Dynamic Structure of a Working Methanol Steam Reforming Catalyst: In Situ Quick-EXAFS on Pd/ZnO Nanoparticles

被引:103
作者
Foettinger, Karin [1 ,2 ]
van Bokhoven, Jeroen A. [2 ,3 ]
Nachtegaal, Maarten [3 ]
Rupprechter, Guenther [1 ]
机构
[1] Vienna Univ Technol, Inst Mat Chem, A-1060 Vienna, Austria
[2] ETH, Inst Chem & Bioengn, CH-8093 Zurich, Switzerland
[3] Paul Scherrer Inst, CH-5232 Villigen, Switzerland
基金
瑞士国家科学基金会;
关键词
SUPPORTED PALLADIUM CATALYSTS; PD-ZN; PARTIAL OXIDATION; ALLOY CATALYSTS; METAL-CATALYSTS; PD(111); GROWTH; DEHYDROGENATION; HYDROGEN; LAYERS;
D O I
10.1021/jz101751s
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
Combining time-resolved X-ray absorption spectroscopy (XAS) with simultaneous mass spectrometric activity measurements, both performed during catalytic methanol steam reforming, we have studied the dynamic changes of Pd nanoparticles supported on ZnO. The formation of the catalytically active phase PdZn was unambiguously monitored in real time. We thus directly prove for the first time that the PdZn alloy formed in the course of the catalytic reaction is responsible for the excellent selectivity to H-2 and CO2. Alloying started at the nanoparticle surface and proceeded "inwards" toward the particle center. On the basis of extended X-ray absorption fine structure (EXAFS) analysis, the extent of PdZn alloy formation was estimated. Alloying was reversible. In contact with oxygen, PdZn segregated into palladium metal and ZnO. The XAS data were corroborated by Fourier transform infrared (FTIR) spectroscopy. It is demonstrated that the application of operando quick-EXAFS is a powerful tool for studying nanomaterials and their dynamic adaptation to reactive environments.
引用
收藏
页码:428 / 433
页数:6
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