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Reduced graphene oxide-supported cobalt oxide decorated N-doped graphitic carbon for efficient bifunctional oxygen electrocatalysis

机译:将石墨烯氧化物负载的钴氧化物装饰为N掺杂的石墨碳,用于有效双官能氧电催化

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摘要

A high-performance composite bifunctional electrocatalyst for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) has been synthesized via in situ growth of a hybrid precursor of graphene oxide (GO) and cobalt-based zeolite imidazolium framework (ZIF-67) under hydrothermal condition, followed by calcination at elevated temperature. The as-prepared composite bifunctional catalyst is confirmed to possess a structure of N-GC/Co@CoO/rGO, with core–shell nanoparticles of Co@CoO encapsulated in nitrogen-doped graphitic carbon (N-GC) thin layers which are then overall supported by reduced graphene oxide (rGO) sheets. With N-GC furnishing high population of ORR active sites, CoO being active for OER which is further enhanced by a highly conductive metal core, rGO sheets enhancing the overall electronic conduction, as well as the multiple synergistic couplings in the composite materials, pronounced ORR and OER catalytic activities with superior stability have been achieved. The catalysts also showed excellent tolerance to the crossover effect to methanol, showing great potential in energy-related applications requiring efficient oxygen electrocatalysis.
机译:用于氧还原反应(ORR)和氧气进化反应(OER)的高性能复合双功能电催化剂通过石墨烯(GO)和钴基沸石咪唑鎓框架(ZIF-67)的杂交前体(ZIF-67)的原位生长合成在水热条件下,然后在升高温度下进行煅烧。确认AS制备的复合双官能催化剂具有N-GC / CO @ CoO / RGO的结构,其中CO烷基纳米颗粒包封在氮气掺杂的石墨碳(N-GC)薄层中。然后通过还原的石墨烯(RGO)片材总体支撑。利用N-GC提供高矿物活性位点,COO为OER,通过高导电金属芯进一步增强,RGO板增强了整体电子传导,以及复合材料中的多种协同耦合,发音为ORR已经实现了具有卓越稳定性的OER催化活动。催化剂还表现出对甲醇的交叉效果的优异耐受性,显示出需要有效氧电胞电催化的能量相关应用的巨大潜力。

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