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Electroactive P-Ani/core-shell/TiO2/TiO2-WO3 employed surface engineering of Ni-P electrodes for alkaline hydrogen evolution reaction

机译:电活性P-Ani /核壳/ TiO2 / TiO2-WO3采用Ni-P电极的表面工程,用于碱性氢气进化反应

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Ni-P coating (NPC) fabricated by electroless deposition has been widely accepted as an effective electrode for alkaline hydrogen evolution reaction. Among the different strategies reported to improve the catalytic activity of Ni-P electrode (NPE) further, incorporation of inorganic metal oxide composite is a proven method. Herein, we propose a modification of TiO2/TiO2-WO3 core-shell structured composite (a novel entity), by the application of conductive polyaniline (P-Ani), as a continuation of our earlier work on its synthesis and characterization. The as-prepared polymer-metal oxide hybrid nanocomposite is then employed to modify the NPE by electroless deposition method. The improved surface characteristics of the modified NPE, after the incorporation of P-Ani/TiO2/TiO2-WO3 composite with reduced charge transfer resistance and low overpotential for alkaline hydrogen evolution (-65 mV at -10 mA/cm(2)) corroborates its enhanced catalytic behavior. The increase in the number of catalytically active sites on the NPE after modification through P-Ani composite is attributed to the enhanced characteristics for alkaline hydrogen evolution. Our strategy proposes a sustainable and low-cost electrode material, competent to the existing industrial electrocatalysts, for long term hydrogen evolution in alkaline medium. (C) 2020 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights
机译:通过无电沉积制造的Ni-P涂层(NPC)已被广泛接受为碱性氢进化反应的有效电极。据报道的不同策略进一步提高Ni-P电极(NPE)的催化活性,掺入无机金属氧化物复合物是经过验证的方法。在此,我们通过在其早期工作的合成和表征的延续下,提出改性TiO2 / TiO2-WO3核 - 壳结构化合物(一种新实体)。然后采用制备的聚合物 - 金属氧化物杂交纳米复合材料通过无电沉积方法改变NPE。改进的NPE表面特性,在掺入电荷转移电阻和碱性氢进化的低电压和低过电位的P-Ani / TiO 2 / TiO2-WO3复合材料(-65mV At -10mA / cm(2))中其增强的催化行为。通过P-Ani复合材料改性后NPE催化活性位点的数量增加归因于碱性氢进化的增强特性。我们的策略提出了可持续和低成本的电极材料,持有现有的工业电催化剂,用于碱性介质的长期氢气进化。 (c)2020朝鲜工业与工程化学学会。由elsevier b.v出版。所有权利

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