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Co NP/NC hollow nanoparticles derived from yolk-shell structured ZIFs@polydopamine as bifunctional electrocatalysts for water oxidation and oxygen reduction reactions

机译:卵黄结构的ZIFs @ polydopamine衍生的Co NP / NC空心纳米颗粒作为双功能电催化剂,用于水氧化和氧还原反应

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摘要

The pyrolysis under inert atmosphere has been widely used for the synthesis of metal containing heteroatoms doped carbon materials,versatile catalysts for various reactions.However,it is difficult to prevent metal nanoparticles aggregation during pyrolysis process.Herein,we reported the efficient synthesis of nitrogen doped carbon hollow nanospheres with cobalt nanoparticles (Co NP,ca.1Onm in size) distributed uniformly in the shell via pyrolysis of yolk-shell structured Zn-Co-ZIFs@polydopamine (PDA).PDA acted as both protection layer and carbon source,which successfully prevented the aggregation of cobalt nanoparticles during high-temperature pyrolysis process.The Co NP and N containing carbon (Co NP/NC) hollow nanospheres were active for both oxygen evolution reaction (OER) and oxygen reduction reaction (ORR),affording overpotential of 430mY at 10mA/cm2 for OER in 1 M KOH and comparable half-wave potential to that of Pt/C (0.80V vs RHE) for ORR in 0.1 M KOH.The superior performance of carbon hollow nanospheres for both OER and ORR was mainly attributed to its small metal nanoparticles,N-doping and hollow nanostructure.The protection and confinement effect that originated from PDA coating strategy could be extended to the synthesis of other hollow structured carbon materials,especially the ones with small metal nanoparticles.
机译:惰性气氛下的热解反应已被广泛用于合成含金属的杂原子掺杂碳材料,各种反应的多功能催化剂。然而,在热解过程中很难防止金属纳米颗粒的聚集。在此,我们报道了氮掺杂的有效合成。通过卵黄壳结构的Zn-Co-ZIFs @ polydopamine(PDA)的热解,具有钴纳米颗粒(Co NP,尺寸约1Onm)的碳空心纳米球均匀地分布在壳中。PDA既是保护层又是碳源。成功地防止了高温热解过程中钴纳米粒子的聚集。含碳纳米管和碳纳米管(Co NP / NC)对氧释放反应(OER)和氧还原反应(ORR)均具有活性,从而提供了超电势在1 M KOH中的OER为10mA / cm2时为430mY,与在0.1 M KOH中的ORR在Pt / C时具有可比的半波电势(0.80V vs RHE)用于OER和ORR的碳中空纳米球主要归因于其小的金属纳米颗粒,N掺杂和中空纳米结构。源自PDA涂层策略的保护和限制作用可以扩展到其他中空结构碳材料的合成,特别是那些带有小的金属纳米粒子。

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  • 来源
    《天然气化学(英文版)》 |2018年第4期|1261-1267|共7页
  • 作者单位

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    Dalian National Laboratory for Clean Energy, Dalian Institute of Chemical Physics, Chinese Academy of Sciences,Dalian 116023, Liaoning, China;

    The Key Laboratory of Fuel Cell Technology of Guangdong Province(&)The Key Laboratory of New Energy Technology of Guangdong Universities, School of Chemistry and Chemical Engineering,South China University of Technology, Guangzhou 510641, Guangdong, China;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

    State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, Liaoning, China;

  • 收录信息 中国科学引文数据库(CSCD);中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
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