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Epitaxial Growth and Integration of Insulating Metal-Organic Frameworks in Electrochemistry

机译:电化学中绝缘金属 - 有机框架的外延生长和集成

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摘要

With tunable pore size and rich active metal centers, metal-organic frameworks (MOFs) have been regarded as the one of the promising materials for catalysis. Prospectively, employing MOFs in electrochemistry would notably broaden the scope of electrocatalysis. However, this application is largely hindered by MOFs' conventionally poor electrical conductivity. Integrating MOFs without compromising their crystalline superiority holds a grand challenge to unveil their pristine electrocatalytic properties. In this work, we introduce an epitaxial growth strategy to accomplish the efficient integration of the insulating MOFs into electrochemistry. Particularly, with pristine-graphene-templated growth, the two-dimensional (2D) single-crystal MOF possesses a large lateral size of similar to 23 mu m and high aspect ratio up to, similar to 1500 and exhibits a significant electrochemical enhancement, with a charge transfer resistance of similar to 200 ohm and a 30 mA cm(-2) current density at only 0.53 V versus a reversible hydrogen electrode. The epitaxial strategy could be further applied to other 2D substrates, such as MoS2. This MOF/graphene 2D architecture sheds light on integrating insulating MOFs into electrochemical applications.
机译:通过可调谐孔径和丰富的活性金属中心,金属有机框架(MOFS)被认为是催化材料之一。前瞻性地,在电化学中使用MOF将尤其会扩大电催化的范围。然而,该应用主要受到Mofs的传统差的导电性。整合MOF而不损害其结晶优势,呈现出巨大的挑战,以推出其原始电催化性能。在这项工作中,我们介绍了一个外延生长策略,以实现绝缘MOF的有效整合到电化学中。特别是,具有原始 - 石墨烯 - 模板化的生长,二维(2D)单晶MOF具有与23μm和高纵横比相似的大横向尺寸,同样为1500并且具有显着的电化学增强电荷传递电阻与200欧姆和30mA cm(-2)电流密度相似,仅为0.53V而可逆氢电极。外延策略可以进一步应用于其他2D基板,例如MOS2。该MOF /石墨烯2D架构揭示了将绝缘MOF集成到电化学应用中。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2019年第28期|11322-11327|共6页
  • 作者单位

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 Peoples R China|Fudan Univ iChEM Collaborat Innovat Ctr Chem Energy Mat Shanghai 200433 Peoples R China;

    Fudan Univ Dept Chem Shanghai 200433 Peoples R China|Fudan Univ Shanghai Key Lab Mol Catalysis & Innovat Mat Shanghai 200433 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);
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