首页> 外文会议>Conference on optical organic and inorganic materials >Transport features of electrons in thin layers of bis4-(anthraquinone-l-amino)-3-hydroxy-l-thiabutylbenzene
【24h】

Transport features of electrons in thin layers of bis4-(anthraquinone-l-amino)-3-hydroxy-l-thiabutylbenzene

机译:双层中电子的传输特征4-(蒽醌-1-氨基)-3-羟基-1-硫基苯

获取原文

摘要

Derivatives of trinitrofluorenone, bisphenylquinone, thiopyran, oxadiazole, anthraquinone may be mentioned as electron transporting materials (ETM). Because of high crystallization speed of these materials it is difficult to prepare organic electrophotographic layers of high quality. It is a common fault of these ETM. In this work was prepared ETM with good film forming properties by reaction of l-(2,3-epoxypropylamino)anthraquinone and 1,3-benzenedithiol. ETM bis[4-(anthraquinone-l-amino)-3-hydroxy-l-thiabutyl]-benzene was obtained this way. The drift mobility of electrons was measured by a time-of-flight method. The transient of a small charge had a fast relaxation but a characteristic kink, by which the time of transit was determined, was weakly expressed because of a strong degree of dispersion of electron transport. The drift mobility of electrons was 4.6-10~(-7)cm~2/Vs at an electric field strength 8-10~5 V/cm and the temperature of 26 deg C. The photosensitivity of positively charged photoreceptor consisting of the lower photogenerative layer of Y-type titanyl phthalocyanine and an ETM transport layer in the spectral range 600 nm to 860 nm is as high as 80 m~2J~(-1) to 120 m~2J~(-1).
机译:作为电子传输材料(ETM),可以提及三分子氟核酮,双苯基醌,硫吡喃,恶二唑,蒽醌的衍生物。由于这些材料的高结晶速度,难以制备高质量的有机电子照相层。这是这些ETM的常见错误。在这项工作中,通过L-(2,3-环氧丙基氨基)蒽醌和1,3-苯二硫醇的反应,制备具有良好膜形成性能的ETM。通过这种方式获得ETM BIS [4-(蒽醌-1-氨基)-3-羟基-1-硫基丁基] - 苯。通过飞行时间方法测量电子的漂移迁移率。小电荷的瞬态具有快速的弛豫,但是由于电子传输的强度分散,因此确定了传输时间的特征性扭结。电子的漂移迁移率为4.6-10〜(-7)cm〜2 / Vs,电场强度为8-10〜5 v / cm,温度为26℃。由下部的带正电感的感光体的光敏性光谱范围600nm至860nm的光氨基酞菁酞菁和ETM传输层高达80m〜2J〜(-1)至120m〜2J〜(-1)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号