格式化
催化作用
电合成
无机化学
电解质
法拉第效率
硫黄
化学
电化学
可逆氢电极
材料科学
氧化还原
化学工程
反应机理
质子化
选择性
碳纤维
氢
多相催化
电催化剂
纳米技术
制氢
反应中间体
协同催化
电解水
兴奋剂
分解水
作者
Mingliang Hu,Yu Zhang,Hao Wei,Ruiying Ding,Jianlong Lin,Sheng Zhang,Zhicheng Zhang
摘要
ABSTRACT Electrocatalytic reduction of CO 2 to formate offers a sustainable route for carbon utilization, converting a greenhouse gas into a valuable chemical feedstock. Although Sn‑based catalysts are among the most promising candidates, their formate selectivity often suffers a marked decline at ampere‑level current densities, and operating efficiently in various electrolytes, especially acidic media, remains a major challenge. In this work, we report a grain boundary‑rich sulfur (S)‐doped SnO 2 catalyst that enables CO 2 ‐to‐formate electrosynthesis at ampere‐level current densities across alkaline, neutral, and acidic electrolytes. The catalyst achieves formate Faradaic efficiencies exceeding 90% at 1 A cm −2 in acidic, neutral, and alkaline electrolytes. In situ spectroscopy and theoretical calculations reveal that S doping reduces the reaction free energy change for the key *OCHO intermediate and promotes its protonation to formate. Meanwhile, S‑doped SnO 2 with abundant grain boundaries facilitates the formation of an enhanced interfacial hydrogen‐bonding network, which promotes efficient proton transfer while suppressing the competing hydrogen evolution reaction (HER). This work provides new insights into the design of high‐performance electrocatalysts through elemental doping and elucidates the governing role of the interfacial microenvironment in reaction activity and selectivity, offering design principles applicable to broader electrochemical syntheses.
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