首页> 外文期刊>Electrochimica Acta >Ultrafine Co2P anchored on porous CoWO4 nanofiber matrix for hydrogen evolution: Anion-induced compositional/morphological transformation and interfacial electron transfer
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Ultrafine Co2P anchored on porous CoWO4 nanofiber matrix for hydrogen evolution: Anion-induced compositional/morphological transformation and interfacial electron transfer

机译:超细CO2P锚定在多孔牛仔4纳米纤维基质上进行氢气进化:阴离子诱导的组成/形态转化和界面电子转移

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摘要

Even though transition metal phosphides (TMPs) have been regarded as very promising catalysts for hydrogen evolution reaction (HER), exploring highly reactive TMPs-based catalysts with reliable stability in alkaline media remains an enormous challenge. Herein, using wafer-like Co(CO3)(0.5)(OH)center dot 0.11H(2)O as template followed by anion-exchange and further phosphorization process, it is synthesized a three-dimensional (3D) hierarchical porous heterostructure with highly dispersed ultrafine metallic Co2P nanoparticles uniformly anchored on porous conductive CoWO4 nanofiber matrix, which not only promotes the electron transfer, but also avoids the deterioration of phosphide. In addition, the electron densities re-distribution within the heterostructure also contributes to the improved catalytic activity. Furthermore, the doping of W into Co2P gives proper H adsorption free energy Delta G(H). Impressively, the Co2P/CoWO4/Ni foam (NF) exhibits an overpotential of 81 mV at -10 mA cm(-2) and a Tafel slop of 47 mV dec(-1) along with supreme long-term durability at -40 mA cm(-2). The present work also demonstrates different dosages of Na2WO4 in the anion-exchange step will lead to different phase compositions and morphologies, giving rise to different HER electrocatalytic performances of the phosphorized samples. (C) 2019 Elsevier Ltd. All rights reserved.
机译:尽管过渡金属磷化物(TMPS)已经被认为是用于析氢反应非常有前途的催化剂(HER),探索高反应性TMPS基于与在碱性介质可靠稳定性催化剂仍然是一个巨大的挑战。在本文中,使用晶片状的Co(CO 3)(0.5)(OH)中心点0.11H(2)O作为模板,然后阴离子交换和进一步磷化过程中,它被合成的三维(3D)分级多孔异质结构高度分散的金属超微粒子Co2P均匀地锚定在多孔质导电性纳米纤维CoWO4矩阵,这不仅促进了电子转移,但还避免了磷化物的劣化。另外,电子密度重新分布的异质结构内也有助于改进催化活性。此外,W的掺杂成Co2P给出适当的吸附H自由能德尔塔G(H)。令人印象深刻的Co2P / CoWO4 /镍泡沫(NF)表现出的超电势81毫伏在-10毫安厘米(-2)和47毫伏分解(-1)与最高在长期耐久性沿塔菲尔斜率-40毫安厘米(-2)。目前的工作还表明在阴离子交换步骤钨酸钠的不同剂量将导致不同的相组成和形貌,从而产生了磷化样品的不同HER电催化性能。 (c)2019 Elsevier Ltd.保留所有权利。

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