Joule-heating Pyrolysis-derived Fe, N Co-doped Carbon and Its Performance in Direct Peroxide-Peroxide Fuel Cells

被引:3
作者
Cheng, Wendong [1 ]
Hou, Shuai [1 ]
Guo, Fen [1 ]
机构
[1] Wuhan Univ Sci & Technol, Sch Chem & Chem Engn, Key Lab Hubei Prov Coal Convers & New Carbon Mat, Wuhan 430081, Peoples R China
关键词
OXYGEN REDUCTION REACTION; H2O2; ELECTROREDUCTION; POLYANILINE; CATALYSTS; NICKEL; MECHANISM; FILMS; ANODE;
D O I
10.1149/1945-7111/ac90ef
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The traditional electric furnace pyrolysis to produce heteroatom doped carbon faces the time-consuming issue due to the fixed size of furnace chamber and indirect heat transfer. Herein a fast Joule-heating pyrolysis method, viz., powering on the C, N, Fe-containing, conductive polyaniline precursor at fixed direct current (DC) voltage for a specific time, is put forward. The polyaniline precursor begins to decompose thermally when being powered with a DC voltage of 5.0 V upwards. In the pyrolysis products, Fe and N co-doping of carbon material leads to C-N bonding and C-Fe bonding in a certain way. The direct peroxide-peroxide fuel cell (DPPFC) with the optimal Fe, N codoped carbon material as anode and cathode can generate an open circuit voltage of 0.85 V and a peak power density of 29.7 mW cm(-2) in ambient temperature, which is highly competitive compared with other DPPFCs with anode and/or cathode made of noble metals.
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页数:9
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