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Polyaniline engineering defect-induced nitrogen doped carbon-supported Co_3O_4 hybrid composite as a high-efficiency electrocatalyst for oxygen evolution reaction

机译:聚苯胺工程缺陷诱导的氮掺杂碳负载的CO_3O_4杂化复合材料作为氧进化反应的高效电催化剂

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摘要

The development of earth-abundance electrocatalyst with high performance for oxygen evolution reaction (OER) is of paramount importance in sustainable water splitting. Herein, the novel defect-induced nitrogen-doped carbon-supported Co(3)O(4 )nanoparticles is successfully fabricated as OER electrocatalyst (denoted as Co3O4/CN HNPs) through a wetness-impregnation treatment of Co/polyaniline (PANI) followed by a thermal annealing. This advanced architecture of Co3O4/CN HNPs can not only improve its conductivity and electrocatalytically active sites but also generate a large number of oxygen-vacancy defects and crystal defects, which effectively exert the preponderance in facilitating interfacial electronic transfer and optimizing the adsorption energy for intermediates, thus imparting the extraordinary activities in catalyzing OER. In addition, there are evidences demonstrating the formation of C-N coordination bonds through the strong interaction of the interconnected interface and the generation of pyridinic-N species after the annealing treatment, which enables the structural stability to get further strengthened and accelerates oxygen releasing for reduction of OER overpotential, respectively. Benefiting from the above desirable properties, the Co3O4/CN HNPs affords a lower overpotential of 290 mV at a current density of 10 mA cm(-2) as compared to those of pure Co(3)O(4 )and PANI, outperforming commercial IrO2 and the representative Co3O4-based OER electrocatalysts as recently reported. Moreover, the Co3O4/CN HNPs also exhibits long durability with negligible activity degeneration at a current density of 10 mA cm(-2) for 20 h.-.
机译:具有高性能的氧气进化反应(OER)的地球丰富电催化剂的发展对可持续水分裂至关重要。在此,通过湿润 - 浸渍处理,新建的缺陷诱导的氮掺杂碳负载的CO(3)α纳米颗粒被成功地制造为Oer电催化剂(表示为CO3O4 / CN HNPS),润湿浸渍处理通过热退火。 Co3O4 / CN HNPS的这种先进架构不仅可以改善其电导率和电象性活性地点,而且还产生大量的氧气空位缺陷和晶体缺陷,这有效地施加了促进界面电子转移和优化中间体吸附能量的优势,从而赋予催化Oer中的非凡活动。此外,还有证据表明通过互连的界面和退火处理后的吡啶-N物种的强相互作用形成CN配位键,这使得结构稳定性能够进一步加强并加速氧气释放以减少氧气OER过幂。受益于上述理想性质,与纯CO(3)O(4)和PANI相比,CO 3O4 / CN HNPS在10mA cm(-2)的电流密度下,290 mV的下电位为290 mV,相比IRO2和基于代表的CO3O4的OER电催化剂如最近报道。此外,CO 3 O 4 / CN HNPS还表现出长期耐久性,其在电流密度为10mA cm(-2)的可忽略不计的活性变性。

著录项

  • 来源
    《Applied Surface Science》 |2020年第1期|146626.1-146626.9|共9页
  • 作者单位

    Dongguan Univ Technol Sch Mat Sci & Engn Dongguan 523808 Guangdong Peoples R China|Univ Technol Sydney Fac Sci Ctr Clean Energy Technol Sch Math & Phys Sci Sydney NSW 2007 Australia|Xi An Jiao Tong Univ Sch Sci Dept Appl Chem Xian 710049 Peoples R China;

    ShanghaiTech Univ Sch Phys Sci & Technol Shanghai 201210 Peoples R China;

    Dongguan Univ Technol Sch Mat Sci & Engn Dongguan 523808 Guangdong Peoples R China|Univ Technol Sydney Fac Sci Ctr Clean Energy Technol Sch Math & Phys Sci Sydney NSW 2007 Australia;

    Donghua Univ Coll Mat Sci & Engn State Key Lab Modificat Chem Fibers & Polymer Mat Innovat Ctr Text Sci & Technol Shanghai 201620 Peoples R China;

    Dongguan Univ Technol Sch Mat Sci & Engn Dongguan 523808 Guangdong Peoples R China;

    Univ Technol Sydney Fac Sci Ctr Clean Energy Technol Sch Math & Phys Sci Sydney NSW 2007 Australia;

    Donghua Univ Coll Mat Sci & Engn State Key Lab Modificat Chem Fibers & Polymer Mat Innovat Ctr Text Sci & Technol Shanghai 201620 Peoples R China;

    Donghua Univ Coll Mat Sci & Engn State Key Lab Modificat Chem Fibers & Polymer Mat Innovat Ctr Text Sci & Technol Shanghai 201620 Peoples R China;

    Univ Technol Sydney Fac Sci Ctr Clean Energy Technol Sch Math & Phys Sci Sydney NSW 2007 Australia;

    Dongguan Univ Technol Sch Mat Sci & Engn Dongguan 523808 Guangdong Peoples R China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    OER; Co3O4/CN HNPs; Crystal defect sites; Oxygen-vacancy sites; Strong interactions;

    机译:oer;co3o4 / cn hnps;晶体缺陷网站;氧空位;强烈的相互作用;

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