Copper oxide photocathodes prepared by a solution based process

被引:90
作者
Chiang, Chia-Ying [1 ]
Shin, Yoon [1 ]
Aroh, Kosi [1 ]
Ehrman, Sheryl [1 ]
机构
[1] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
Hydrogen energy; Photoelectrochemical cell; Copper oxide; Water splitting; THIN-FILMS; CUO; CU2O; WATER;
D O I
10.1016/j.ijhydene.2012.02.049
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Solution based processes are well known by their low-cost trait to fabricate semiconductor devices. In this study, we devised an economical solution based route to photoelectrochemical (PEC) cells, taking copper nitrate as the copper ion source and adding an alkali hydroxide, here NaOH, to produce high aspect ratio (3.1-9.7) CuO nanoparticles. These CuO particles were used for splitting water and generation of hydrogen via a PEC cell. CuO nanoparticle morphology, i.e. rod-like, spindle-like, and needle-like, was dependent on the processing temperature. Sintering the spin coated CuO films, improved crystallinity. The bandgaps for these films were estimated to be 1.35 eV and 1.64 eV for sintering temperatures of 600 degrees C and 400 degrees C for 1 h, respectively. The porous structure of the nano-sized CuO films increased surface area and thus led to a high photocurrent, i.e. 1.20 mA/cm(2), for powder prepared at 60 degrees C and sintered at 600 degrees C for 1 h. These films demonstrated 0.91% solar conversion efficiency at an applied voltage of -0.55 V vs. Ag/AgCl in 1 M KOH electrolyte with 1 sun (AM1.5G) illumination. The charge carrier density was estimated to be 6.1 x 10(20) cm(-3). This relatively high charge carrier density may be due to the high surface area and short transport distance to the electrode/electrolyte interface in the porous nanostructure. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:8232 / 8239
页数:8
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