Huang Minghong, Zhou Sheng-Hua, Yang Cheng-Jie, Dong Chung-Li, He Yingchun, Wei Wenbo, Li Xiaofang, Zhu Qi-Long, Huang Zhenguo
School of Civil and Environmental Engineering, University of Technology Sydney, Ultimo, New South Wales 2007, Australia.
State Key Laboratory of Structural Chemistry, Fujian Institute of Research on the Structure of Matter, Chinese Academy of Sciences (CAS), Fuzhou 350002, China.
ACS Nano. 2024 Dec 3;18(48):33210-33219. doi: 10.1021/acsnano.4c12576. Epub 2024 Nov 1.
Single-atom catalysts are promising for electrocatalytic CO conversion but face challenges in controllable syntheses. Herein, a facile selenic acid etching-assisted strategy has been developed to fabricate a hybrid metal-semimetal dual single-atom catalyst for electrocatalytic CO reduction. This strategy enables the simultaneous generation of monodisperse active sites and hierarchical morphologies with hollow nanostructures. The as-obtained catalyst with Fe-Se dual single-atom sites supported by porous nitrogen-doped carbon (FeSe-NC) shows exceptional catalytic activity and CO selectivity, delivering a Faradaic efficiency (FE) of >97% with industrially comparable , superior to the Fe single-atom catalyst. Moreover, the FeSe-NC-based rechargeable Zn-CO battery delivers a high power density (2.01 mW cm) and outstanding FE (>90%), as well as excellent cycling stability. Experimental results together with theoretical calculations reveal that the etching-induced defects and the Se-modulated Fe centers with asymmetrical polarized charge distributions synergistically facilitate the key intermediate *CO desorption and thus accelerate the CO-to-CO conversion.
单原子催化剂在电催化CO转化方面具有潜力,但在可控合成方面面临挑战。在此,开发了一种简便的硒酸蚀刻辅助策略,用于制备用于电催化CO还原的混合金属-半金属双单原子催化剂。该策略能够同时生成具有中空纳米结构的单分散活性位点和分级形态。所制备的由多孔氮掺杂碳负载的具有Fe-Se双单原子位点的催化剂(FeSe-NC)表现出优异的催化活性和CO选择性,在工业可比条件下法拉第效率(FE)>97%,优于Fe单原子催化剂。此外,基于FeSe-NC的可充电Zn-CO电池具有高功率密度(2.01 mW cm)、出色的FE(>90%)以及优异的循环稳定性。实验结果与理论计算表明,蚀刻诱导的缺陷和具有不对称极化电荷分布的Se调制Fe中心协同促进关键中间体*CO的脱附,从而加速CO到CO的转化。