Experimental investigation of a solar tower based photocatalytic hydrogen production system

被引:13
作者
Shamim, R. O. [1 ]
Dincer, I. [1 ]
Naterer, G. F. [2 ]
Zamfirescu, C. [1 ]
机构
[1] Univ Ontario Inst Technol, Fac Engn & Appl Sci, Oshawa, ON L1H 7K4, Canada
[2] Mem Univ Newfoundland, Fac Engn & Appl Sci, St John, NF A1C 5S7, Canada
关键词
Solar energy; Hydrogen production; Photocatalysis; Efficiency; WATER-SPLITTING REACTOR; QUANTUM EFFICIENCY; SOLID-SOLUTION; ENERGY; CONVERSION;
D O I
10.1016/j.ijhydene.2014.01.135
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, production of hydrogen from concentrated solar radiation is examined by a laboratory scale solar tower system that is capable of handling continuous flow photocatalysis. The system is built and studied under a solar simulator with an aiming area of 20 x 20 cm(2). The fraction of solar spectrum useful for water splitting depends on the energy band gap of the selected photocatalyst. Two types of nano-particulate photocatalysts are used in this work: ZnS (3.6 eV) and CdS (2.4 eV). The effect of light concentration on photocatalysis performance is studied using Alfa Aesar 99.99% pure grade, 325 mesh ZnS nano-particles. An improved quantum efficiency of 73% is obtained as compared to 45% with the same sample under non-concentrated light in a previous study. Only 1.1% of the energy of the solar radiation spectrum can be used by ZnS catalyst. A mixture of CdS and ZnS nano-particulate photocatalysts (both Alfa Aesar 99.99% pure grade, 325 mesh) is used to conduct a parametric study for a wider spectrum capture corresponding to 18% of the incident energy. Hydrogen production increases from 0.1 mmol/h to 0.21 mmol/h when the operating conditions are varied from 25 degrees C and 101 kPa to 40 degrees C and 21 kPa absolute pressures. Furthermore, the implementation of a continuous flow process results in an improvement in the energy efficiency by a factor of 5.5 over the batch process. Copyright (C) 2014, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:5546 / 5556
页数:11
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