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一种基于金属有机框架的、用于析氢和析氧反应的、由嵌入氮掺杂竹节状碳纳米管的硒化钴纳米颗粒构成的高效双功能催化剂。

A highly effective bifunctional catalyst of cobalt selenide nanoparticles embedded nitrogen-doped bamboo-like carbon nanotubes toward hydrogen and oxygen evolution reactions based on metal-organic framework.

作者信息

Ding Hui, Xu Guancheng, Zhang Li, Wei Bei, Hei Jincheng, Chen Liang

机构信息

Key Laboratory of Energy Materials Chemistry, Ministry of Education, Key Laboratory of Advanced Functional Materials, Autonomous Region, Institute of Applied Chemistry, Xinjiang University, Urumqi 830046, Xinjiang, PR China.

Key Laboratory of Energy Materials Chemistry, Ministry of Education, Key Laboratory of Advanced Functional Materials, Autonomous Region, Institute of Applied Chemistry, Xinjiang University, Urumqi 830046, Xinjiang, PR China.

出版信息

J Colloid Interface Sci. 2020 Apr 15;566:296-303. doi: 10.1016/j.jcis.2020.01.096. Epub 2020 Jan 25.

DOI:10.1016/j.jcis.2020.01.096
PMID:32007740
Abstract

Metal selenides as highly efficient bifunctional electrocatalysts were extensively applied to water-splitting technology. In present work, N-doped graphitized carbon wrapped CoSe nanoparticles (NPs) with in-situ grown bamboo-like carbon nanotube (CoSe@N/C-CNT) was successfully synthesized via a Co-Ade (Adenine) MOF-derived selenylation strategy. Each CNT was capped with CoSe NP, which not only effectively avoided self-agglomeration of CoSe NPs but also protected the CoSe NPs from electrolyte etching. The synergism of bamboo-like CNT with high conductivity and the uniformly distributed CoSe NPs endowed CoSe@N/C-CNT the better bifunctional electrocatalytic activities toward both HER (hydrogen evolution reaction) and OER (oxygen evolution reaction). To generate a current density of 10 mA cm, CoSe@N/C-CNT exerted as low as overpotential (η) of 185 mV vs. RHE (reversible hydrogen electrode) and 340 mV vs. RHE for HER and OER, the corresponding Tafel slopes were 98 and 107 mV dec respectively. In addition, CoSe@N/C-CNT exhibited superior durability with negligible attenuation after long-term stability test.

摘要

金属硒化物作为高效双功能电催化剂被广泛应用于水分解技术。在本工作中,通过一种基于钴 - 腺嘌呤(Adenine)金属有机框架(MOF)衍生的硒化策略,成功合成了原位生长竹节状碳纳米管包裹的氮掺杂石墨化碳包覆的硒化钴纳米颗粒(CoSe@N/C-CNT)。每个碳纳米管都被硒化钴纳米颗粒覆盖,这不仅有效避免了硒化钴纳米颗粒的自团聚,还保护了硒化钴纳米颗粒免受电解质侵蚀。具有高导电性的竹节状碳纳米管与均匀分布的硒化钴纳米颗粒之间的协同作用,赋予了CoSe@N/C-CNT对析氢反应(HER)和析氧反应(OER)更好的双功能电催化活性。为了产生10 mA cm的电流密度,CoSe@N/C-CNT对HER和OER的过电位(η)分别低至相对于可逆氢电极(RHE)为185 mV和340 mV,相应的塔菲尔斜率分别为98和107 mV dec。此外,CoSe@N/C-CNT在长期稳定性测试后表现出优异的耐久性,衰减可忽略不计。

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引用本文的文献

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Cobalt-Based Metal-Organic Frameworks and Their Derivatives for Hydrogen Evolution Reaction.
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Front Chem. 2020 Nov 20;8:592915. doi: 10.3389/fchem.2020.592915. eCollection 2020.