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)H 2 O] 2+ ) which deactivates enzymes deteriorates the whole process efficiency. Herein, we report the immobilization of electron mediator ([Cp*Rh(bpy)H 2 O] 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·g COF −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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