制氢
材料科学
氢
电子转移
光催化
光敏剂
化学工程
光化学
纳米技术
催化作用
化学
有机化学
工程类
作者
Xingxing Lv,Danqing Liu,Rui Chen,Haoxin Liu,Ling Weng,Liangcan He,Shaoqin Liu
标识
DOI:10.1021/acsami.4c02788
摘要
Photosynthetic inorganic biohybrid systems (PBSs) combining an inorganic photosensitizer with intact living cells provide an innovative view for solar hydrogen production. However, typical whole-cell biohybrid systems often suffer from sluggish electron transfer kinetics during transmembrane diffusion, which severely limits the efficiency of solar hydrogen production. Here, a unique biohybrid system with a quantum yield of 8.42% was constructed by feeding bismuth-doped carbon dots (Bi@CDS) to Escherichia coli (E. coli). In this biohybrid system, Bi@CDS can enter the cells and transfer the electrons upon light irradiation, greatly reducing the energy loss and shortening the distance of electron transfer. More importantly, the photocatalytic hydrogen production of the E. coli–Bi@CDs biohybrid system reached up to 0.95 mmol within 3 h under light irradiation (420–780 nm, 2000 W m–2), which is 1.36 and 2.38 times higher than that in the E. coli–CDs biohybrid system and the E. coli system, respectively. In addition, the mechanism of enhanced hydrogen production was further explored. It was found that the accelerated decomposition of glucose, the accelerated production of pyruvate, the inhibition of lactic acid, and the increase of formic acid were the reasons for the increase of hydrogen production. This work provides a novel strategy for improving the hydrogen production in photosynthetic inorganic biohybrid systems.
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