首页 | 本学科首页   官方微博 | 高级检索  
     

聚3-氯噻吩修饰CdSe纳米棒复合膜电极光电化学性能研究
引用本文:郝彦忠,殷志刚. 聚3-氯噻吩修饰CdSe纳米棒复合膜电极光电化学性能研究[J]. 高等学校化学学报, 2007, 28(6): 1117-1121
作者姓名:郝彦忠  殷志刚
作者单位:河北科技大学理学院,石家庄,050018;河北科技大学化学与制药工程学院,石家庄,050018
基金项目:国家自然科学基金 , 河北省自然科学基金 , 河北省教育厅指导性项目
摘    要:采用水热法制备了具有闪锌矿和纤维锌矿结构的CdSe纳米棒. 纳米棒直径约为100 nm, 长度约为300 nm. 当外加电极电势为-0.6 V 时, 经聚3-氯噻吩[Poly(3-chlorothiophene), P3CT]修饰的CdSe纳米棒具有最大光电流, 并且CdSe/P3CT复合膜电极最高光电转换效率(IPCE)为13.5%, 低于CdSe纳米棒膜电极17.7%的最高IPCE. CdSe/P3CT复合膜电极中存在p-n异质结, p-n异质结的存在使得CdSe/P3CT复合膜电极在长波区(>410 nm)的IPCE整体高于CdSe纳米棒薄膜电极的IPCE.

关 键 词:聚3-氯噻吩  CdSe/P3CT复合膜电极  光电化学
文章编号:0251-0790(2007)06-1117-05
收稿时间:2006-08-03
修稿时间:2006-08-03

Photoelectrochemical Studies of P3CT Modified CdSe Nanorod Composite Film Electrode
HAO Yan-Zhong,YIN Zhi-Gang. Photoelectrochemical Studies of P3CT Modified CdSe Nanorod Composite Film Electrode[J]. Chemical Research In Chinese Universities, 2007, 28(6): 1117-1121
Authors:HAO Yan-Zhong  YIN Zhi-Gang
Affiliation:1.College of Science, 2. College of Chemical and Pharmaceutical Engineering, Hebei University of Science and Technology, Shijiazhuang 050018, China
Abstract:CdSe nanorods(zinc blende and wulitize) were prepared via hydrothermal method.The CdSe nanorod was formed with a diameter about 100 nm and a length about 300 nm.The photoelectrochemical pro-perties of the CdSe nanorods/P3CT composite film electrode were investigated.The results show that the maximum value of photocurrent appeared at an electrode potential of-0.6 V.The maximum IPCE(13.5%) of the modified film electrode was lower than that of 17.7% CdSe nanorord film electrode.The p-n heterojunction was existed in the CdSe/P3CT composite film electrode.Because of the existence of p-n heterojunction,under certain condition the IPCE of P3CT modified CdSe nanorod was larger than that of CdSe film electrode in the whole long wavelength region(>410 nm).
Keywords:Poly(3-chlorothiophene)  CdSe/P3CT composite film electrode  Photoelectrochemistry
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《高等学校化学学报》浏览原始摘要信息
点击此处可从《高等学校化学学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号