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Published on: August 18, 2020
Enhancing C2 Selectivity in Electrocatalytic CO2 Reduction Via Synergy of Plasmonic Hot Electrons and Photothermal
Linlin Chen1,2, Cenfeng Fu3, Canyu Hu1
1USTC Center for Micro- and Nanoscale Research and Fabrication, Hefei National Research Center for Physical Sciences at the Microscale, Key Laboratory of Precision and Intelligent Chemistry, School of Chemistry and Materials Science, National Synchrotron Radiation Laboratory, School of Nuclear Science and Technology, The Experimental Center of Engineering and Material Sciences, University of Science and Technology of China, Hefei, 230026, China.
Abstract:
Surface plasmon-enhanced electrocatalytic CO2 reduction offers an attractive dimension beyond conventional electrocatalytic methods by optimizing photon utilization to simplify electrocatalytic reactor designs and enhance reaction activity/selectivity. However, the synergistic regulation mechanism of the complex multiple plasmonic effects on the CO2 reduction reaction, particularly under electrochemical bias, remains to be thoroughly investigated. This study, based on copper plasmonic electrodes, reveals the key role of localized surface plasmon resonance (LSPR) in enhancing CO2 conversion and facilitating the transition of the key intermediate *CO from bridge to atop adsorption configuration. Through a combination of experiments and density functional theory calculations, we show that the synergy of plasmonic hot electrons and photothermal effect effectively reduces the C─C coupling energy barrier. Systematic measurements clarify the correlation between the plasmonic excitation of the electrode and the enhanced selectivity of C2 products. Under optimized conditions, synergetic plasmonic effects significantly promote the CO2 conversion and enhance the Faradaic efficiency (FE) of C2 products, with a maximum increase from 57% to 87%. This work not only provides a new perspective for understanding the complex synergistic mechanisms of plasmonic effects, but also opens a new avenue for achieving selective electrocatalytic CO2 conversion.
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