N-Doped Carbon-Supported CoCu-Layered Double Hydroxide Nanosheets as Antibacterial Oxygen Reduction Catalysts for Microbial Fuel Cells

氢氧化物 催化作用 碳纤维 氧还原 氧还原反应 氧气 微生物燃料电池 材料科学 燃料电池 兴奋剂 化学工程 无机化学 化学 有机化学 电化学 复合数 电极 复合材料 工程类 光电子学 物理化学 阳极
作者
Liang Li,Demin Jiang,sainan cai,Shikuo Li,Yuqiao Wang
出处
期刊:ACS applied energy materials [American Chemical Society]
卷期号:7 (7): 2854-2861 被引量:1
标识
DOI:10.1021/acsaem.4c00061
摘要

The sluggish reaction kinetics of the oxygen reduction reaction (ORR) and the formation of a biofilm on the cathode prevent efficient and stable operation of microbial fuel cells (MFCs). In this work, zeolitic imidazolate framework-derived N-doped carbon-supported CoCu-layered double hydroxide nanosheets (CoCu-LDH@NC) were synthesized as a bifunctional cathode catalyst for MFCs. CoCu-LDH supported on CoO@NC induced the production of carbon nanotubes (CNTs) from the NC matrix. CNTs and CoCu-LDH nanosheets improved the atomic reaction efficiency and active area for the ORR. The high-speed electron-transfer channel was attributed to two-dimensional CoCu-LDH nanosheets and one-dimensional CNTs. The catalytic activity and stability of CoO@NC were sustained through the incorporation of CoCu-LDH nanosheets. The electronic interaction of CoCu-LDH and CoO@NC enhanced the ORR catalytic activities. CoCu-LDH nanosheets generated reactive oxygen species (ROS) and Cu+, improving the antibacterial activity to prevent the growth of biofilm for MFCs. CoCu-LDH@NC demonstrated superior oxygen reduction activity with a half-wave potential of 0.84 V and an onset potential of 0.89 V. The maximum power density and operating cycle of the MFCs assembled with CoCu-LDH@NC reached 1012 mW m–2 and 170 h, respectively. This work offers guidance to enhancing the ORR catalytic activity and stability by designing antibacterial ORR catalysts.
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