Breaking Anionic Solvation Barrier for Safe and Durable Potassium-ion Batteries Under Ultrahigh-Voltage Operation

Yong-Li Heng, Dr. Zhen-Yi Gu, Han-Hao Liu, Dr. Hao-Jie Liang, Yating Deng, Prof. Jian Zhao, Xiao-Tong Wang, Zi-Hang Xue, Dr. Hong-Yan Lü, Prof. Xing-Long Wu
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Abstract

Ultrahigh-voltage potassium-ion batteries (PIBs) with cost competitiveness represent a viable route towards high energy battery systems. Nevertheless, rapid capacity decay with poor Coulombic efficiencies remains intractable, mainly attributed to interfacial instability from aggressive potassium metal anodes and cathodes. Additionally, high reactivity of K metal and flammable electrolytes pose severe safety hazards. Herein, a weakly solvating fluorinated electrolyte with intrinsically nonflammable feature is successfully developed to enable an ultrahigh-voltage (up to 5.5 V) operation. Through breaking the anionic solvation barrier, synergistic interfacial modulation can be achieved by the formation of robust anion-derived inorganic-rich electrode-electrolyte interfaces on both the cathode and anode. As proof of concept, a representative KVPO4F cathode can sustain 1600 cycles with 84.4 % of capacity retention at a high cutoff voltage of 4.95 V. Meanwhile, K plating/stripping process in our designed electrolyte also demonstrates optimized electrochemical reversibility and stability with effectively inhibited potassium dendrites. These findings underscore the critical impact of anion-dominated solvation configuration on synergistic interfacial modulation and electrochemical properties. This work provides new insights into rational design of ultrahigh-voltage and safe electrolyte for advanced PIBs.

打破阴离子溶解障碍,打造超高电压下安全耐用的钾离子电池
具有成本竞争力的超高压钾离子电池(PIBs)是实现高能电池系统的可行途径。然而,库仑效率差的快速容量衰减仍然是难以解决的问题,主要是由于侵略性钾金属阳极和阴极的界面不稳定。此外,K金属的高反应性和易燃电解质构成严重的安全隐患。本文成功地开发了一种具有本质不可燃特性的弱溶剂化氟化电解质,以实现超高压(高达5.5 V)的工作。通过打破阴离子溶剂化屏障,可以通过在阴极和阳极上形成强大的阴离子衍生的富无机电极-电解质界面来实现协同界面调制。作为概念验证,典型的KVPO4F阴极在4.95 V的高截止电压下可以维持1600次循环,容量保持率为84.4%。同时,在我们设计的电解液中镀/剥离K的过程也表现出优化的电化学可逆性和稳定性,有效地抑制了钾枝晶。这些发现强调了阴离子主导的溶剂化构型对协同界面调制和电化学性能的关键影响。本研究为先进pib超高压安全电解液的合理设计提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Angewandte Chemie
Angewandte Chemie 化学科学, 有机化学, 有机合成
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