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首页> 外文期刊>Advanced Functional Materials >Two Birds with One Stone: Metal-Organic Framework Derived Micro-/Nanostructured Ni_2P/Ni Hybrids Embedded in Porous Carbon for Electrocatalysis and Energy Storage
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Two Birds with One Stone: Metal-Organic Framework Derived Micro-/Nanostructured Ni_2P/Ni Hybrids Embedded in Porous Carbon for Electrocatalysis and Energy Storage

机译:两鸟一石:金属有机骨架衍生的微/纳米结构Ni_2P / Ni杂化物嵌入多孔碳中进行电催化和储能

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摘要

The construction of bifunctional electrode materials for hydrogen evolution reaction (HER) and lithium-ion batteries (LIBs) has been a hot topic of research. Herein, metal-organic frameworks (MOFs) derived micro-anostructured Ni2P/Ni hybrids with a porous carbon coating (denoted as Ni2P/Ni@C) are prepared using a feasible pyrolysis-phosphidation strategy. On the one hand, the optimal Ni2P/Ni@C catalyst exhibits superior HER performance with a low overpotential of 149 mV versus a reversible hydrogen electrode (RHE) at 10 mA cm(-2) and excellent durability. The density functional theory computations verify that the strong synergistic effect between Ni2P and Ni could optimize the electronic structure, thus rendering the enhanced electrocatalytic performance. On the other hand, the Ni2P/Ni@C electrode displays a reversible capacity of 597 mAh g(-1) after 1000 cycles at 1000 mA g(-1) and improved rate capability as an anode for LIBs, owing to the well-organized micro-anostructure and conductive Ni core. In addition, the electrochemical reaction mechanism of the Ni2P/Ni@C electrode upon lithiation/delithiation is investigated in detail via ex situ X-ray powder diffraction and X-ray photoelectron spectroscopy methods. It is expected that the facile and controllable approach can be extended to fabricate other MOF-based metal phosphides/metal hybrids for electrochemical energy storage and conversion systems.
机译:用于氢析出反应(HER)和锂离子电池(LIB)的双功能电极材料的构造已成为研究的热点。在本文中,使用可行的热解-磷酸化策略制备了具有多孔碳涂层(表示为Ni2P / Ni @ C)的金属/有机骨架(MOF)衍生的微/纳米结构Ni2P / Ni杂化物。一方面,最佳的Ni2P / Ni @ C催化剂表现出卓越的HER性能,与10mA cm(-2)的可逆氢电极(RHE)相比,具有149 mV的低过电势和出色的耐久性。密度泛函理论计算证明,Ni2P和Ni之间的强协同作用可以优化电子结构,从而增强电催化性能。另一方面,Ni2P / Ni @ C电极在1000 mA g(-1)下循环1000次后,可逆容量为597 mAh g(-1),并且由于锂离子电池的阳极效应,其作为LIBs阳极的速率能力得到了改善。有组织的微/纳米结构和导电镍芯。此外,通过异位X射线粉末衍射和X射线光电子能谱方法,详细研究了Ni2P / Ni @ C电极在锂化/脱锂过程中的电化学反应机理。期望可以将这种容易且可控制的方法扩展到制造用于电化学能量存储和转换系统的其他基于MOF的金属磷化物/金属杂化物。

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  • 来源
    《Advanced Functional Materials 》 |2019年第35期| 1901510.1-1901510.9| 共9页
  • 作者单位

    Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100083, Peoples R China;

    Tsinghua Univ, Sch Mat Sci & Engn, Beijing 100084, Peoples R China;

    Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100083, Peoples R China;

    Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100083, Peoples R China;

    Tsinghua Univ, Sch Mat Sci & Engn, Beijing 100084, Peoples R China;

    Univ Sci & Technol Beijing, Inst Adv Mat & Technol, Beijing Adv Innovat Ctr Mat Genome Engn, Beijing 100083, Peoples R China;

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

    hydrogen evolution reaction; Li storage; metal-organic framework; micro-; nanostructure;

    机译:氢气进化反应;李储存;金属 - 有机框架;微型;纳米结构;

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