Chen Jingyi, Fan Lei, Zhao Yilin, Yang Haozhou, Wang Di, Hu Bihao, Xi Shibo, Wang Lei
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, 117585, Singapore.
Institute of Sustainability for Chemicals, Energy and Environment, A*STAR, 1 Pesek Road, Jurong Island, 627833, Singapore.
Chem Commun (Camb). 2024 Mar 14;60(23):3178-3181. doi: 10.1039/d3cc05972c.
Electrochemical CO reduction (COR) to valuable products provides a promising strategy to enable CO utilization sustainably. Here, we report the strategy of using Cu-DAT (3,5-diamino-1,2,4-triazole) as a catalyst precursor for efficient CO reduction, demonstrating over 80% selectivity towards multicarbon products at 400 mA cm, with intrinsic activity over 19 times higher than that of Cu nanoparticles. The catalysts active phase is determined to be metallic copper wrapped with the DAT ligand. We attribute this enhanced COR performance to the accelerated steps of *CO adsorption and C-C coupling induced by the closely cooperated DAT ligand.
将电化学CO还原(COR)为有价值的产物提供了一种可持续利用CO的有前景的策略。在此,我们报道了使用Cu-DAT(3,5-二氨基-1,2,4-三唑)作为高效CO还原催化剂前体的策略,在400 mA cm下对多碳产物的选择性超过80%,其本征活性比Cu纳米颗粒高19倍以上。确定催化剂的活性相为被DAT配体包裹的金属铜。我们将这种增强的COR性能归因于紧密配合的DAT配体诱导的*CO吸附和C-C偶联步骤的加速。