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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >In situ nitridated porous nanosheet networked Co3O4-Co4N heteronanostructures supported on hydrophilic carbon cloth for highly efficient electrochemical hydrogen evolution
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In situ nitridated porous nanosheet networked Co3O4-Co4N heteronanostructures supported on hydrophilic carbon cloth for highly efficient electrochemical hydrogen evolution

机译:原位氮化多孔纳米片网络化CO3O4-CO4N杂酐,支持高效电化学氢气进化的亲水性碳布

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摘要

Three-dimensional Co3O4-Co4N porous nanosheet network (PNSN) heterostructures were controllably prepared on hydrophilic carbon cloth (HCC) through in situ plasma nitridation of cobalt hydroxide, and the Co4N grains were observed to grow epitaxially on Co3O4 with an orientation relationship of Co3O4 (331)//Co4N (111). To achieve effective loading of active materials, we demonstrated a simpler and more eco-friendly approach to ameliorate the hydrophilicity of carbon cloth through hydrogen plasma treatment. The Co3O4-Co4N PNSNs/HCC obtained under optimized conditions showed high catalytic activity and excellent stability for the hydrogen evolution reaction (HER) under basic conditions, e.g., a low overpotential of 90 mV at 10 mA cm(-2) and a low Tafel slope of 57.8 mV dec(-1). It was revealed that the electron transfer from Co3O4 to Co4N enabled the nanohybrid to have a synergistic effect in terms of the desorption of H-ad and the release of OH- during the HER, leading to an enhanced intrinsic activity. Moreover, a large number of active sites and a fast charge transport capability of the hybrid system also played beneficial roles in achieving an outstanding HER performance. The in situ plasma nitridation technique provides an alternative approach for developing new nitride-hybridized catalysts based on earth-abundant materials for electrolytic hydrogen production.
机译:通过氢氧化钴的硫化碳布(HCC)对亲水碳布(HCC)进行三维CO3O4-CO4N多孔纳米型网络(PNSN)异质结构,并且观察到CO 4N晶粒在CO3O4的取向关系上外延生长( 331)// CO4N(111)。为实现有效负载活性材料,我们证明了一种更简单和更环保的方法来改善碳布通过氢等离子体处理的亲水性。在优化条件下获得的CO 3 O 4-CO 4N PNSNS / HCC显示出高催化活性和在基本条件下的氢进化反应(她)的优异稳定性,例如,在10 mA cm(-2)和低Tafel下为90mV的低过电位57.8 mV Dec(-1)坡度。据透露,来自CO3O4至CO 4N的电子转移使纳米冬小化在H-AD的解吸方面具有协同效应和在她们期间的OH-释放,导致增强的内在活性。此外,混合系统的大量积极场所和快速充电传输能力也在实现优异的性能方面发挥了有益的作用。原位等离子体氮化技术提供了一种替代方法,用于基于用于电解氢生产的土坯材料的新型氮化物杂交催化剂的替代方法。

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    City Univ Hong Kong Dept Mat Sci &

    Engn Ctr Super Diamond &

    Adv Films COSDAF Kowloon Tat Chee Ave Hong Kong Peoples R China;

    City Univ Hong Kong Dept Mat Sci &

    Engn Ctr Super Diamond &

    Adv Films COSDAF Kowloon Tat Chee Ave Hong Kong Peoples R China;

    Hong Kong Univ Sci &

    Technol Inst Mol Funct Mat Inst Adv Study Dept Chem Div Biomed Engn Kowloon Clear Water Bay Hong Kong Peoples R China;

    City Univ Hong Kong Dept Mech &

    Biomed Engn Kowloon Tat Chee Ave Hong Kong Peoples R China;

    City Univ Hong Kong Dept Chem Ctr Super Diamond &

    Adv Films COSDAF Kowloon Tat Chee Ave Hong Kong Peoples R China;

    City Univ Hong Kong Dept Chem Ctr Super Diamond &

    Adv Films COSDAF Kowloon Tat Chee Ave Hong Kong Peoples R China;

    Anhui Univ Technol Sch Chem &

    Chem Engn Maanshan 243032 Anhui Peoples R China;

    City Univ Hong Kong Dept Mat Sci &

    Engn Ctr Super Diamond &

    Adv Films COSDAF Kowloon Tat Chee Ave Hong Kong Peoples R China;

    City Univ Hong Kong Dept Mech &

    Biomed Engn Kowloon Tat Chee Ave Hong Kong Peoples R China;

    City Univ Hong Kong Dept Chem Ctr Super Diamond &

    Adv Films COSDAF Kowloon Tat Chee Ave Hong Kong Peoples R China;

    City Univ Hong Kong Dept Mat Sci &

    Engn Ctr Super Diamond &

    Adv Films COSDAF Kowloon Tat Chee Ave Hong Kong 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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