法拉第效率
电化学
催化作用
阴极保护
电流密度
材料科学
电极
还原(数学)
化学工程
聚合物
氧化还原
二氧化碳电化学还原
纳米技术
化学
一氧化碳
物理化学
有机化学
物理
复合材料
冶金
几何学
数学
量子力学
工程类
作者
Junmei Chen,Haoran Qiu,Yilin Zhao,Haozhou Yang,Lei Fan,Zhihe Liu,Shibo Xi,Guangtai Zheng,Jiayi Chen,Lei Chen,Ya Liu,Liejin Guo,Lei Wang
标识
DOI:10.1038/s41467-024-50269-1
摘要
Abstract Controlling the concentrations of H 2 O and CO 2 at the reaction interface is crucial for achieving efficient electrochemical CO 2 reduction. However, precise control of these variables during catalysis remains challenging, and the underlying mechanisms are not fully understood. Herein, guided by a multi-physics model, we demonstrate that tuning the local H 2 O/CO 2 concentrations is achievable by thin polymer coatings on the catalyst surface. Beyond the often-explored hydrophobicity, polymer properties of gas permeability and water-uptake ability are even more critical for this purpose. With these insights, we achieve CO 2 reduction on copper with Faradaic efficiency exceeding 87% towards multi-carbon products at a high current density of −2 A cm −2 . Encouraging cathodic energy efficiency (>50%) is also observed at this high current density due to the substantially reduced cathodic potential. Additionally, we demonstrate stable CO 2 reduction for over 150 h at practically relevant current densities owning to the robust reaction interface. Moreover, this strategy has been extended to membrane electrode assemblies and other catalysts for CO 2 reduction. Our findings underscore the significance of fine-tuning the local H 2 O/CO 2 balance for future CO 2 reduction applications.
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