歧化
甲酸
化学
电解
甲醛
阳极
电化学
无机化学
甲醇
双功能
阴极
双金属片
法拉第效率
脱质子化
甲醛脱氢酶
电解水
制氢
氢
格式化
化学工程
光化学
计时安培法
反应机理
催化作用
铜
本体电解
作者
Yun Song,Zhaohua Zhu,Tridip Das,Aarya D. Riasati,Jianjun Su,Weihua Guo,Yong Liu,Geng Li,Yinger Xin,Qiang Zhang,Mingming He,R. Wang,Rui Xue,Shenlong Zhao,Chuan Xia,Ben Zhong Tang,Marc Robert,Xin Eric Wang,William A. Goddard,R. Ye
标识
DOI:10.1038/s41467-026-70739-y
摘要
Abstract Formaldehyde (FA) electrolysis is attractive for paired production of value‑added chemicals. However, conventional electrolysis adopts alkaline electrolytes, which triggers FA self-disproportionation and severe feed loss. Here we introduce a sustainable and selective strategy for valorizing FA through electrochemically mediated disproportionation in acidic electrolytes. By leveraging a dual-electrode system consisting of a hydrophobic copper tetraminophthalocyanine layer (CuTAPc-layer) cathode and a Pt 2 Ru bimetallic anode, we efficiently convert FA into methanol and formic acid at high Faradaic efficiencies of 93.2% and 91.3%, respectively. Compared with alkaline FA oxidation, which can lose up to 76% FA and complicate downstream separation, the acidic system suppresses side reactions to ensure high product purity. Mechanism studies reveal that the hydrophobic microenvironment of CuTAPc-layer suppresses hydrogen evolution, while the stronger oxophilicity of Pt 2 Ru enhances FA activation and lowers the key deprotonation barrier for FA oxidation. The integrated device demonstrates application potential in polyoxymethylene upgrading, delivering 374.2 mA at 4 V with ~90% single-pass conversion, establishing a scalable and eco-friendly electrochemical pathway for chemical upcycling.
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