Self-assembly of cell-embedding reduced graphene oxide/ polypyrrole hydrogel as efficient anode for high-performance microbial fuel cell

聚吡咯 石墨烯 材料科学 微生物燃料电池 化学工程 电化学 电极 纳米复合材料 舍瓦内拉 氧化物 聚合 生物相容性 纳米技术 阳极 原位聚合 化学 聚合物 复合材料 冶金 细菌 物理化学 工程类 生物 遗传学
作者
C. Joseph Kirubaharan,Jianwei Wang,Syed Zaghum Abbas,Syed Bilal Shah,Yafei Zhang,Jing‐Xian Wang,Yang‐Chun Yong
出处
期刊:Chemosphere [Elsevier]
卷期号:326: 138413-138413 被引量:9
标识
DOI:10.1016/j.chemosphere.2023.138413
摘要

A three-dimensional (3D) macroporous reduced graphene oxide/polypyrrole (rGO/Ppy) hydrogel assembled by bacterial cells was fabricated and applied for microbial fuel cells. By taking the advantage of electroactive cell-induced bioreduction of graphene oxide and in-situ polymerization of Ppy, a facile self-assembly by Shewanella oneidensis MR-1and in-situ polymerization approach for 3D rGO/Ppy hydrogel preparation was developed. This facile one-step self-assembly process enabled the embedding of living electroactive cells inside the hydrogel electrode, which showed an interconnected 3D macroporous structures with high conductivity and biocompatibility. Electrochemical analysis indicated that the self-assembly of cell-embedding rGO/Ppy hydrogel enhanced the electrochemical activity of the bioelectrode and reduced the electron charge transfer resistance between the cells and the electrode. Impressively, extremely high power output of 3366 ± 42 mW m-2 was achieved from the MFC with cell-embedding rGO/Ppy hydrogel rGO/Ppy, which was 8.6 times of that delivered from the MFC with bare electrode. Further analysis indicated that the increased cell loading by the hydrogel and improved electrochemical activity by the rGO/Ppy composite would be the underlying mechanism for this performance improvement. This study provided a facile approach to fabricate the biocompatible and electrochemical active 3D nanocomposites for MFC, which would also be promising for performance optimization of various bioelectrochemical systems.
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