Yumin Da, Jie Chen, Lei Fan, Rui Jiang, Yukun Xiao, Meng Wang, Ganwen Chen, Zhangliu Tian, Hanqian Zhang, Hongqiang Jin, Xiang Chen, Chenrui Ji, Shibo Xi, Prof. Yanwei Lum, Prof. Lei Wang, Tong Zhu, Prof. Jia Zhang, Prof. Wei Chen
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引用次数: 0
摘要
乙醇具有较高的市场价值和稳定的全球需求,是一种有吸引力的电催化二氧化碳还原产品。然而,在工业电流密度下实现高乙醇选择性和能源效率仍然具有挑战性。在这项研究中,我们采用混合阴离子调制策略来提高二氧化碳到乙醇转化的选择性和能源效率。在由2 M KOH和1 M KCl组成的混合电解质中,在700 mA cm−2的温度下,Cu2(OH)3F预催化剂对乙醇和C2+的法拉第效率分别为50%和93%。综合电化学测试、现场表征和理论分析表明,氯化物和氢氧化物增加了*CO覆盖率,实现了高效的C─C耦合。此外,氢氧化物通过与催化剂表面吸附的氢氧化物形成氢键来稳定*CHCOH中间体,而Cl则通过促进水向乙醇途径解离来协同增强其反应活性。
Selective and Energy Efficient Electrocatalytic CO2-to-Ethanol Conversion through Anion Modulation
Ethanol, with its high market value and stable global demand, stands out as an attractive product of electrocatalytic CO2 reduction. However, achieving high ethanol selectivity and energy efficiency at industrial current densities remains challenging. In this study, we employed a blended anion modulation strategy to enhance the selectivity and energy efficiency of CO2-to-ethanol conversion. The Cu2(OH)3F pre-catalyst achieved Faradaic efficiencies of 50% and 93% for ethanol and C2+, respectively, at 700 mA cm−2 in a blended electrolyte consisting of 2 M KOH and 1 M KCl. Comprehensive electrochemical tests, combined with in situ characterizations and theoretical analysis, revealed that chloride and hydroxide increased *CO coverage for efficient C─C coupling. Moreover, hydroxide stabilizes the *CHCOH intermediate through hydrogen bonding with the adsorbed hydroxide on the catalyst surface, while Cl synergistically enhances its reactivity by promoting water dissociation toward the ethanol pathway.