Oxygen reduction to hydrogen peroxide on Fe3O4 nanoparticles supported on Printex carbon and Graphene

被引:136
作者
Barros, Willyam R. P. [1 ,2 ]
Wei, Qiliang [2 ]
Zhang, Gaixia [2 ]
Sun, Shuhui [2 ]
Lanza, Marcos R. V. [1 ]
Tavares, Ana C. [2 ]
机构
[1] Univ Sao Paulo, Inst Quim Sao Carlos, BR-13566590 Sao Carlos, SP, Brazil
[2] Inst Natl Rech Sci Energie Mat & Telecommun, Varennes, PQ J3X 1S2, Canada
基金
巴西圣保罗研究基金会;
关键词
Fe3O4; oxygen reduction reaction; 2 electron pathway; Printex 6L carbon; graphene; RETICULATED VITREOUS CARBON; GAS-DIFFUSION CATHODE; EFFICIENT ELECTROCATALYST; OXIDE NANOPARTICLES; ELECTRODES; ELECTROGENERATION; CATALYST; IRON; ELECTROREDUCTION; H2O2;
D O I
10.1016/j.electacta.2015.02.175
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Fe3O4 nanoparticles supported on graphene (Fe3O4/graphene) and Printex carbon (Fe3O4/Printex) are reported as promising catalysts for oxygen reduction reaction (ORR) to H2O2 in alkaline medium. The catalysts were synthesized by a simple precipitation method using NaBH4 as reducing agent to favor the formation of the magnetite phase. The structure and morphology of the catalysts was evaluated by x-ray diffraction, transmission electron microscopy and small angle electron diffraction. The electrocatalytic activity towards ORR was investigated by means of cyclic and linear voltammetries in 1 mol L (-1) KOH. The linear polarization curves highlighted the synergetic effect between the oxide and the carbon supports. Analysis of the polarization curves showed that electro-catalytic activity of the materials towards oxygen reduction expressed by the current density at -0.3 V vs SCE increases from Printex (0.29 mA cm (-2)) < Fe3O4/Printex (0.38 mA cm (-2)) < graphene (0.85 mA cm (-2)) < Fe3O4/graphene (1.12 mA cm (-2)). The number of exchanged electrons was close to 2.7 for both catalysts, and the % H2O2 electro-generated above 60% in the -0.2 to -0.7 V (vs SCE) potential range. Furthermore, both Fe3O4/graphene and Fe3O4/ Printex catalysts show excellent durability. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:263 / 270
页数:8
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