Cheng Yuqing, Shi Jiafu, Wu Yizhou, Wang Xueying, Sun Yiying, Cai Ziyi, Chen Yu, Jiang Zhongyi
Key Laboratory for Green Chemical Technology of Ministry of Education, School of Chemical Engineering and Technology, Tianjin University, 92 Weijin Road, Nankai District, Tianjin 300072, China.
Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), 92 Weijin Road, Nankai District, Tianjin 300072, China.
Research (Wash D C). 2021 Feb 18;2021:8175709. doi: 10.34133/2021/8175709. eCollection 2021.
Solar-driven photocatalytic regeneration of cofactors, including reduced nicotinamide adenine dinucleotide (NADH), reduced nicotinamide adenine dinucleotide phosphate (NADPH), and reduced flavin adenine dinucleotide (FADH), could ensure the sustainable energy supply of enzymatic reactions catalyzed by oxidoreductases for the efficient synthesis of chemicals. However, the elevation of cofactor regeneration efficiency is severely hindered by the inefficient utilization of electrons transferred on the surface of photocatalysts. Inspired by the phenomenon of ferredoxin-NADP reductase (FNR) anchoring on thylakoid membrane, herein, a homogeneous catalyst of rhodium (Rh) complex, [Cp∗Rh(bpy)HO], was anchored on polymeric carbon nitride (PCN) mediated by a tannic acid/polyethyleneimine (TA/PEI) adhesive layer, acquiring PCN@TA/PEI-Rh core@shell photocatalyst. Illuminated by visible light, electrons were excited from the PCN core, then transferred through the TA/PEI shell, and finally captured by the surface-anchored Rh for instant utilization during the regeneration of NADH. The TA/PEI-Rh shell could facilitate the electron transfer from the PCN core and, more importantly, achieved ~1.3-fold elevation of electron utilization efficiency compared with PCN. Accordingly, the PCN@TA/PEI-Rh afforded the NADH regeneration efficiency of 37.8% after 20 min reaction under LED light (405 nm) illumination, over 1.5 times higher than PCN with free Rh. Coupling of the NADH regeneration system with formate dehydrogenase achieved continuous production of formate from carbon dioxide (CO). Our study may provide a generic and effective strategy to elevate the catalytic efficiency of a photocatalyst through intensifying the electron utilization.
太阳能驱动的辅因子光催化再生,包括还原型烟酰胺腺嘌呤二核苷酸(NADH)、还原型烟酰胺腺嘌呤二核苷酸磷酸(NADPH)和还原型黄素腺嘌呤二核苷酸(FADH),可以确保氧化还原酶催化的酶促反应的可持续能量供应,以实现化学品的高效合成。然而,光催化剂表面转移电子的低效利用严重阻碍了辅因子再生效率的提高。受铁氧还蛋白-NADP还原酶(FNR)锚定在类囊体膜上这一现象的启发,在此,一种铑(Rh)配合物的均相催化剂[Cp∗Rh(bpy)HO]通过单宁酸/聚乙烯亚胺(TA/PEI)粘合剂层锚定在聚合氮化碳(PCN)上,获得了PCN@TA/PEI-Rh核壳光催化剂。在可见光照射下,电子从PCN核被激发,然后通过TA/PEI壳层转移,最终被表面锚定的Rh捕获,以便在NADH再生过程中即时利用。TA/PEI-Rh壳层可以促进电子从PCN核的转移,更重要的是,与PCN相比,电子利用效率提高了约1.3倍。因此,在LED灯(405nm)照射下反应20分钟后,PCN@TA/PEI-Rh的NADH再生效率达到37.8%,比含有游离Rh的PCN高出1.5倍以上。NADH再生系统与甲酸脱氢酶的耦合实现了从二氧化碳(CO)连续生产甲酸。我们的研究可能提供一种通用且有效的策略,通过强化电子利用来提高光催化剂的催化效率。