期刊
NANO RESEARCH
卷 10, 期 6, 页码 2181-2191出版社
TSINGHUA UNIV PRESS
DOI: 10.1007/s12274-017-1514-6
关键词
carbon-dioxide electroreduction; Pd nanoparticles; active phase; selectivity fluctuation
类别
资金
- National Basic Research Program of China [2016YFB0600901, 2013CB733501]
- National Natural Science Foundation of China [21136001, 21573222, 91545202, 91334103]
- Chinese Academy of Sciences [XDB17020200]
- CAS Youth Innovation Promotion Association
Active-phase engineering is regularly utilized to tune the selectivity of metal nanoparticles (NPs) in heterogeneous catalysis. However, the lack of understanding of the active phase in electrocatalysis has hampered the development of efficient catalysts for CO2 electroreduction. Herein, we report the systematic engineering of active phases of Pd NPs, which are exploited to select reaction pathways for CO2 electroreduction. In situ X-ray absorption spectroscopy, in situ attenuated total reflection-infrared spectroscopy, and density functional theory calculations suggest that the formation of a hydrogen-adsorbed Pd surface on a mixture of the a-and a-phases of a palladium-hydride core (alpha+beta PdHx@PdHx) above -0.2 V (vs. a reversible hydrogen electrode) facilitates formate production via the HCOO* intermediate, whereas the formation of a metallic Pd surface on the a-phase Pd hydride core (beta PdHx@Pd) below -0.5 V promotes CO production via the COOH* intermediate. The main product, which is either formate or CO, can be selectively produced with high Faradaic efficiencies (> 90%) and mass activities in the potential window of 0.05 to -0.9 V with scalable application demonstration.
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