Coordination Chemistry of [Co(acac)2] with N-Doped Graphene: Implications for Oxygen Reduction Reaction Reactivity of Organo-metallic Co-O4-N Species

被引:92
作者
Han, Jongwoo [1 ]
Sa, Young Jin [2 ]
Shim, Yeonjun [1 ]
Choi, Min [4 ,5 ]
Park, Noejung [1 ,4 ,5 ]
Joo, Sang Hoon [2 ,3 ]
Park, Sungjin
机构
[1] Inha Univ, Dept Chem & Chem Engn, Inchon 402751, South Korea
[2] Ulsan Natl Inst Sci & Technol, Dept Chem, Ulsan 689798, South Korea
[3] UNIST, Sch Energy & Chem Engn, Ulsan 689798, South Korea
[4] UNIST, Dept Phys, Ulsan 689798, South Korea
[5] UNIST, Ctr Multidimens Carbon Mat, Ulsan 689798, South Korea
基金
新加坡国家研究基金会;
关键词
cobalt; electrocatalysis; heterogeneous catalysis; nanomaterials; solid-state NMR; HIGH-PERFORMANCE ELECTROCATALYSTS; FUEL-CELLS; CATALYSTS; COBALT; CARBON; GENERATION; IRON; POLYMERIZATION; COMPOSITE; OXIDE;
D O I
10.1002/anie.201504707
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hybridization of organometallic complexes with graphene-based materials can give rise to enhanced catalytic performance. Understanding the chemical structures within hybrid materials is of primary importance. In this work, archetypical hybrid materials are synthesized by the reaction of an organometallic complex, [Co-II(acac)(2)] (acac=acetylacetonate), with N-doped graphene-based materials at room temperature. Experimental characterization of the hybrid materials and theoretical calculations reveal that the organometallic cobalt-containing species is coordinated to heterocyclic groups in N-doped graphene as well as to its parental acac ligands. The hybrid material shows high electrocatalytic activity for the oxygen reduction reaction (ORR) in alkaline media, and superior durability and methanol tolerance to a Pt/C catalyst. Based on the chemical structures and ORR experiments, the catalytically active species is identified as a Co-O-4-N structure.
引用
收藏
页码:12622 / 12626
页数:5
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