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首页> 外文期刊>ACS nano >Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction
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Vacancy Occupation-Driven Polymorphic Transformation in Cobalt Ditelluride for Boosted Oxygen Evolution Reaction

机译:用于增强氧气进化反应的钴Ditellide中空位占用的多态性转化

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摘要

Transition-metal dichalcogenides (TMDs) hold great potential as an advanced electrocatalyst for oxygen evolution reaction (OER), but to date the activity of transition metal telluride catalysts are demonstrated to be poor for this reaction. In this study, we report the activation of CoTe2 for OER by doping secondary anions into Te vacancies to trigger a structural transition from the hexagonal to the orthorhombic phase. The achieved orthorhombic CoTe2 with partial vacancies occupied by P-doping exhibits an exceptional OER catalytic activity with an overpotential of only 241 mV at 10 mA cm(-2) and a robust stability more than 24 h. The combined experimental and theoretical studies suggest that the defective phase transformation is controllable and allows the synergism of vacancy, doping as well as the reconstructed crystallographic structure, ensuring more exposure of catalytic active sites, rapid charge transfer, and energetically favorable intermediates. This vacancy occupation-driven strategy of structural transformation can also be manipulated by S- and Se-doping, which may offer useful guidance for developing tellurides-based electrocatalyst for OER.
机译:过渡金属二甲硅藻(TMDS)作为氧气进化反应(oer)的先进电催化剂保持巨大潜力,但迄今为止过渡金属碲化酯催化剂的活性被证明在该反应中差。在这项研究中,我们通过将二次阴离子掺杂到Te空位中来报告OER的COTE2激活,以触发从六边形到正交相位的结构转变。通过p掺杂占用的部分空位的实现的正交蛋白质具有出色的oer催化活性,其具有在10 mA cm(-2)的241mV的过电位,并且稳健的稳定性超过24小时。该组合的实验和理论研究表明,缺陷相变度是可控的,并且允许空位,掺杂以及重建的晶体结构的协同作用,确保更多地暴露催化活性位点,快速电荷转移和能量有利的中间体。这种空缺职业驱动的结构转化策略也可以通过S-和SE掺杂来操纵,这可能为oer提供基于碲化物的电催化剂提供有用的指导。

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