Selective CO 2 electrolysis to CO using isolated antimony alloyed copper.
Jiawei LiHongliang ZengXue DongYimin DingSunpei HuRunhao ZhangYizhou DaiPei-Xin CuiZhou XiaoDonghao ZhaoLiujiang ZhouTingting ZhengJianping XiaoJie ZengChuan XiaPublished in: Nature communications (2023)
Renewable electricity-powered CO evolution from CO 2 emissions is a promising first step in the sustainable production of commodity chemicals, but performing electrochemical CO 2 reduction economically at scale is challenging since only noble metals, for example, gold and silver, have shown high performance for CO 2 -to-CO. Cu is a potential catalyst to achieve CO 2 reduction to CO at the industrial scale, but the C-C coupling process on Cu significantly depletes CO* intermediates, thus limiting the CO evolution rate and producing many hydrocarbon and oxygenate mixtures. Herein, we tune the CO selectivity of Cu by alloying a second metal Sb into Cu, and report an antimony-copper single-atom alloy catalyst (Sb 1 Cu) of isolated Sb-Cu interfaces that catalyzes the efficient conversion of CO 2 -to-CO with a Faradaic efficiency over 95%. The partial current density reaches 452 mA cm -2 with approximately 91% CO Faradaic efficiency, and negligible C 2+ products are observed. In situ spectroscopic measurements and theoretical simulations reason that the atomic Sb-Cu interface in Cu promotes CO 2 adsorption/activation and weakens the binding strength of CO*, which ends up with enhanced CO selectivity and production rates.