铜
电催化剂
催化作用
选择性
价(化学)
化学
无机化学
氧化物
材料科学
电解
金属
氮化硼
电子结构
电化学
物理化学
纳米技术
电极
计算化学
冶金
有机化学
生物化学
电解质
作者
Yixiang Zhou,Yebo Yao,Rui Zhao,Xiaoxuan Wang,Zhenzhen Fu,Dewei Wang,Huaizhi Wang,Liang Zhao,Wei Ni,Zhiyu Yang,Yi‐Ming Yan
标识
DOI:10.1002/anie.202205832
摘要
Copper oxide-based materials effectively electrocatalyze carbon dioxide reduction (CO2 RR). To comprehend their role and achieve high CO2 RR activity, Cu+ in copper oxides must be stabilized. As an electrocatalyst, Cu2 O nanoparticles were decorated with hexagonal boron nitride (h-BN) nanosheets to stabilize Cu+ . The C2 H4 /CO ratio increased 1.62-fold in the CO2 RR with Cu2 O-BN compared to that with Cu2 O. Experimental and theoretical studies confirmed strong electronic interactions between the two components in Cu2 O-BN, which strengthens the Cu-O bonds. Electrophilic h-BN receives partial electron density from Cu2 O, protecting the Cu-O bonds from electron attack during the CO2 RR and stabilizing the Cu+ species during long-term electrolysis. The well-retained Cu+ species enhanced the C2 product selectivity and improved the stability of Cu2 O-BN. This work offers new insight into the metal-valence-state-dependent selectivity of catalysts, enabling the design of advanced catalysts.
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