首页> 外文期刊>Journal of Colloid and Interface Science >Metal-organic framework derived Fe/Fe3C@N-doped-carbon porous hierarchical polyhedrons as bifunctional electrocatalysts for hydrogen evolution and oxygen-reduction reactions
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Metal-organic framework derived Fe/Fe3C@N-doped-carbon porous hierarchical polyhedrons as bifunctional electrocatalysts for hydrogen evolution and oxygen-reduction reactions

机译:金属有机框架衍生Fe / Fe3C @ N-掺杂碳多孔等级分层多面体作为氢气进化和氧还原反应的双官能电催化剂

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The development of simple and cost-effective synthesis methods for electrocatalysts of hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR) is critical to renewable energy technologies. Herein, we report an interesting bifunctional HER and ORR electrocatalyst of Fe/Fe3C@N-doped-carbon porous hierarchical polyhedrons (Fe/Fe3C@N-C) by a simple metal-organic framework precursor route. The Fe/Fe3C@N-C polyhedrons consisting of Fe and Fe3C nanocrystals enveloped by N-doped carbon shells and accompanying with some carbon nanotubes on the surface were prepared by thermal annealing of Zn-3[Fe(CN)(6)](2)center dot xH(2)O polyhedral particles in nitrogen atmosphere. This material exhibits a large specific surface area of 182.5 m(2) g(-1) and excellent ferromagnetic property. Electrochemical tests indicate that the Fe/Fe3C@N-C hybrid has apparent HER activity with a relatively low overpotential of 236 mV at the current density of 10 mA cm(-2) and a small Tafel slope of 59.6 mV decade(-1). Meanwhile, this material exhibits excellent catalytic activity toward ORR with an onset potential (0.936 V vs. RHE) and half-wave potential (0.804 V vs. RHE) in 0.1 M KOH, which is comparable to commercial 20 wt% Pt/C (0.975 V and 0.820 V), and shows even better stability than the Pt/C. This work provides a new insight to developing multi-functional materials for renewable energy application. (C) 2018 Elsevier Inc. All rights reserved.
机译:用于氢化反应(她)和氧还原反应(ORR)的氢催化剂的简单且经济高效的合成方法的开发对于可再生能源技术至关重要。在此,我们通过简单的金属 - 有机框架前体途径向N-FE3C @ N-掺杂碳多孔分层多篮(Fe / Fe3C @ N-C)报告有趣的双官能的双官能催化剂。由Zn-3 [Fe(CN)(6)(6)(6)](2)的热退火制备由由N掺杂的碳壳包覆的Fe和Fe 3C纳米晶体组成的Fe / Fe 3C纳米晶体组成的Fe和Fe 3C纳米晶体组成的Fe和Fe 3C纳米晶体由表面的热退火制备中心点XH(2)o氮气氛中的多面体颗粒。该材料具有182.5m(2 )g(-1)和优异的铁磁性性能的大比表面积。电化学试验表明Fe / Fe3C @ N-C杂种具有表观她的活性,其活性相对较低,在10mA cm(-2)的电流密度下,小Tafel斜率为59.6 mV十年(-1)。同时,该材料表现出优异的催化活性,朝向ORR具有发病势(0.936V与RHE)和0.1M KOH的半波电位(0.804V与RHE),其与商业20wt%Pt / c相当( 0.975 V和0.820 V),表明甚至比PT / C更好的稳定性。这项工作为开发可再生能源应用的多功能材料提供了新的洞察力。 (c)2018 Elsevier Inc.保留所有权利。

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