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首页> 外文期刊>Advanced Functional Materials >Molybdenum and Phosphorous Dual Doping in Cobalt Monolayer Interfacial Assembled Cobalt Nanowires for Efficient Overall Water Splitting
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Molybdenum and Phosphorous Dual Doping in Cobalt Monolayer Interfacial Assembled Cobalt Nanowires for Efficient Overall Water Splitting

机译:钴单层界面组装钴纳米线中的钼和磷双掺杂,用于高效整体水分裂

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摘要

The necessity for better water splitting requires speedy development of efficient catalysts with high activity, long-term stability, and cost effectiveness. In this work, a bifunctional catalyst originating from the interfacial assembly of a thin Mo,P-codoped Co layer (approximate to 50 nm) shelled Co nanowire (Co-Mo-P/CoNWs) network is fabricated via a facile approach. The catalyst exhibits low overpotentials of 0.08 and 0.27 V to reach a current response of 20 mA cm(-2)for the hydrogen evolution reaction and oxygen evolution reaction, respectively, together with long-term stability in 1.0mKOH medium. The outstanding performance is further demonstrated by a Co-Mo-P/CoNWs-based electrolyzer, which enables a cell voltage of only 1.495 V to reach 10 mA cm(-2), superior to one derived from commercial (Pt/C + RuO2/C) as well as to various reports recently published elsewhere. It is recognized that the formation of multiactive centers together with the increased active site number caused by Mo and P dual doping synergistically promote both hydrogen and oxygen evolution performance. Such a hybrid material opens a new approach for developing efficient and cost-effective catalysts for water splitting application.
机译:更好的水分分裂的必要性需要快速发展高效,长期稳定性和成本效益的高效催化剂。在这项工作中,通过容易的方法制造源自薄Mo的薄Mo,P型Popeed Co层(近似至50nm)壳Co纳米线(Co-Mo-P / CoWs)网络的双官能催化剂。催化剂表现出0.08和0.27V的低过电位,以达到氢进化反应和氧进化反应的20mA cm(-2)的电流响应,以及在1.0MKOH培养基中的长期稳定性。基于CO-MO-P / CONWS的电解槽进一步证明了出色的性能,这使得仅1.495V的电池电压达到10 mA cm(-2),优于来自商业广告(PT / C + RUO2 / c)以及最近在其他地方发布的各种报告。人们认识到,组成多功率中心以及由Mo和P双掺杂引起的增加的活性位点协同促进氢气和氧气进化性能。这种混合材料开辟了一种新方法,用于开发用于水分裂施用的高效且经济高效的催化剂。

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  • 来源
    《Advanced Functional Materials》 |2020年第34期|2002533.1-2002533.12|共12页
  • 作者单位

    Jeonbuk Natl Univ Adv Mat Inst BIN Convergence Technol BK21 Plus Global Program Dept BIN Convergence Technol Jeonju 54896 Jeonbuk South Korea;

    Jeonbuk Natl Univ Adv Mat Inst BIN Convergence Technol BK21 Plus Global Program Dept BIN Convergence Technol Jeonju 54896 Jeonbuk South Korea;

    Jeonbuk Natl Univ Adv Mat Inst BIN Convergence Technol BK21 Plus Global Program Dept BIN Convergence Technol Jeonju 54896 Jeonbuk South Korea;

    Jeonbuk Natl Univ Div Sci Educ Jeonju 54896 Jeonbuk South Korea;

    Jeonbuk Natl Univ Adv Mat Inst BIN Convergence Technol BK21 Plus Global Program Dept BIN Convergence Technol Jeonju 54896 Jeonbuk South Korea;

    Jeonbuk Natl Univ Adv Mat Inst BIN Convergence Technol BK21 Plus Global Program Dept BIN Convergence Technol Jeonju 54896 Jeonbuk South Korea|Jeonbuk Natl Univ Carbon Composite Res Ctr Dept Polymer Nano Sci & Technol Jeonju 54896 Jeonbuk South Korea;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    bifunctional electrocatalysts; core@shell structured networks; Molybdenum; overall water splitting; P-codoped Co layers;

    机译:双功能电催化剂;核心@ shell结构网络;钼;整体水分裂;p-copoped co层;

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