期刊
CARBON
卷 116, 期 -, 页码 655-669出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2017.02.045
关键词
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资金
- The National Science Centre (Poland) [2013/09/D/ST5/03889, 2012/04/A/ST4/00287, DEC-2013/09/D/ST5/03889]
- National Science Centre (Poland) [2012/04/A/ST4/00287]
(Co)polycondensation of resorcinol and heterocyclic aldehydes yields heteroaromatic porous polymers. Carbonization of such polymers results in N-doped, S-doped, N/S-co-doped or undoped carbon gels depending on the starting composition of reactants. If the (co)polycondensation is initiated with FeC13, Fe-containing carbon gels are obtained. Depending on the nature of the heteroatom doping (solely N or S, both N and S or no heteroatom) the Fe-containing carbon gels exhibit distinct structural properties. While the presence of sulfur hinders Fe-driven graphitization, yielding carbons with high specific surface area (SSA), N-doping exhibits the contrary effect, resulting in highly graphitic structures with low SSAs. More importantly, increasing the Fe content in the N/S-co-doped carbons results in remarkable increases in microporosity, yielding materials with SSA of up to 1240 m(2)g(4). The Fe-containing carbon gels are considered non-precious metal catalysts for the oxygen reduction reaction. It is demonstrated that in the case of Fe/N/C/S type catalysts, the interaction between S, C and Fe (at the pyrolysis stage) results in the enhancement of microporosity, where S acts as a soft oxidant toward carbon, while Fe recaptures the sulfur- and carbon-containing pyrolytic gases. The incidental deposition of pyrolytic gases contributes significantly to the final structure of the catalysts. (C) 2017 Elsevier Ltd. All rights reserved.
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