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In relation to this article, we declare that there is no conflict of interest.
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Received May 9, 2008
Accepted October 23, 2008
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Xerographic properties of metal/metal-free phthalocyanine composites in a double-layered photoconductor

Department of Chemical Engineering, Chungbuk National University, Cheongju 361-763, Korea 1Neo Photocon, 416-5, GeunChang-ri, Baekam-myun, CheIn-gu, Yongin-shi, Gyeonggi-do 449-861, Korea
jdlee@cbu.ac.kr
Korean Journal of Chemical Engineering, May 2009, 26(3), 673-678(6), 10.1007/s11814-009-0112-z
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Abstract

The electrophotographic properties of a negatively charged double-layered photoconductor that consisted of y-type metal phthalocyanine (TiOPc) and x-type metal-free phthalocyanine (H2Pc) composites were studied. The undercoating layer (UCL) was fabricated by a dip-coating method with Al2O3 and polyamide, and the charge transport layer (CTL) was prepared from N,N'-Bis-(3-methylpenyl)-N,N"-bis-(phenyl)-benzidine (TPD), polycarbonate (PC), and polyester (PE). In the charge generation layer (CGL), the dispersion state becomes more homogeneous with increasing amounts of non-metal phthalocyanine (H2Pc). The electrophotographic properties of the photoconductor were obtained by using photo-induced discharge curves (PIDC) of charge acceptance, dark decay, photosensitivity, and photofatigue. It was found that the initial charge potential was not dependent on the compositional ratio of the charge generating material. However, the dark decaying rates and the photosensitivity were proportional to the content of TiOPc in the organic photoconductors.

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