CoP-Fe2O3/g-C3N4 photocathode enhances the microbial electrosynthesis of polyhydroxybutyrate production via CO2 reduction
文献类型: 外文期刊
作者: Zhang, Kang 1 ; Xu, Xingchao 1 ; Li, Xiang Ling 1 ; Song, Tianshun 1 ; Xie, Jingjing 1 ; Guo, Ting 4 ;
作者机构: 1.Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
2.Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, Nanjing 211816, Peoples R China
3.Jiangsu Natl Synerget Innovat Ctr Adv Mat SICAM, Nanjing 211816, Peoples R China
4.Jiangsu Acad Agr Sci, Nanjing 210014, Peoples R China
关键词: Microbial electrosynthesis; Photoelectrocatalytic; PHB
期刊名称:FUEL ( 影响因子:7.4; 五年影响因子:7.0 )
ISSN: 0016-2361
年卷期: 2024 年 357 卷
页码:
收录情况: SCI
摘要: The hydrogen energy and CO2 reduction in-situ recombination has drawn increasing attention. Microbial elec-trosynthesis (MES) integrated with photocatalytic materials is a novel technology for CO2 utilization. Here, MES with the photocathode CoP-Fe2O3/g-C3N4 was constructed using Ralstonia eutropha as biocatalyst to generate polyhydroxybutyrate (PHB). The integration of CoP and Fe2O3/g-C3N4 facilitated electron-hole pair separation and electron transfer, which enhanced hydrogen evolution reaction and provided additional reducing power for CO2 conversion. Simultaneously, the concentration of reactive oxygen species was also considerably reduced, increasing the production of PHB. In particular, 87.54 mg/L of PHB was obtained in CoP-Fe2O3/g-C3N4 at -1.05 V, which is about three times higher than that in carbon felt. At -0.9 V, PHB concentration further increased to 142.20 mg/L. This study provides a new approach for converting CO2 into multicarbon compounds in situ electrolysis of water under visible light.
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