Highly Active Small Palladium Clusters Supported on Ferric Hydroxide for Carbon Monoxide-Tolerant Hydrogen Oxidation

被引:32
作者
Qiao, Botao [1 ,2 ]
Lin, Jian [1 ]
Li, Lin [1 ]
Wang, Aiqin [1 ]
Liu, Jingyue [1 ,2 ]
Zhang, Tao [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[2] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA
关键词
nanoparticles; hydrogen; CO-tolerant; oxidation; palladium; ALCOHOL FUEL-CELLS; CO TOLERANCE; PREFERENTIAL OXIDATION; ANODE ELECTROCATALYSTS; PD; ADSORPTION; NANOPARTICLES; CATALYSTS; H-2; SPECTROSCOPY;
D O I
10.1002/cctc.201300947
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Proton-exchange membrane fuel cells have been regarded as one of the most promising candidates for efficient energy conversion. However, the CO poisoning of the anode and the scarcity of the Pt metal are two major barriers to their commercialization. Development of CO-tolerant Pd electrocatalysts is considered to be a plausible approach to overcome these problems. Herein we report that for the CO-tolerant H-2 oxidation, sub-2-nm size Pd clusters as well as single atoms, supported on FeOx nanocrystallites, are highly active and durable at a wide temperature range of 20-120 degrees C. Experimental data demonstrated that CO preferentially adsorbs on these small Pd clusters or single atoms linearly, resulting in weakened CO binding and enhanced H-2 competitive adsorption. Therefore, FeOx-supported small Pd clusters or single atoms provide a higher CO-tolerant performance. This finding may offer a new strategy to develop CO-tolerant Pd-based electrodes.
引用
收藏
页码:547 / 554
页数:8
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