电合成
法拉第效率
催化作用
电催化剂
吸附
化学工程
电化学
材料科学
金属有机骨架
化学
电子转移
无机化学
纳米技术
产量(工程)
氧化还原
镍
拉曼光谱
吸收(声学)
阴极
原位
过渡金属
组合化学
生产率
二氧化碳电化学还原
过程(计算)
限制电流
限制
作者
Guangye Zhou,Jonathan R. Humphreys,Dongfang Cheng,Shan Jiang,Wei-Ling Huang,Guangming Cheng,Nan Yao,Wei Xiong,Jeffrey T. Miller,Katherine Chou,Johannes B. M. Klok,Hongxu Chen,James Christopher Dykstra,Zhiyong Jason Ren
标识
DOI:10.1038/s41467-026-68358-8
摘要
Hybrid systems that integrate electrochemical CO2 reduction with microbial upgrading offer a viable route to high value organic compounds from CO2 at ambient conditions. However, electrocatalyst deactivation in microbial growth media remains a key barrier, limiting efficiency and increasing cost. Here we show that a bioadaptive single-atom nickel catalyst (Ni SAC), coupled with genetically engineered Clostridium ljungdahlii, enables robust electrosynthesis of isopropanol (IPA) from CO2 via a CO-mediated pathway. Instead of relying on H2 as an electron carrier, the system applies high-rate CO formation in complex growth media, maintaining a tunable CO Faradaic efficiency up to 92%, which is 9.4 to 52.7 times greater than conventional Ag catalysts. This performance supports stable IPA production at current density of 10.8 A/m2 and production rate of 161.3 mg/L/day. In situ Raman and X-ray absorption spectroscopy, together with theoretical calculations, indicate that the Ni SAC can resist competing organic adsorption and retain its coordination structure during CO2 reduction in bioelectrolytes, providing a mechanistic basis for the catalyst stability and integrated process performance.
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