Fang Qiang, Jia Yunzhen, Lang Xuelei, Li Geng, Zhao Tao, Zhong Dazhong, Li Jinping, Zhao Qiang
College of Chemistry and Chemical Engineering, Shanxi Key Laboratory of Gas Energy Efficient and Clean Utilization, Taiyuan University of Technology, Taiyuan, Shanxi, 030024, P. R. China.
Adv Sci (Weinh). 2025 Jul 26:e10161. doi: 10.1002/advs.202510161.
Acidic electrocatalytic CO reduction (CORR) faces slow C-C coupling kinetics and dominant hydrogen evolution, resulting in low C yields and selectivity. Here, the porous copper nanosheets (pCu NS) are reported with abundant Cu(100) and defect sites for efficient acidic CORR to C products. In a membrane electrode assembly (MEA), the pCu NS electrodes achieved a remarkable 75.01% C production Faradaic efficiency (FE) at a current density of 300 mA cm with a full-cell voltage of 3.8 V. A CO single-pass conversion efficiency of up to 74.38% is achieved. In situ Raman spectra and density functional theory calculations revealed that pCu NS not only gives abundant nanopores and defect sites but also preferentially exposes Cu(100) facets, synergistically creating local alkaline microenvironment, maximizing the *CO intermediate coverage, and promoting *CO hydrogenation for C production. This work offers a crucial insight for designing an efficient catalyst for efficient acidic CO-to-C conversion.
酸性电催化CO还原(CORR)面临着缓慢的C-C偶联动力学和占主导地位的析氢反应,导致C的产率和选择性较低。在此,报道了具有丰富Cu(100)和缺陷位点的多孔铜纳米片(pCu NS),用于将酸性CORR高效转化为C产物。在膜电极组件(MEA)中,pCu NS电极在300 mA cm的电流密度和3.8 V的全电池电压下,实现了高达75.01%的C生成法拉第效率(FE)。CO单程转化效率高达74.38%。原位拉曼光谱和密度泛函理论计算表明,pCu NS不仅具有丰富的纳米孔和缺陷位点,还优先暴露Cu(100)晶面,协同创造局部碱性微环境,使CO中间体覆盖率最大化,并促进CO加氢生成C。这项工作为设计一种高效的酸性CO到C转化催化剂提供了关键见解。