首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Conceptual design of three-dimensional CoN/Ni3N-coupled nanograsses integrated on N-doped carbon to serve as efficient and robust water splitting electrocatalysts
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Conceptual design of three-dimensional CoN/Ni3N-coupled nanograsses integrated on N-doped carbon to serve as efficient and robust water splitting electrocatalysts

机译:基于N掺杂碳的三维CON / NI3N耦合纳米草的概念设计用作高效且鲁棒的水分裂电催化剂

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Developing binder-free, low-cost, and efficient electrocatalysts for water splitting is very important to meet the ever-increasing global energy demands. We have judiciously designed a polyaniline (PANI)-mediated protocol for the synthesis of nickel-cobalt nitride (NCN) heterostructures on carbon cloth (CC) to be applied as catalysts for full electrochemical splitting of water. Controlled pyrolyzation of the nickel-cobalt precursor on PANI-coated CC generates assembled grass-like nanostructures of cobalt nitride (CoN) and nickel nitride (Ni3N) along with beneficial, conductive nitrogen-doped carbon layers on CC for improved electrochemical activity. The generation of numerous catalytically active centers with expeditious charge and mass transportation due to the incorporated nickel and high mechanical stability owing to the self-supporting nature of the designed material result in excellent and stable electrocatalytic performance. The designed NCN/CC electrode requires low overpotentials (eta(10)) of 247 and 68 mV to attain a current density of 10 mA cm(-2) during oxygen evolution and hydrogen evolution reactions, respectively, with appreciable stability ( 90% retention of the initial current density) over a 24 h long electrochemical test in 1.0 M KOH. Finally, the NCN/CC electrocatalyst is utilized to demonstrate full alkaline water splitting at a cell voltage of 1.56 V to deliver the current density of 10 mA cm(-2) with tremendous stability over 240 h. Moreover, NCN/CC could afford a stable current density of 10 mA cm(-2) towards full water splitting at 1.59 V cell voltage in acidic electrolyte with 100 h long-term stability. These results suggest its prospects as a substitute for expensive noble-metal-based water splitting electrocatalysts in practical applications.
机译:开发无粘合剂,低成本和有效的水裂缝的有效电催化剂对于满足不断增加的全球能源需求非常重要。我们明智地设计了一种聚苯胺(PANI)介导的方案,用于合成碳布(CC)上的氮化镍氮化镍(NCN)异质结构,以施加为催化剂,用于全电化学分裂的水。粘合涂层CC上的镍 - 钴前体的受控热解产生CC上的有益的导电氮气(Ni3N)的组装格式的氮化物(Con)和氮化镍(Ni3N)的组装草状纳米结构,以改善电化学活性。由于设计材料的自支撑性质而导致掺入的镍和高机械稳定性,具有迅速的电荷和质量运输的许多催化活性中心的产生导致电催化性能优异且稳定的电催化性能。设计的NCN / CC电极需要247和68mV的低过电(ETA(10)),以分别在氧化过程中获得10 mA cm(-2)的电流密度,分别具有可观的稳定性(& 90初始电流密度的百分比%在1.0 m KOH中超过24小时电化学试验。最后,利用NCN / CC电催化剂在1.56V的电池电压下展示全碱性水分解,以提供10 mA cm(-2)的电流密度,具有巨大稳定性超过240小时。此外,NCN / CC可以在酸性电解质中为1.59V细胞电压的稳定电流密度为10 mA cm(-2),以100h的长期稳定性。这些结果表明,其前景作为实际应用中昂贵的贵金属水分水分裂电催化剂的替代。

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