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首页> 外文期刊>ACS nano >Active Sites Implanted Carbon Cages in Core Shell Architecture: Highly Active and Durable Electrocatalyst for Hydrogen Evolution Reaction
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Active Sites Implanted Carbon Cages in Core Shell Architecture: Highly Active and Durable Electrocatalyst for Hydrogen Evolution Reaction

机译:活性部位在碳核壳结构中植入碳笼:用于氢释放反应的高活性和持久性电催化剂

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摘要

Low efficiency and poor stability are two major challenges we encounter in the exploration of non-noble metal electrocatalysts for the hydrogen evolution reaction (HER) in both acidic and alkaline environment. Herein, the hybrid of cobalt encapsulated by N, B codoped ultrathin carbon cages (Co@BCN) is first introduced as a highly active and durable nonprecious metal electrocatalysts for HER, which is constructed by a bottom-up approach using metal organic frameworks (MOFs) as precursor and self-sacrificing template. The optimized catalyst exhibited remarkable electrocatalytic performance for hydrogen production from both both acidic and alkaline media. Stability investigation reveals the overcoating of carbon cages can effectively avoid the corrosion and oxidation of the catalyst under extreme acidic and alkaline environment. Electrochemical active surface area (EASA) evaluation and density functional theory (DFT) calculations revealed that the synergetic effect between the encapsulated cobalt nanoparticle and the N, B codoped carbon shell played the fundamental role in the superior HER catalytic performance.
机译:低效率和差的稳定性是我们在探索用于酸性和碱性环境中的析氢反应(HER)的非贵金属电催化剂时遇到的两个主要挑战。在此,首先引入了由N,B共掺杂的超薄碳笼(Co @ BCN)封装的钴​​的杂化物,作为HER的高活性和耐用性非贵金属电催化剂,它是通过自下而上的方法使用金属有机骨架(MOF)构建)作为先驱和自我牺牲的模板。优化的催化剂对于从酸性和碱性介质中制氢均表现出卓越的电催化性能。稳定性研究表明,碳笼罩的外涂层可以有效避免催化剂在极端酸性和碱性环境下的腐蚀和氧化。电化学活性表面积(EASA)评估和密度泛函理论(DFT)计算表明,封装的钴纳米颗粒与N,B共掺杂的碳壳之间的协同作用在优异的HER催化性能中起着基本作用。

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