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由BiOCO和MXene组装而成的异质结构通过激发内建电场增强钾离子存储性能

Heterostructures Assembled from BiOCO and MXene for Boosted Potassium-Ion Storage by Arousing the Built-in Electric Field.

作者信息

Chen Song, Ma Heping, Du Yibo, Tian Miao, Wang Zhitao, Fan Shuang, Zhang Wenming, Yang Hui Ying

机构信息

Hebei Key Laboratory of Optic-Electronic Information and Materials, National & Local Joint Engineering Laboratory of New Energy Photoelectric Devices, College of Physics Science and Technology, Hebei University, Baoding, 071002, China.

Hebei Key Laboratory of Optic-Electronic Information Materials, College of Physics Science and Technology, Hebei University, Baoding, 071002, China.

出版信息

Small. 2024 Aug;20(34):e2401314. doi: 10.1002/smll.202401314. Epub 2024 Apr 22.

Abstract

Bismuth-based materials have been recognized as the appealing anodes for potassium-ion batteries (PIBs) due to their high theoretical capacity. However, the kinetics sluggishness and capacity decline induced by the structure distortion predominately retard their further development. Here, a heterostructure of polyaniline intercalated BiOCO/MXene (BOC-PA/MXene) hybrids is reported via simple self-assembly strategy. The ingenious design of heterointerface-rich architecture motivates significantly the interior self-built-in electric field (IEF) and high-density electron flow, thus accelerating the charge transfer and boosting ion diffusion. As a result, the hybrids realize a high reversible specific capacity, satisfying rate capability as well as long-term cycling stability. The in/ex situ characterizations further elucidate the stepwise intercalation-conversion-alloying reaction mechanism of BOC-PA/MXene. More encouragingly, the full cell investigation further highlights its competitive merits for practical application in further PIBs. The present work not only opens the way to the design of other electrodes with an appropriate working mechanism but also offers inspiration for built-in electric-field engineering toward high-performance energy storage devices.

摘要

铋基材料因其高理论容量而被认为是钾离子电池(PIB)有吸引力的阳极。然而,结构畸变引起的动力学迟缓以及容量下降主要阻碍了它们的进一步发展。在此,通过简单的自组装策略报道了一种聚苯胺插层的BiOCO/MXene(BOC-PA/MXene)杂化物的异质结构。富含异质界面结构的巧妙设计极大地激发了内部自建立电场(IEF)和高密度电子流,从而加速了电荷转移并促进了离子扩散。结果,该杂化物实现了高可逆比容量、良好的倍率性能以及长期循环稳定性。原位/非原位表征进一步阐明了BOC-PA/MXene的逐步插层-转化-合金化反应机制。更令人鼓舞的是,全电池研究进一步突出了其在进一步的PIB实际应用中的竞争优势。本工作不仅为设计具有适当工作机制的其他电极开辟了道路,也为高性能储能器件的内建电场工程提供了灵感。

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