Co anchored on porphyrinic triazine-based frameworks with excellent biocompatibility for conversion of CO_(2)in H_(2)-mediated microbial electrosynthesis  

作　　者：Folin Liu Shaohua Feng Siyuan Xiu Bin Yang Yang Hou Lecheng Lei Zhongjian Li 

机构地区：[1]College of Chemical and Biological Engineering,Key Laboratory of Biomass Chemical Engineering of Ministry of Education,Zhejiang University,Hangzhou 310027,China [2]Institute of Zhejiang University—Quzhou,Quzhou 324000,China [3]Academy of Ecological Civilization,Zhejiang University,Hangzhou 310027,China

出　　处：《Frontiers of Chemical Science and Engineering》2022年第12期1761-1771,共11页化学科学与工程前沿（英文版）

基　　金：This project was supported by the National Natural Science Foundation of China(Grant Nos.22122812,22075245 and 21961160742)。

摘　　要：Microbial electrosynthesis is a promising alternative to directly convert CO_(2)into long-chain compounds by coupling inorganic electrocatalysis with biosynthetic systems.However,problems arose that the conventional electrocatalysts for hydrogen evolution may produce extensive by-products of reactive oxygen species and cause severe metal leaching,both of which induce strong toxicity toward microorganisms.Moreover,poor stability of electrocatalysts cannot be qualified for long-term operation.These problems may result in poor biocompatibility between electrocatalysts and microorganisms.To solve the bottleneck problem,Co anchored on porphyrinic triazine-based frameworks was synthesized as the electrocatalyst for hydrogen evolution and further coupled with Cupriavidus necator H16.It showed high selectivity for a four-electron pathway of oxygen reduction reaction and low production of reactive oxygen species,owing to the synergistic effect of Co–Nx modulating the charge distribution and adsorption energy of intermediates.Additionally,low metal leaching and excellent stability were observed,which may be attributed to low content of Co and the stabilizing effect of metalloporphyrins.Hence,the electrocatalyst exhibited excellent biocompatibility.Finally,the microbial electrosynthesis system equipped with the electrocatalyst successfully converted CO_(2)to poly-β-hydroxybutyrate.This work drew up a novel strategy for enhancing the biocompatibility of electrocatalysts in microbial electrosynthesis system.

关 键 词：microbial electrosynthesis hydrogen evolution reaction METALLOPORPHYRINS BIOCOMPATIBILITY CO_(2)conversion 

分 类 号：O64[理学—物理化学]