首页> 外文期刊>International journal of hydrogen energy >Iron-substituted Co-Ni phosphides immobilized on Ni foam as efficient self-supported 3D hierarchical electrocatalysts for oxygen evolution reaction
【24h】

Iron-substituted Co-Ni phosphides immobilized on Ni foam as efficient self-supported 3D hierarchical electrocatalysts for oxygen evolution reaction

机译:固定在镍泡沫上的铁取代的Co-Ni磷化物作为用于氧气析出反应的高效自支撑3D分层电催化剂

获取原文
获取原文并翻译 | 示例
           

摘要

Electrocatalytic water splitting for hydrogen evolution is significantly impeded by the kinetically sluggish oxygen evolution reaction (OER). Thus, the development of highly efficient and durably stable non-noble-metal OER electrocatalyst is necessary and challenging for the large-scale electrocatalytic water splitting. Herein, a series of iron-substituted cobalt-nickel phosphides grown on Ni foam (FeCoNi-P/NFs) were easily prepared though successive hydrothermal and phosphorization treatments. The chemical compositions, crystalline and electronic structures as well as surface morphologies of these resulting electrocatalysts are strongly related with the iron substitution ratio. More interestingly, the FeCoNi-P/NF-2 nanosheet arrays prepared from equivalent molar ratio of iron and cobalt precursors exhibit the best OER performance with a low overpotential of 266 mV to produce a current density of 50 mA cm(-2) and a low Tafel slope of 61.2 mV dec(-1) in 1.0 M KOH condition, which is comparable to the reported state-of-the-art OER electrocatalysts. Additionally, the FeCoNi-P/NF-2 nanosheet arrays also show satisfactory long-term durability over 60 h. The superior OER activity of the electrocatalyst is essentially attributed to the heteroatomic substitution and the unique three-dimensional hierarchical morphology, which greatly increase the electrical conductivity, afford more active sites and facilitate the efficient charge transfer ability. (C) 2019 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:动力学缓慢的氧气逸出反应(OER)严重阻碍了用于氢气逸出的电催化水分解。因此,对于大规模的电催化水分解,开发高效且持久稳定的非贵金属OER电催化剂是必要的,也是挑战。在此,通过连续的水热处理和磷化处理,可以容易地制备在镍泡沫上生长的一系列铁取代的钴镍磷化物(FeCoNi-P / NFs)。这些所得电催化剂的化学组成,晶体和电子结构以及表面形态与铁取代率密切相关。更有趣的是,由铁和钴前体的当量摩尔比制备的FeCoNi-P / NF-2纳米片阵列表现出最佳的OER性能,具有266 mV的低过电势,产生50 mA cm(-2)的电流密度和在1.0 M KOH条件下的低Tafel斜率为61.2 mV dec(-1),与报道的最新OER电催化剂相当。此外,FeCoNi-P / NF-2纳米片阵列在60小时内也显示出令人满意的长期耐久性。电催化剂优异的OER活性基本上归因于杂原子取代和独特的三维层次形态,这极大地提高了电导率,提供了更多的活性位点并促进了有效的电荷转移能力。 (C)2019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》 |2019年第16期|8156-8165|共10页
  • 作者单位

    Tianjin Normal Univ, Coll Chem, Key Lab Inorgan Organ Hybrid Funct Mat Chem, Minist Educ,Tianjin Key Lab Struct & Performance, Tianjin 300387, Peoples R China;

    Tianjin Normal Univ, Coll Chem, Key Lab Inorgan Organ Hybrid Funct Mat Chem, Minist Educ,Tianjin Key Lab Struct & Performance, Tianjin 300387, Peoples R China;

    Tianjin Normal Univ, Coll Chem, Key Lab Inorgan Organ Hybrid Funct Mat Chem, Minist Educ,Tianjin Key Lab Struct & Performance, Tianjin 300387, Peoples R China;

    Tianjin Normal Univ, Coll Chem, Key Lab Inorgan Organ Hybrid Funct Mat Chem, Minist Educ,Tianjin Key Lab Struct & Performance, Tianjin 300387, Peoples R China;

    Tianjin Normal Univ, Coll Chem, Key Lab Inorgan Organ Hybrid Funct Mat Chem, Minist Educ,Tianjin Key Lab Struct & Performance, Tianjin 300387, Peoples R China|Collaborat Innovat Ctr Chem Sci & Engn, Tianjin 300071, Peoples R China;

    Tianjin Normal Univ, Coll Chem, Key Lab Inorgan Organ Hybrid Funct Mat Chem, Minist Educ,Tianjin Key Lab Struct & Performance, Tianjin 300387, Peoples R China;

  • 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

    Trimetallic phosphide; Fe-substitution; Hierarchical nanomaterials; Oxygen evolution reaction;

    机译:三金属磷化物;铁​​取代;递阶纳米材料;析氧反应;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号