five

Supplementary Information Files for 'Acetate production from inorganic carbon (HCO3-) in photo-assisted biocathode microbial electrosynthesis systems using WO3/MoO3/g-C3N4 heterojunctions and Serratia marcescens species.'

收藏
DataCite Commons2024-02-15 更新2024-07-13 收录
下载链接:
https://repository.lboro.ac.uk/articles/dataset/Supplementary_Information_Files_for_Acetate_production_from_inorganic_carbon_HCO3-_in_photo-assisted_biocathode_microbial_electrosynthesis_systems_using_WO3_MoO3_g-C3N4_heterojunctions_and_Serratia_marcescens_species_/11798829
下载链接
链接失效反馈
官方服务:
资源简介:
Supplementary Information Files for 'Acetate production from inorganic carbon (HCO3-) in photo-assisted biocathode microbial electrosynthesis systems using WO3/MoO3/g-C3N4 heterojunctions and Serratia marcescens species.'<br>Abstract:The efficient production of acetate from HCO3− is demonstrated in a photo-assisted microbial electrosynthesis system (MES) incorporating a WO3/MoO3/g-C3N4 heterojunction photo-assisted biocathode supporting Serratia marcescens Q1 electrotroph. The WO3/MoO3/g-C3N4 structured electrode consisting of a layer of g-C3N4 coated on graphite felt decorated with W/Mo oxides nanoparticles exhibited stable photocurrents, 4.8 times higher than the g-C3N4 electrode and acetate production of 3.12 ± 0.20 mM/d with a CEacetate of 73 ± 4 % and current of 2.5 ± 0.3 A/m2. Photo-induced electrons on the conduction bands of WO3/MoO3/g-C3N4 favoured hydrogen evolution, which was metabolized by S. marcescens with HCO3− to acetate, while the holes were refilled by the electrons travelling from the anode. Such mechanism reduced the interfacial resistances creating a supplementary driving force leading to higher acetate production. The biocompatible components of WO3/MoO3/g-C3N4 synergistically couple light-harvesting and further catalyze S. marcescens to acetate from HCO3−, providing a feasible strategy for achieving sustainable high rates of acetate production.<br>

本文件为《使用WO3/MoO3/g-C3N4异质结与粘质沙雷氏菌(Serratia marcescens)的光辅助生物阴极微生物电合成系统中以无机碳(HCO3-)合成乙酸盐》的补充信息文件。<br>摘要:本研究在搭载负载粘质沙雷氏菌(Serratia marcescens)Q1电营养菌的WO3/MoO3/g-C3N4异质结光辅助生物阴极的微生物电合成系统(MES)中,实现了以碳酸氢根(HCO3-)为原料高效合成乙酸盐。该WO3/MoO3/g-C3N4结构化电极以负载钨/钼氧化物纳米颗粒的石墨毡为基底,表面覆有类石墨相氮化碳(g-C3N4)涂层,展现出稳定的光电流,其强度为纯g-C3N4电极的4.8倍;配套系统的乙酸盐产率可达3.12 ± 0.20 mM/d,乙酸盐电流效率(CEacetate)为73 ± 4%,电流密度为2.5 ± 0.3 A/m²。WO3/MoO3/g-C3N4导带上的光生电子可促进析氢反应,粘质沙雷氏菌可利用该反应产物与碳酸氢根代谢合成乙酸盐;而价带上的空穴则由从阳极迁移而来的电子补充。该机制降低了界面电阻,形成额外驱动力,从而提升了乙酸盐产率。WO3/MoO3/g-C3N4的生物相容性组分可协同实现光捕获,并进一步催化粘质沙雷氏菌以碳酸氢根为原料合成乙酸盐,为实现可持续的乙酸盐高产率制备提供了可行策略。
提供机构:
Loughborough University
创建时间:
2020-02-04
二维码
社区交流群
二维码
科研交流群
商业服务