigonal selenium containing a mixture of an alkali metal selenite and an alkali metal carbonate. This layer can be the charge generation layer of an imaging member also having a charge transport layer in contact therewith.
An imaging member comprising a layer of particulate photoconductive material dispersed in an organic resinous binder, said photoconductive material comprising trigonal selenium containing a mixture of alkali metal selenite and alkali metal carbonate of from about 0.01 to about 12.0 percent total weight based on the weight of the trigonal selenium wherein ratio of the selenite to carbonate ranges from 90 to 10 parts by weight to 10 to 90 parts by weight.
An imaging member comprising a charge generation layer comprising a particulate photoconductive material comprising trigonal selenium dispersed in an organic resinous binder, said trigonal selenium containing a mixture of alkali metal selenite and alkali metal carbonate of from about 0.01 to about 12.0 percent total weight based on the weight of trigonal selenium wherein the ratio of the selenite to carbonate ranges from 90 to 10 parts by weight to 10 to 90 parts by weight and a contiguous charge transport layer, said photoconductive material exhibiting the capability of photogeneration of charge carriers and injection of said charge carriers and said charge transport layer being substantially nonabsorbing in the spectral region at which the photoconductive material generates and injects photogenerated charge carriers but being capable of supporting the injection of photogenerated charge carriers from said photoconductive material and transporting said charge carriers through said charge transport layer.
Dependencies are inferred from the claim text.
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From the US filing history. Foreign family members aren’t listed.
Characterised by the photoconductive material being inorganic: and being incorporated in an organic bonding material
Electrography
Term ended 4 Nov 1997 (estimated)
USPTO file history isn’t available for this patent, so only indexed dates are shown.
This invention relates in general to xerography and more specifically to a novel photosensitive device.
Vitreous and amorphous selenium is a photoconductive material which has had wide use as a reusable photoconductor in commercial xerography. However, its spectral response is limited largely to the blue-green portion of the visible spectrum, i.e. below 5200 angstrom units.
Selenium also exists in a crystalline form known as trigonal or hexagonal selenium. Trigonal selenium is well known in the semiconductor art for use in the manufacture of selenium rectifiers.
FIG. 1 is a schematic illustration of one of the members of the instant invention which comprises particulate trigonal selenium randomly dispersed in a resinous binder overlying a substrate.
FIG. 2 is a schematic illustration of one of the members of the instant invention wherein the particulate trigonal selenium is geometrically dispersed within an electrically insulating organic binder. This layer overlies the substrate.
FIG. 3 is a schematic illustration of one of the members of the instant invention illustrating a composite photoreceptor comprising a charge carrier generation layer overcoated with a charge transport layer. The charge carrier generation layer comprises the selenite and carbonate modified trigonal selenium dispersed in an organic resinous binder as the charge carrier generation layer.
For a better understanding of the Figures, several terms should be defined. The term "rested dark decay" when used in this application means that it is the amount of voltage drop, i.e. surface potential drop, of a member which has been rested and then charged initially to an initial surface potential, measured in voltage, and then allowed to remain in the dark. The drop in potential is measured 0.06 seconds after charging, 0.22 seconds after charging, and 0.66 seconds after charging. This "rested dark decay" means that the photoreceptor has been rested in the dark for at least 30 minutes prior to testing i.e. cycling in a xerographic mode.
"Fatigue dark decay" means, for purpose of this application, a drop in surface potential 0.06 seconds after charging, then after 0.22 seconds and then after 0.66 seconds. These measurements are made while the photoreceptor remains in the dark. "Fatigue dark decay" further means that the photoreceptor has been cycled at least one time through a xerographic cycle and then discharged, i.e. erased, and then is tested before the photoreceptor has rested, preferably before 30 minutes has passed after charging the photoreceptor. The process speed of the photoreceptor is 30 inches per second.
Referring to FIG. 1, reference character 10 designates an imaging member which comprises a supporting substrate 11 having a binder layer 12 thereon. Substrate 11 is preferably comprised of any suitable conductive material. Typical conductors comprise aluminum, steel, nickel, brass or the like. The substrate may be rigid or flexible and of any conventional thickness. Typical substrates include flexible belts of sleeves, sheets, webs, plates, cylinders and drums. The substrate or support may also comprise a composite structure such as a thin conductive coating contained on a paper base; a plastic coated with a thin conductive layer such as aluminum, nickel or copper iodine; or glass coated with a thin conductive coating of chromium or tin oxide.