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Seamlessly Conductive 3D Nanoarchitecture of Core-Shell Ni-Co Nanowire Network for Highly Efficient Oxygen Evolution

机译:核-壳Ni-Co纳米线网络的无缝导电3D纳米体系结构,可高效释放氧气

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摘要

Electrochemical splitting of water is an attractive way to produce hydrogen fuel as a clean and renewable energy source. However, a major challenge is to accelerate the sluggish kinetics of the anodic half-cell reaction where oxygen evolution reaction (OER) takes place. Here, a seamlessly conductive 3D architecture is reported with a carbon-shelled Ni-Co nanowire network as a highly efficient OER electrocatalyst. Highly porous and granular Ni-Co nanowires are first grown on a carbon fiber woven fabric utilizing a cost-effective hydrothermal method and then conductive carbon shell is coated on the Ni-Co nanowires via glucose carbonization and annealing processes. The conductive carbon layer surrounding the nanowires is introduced to provide a continuous pathway for facile electron transport throughout the whole of the integrated 3D catalyst. This 3D hierarchical structure provides several synergistic effects and beneficial functions including a large number of active sites, easy accessibility of water, fast electron transport, rapid release of oxygen gas, enhanced electrochemical durability, and stronger structural integrity, resulting in a remarkable OER activity that delivers an overpotential of 302 mV with a Tafel slope of 43.6 mV dec(-1) at a current density of 10 mA cm(-2) in an alkaline medium electrolyte (1 m KOH).
机译:水的电化学分解是生产氢燃料作为清洁和可再生能源的一种有吸引力的方式。然而,主要的挑战是加速发生氧释放反应(OER)的阳极半电池反应的缓慢动力学。在此,报道了一种无缝导电的3D体系结构,该结构具有碳壳Ni-Co纳米线网络,是一种高效的OER电催化剂。首先使用经济高效的水热法在碳纤维机织织物上生长高度多孔且颗粒状的Ni-Co纳米线,然后通过葡萄糖碳化和退火工艺将导电碳壳包覆在Ni-Co纳米线上。引入围绕纳米线的导电碳层以提供连续的路径,用于在整个集成的3D催化剂中轻松进行电子传输。这种3D分层结构提供了多种协同效应和有益功能,包括大量的活性位点,水的易接近性,快速的电子传输,氧气的快速释放,增强的电化学耐久性以及更强的结构完整性,从而产生了卓越的OER活性,在碱性介质电解质(1 m KOH)中以10 mA cm(-2)的电流密度提供302 mV的过电势和43.6 mV dec(-1)的Tafel斜率。

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  • 来源
    《Advanced energy materials》 |2017年第1期|1601492.1-1601492.11|共11页
  • 作者单位

    Korea Adv Inst Sci & Technol, Creat Res Initiat Ctr Functionally Antagonist Nan, Dept Mech Engn, Daehak Ro 291, Daejeon 34141, South Korea;

    Korea Adv Inst Sci & Technol, Creat Res Initiat Ctr Functionally Antagonist Nan, Dept Mech Engn, Daehak Ro 291, Daejeon 34141, South Korea;

    Univ Paris Diderot, Sorbonne Paris Cite, CNRS, ITODYS,UMR 7086, 15 Rue Jean Antoine Baif, F-75205 Paris 13, France;

    Inst for Basic Sci Korea, Ctr Nanomat & Chem React, Daejeon 34141, South Korea|Korea Adv Inst Sci & Technol, Grad Sch EEWS, Daejeon 34141, South Korea;

    Inst for Basic Sci Korea, Ctr Nanomat & Chem React, Daejeon 34141, South Korea|Korea Adv Inst Sci & Technol, Grad Sch EEWS, Daejeon 34141, South Korea;

    Korea Adv Inst Sci & Technol, Creat Res Initiat Ctr Functionally Antagonist Nan, Dept Mech Engn, Daehak Ro 291, Daejeon 34141, South Korea;

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