首页> 外文期刊>International journal of hydrogen energy >Syntheses of nickel sulfides from 1,2-bis(diphenylphosphino)ethane nickel(Ⅱ)dithiolates and their application in the oxygen evolution reaction
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Syntheses of nickel sulfides from 1,2-bis(diphenylphosphino)ethane nickel(Ⅱ)dithiolates and their application in the oxygen evolution reaction

机译:1,2-双(二苯基膦基)乙烷二硫代镍(Ⅱ)的硫化镍的合成及其在产氧反应中的应用

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摘要

In this work, four heteroleptic Ni(II)dppe dithiolates complexes, [Ni(NED)(dppe)] (Ni-NED), [Ni(ecda)(dppe)] (Ni-ecda), [Ni(i-mnt)(dppe)] (Ni-i-mnt) and [Ni(cdc)(dppe)] (Ni-cdc) (dppe = 1,2-bis(diphenylphosphino)ethane; NED = 1-nitroethylene-2,2-dithiolate; ecda = 1-ethoxycarbonyl-1-cyanoethyelene-2,2-dithiolate; i-mnt = 1,1-dicyanoethylene-2,2-dithiolate and cdc = cyanodithioimidocarbonate), have been synthesized and characterized by analytical and spectroscopic techniques (Elemental analysis, vibrational, electronic absorption and multinuclear NMR spectroscopy). Structural characterization of all the four complexes by single crystal X-ray diffraction study suggests distortion in regular square planar geometry at Ni(II) center by coordination with two phosphorus of the dppe and two sulfur of the dithiolate ligands, respectively. The decomposition of all four complexes have been done to produce nickel sulfides and the resulting nickel sulfides have been utilized for electrocatalytic oxygen evolution reaction (OER). The nickel sulfide obtained by decomposing Ni-cdc shows best activity with overpotential n = 222 mV at j = 10 mA cm(-2) and a Tafel slope of 44.2 mV dec(-1) while other catalysts shows n 470 mV at j = 5 mA cm(-2) and eta 600 mV at j = 10 mA cm(-2) at loading of 1.3 mg cm(-2). (C) 2018 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:在这项工作中,四个杂合的Ni(II)dppe二硫盐复合物[Ni(NED)(dppe)](Ni-NED),[Ni(ecda)(dppe)](Ni-ecda),[Ni(i-mnt) )(dppe)](Ni-i-mnt)和[Ni(cdc)(dppe)](Ni-cdc)(dppe = 1,2-双(二苯基膦基)乙烷; NED = 1-硝基乙烯-2,2-二硫醇盐; ecda = 1-乙氧基羰基-1-氰基噻吩-2,2-二硫醇盐; i-mnt = 1,1-二氰亚乙基-2,2-二硫醇盐和cdc =氰基二硫代亚氨基碳酸酯),已通过分析和光谱技术进行了合成和表征(元素分析,振动,电子吸收和多核NMR光谱)。通过单晶X射线衍射研究对所有四个配合物的结构表征表明,Ni(II)中心的规则正方形平面几何结构中的畸变是通过分别与dppe的两个磷和二硫醇盐配体的两个硫配位而实现的。已经完成所有四种配合物的分解以产生硫化镍,并且所得的硫化镍已经用于电催化氧释放反应(OER)。通过分解Ni-cdc所获得的硫化镍表现出最佳的活性,在j = 10 mA cm(-2)时超电势n = 222 mV,Tafel斜率为44.2 mV dec(-1),而其他催化剂在j时n> 470 mV。在1.3 mg cm(-2)的负载下,j = 10 mA cm(-2)时= 5 mA cm(-2)且eta> 600 mV。 (C)2018氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2018年第12期|5985-5995|共11页
  • 作者单位

    Univ Lucknow, Dept Chem, Fac Sci, Lucknow 226007, Uttar Pradesh, India;

    Univ Lucknow, Dept Chem, Fac Sci, Lucknow 226007, Uttar Pradesh, India;

    Univ Bath, Chem Characterisat & Anal Facil, Bath BA2 7AY, Avon, England;

    Univ Delhi, Dept Chem, Delhi, India;

    Banaras Hindu Univ, Sch Mat Sci & Technol, Indian Inst Technol, Varanasi 221005, Uttar Pradesh, India;

    Banaras Hindu Univ, Sch Mat Sci & Technol, Indian Inst Technol, Varanasi 221005, Uttar Pradesh, India;

    Univ Lucknow, Dept Chem, Fac Sci, Lucknow 226007, Uttar Pradesh, India;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Nickel sulfides; Single-source precursors; Dithiolate; X-ray; OER;

    机译:硫化镍;单源前驱体;二硫代盐;X射线;OER;
  • 入库时间 2022-08-18 00:18:12

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