Liu Li-Xia, Li Xiang, Cai Yanming, Du Huitong, Liu Fuqiang, Zhang Jian-Rong, Fu Jiaju, Zhu Wenlei
State Key Laboratory of Pollution Control and Resource Reuse, State Key Laboratory of Analytical Chemistry for Life Science, the Frontiers Science Center for Critical Earth Material Cycling, School of the Environment, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, People's Republic of China.
Nanoscale. 2022 Sep 29;14(37):13679-13688. doi: 10.1039/d2nr03433f.
Electrochemical reduction of CO into liquid fuels is a promising approach to achieving a carbon-neutral energy cycle but remains a great challenge due to the lack of efficient catalysts. Here, the hierarchical architectures assembled by ultrathin and porous S-modified Cu nanoflakes (Cu-S NFs) are designed and constructed as an efficient electrocatalyst for CO conversion to formate with high partial current density. Specifically, when integrated into a gas diffusion electrode in a flow cell, Cu-S NFs are capable of delivering the ultrahigh formate current density up to 404.1 mA cm with a selectivity of 89.8%. Electrochemical tests and theoretical calculations indicate that the superior performance of the designed catalysts may be attributed to the unique structure, which can provide abundant active sites, fast charge transfer, and highly active edge sites.
将CO电化学还原为液体燃料是实现碳中性能量循环的一种有前景的方法,但由于缺乏高效催化剂,仍然是一个巨大的挑战。在此,由超薄多孔S修饰的Cu纳米片(Cu-S NFs)组装而成的分级结构被设计并构建为一种高效的电催化剂,用于将CO转化为甲酸盐,具有高的分电流密度。具体而言,当集成到流动池中气体扩散电极时,Cu-S NFs能够提供高达404.1 mA cm的超高甲酸盐电流密度,选择性为89.8%。电化学测试和理论计算表明,所设计催化剂的优异性能可能归因于其独特的结构,该结构可提供丰富的活性位点、快速的电荷转移和高活性的边缘位点。