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Amorphous MoS_2 nanosheets on MoO_2 films/Mo foil as free-standing electrode for synergetic electrocatalytic hydrogen evolution reaction

机译:Amorphous MOS_2纳米型在MOO_2薄膜/ MO箔上作为单独的直接电极,用于协同电催化氢进化反应

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摘要

A facile oxidation-sulfidation strategy is proposed to fabricate the vertically aligned amorphous MoS2 nanosheets on MoO2 films/Mo foil (MF) as free-standing electrode, which features as the integration of three merits (high conductivity, abundant exposures of active sites, and enhanced mass transfer) into one electrode for hydrogen evolution reaction (HER). Density functional theory (DFT) calculations reveal the strong interaction between MoS2 and MoO2, which can enhance the intrinsic conductivity with narrow bandgap, and decreases hydrogen adsorption free energy (Delta G(H). = similar to 0.06 eV) to facilitate the HER process. Benefiting from the unique hierarchical structure with amorphous MoS2 nanosheets on conductive MoO2 films/MF to facilitate the electron/mass transfer by eliminate contact resistance, controllable number of stacking layers and size of MoS2 slabs to expose more edge sites, the optimal MoS2/MoO2/MF exhibits outstanding activity with overpotential of 154 mV at the current density of 10 mA cm(-2), Tafel slope of 52.1 mV dec(-1), and robust stability. Furthermore, the intrinsic HER activity (us. ECSA) on MoS2/MoO2 /MF is significantly enhanced, which shows 4.5 and 18.6 times higher than those of MoS2/MF and MoO2/MF at overpotential of 200 mV, respectively. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:提出了一种容易氧化 - 硫化策略,用于在MOO2薄膜/ MO箔(MF)上作为独立电极制造垂直对齐的无定形MOS2纳米片,其具有三种优点的整合(高导电性,活性位点暴露,以及增强的传质)进入一个电极,用于氢化反应(她)。密度函数理论(DFT)计算揭示MOS2和MOO2之间的强相互作用,其可以增强具有窄带隙的内在电导率,并降低氢吸收自由能量(Delta G(H)。=类似于0.06eV)以促进她的过程。从独特的层次结构受益于导电MOO2薄膜/ MF上的无晶态MOS2纳米片,以促进通过消除接触电阻,可控数量的堆叠层和MOS2板的尺寸来促进电子/质量传递,以露出更多的边缘位点,最佳MOS2 / MOO2 / MF在10 mA cm(-2)的电流密度为154 mV的过电位,TAFEL斜率为52.1mV(-1),稳定稳定性,呈现出优异的活动。此外,MOS2 / MOO2 / MF上的内在活动(ECSA)显着增强,分别显示4.5%和18.6倍,分别在200mV的过电位下的MOS2 / MF和MOO2 / MF的4.5%和18.6倍。 (c)2020氢能源出版物LLC。 elsevier有限公司出版。保留所有权利。

著录项

  • 来源
    《International journal of hydrogen energy》 |2020年第35期|17422-17433|共12页
  • 作者单位

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 Peoples R China;

    China Univ Petr State Key Lab Heavy Oil Proc Beijing 102249 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

    Amorphous MoS2 nanosheets; Conductive MoO2 films/Mo; Self-supported electrode; Hydrogen evolution reaction; Density functional theory;

    机译:无定形MOS2纳米片;导电MOO2薄膜/ MO;自支撑电极;氢气进化反应;密度函数理论;

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