电解质
相间
材料科学
碳酸盐
钾
碳酸钾
化学工程
离子
无机化学
电极
纳米技术
冶金
物理化学
有机化学
化学
遗传学
生物
工程类
作者
Ling Ni,Shu Zhang,Chuanchuan Li,Jie Lü,Junfeng Li,Jinzhi Wang,Shenghang Zhang,Guansheng Chen,Zengqi Zhang,Sun Fu,Gaojie Xu,Zili Cui,Guanglei Cui
标识
DOI:10.1002/adfm.202400570
摘要
Abstract Potassium batteries have received extensive attention as a promising grid‐level storage technology. However, the anodes in potassium batteries using conventional carbonate‐based electrolyte systems always suffer from severe capacity deterioration, due to the heterogeneous and highly swollen solid‐electrolyte interphase (SEI) layer. Herein, a rigid‐flexible compact SEI consisting of rigid inner KF layer and flexible crosslinked oligomeric K–B(OCH 2 CH 2 ) n (modified KEO), is designed by tailoring cation–anion coordination in 1 m carbonate electrolyte based on the main salt—potassium perfluorinated pinacolatoborate, (KB(O 2 C 2 (CF 3 ) 4 ) 2 , abbreviated as KPFB). Specifically, the KPFB tunes K + −anions coordinated configuration in K + solvation sheaths by unique spatial structure and strong electron‐withdrawing effect of its eight −CF 3 groups. With the assistance of rigid‐flexible compact SEI layer, the potassium metal symmetric cells stably cycle for more than 1600 hours in the conventional carbonate electrolyte (1 m KPFB‐EC/DEC). Moreover, K||graphite and K||Prussian blue (PB) batteries adopting this conventional carbonate electrolyte can operate for more than 500 and 120 cycles with high average Coulombic efficiency of 99.7% and 99.4%, respectively. The work provides new insights in customizing salt anion structure to reinforce SEI layer for high‐performance potassium batteries.
科研通智能强力驱动
Strongly Powered by AbleSci AI