石墨界面的协同动力学调制使超快和耐用的钾离子电池成为可能

IF 19 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Xuemei Ma, Hongwei Fu, Hang Xia, Yongmin He, Dianwei Zhang, Yaqin Wu, Jiawan Zhou, Jiang Zhou, Ling Fan, Bingan Lu
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引用次数: 0

摘要

石墨由于具有较高的理论比容量和良好的充放电平台,被认为是钾离子电池最具商业化前景的负极材料。然而,在传统的基于kpf6的电解质中,钾离子(K+)通过固体电解质间相(SEI)传输缓慢阻碍了实际实施,导致速率能力差和循环耐久性差。在石墨表面(SiO2- graphite)构建纳米结构的SiO2修饰层来调节界面动力学,使其具有更快的K+扩散能力和更低的K+迁移势垒。值得注意的是,在传统的kpf6基电解质中,sio2 -石墨阳极具有高的初始库仑效率(84.1%),优异的循环稳定性(400次循环,容量保持率为71%)和高倍率容量(213 mAh g−1,高电流密度为500 mA g−1)。此外,PB|| sio2 -石墨全电池还表现出良好的循环稳定性(循环600次后容量保持90%)和优异的倍率性能(电流密度为2000 mA g−1时的高比容量),优于大多数先前报道的PIBs系统。这种界面动力学调节策略为提高电极的循环稳定性和速率能力提供了新的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synergistic Kinetics Modulation at Graphite Interface Enables Ultrafast and Durable Potassium-Ion Batteries

Synergistic Kinetics Modulation at Graphite Interface Enables Ultrafast and Durable Potassium-Ion Batteries

Synergistic Kinetics Modulation at Graphite Interface Enables Ultrafast and Durable Potassium-Ion Batteries

Graphite has been considered as the most promising anode material for potassium-ion batteries (PIBs) commercialization due to its high theoretical specific capacity and favorable charge-discharge platform. Nevertheless, in conventional KPF6-based electrolytes, the practical implementation is hindered by sluggish potassium-ion (K+) transport through solid electrolyte interphase (SEI), leading to poor rate capability and inferior cycling durability. A nanostructured SiO2 modification layer is constructed on a graphite surface (SiO2-Graphite) to regulate the interfacial kinetics, which can enable a faster K+ diffusion capability and lower K+ migration barrier. Notably, the SiO2-Graphite anode exhibits high initial Coulombic efficiency (84.1%), excellent cycling stability (400 cycles with a capacity retention of 71%), and high-rate capability (213 mAh g−1 at a high current density of 500 mA g−1) in conventional KPF6-based electrolyte. In addition, the PB||SiO2-Graphite full cell also demonstrates good cycling stability (90% capacity retention after 600 cycles) and excellent rate performance (high specific capacity at a current density of 2000 mA g−1), which outperforms that of most previously reported PIBs systems. This interfacial kinetics regulation strategy provides new insights into improving the cycling stability and rate capability of electrodes.

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来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
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