Fe doped porous triazine as efficient electrocatalysts for the oxygen reduction reaction in acid electrolyte

被引:35
作者
Garcia, Alvaro [1 ]
Retuerto, Maria [1 ]
Dominguez, Carlota [1 ]
Pascual, Laura [2 ]
Ferrer, Pilar [3 ]
Gianolio, Diego [3 ]
Serrano, Aida [4 ]
Assmann, Pia [5 ]
Sanchez, Daniel G. [5 ]
Pena, Miguel A. [5 ]
Rojas, Sergio [5 ]
机构
[1] CSIC, Inst Catalisis & Petroleoquim, Grp Energia & Quim Sostenibles, Marie Curie 2, Madrid 28049, Spain
[2] CSIC, Inst Catalisis & Petroleoquim, Marie Curie 2, Madrid 28049, Spain
[3] Diamond Light Source, Harwell Sci & Innovat Campus, Didcot OX11 0DE, Oxon, England
[4] European Synchrotron, Spanish CRG BM25 Beamline, SpLine, 71 Ave Martyrs, F-38000 Grenoble, France
[5] German Aerosp Ctr DLR, Inst Engn Thermodynam, Pfaffenwaldring 38-40, D-70569 Stuttgart, Germany
基金
欧盟地平线“2020”;
关键词
ORR; NPMC; Triazine; PEMFC; Fe-N; NONPRECIOUS METAL-CATALYSTS; ACTIVE-SITES; CARBON; PERFORMANCE; POLYMER; IRON; FRAMEWORKS; IDENTIFICATION; ELECTROCHEMISTRY; SPECTROSCOPY;
D O I
10.1016/j.apcatb.2019.118507
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this work, we report the synthesis of Fe/N/C electrocatalysts using triazine based porous organic polymers as precursors. Iron-doped triazine porous organic polymers were obtained by in situ polymerization of iron precursor and 1,2- or 1,4- dicyanobenzene (DCB). In order to obtain the actual catalyst, the polymer obtained was subjected to thermal treatment under NH3. The catalysts obtained exhibit activity and durability for the oxygen reduction reaction in acid electrolyte. Thorough characterization of the catalysts reveal the formation of several types of iron species, including metallic iron, iron carbides and Fe-Nx moieties. The latter species is the main responsible for the high activity measured for the oxygen reduction reaction in acid electrolyte. 1,2-DCB results in more active catalysts than 1,4-DCB due to the higher fraction of FeNx ensembles in the former, probably because vicinal positions of N-bearing groups are more prone to coordinate Fe atoms.
引用
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页数:13
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