光催化
醇脱氢酶
光化学
电子转移
化学
人工光合作用
共价键
NAD+激酶
电子供体
丁醇
催化作用
调解人
酶
化学工程
材料科学
组合化学
有机化学
乙醇
生物
内分泌学
工程类
作者
Jiali Liu,Xiaomin Ren,Chunzhi Li,Maodi Wang,He Li,Qihua Yang
标识
DOI:10.1016/j.apcatb.2022.121314
摘要
Photocatalytic regeneration of the high-cost co-factor NADH is a promising method to couple photo-enzyme catalysis, however, the usage of homogeneous electron mediator ([Cp*Rh(bpy)H2O]2+) which deactivates enzymes deteriorates the whole process efficiency. Herein, we report the immobilization of electron mediator ([Cp*Rh(bpy)H2O]2+) on covalent organic frameworks (COFs) by the sequential assembly method. The resultant bi-functional photocatalyst with controlled cascade electron transfer afforded NADH production rate of 9.8 mmol·gCOF−1·h−1, much higher than previously reported ones with integrated electron mediator. The photo-enzyme coupling system with the photocatalyst and alcohol dehydrogenase could continuously produce butanol for at least 180 min under visible light irradiation, implying the potential application of bi-functional photocatalyst in artificial photosynthesis.
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