首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >Templated constructing honeycomb-like V5S8@C anode with multi-scale interfacial coactions and high pseudocapacitive contribution for enhanced potassium storage capability
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Templated constructing honeycomb-like V5S8@C anode with multi-scale interfacial coactions and high pseudocapacitive contribution for enhanced potassium storage capability

机译:模板化构建蜂窝状v5s8 @ c anode,具有多尺度的界面连接和高假型蓄能贡献,可增强钾储存能力

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摘要

Potassium-ion batteries (PIBs) are considered as the promising candidate for lithium-ion batteries (LIBs) nowadays, due to its abundance natural reserves and similar operation mechanisms. However, owing to the larger radius of K+ ions, the nanostructure of anode materials is easily destroyed during repeatedly intercalation/extraction process as well as fast fades of specific capacity. Therefore, constructing rational nanostructure for anode material is a significant approach to enhance the durability of PIBs. In this work, we rationally proposed a dual strategy including inducing numerous regular artificial pores in nanostructure with a honeycomb-like morphology and building multi-scale interfacial coactions between the V5S8 skeleton and exterior graphene nanosheets. Attributing to these advantages, the as-prepared V5S8@C composite exhibits an enhanced potassium storage performances, which delivers an initial charge capacity of 479.1 mAh g(-1) at 0.05 A g(-1) and a capacity of 121.5 mAh g(-1) after 500 cycles at 1 A g(-1). The further reaction kinetics results suggest the electrochemical reaction is mainly dominated by pseudocapacitive charge storage process. Our work has shed light on rational designing nanostructure for advanced electrode material in energy storage fields. (C) 2020 Elsevier B.V. All rights reserved.
机译:钾离子电池(PIB)因其丰富的自然储量和类似的运行机制,被认为是锂离子电池(LIB)的最有希望的候选电池。然而,由于K+离子半径较大,在反复插层/萃取过程中,阳极材料的纳米结构容易被破坏,比容量快速衰减。因此,为阳极材料构建合理的纳米结构是提高PIB耐久性的重要途径。在这项工作中,我们合理地提出了一种双重策略,包括在具有蜂窝状形貌的纳米结构中诱导大量规则的人工孔,以及在V5S8骨架和外部石墨烯纳米片之间建立多尺度界面作用。鉴于这些优势,我们准备好了V5S8@C复合材料的储钾性能增强,在0.05 A g(-1)下的初始充电容量为479.1 mAh g(-1),在1 A g(-1)下进行500次循环后的容量为121.5 mAh g(-1)。进一步的反应动力学结果表明,电化学反应主要由假电容电荷储存过程控制。我们的工作为合理设计储能领域的先进电极材料的纳米结构提供了依据。(C) 2020爱思唯尔B.V.版权所有。

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