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Ordered Macro-Microporous Metal-Organic Framework Single Crystals and Their Derivatives for Rechargeable Aluminum-Ion Batteries

机译:用于可充电铝离子电池的有序宏观-微孔金属-有机骨架单晶及其衍生物

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摘要

Constructing ordered hierarchical porous structures while maintaining their overall crystalline order is highly desirable but remains an arduous challenge. Herein, we successfully achieve the growth of single-crystalline metal-organic frameworks (MOFs) in three-dimensional (3D) ordered macroporous template voids by a saturated solution-based double-solventassisted strategy with precise control over the nucleation process. The as-prepared single-crystalline ordered macro-microporous Co-based MOFs (SOM ZIF-67) exhibit an ordered macro-microporous structure with robust single-crystalline nature. Moreover, SOM ZIF-67 can serve as a precursor to derive 3D-ordered macroporous cobalt diselenide@carbon (3DOM CoSe2@C) through a facile carbonization-selenization treatment. The as-derived 3DOM CoSe2@C can well preserve the 3D-ordered macroporous structure of the precursor. More importantly, CoSe2 nanoparticles could be uniformly confined in the conductive ordered macroporous carbon framework, affording regularly interconnected macroporous channels and large surface area. As a result, when evaluated as a cathode material for aluminum-ion batteries, the ordered macroporous structure could not only effectively facilitate the diffusion of large-sized chloroaluminate anions but also increase the contact area with electrolyte and provide more exposed active sites, thereby exhibiting superior reversible rate capacity (86 mA h g(-1) at 5.0 A g(-1)) and remarkable cycling performance (125 mA h g(-1) after 1000 cycles at 2.0 A g(-1)).
机译:在维持其整体结晶顺序的同时构造有序的分层多孔结构是非常期望的,但是仍然是艰巨的挑战。在本文中,我们通过基于溶液的双溶剂辅助策略以及对成核过程的精确控制,成功实现了三维(3D)有序大孔模板空隙中单晶金属有机骨架(MOF)的增长。所制备的单晶有序大孔微孔Co基MOF(SOM ZIF-67)表现出具有稳健的单晶性质的有序大孔微孔结构。此外,SOM ZIF-67可以作为前体,通过简便的碳化-硒化处理获得3D顺序的大孔二硒化钴@碳(3DOM CoSe2 @ C)。如此衍生的3DOM CoSe2 @ C可以很好地保留前体的3D顺序大孔结构。更重要的是,CoSe2纳米颗粒可以均匀地限制在导电的有序大孔碳骨架中,从而提供规则互连的大孔通道和大表面积。结果,当评价为铝离子电池的正极材料时,有序的大孔结构不仅可以有效地促进大型氯铝酸根阴离子的扩散,而且可以增加与电解质的接触面积并提供更多的暴露活性位,从而展现出出色的可逆速率容量(在5.0 A g(-1)时为86 mA hg(-1))和出色的循环性能(在2.0 A g(-1)时经过1000次循环后为125 mA hg(-1))。

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  • 来源
    《Journal of the American Chemical Society》 |2019年第37期|14764-14771|共8页
  • 作者单位

    South China Univ Technol Sch Chem & Chem Engn Guangzhou 510640 Guangdong Peoples R China;

    Univ Cambridge Dept Engn Cambridge CB3 0FA England;

    South China Univ Technol Analyt & Testing Ctr Guangzhou 510640 Guangdong Peoples R China;

    Jilin Univ Coll Chem State Key Lab Inorgan Synth & Preparat Chem 2699 Qianjin St Changchun 130012 Jilin 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);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 04:58:37

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