己二酸
电催化剂
电解
法拉第效率
电合成
催化作用
电化学
化学
无机化学
单体
阳极
化学工程
材料科学
协同催化
格式化
氢氧化物
氨生产
钝化
电解水
碘化物
析氧
碳纤维
碱性水电解
胺气处理
合成气
二氧化碳电化学还原
作者
Weijin Cao,Changlong Wang,Minwei Song,Hui Li,Min Liu,Yufeng Wu
标识
DOI:10.1038/s41467-026-73913-4
摘要
Adipic acid (AA), a pivotal monomer, is produced via high-temperature nitric acid oxidation of cyclohexanone–cyclohexanol mixture (KA oil); a NO2-intensive process with a large carbon footprint. Electricity-powered electro-oxidative upgrading of KA is appealing, but impractical due to poor O2 utilization, oxygen evolution, and rapid catalyst passivation under potentials, causing an activity–stability–selectivity trade-off. We present an integrated electrocatalytic platform combining an α-FeOOH/NiFe layered double hydroxide (NiFe-LDH) heterojunction catalyst with pulsed electrolysis (PE) for green, efficient AA production. The heterointerface directs electron bridging between α-FeOOH and NiFe-LDH, lowering energy barriers for C–C scission, and creating surface sites for selective AA. PE mode decouples electro-oxidation from catalytic-site regeneration, cyclically refreshing poisoned centers to prevent intermediate accumulation. This strategy achieves 6.73 mmol h−1 cm−2 AA yield with 90.06% Faradaic efficiency over 300 h. Moreover a flow electrolyzer coupling anodic AA synthesis with cathodic CO2-to-formate conversion at 300 mA cm−2 enables scalable, sustainable nylon-monomer production. The electrochemical synthesis of nylon monomer adipic acid is limited by the activity-selectivity-stability tradeoff under constant potential. Here, the authors report a synergistic pulsed electrosynthesis by α-FeOOH/NiFe-LDH heterjunction which is paired with carbon dioxide to formate conversion.
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