Catalytic investigation of ceria-zirconia solid solutions for solar hydrogen production

被引:119
|
作者
Le Gal, Alex [1 ]
Abanades, Stephane [1 ]
机构
[1] CNRS, PROMES, Proc Mat & Solar Energy Lab, F-66120 Font Romeu, France
关键词
Thermochemical cycle; Water-splitting; Hydrogen; Doped ceria; Kinetics; HYDROTHERMAL SYNTHESIS; H-2; GENERATION; 2-STEP; REDUCTION; OXIDATION; OXIDES; CYCLES; CU;
D O I
10.1016/j.ijhydene.2011.01.078
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
This study addresses the solar thermochemical production of hydrogen from water-splitting cycles using ceria-zirconia solid solutions prepared via soft chemistry methods. The effect of zirconium doping on the catalytic activity of ceria for hydrogen production was studied using thermogravimetric analysis. The influence of the zirconium content between 10% and 50% on the redox properties of the Ce1-delta Zr delta O2 material was investigated. The higher the amount of zirconium, the higher the reduction yields. The reduction yield at 1400 degrees C in inert atmosphere was 9% for 10% Zr, 16% for 25% Zr, and 28% for 50% Zr. However, increasing the Zr content did not automatically lead to the highest amount of hydrogen produced during cycling. Indeed, the powder with 25% Zr produced 334 and 298 mu mol H-2/g at 1050 degrees C during the first and the second cycle, respectively. In contrast, the powder with 50% Zr yielded 468 and 266 mu mol H-2/g during the two successive cycles. Moderate Zr contents thus favored H-2 production during repeated cycles without any significant reactivity losses. A kinetic study of the reduction and the hydrolysis steps was proposed. The activation energies for the thermal reduction and the hydrolysis of Ce0.75Zr0.25O2 were 221 kJ/mol and 51 kJ/mol, respectively. Finally, the use of a template molecule during synthesis was considered, which improved the reduction yield markedly (up to 52%) but strong sintering phenomena limited the hydrogen production and the material cyclability. Copyright (C) 2011, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:4739 / 4748
页数:10
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