过电位
化学
格式化
电化学
选择性
法拉第效率
极限抗拉强度
电催化剂
无机化学
化学工程
催化作用
物理化学
电极
有机化学
冶金
工程类
材料科学
作者
Jinsol Bok,Si Young Lee,Byoung‐Hoon Lee,Cheonghee Kim,Dang Le Tri Nguyen,Ji Won Kim,Euiyeon Jung,Chan Woo Lee,Yoon Seok Jung,Hyeon Seok Lee,Jiheon Kim,Kangjae Lee,Wonjae Ko,Young Seong Kim,Sung‐Pyo Cho,Jong Suk Yoo,Taeghwan Hyeon,Yun Jeong Hwang
摘要
Pd is one of the most effective catalysts for the electrochemical reduction of CO 2 to formate, a valuable liquid product, at low overpotential. However, the intrinsically high CO affinity of Pd makes the surface vulnerable to CO poisoning, resulting in rapid catalyst deactivation during CO 2 electroreduction. Herein, we utilize the interaction between metals and metal–organic frameworks to synthesize atomically dispersed Au on tensile-strained Pd nanoparticles showing significantly improved formate production activity, selectivity, and stability with high CO tolerance. We found that the tensile strain stabilizes all reaction intermediates on the Pd surface, whereas the atomically dispersed Au selectively destabilizes CO* without affecting other adsorbates. As a result, the conventional COOH* versus CO* scaling relation is broken, and our catalyst exhibits 26- and 31-fold enhancement in partial current density and mass activity toward electrocatalytic formate production with over 99% faradaic efficiency, compared to Pd/C at −0.25 V versus RHE.
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