过电位
纳米材料基催化剂
电化学
法拉第效率
材料科学
氧化还原
催化作用
化学工程
纳米结构
粒子(生态学)
氢
胶体
电极
纳米颗粒
纳米技术
无机化学
化学
物理化学
冶金
有机化学
海洋学
地质学
工程类
作者
Dong‐Rui Yang,Ling Liu,Qian Zhang,Yi Shi,Yue Zhou,Chungen Liu,Feng‐Bin Wang,Xing‐Hua Xia
标识
DOI:10.1016/j.scib.2020.01.015
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI