材料科学
制氢
化学工程
光化学
纳米技术
氢
化学
有机化学
工程类
作者
Kemeng Xiao,Tsz Ho Tsang,Dong Sun,Jun Liang,Hui Zhao,Zhifeng Jiang,Bo Wang,Jimmy C. Yu,Po Keung Wong
标识
DOI:10.1002/aenm.202100291
摘要
Abstract The recently emerged photosynthetic biohybrid systems (PBSs) integrate the advantages of the light‐harvesting ability of semiconductors and the catalytic power of biological metabolism. Herein, negatively charged iodine‐doped hydrothermally carbonized carbon (I‐HTCC) is interfaced with surface modified Escherichia coli cells through a facile “add‐on” mode via electrostatic interactions. As a result of the photoexcited electrons, the self‐assembled I‐HTCC@ E. coli biohybrid shows enhanced hydrogen production efficiency with a quantum efficiency of 9.11% under irradiation. The transduction of photoelectrons from I‐HTCC to cells is the rate‐limiting step for H 2 production and is delivered through both direct injection and the NADH/NAD + ‐mediated pathways. The injected photoelectrons fine‐tune the H 2 production through the formate and NADH pathways in a subtle manner. The excellent biocompatibility and photostability of the I‐HTCC@ E. coli biohybrid demonstrate its potential real‐world application under sunlight. In addition, the proposed “add‐on” mode is extended to a series of negatively charged common carbon‐based materials with different levels of promotion effects compared with that of pure bacterial cultures. This facile and effective mode provides an insight into the rational design of the whole‐cell PBSs with various semiconductors for H 2 production.
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