碳纤维
微生物燃料电池
氮气
氧还原反应
氧气
氧还原
燃料电池
化学
纳米结构
还原(数学)
化学工程
材料科学
环境化学
无机化学
纳米技术
有机化学
电化学
工程类
电极
几何学
数学
物理化学
复合数
阳极
复合材料
作者
Hai-Xia Liao,Hui-Xu Wei,Shu-Qi Zhou,Hao-Wen Zhou,Yi-Ting Cao,Nan Li
标识
DOI:10.1021/acsanm.4c06339
摘要
Iron–nitrogen codoped carbon (Fe–N–C) nanostructure materials, enhancing catalytic performance by creating active metal center sites, serve as a promising alternative to noble metal catalysts in the oxygen reduction reaction (ORR). In this study, nitrogen-doped carbon dots (NCDs) with an average size of 3.3 ± 0.03 nm and cyanide-functionalized surfaces were utilized to synthesize a nitrogen-doped carbon-dot-modified Fe–N–C nanostructure (NCDM–Fe–N-C). The synthesis leveraged the interactions between cyanide groups on the NCD surfaces and iron ions, resulting in the enrichment of the nanostructure with Fe–Nx reactive species. Under neutral conditions, the optimal NCDM–Fe–N-C-2 sample exhibited significantly enhanced performance compared to conventionally prepared Fe–N–C and commercial 20% Pt/C. The half-wave potential reached 0.75 V vs RHE, and the kinetic current density at 0.70 V stood at 16.4 mA cm–2, surpassing Fe–N–C (0.71 V vs RHE and 4.8 mA cm–2) and 20% Pt/C (0.70 V vs RHE and 3.9 mA cm–2). Furthermore, integrating NCDM–Fe–N-C-2 into microbial fuel cells (MFCs) notably improved the ORR performance at the cathode and enhanced biocompatibility at the anode, resulting in an impressive MFC power density of 959.5 ± 18.6 mW m–2. This study introduces an effective approach to augment ORR activity in Fe–N–C materials and presents a successful concept for advancing MFC development.
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