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Electrochemically assisted synthesis of three-dimensional FeP nanosheets to achieve high electrocatalytic activity for hydrogen evolution reaction

机译:电化学辅助合成三维FeP纳米片以实现高的氢分解反应电催化活性

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摘要

Iron phosphide (FeP) is a promising alternative catalyst for electrocatalytic hydrogen evolution reaction (HER) due to its low price, highly active catalytic sites and long-term anti acid corrosion. Herein, we report a very facile strategy to fabricate novel FeP nanosheets as a HER electrocatalyst. Three-dimensional interconnected nanosheet structures of Fe2O3 (3D Fe2O3 NS) were directly exfoliated from metal Fe wires by alternating current (AC) voltage disturbance, and a simple subsequent phosphorization process could easily convert gamma-Fe2O3 into FeP phase, which also maintained the 3D NS structure. Importantly, increasing the AC voltage resulted in the evolution of iron-containing nanostructures from nanoparticles to 2D nanosheets until the formation of 3D NS structure. Owing to the large specific surface area, enriched active sites and abundant hierarchical porous channels, as prepared 3D FeP NS has exhibited significantly enhanced electrocatalytic HER activities such as a cathode current density of 10 mA cm(-2) at a small overpotential of 88 mV, low Tafel slope (47.7 mV dec(-1)) and satisfactory long-term stability in acidic electrolyte. We expect that this simple and green synthetic strategy of transition metal phosphides will provide a promising prospect to innovate nonprecious HER electrocatalysts. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:磷化铁(FeP)价格低廉,具有高活性的催化位点和长期的抗酸腐蚀性能,是电催化制氢反应(HER)的有希望的替代催化剂。本文中,我们报道了一种非常简便的策略来制备新型FeP纳米片作为HER电催化剂。通过交流电(AC)电压干扰直接从金属铁丝上剥落3D互连的Fe2O3(3D Fe2O3 NS)纳米片结构,随后进行简单的磷化处理很容易将γ-Fe2O3转变为FeP相,从而保持了3D NS结构。重要的是,增加交流电压会导致含铁的纳米结构从纳米颗粒演变为2D纳米片,直到形成3D NS结构。由于具有较大的比表面积,富集的活性位点和丰富的分层多孔通道,如制备的3D FeP NS所示,在88 mV的小超电势下,其电催化HER活性显着增强,例如阴极电流密度为10 mA cm(-2) ,低Tafel斜率(47.7 mV dec(-1))和令人满意的酸性电解质长期稳定性。我们希望,这种简单而绿色的过渡金属磷化物合成策略将为创新非贵金属HER电催化剂提供有希望的前景。 (C)2019氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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