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Highly Efficient Electrocatalysts for Oxygen Reduction Reaction Based on 1D Ternary Doped Porous Carbons Derived from Carbon Nanotube Directed Conjugated Microporous Polymers

机译:基于碳纳米管定向共轭微孔聚合物衍生的一维三元掺杂多孔碳的高效氧还原反应催化剂

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摘要

One-dimensional (1D) porous materials have shown great potential for gas storage and separation, sensing, energy storage, and conversion. However, the controlled approach for preparation of 1D porous materials, especially porous organic materials, still remains a great challenge due to the poor dispersibility and solution processability of the porous materials. Here, carbon nanotube (CNT) templated 1D conjugated microporous polymers (CMPs) are prepared using a layer-by-layer method. As-prepared CMPs possess high specific surface areas of up to 623 m(2) g(-1) and exhibit strong electronic interactions between p-type CMPs and n-type CNTs. The CMPs are used as precursors to produce heteroatom-doped 1D porous carbons through direct pyrolysis. As-produced ternary heteroatom-doped (B/N/S) 1D porous carbons possess high specific surface areas of up to 750 m2 g-1, hierarchical porous structures, and excellent electrochemical-catalytic performance for oxygen reduction reaction. Both of the diffusion-limited current density (4.4 mA cm(-2)) and electron transfer number (n = 3.8) for three-layered 1D porous carbons are superior to those for random 1D porous carbon. These results demonstrate that layered and core-shell type 1D CMPs and related heteroatomdoped 1D porous carbons can be rationally designed and controlled prepared for high performance energy-related applications.
机译:一维(1D)多孔材料在气体存储和分离,传感,能量存储和转换方面显示出巨大潜力。然而,由于多孔材料的差的分散性和溶液加工性,用于制备一维多孔材料,特别是多孔有机材料的受控方法仍然仍然是巨大的挑战。在此,使用逐层方法制备碳纳米管(CNT)模板化的一维共轭微孔聚合物(CMP)。制备的CMP具有高达623 m(2)g(-1)的高比表面积,并在p型CMP和n型CNT之间表现出强大的电子相互作用。 CMP用作通过直接热解生产杂原子掺杂的一维多孔碳的前驱体。所生产的三元杂原子掺杂(B / N / S)一维多孔碳具有高达750 m2 g-1的高比表面积,分层的多孔结构以及对氧还原反应的出色电化学催化性能。三层一维多孔碳的扩散极限电流密度(4.4 mA cm(-2))和电子转移数(n = 3.8)均优于无序一维多孔碳。这些结果表明,可以合理地设计和控制层状和核壳型1D CMP以及相关的杂原子掺杂的1D多孔碳,以准备与高性能能源相关的应用。

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  • 来源
    《Advanced Functional Materials》 |2016年第45期|8255-8265|共11页
  • 作者单位

    Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai Key Lab Elect Insulat & Thermal Ageing, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

    Max Planck Inst Polymer Res, Max Planck Res Grp Organ Optoelect, Ackermannweg 10, D-55128 Mainz, Germany;

    Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China;

    Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai Key Lab Elect Insulat & Thermal Ageing, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

    Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai Key Lab Elect Insulat & Thermal Ageing, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

    Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai Key Lab Elect Insulat & Thermal Ageing, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

    Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai Key Lab Elect Insulat & Thermal Ageing, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

    Max Planck Inst Polymer Res, Max Planck Res Grp Organ Optoelect, Ackermannweg 10, D-55128 Mainz, Germany;

    Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai Key Lab Elect Insulat & Thermal Ageing, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China|Jilin Univ, Coll Chem, State Key Lab Inorgan Synth & Preparat Chem, Changchun 130012, Peoples R China;

    Shanghai Jiao Tong Univ, State Key Lab Met Matrix Composites, Shanghai Key Lab Elect Insulat & Thermal Ageing, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China;

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