Facile synthesis of cobalt oxide as electrocatalyst for the oxygen reduction reaction in microbial fuel cells

被引:28
|
作者
Xia, Xue [1 ,2 ]
Li, Mengchen [1 ]
Liu, Tao [1 ]
Liang, Peng [1 ]
Huang, Xia [1 ]
机构
[1] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China
[2] Chinese Acad Sci, Res Ctr Eco Environm Sci, Key Lab Environm Biotechnol, Beijing 100085, Peoples R China
基金
中国国家自然科学基金;
关键词
Microbial fuel cell; Oxygen reduction reaction; Air-cathode; Catalyst; Cobalt oxide; WASTE-WATER TREATMENT; CATHODE CATALYST; ACTIVATED CARBON; GENERATION; GRAPHENE; PHTHALOCYANINE; NANOPARTICLES; PLATINUM; COTMPP; IRON;
D O I
10.1016/j.cej.2018.02.092
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Cost-effective cobalt oxides were synthesized at mild condition as alternatives to platinum catalyst for oxygen reduction in microbial fuel cells (MFCs). The catalysts were prepared by heating Co(NO3)(2) above its decomposition temperature together with carbon black (CB). At a catalyst loading of 5 mg/cm(2), cobalt oxide cathodes with a Co(NO3)(2) to CB ratio of 0.732:1 produced a maximum power density of 1220 mW/m(2), which was slightly lower than that of Pt/C cathodes (1360 mW/m(2)). Further increase in the loading of cobalt oxides resulted in an increase in performance. The maximum power densities produced by cobalt oxide cathodes increased to 1400 mW/m(2) at a catalyst loading of 20 mg/cm(2) and 1540 mW/m(2) at 30 mg/cm(2), which outperformed the Pt/C control. The durability of cobalt oxide catalysts was comparable to that of Pt/C in single-chamber MFCs with biological contamination. The costs of cobalt oxide catalysts were much lower than that of Pt/C catalyst, even when the loading of cobalt oxides was several times higher than Pt/C catalyst. These findings show that the facilely synthesized cobalt oxides were cost-effective catalysts for oxygen reduction in air-cathode MFCs.
引用
收藏
页码:395 / 400
页数:6
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