Importance of Au nanostructures in CO2 electrochemical reduction reaction

• Published in: Science bulletin (Beijing) 2020-05, Vol.65 (10), p.796-802
• Main Authors: Yang, Dong-Rui, Liu, Ling, Zhang, Qian, Shi, Yi, Zhou, Yue, Liu, Chungen, Wang, Feng-Bin, Xia, Xing-Hua
• Format: Article
• Language: English
• Subjects: CO2 reduction reaction (CO2RR); Electrocatalysis; Gold nanostructures; Morphological effect; Size effect
• ISSN: 2095-9273
• DOI: 10.1016/j.scib.2020.01.015

Based on experimental and theoretical results, we find that the high-index (2 2 1) facets and the low-coordinated edge sites of gold nanoparticles are more favorable for the reduction of CO2 to CO by comparing the performance of Au colloids with Au trisoctahedron of different sizes. [Display omitted] Electrochemical conversion of CO2 into fuels is a promising means to solve greenhouse effect and recycle chemical energy. However, the CO2 reduction reaction (CO2RR) is limited by the high overpotential, slow kinetics and the accompanied side reaction of hydrogen evolution reaction. Au nanocatalysts exhibit high activity and selectivity toward the reduction of CO2 into CO. Here, we explore the Faradaic efficiency (FE) of CO2RR catalyzed by 50 nm gold colloid and trisoctahedron. It is found that the maximum FE for CO formation on Au trisoctahedron reaches 88.80% at −0.6 V, which is 1.5 times as high as that on Au colloids (59.04% at −0.7 V). The particle-size effect of Au trisoctahedron has also been investigated, showing that the FE for CO decreases almost linearly to 62.13% when the particle diameter increases to 100 nm. The X-ray diffraction characterizations together with the computational hydrogen electrode (CHE) analyses reveal that the (2 2 1) facets on Au trisoctahedron are more feasible than the (1 1 1) facets on Au colloids in stabilizing the critical intermediate COOH*, which are responsible for the higher FE and lower overpotential observed on Au trisoctahedron.