格式化
电解
甲酸脱氢酶
化学
阳极
流动化学
法拉第效率
水溶液
胺化
本体电解
电化学
化学工程
阴极
无机化学
电解槽
烯烃
材料科学
产量(工程)
碳纤维
微生物电解槽
间歇式反应器
水解
有机化学
歧化过程
作者
Beverly Qian Ling Low,Santiago Rodríguez‐Jiménez,Andrea Rogolino,Samuel J. Cobb,Han Chen,Guilherme Martins,Inês A. C. Pereira,Erwin Reisner
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-09-24
卷期号:64 (46): e202515810-e202515810
被引量:1
标识
DOI:10.1002/anie.202515810
摘要
Abstract Paired electrolysis enables the simultaneous coupling of CO 2 reduction with anodic waste upcycling to form valuable products. However, achieving selective, efficient, and stable product formation and coupling to downstream valorization remains a challenge. In this study, W‐containing formate dehydrogenase from Nitratidesulfovibrio vulgaris Hildenborough is immobilized onto a cathode made from carbon felt coated with porous TiO 2 and paired with a commercial Ni foam anode to assemble a semiartificial flow electrolyzer for the simultaneous conversion of CO 2 and waste (plastic and biomass) to the single product formate. The enzymatic flow electrolyzer achieved an initial cell faradaic efficiency toward formate of almost 200%, a maximum CO 2 conversion yield of 18% and can operate at a low full‐cell voltage of −1.5 V for 122 h, which allows for bias‐free operation with a silicon photovoltaic cell. The aqueous formate produced in the enzymatic electrolyzer was subsequently utilized downstream as a C 1 building block in the photocatalytic hydrocarboxylation of alkenes, providing a path for the domino valorization of CO 2 and waste toward bulk and fine chemical synthesis.
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