Performance evaluation of a photoelectrochemical hydrogen production reactor under concentrated and non-concentrated sunlight conditions

被引:14
作者
Bicer, Yusuf [1 ]
Dincer, Ibrahim [1 ]
机构
[1] Univ Ontario Inst Technol, Clean Energy Res Lab, Fac Engn & Appl Sci, 2000 Simcoe St North, Oshawa, ON L1H 7K4, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Hydrogen production; Solar energy; Photoelectrochemical process; Renewable energy; Performance assessment; PRODUCTION SYSTEM; SOLAR; WATER; PHOTOANODE; EFFICIENCY; CONVERSION; CELLS; LIGHT; OXIDE; DEVICE;
D O I
10.1016/j.ijhydene.2017.08.122
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
In this paper, we present the experimental performance evaluations of a newly developed photoelectrochemical (PEC) reactor for the production of hydrogen under no-light and concentrated solar radiation conditions. With a newly developed experimental setup, the solar light is concentrated about ten times, and the spectrum is divided using cold mirrors for better sunlight utilization. The photoelectrochemical reactor is examined at different applied potentials and the hydrogen production quantities are measured. Copper oxide, which is used as a light-sensitive material, is electrochemically coated on the cathode metal plate to increase the rate of hydrogen evolution under illumination. The present experiments are conducted to investigate the variation of reactor performance with intensified light conditions and the obtained results are compared with the dark conditions. The results of this study reveal that the hydrogen evolution rate was 41.34 mg/h for concentrated light measurement and 34.73 mg/h for no-light measurements at 2.5 V applied potential. The corresponding photocurrent generated under concentrated light at 2.5 V is found to be 0.63 mA/cm(2). Under the concentrated sunlight, the hydrogen production rates increase considerably which is led by the positive effect of the photocurrent contribution. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:10258 / 10267
页数:10
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