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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >A synergetic strategy for an advanced electrode with Fe3O4 embedded in a 3D N-doped porous graphene framework and a strong adhesive binder for lithium/potassium ion batteries with an ultralong cycle lifespan
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A synergetic strategy for an advanced electrode with Fe3O4 embedded in a 3D N-doped porous graphene framework and a strong adhesive binder for lithium/potassium ion batteries with an ultralong cycle lifespan

机译:具有Fe3O4的高级电极的协同策略,嵌入3D n掺杂多孔石墨烯框架和具有超强循环寿命的锂/钾离子电池的强粘合剂粘合剂

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摘要

Fe3O4 is considered to be a prospective anode material with superior capabilities for both lithium (Li) and potassium (K) storage, but its inferior conductivity and drastic volume change upon lithiation/potassiation bring great challenges to the realization of high capacity and stable cycling. Given these circumstances, we present a facile chemical blowing method to construct a three-dimensional N-doped porous graphene framework decorated with Fe3O4 nanoparticles (Fe3O4/3DNPGF). In particular, the well-designed NPGF with massive pores and void space can not only buffer the volume variation of the embedded Fe3O4 nanoparticles associated with Li+/K+ insertion and extraction, but also reduce the steric effect, to enhance electron/ion transportation. In addition, the N-doping provides prolific active sites for electrochemical reactions and improves the electronic conductivity of the NPGF. More importantly, by introducing a novel binder material, a synergetic strategy was used to prepare robust electrodes with stronger adhesion between the active materials, conductive agents and binder material for greater tolerance towards volume change during cycling. Thus, the Fe3O4/3DNPGF electrodes demonstrated exceptional electrochemical activity in terms of high capacity, rate performance and prolonged lifespan in both lithium ion batteries (377.1 mA h g(-1) at 10 A g(-1) over 5000 cycles) and potassium ion batteries (154.6 mA h g(-1) at 1 A g(-1) over 500 cycles).
机译:Fe3O4被认为是前瞻性阳极材料,具有锂(Li)和钾(K)储存的优异能力,但其在锂化/钾的较差和剧烈体积变化会对实现高容量和稳定循环产生巨大挑战。鉴于这些情况,我们提出了一种容易化学吹塑方法,构建用Fe3O4纳米颗粒(Fe3O4 / 3DNPGF)装饰的三维N掺杂多孔石墨烯框架。特别地,具有大规模孔隙和空隙空间的精心设计的NPGF不能缓冲与Li + / K +插入和提取相关的嵌入式Fe3O4纳米颗粒的体积变化,但也降低了空间效应,以增强电子/离子运输。此外,n掺杂为电化学反应提供多平的活性位点,提高NPGF的电子电导率。更重要的是,通过引入一种新型粘合剂材料,使用协同策略来制备具有更强的粘附性,在活性材料,导电剂和粘合剂材料之间具有更强的粘附性,以便在循环期间对体积变化进行更大的耐受性。因此,Fe3O4 / 3DNPGF电极在锂离子电池(377.1mA Hg(-1)以上超过5000次循环)和钾离子的高容量,速率性能和延长的寿命方面表现出具有卓越的电化学活性。和钾离子电池(154.6 mA Hg(-1),在500次以上1Ag(-1))。

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    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

    Southwest Univ Sci &

    Technol Sch Mat Sci &

    Engn Mianyang 621010 Sichuan Peoples R China;

    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

    Univ Sci &

    Technol Beijing Beijing Adv Innovat Ctr Mat Genome Engn Inst Adv Mat &

    Technol Beijing 100083 Peoples R China;

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  • 正文语种 eng
  • 中图分类 工程材料学;
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