摘要
Although graphite anodes operated with representative de/intercalation patterns at low potentials are considered highly desirable for K-ion batteries,the severe capacity fading caused by consecutive reduction reactions on the aggressively reactive surface is inevitable given the scarcity of effective protecting layers.Herein,by introducing a flame-retardant localized high-concentration electrolyte with retentive solvation configuration and relatively weakened anion-coordination and non-solvating fluorinated ether,the rational solid electrolyte interphase characterized by well-balanced inorganic/organic components is tailored in situ.This effectively prevented solvents from excessively decomposing and simultaneously improved the resistance against K-ion transport.Consequently,the graphite anode retained a prolonged cycling capability of up to 1400 cycles(245 mA h g,remaining above 12 mon)with an excellent capacity retention of as high as 92.4%.This is superior to those of conventional and high-concentration electrolytes.Thus,the optimized electrolyte with moderate salt concentration is perfectly compatible with graphite,providing a potential application prospect for K-storage evolution.
在钾离子电池石墨负极中,钾离子在石墨层间嵌入/脱出的模式能够实现储能,且具有较低工作电位和廉价等优势,表现出巨大的吸引力.然而,在缺乏足够界面保护等条件下,石墨负极在传统碳酸酯类电解液中容易发生连续的副反应,充放电容量会面临严重的持续衰减.本文从电解液设计的角度出发,针对石墨负极的钾离子存储问题,配制了阻燃的局部高浓度电解液,其特有的溶剂化结构可调控石墨表面固体电解质界面相,改善界面的结构稳定性和离子传导特性,从而实现石墨负极储钾的高稳定循环.同时,电解液的高阻燃特性也为钾离子电池的高安全性提供了保障.
作者
Hao-Jie Liang
Zhen-Yi Gu
Xin-Xin Zhao
Jin-Zhi Guo
Jia-Lin Yang
Wen-Hao Li
Bao Li
Zhi-Ming Liu
Zhong-Hui Sun
Jing-Ping Zhang
Xing-Long Wu
梁皓杰;谷振一;赵欣欣;郭晋芝;杨佳霖;李文灏;李苞;刘治明;孙中辉;张景萍;吴兴隆(Key Laboratory for UV Light-Emitting Materials and Technology of Ministry of Education,Northeast Normal University,Changchun 130024,China;Department of Chemistry,Northeast Normal University,Changchun 130024,China;School of Chemistry and Chemical Engineering,Henan Normal University,Xinxiang 453007,China;College of Electromechanical Engineering,Shandong Engineering Laboratory for Preparation and Application of High-performance Carbon-Materials,Qingdao University of Science and Technology,Qingdao 266061,China;Center for Advanced Analytical Science,School of Chemistry and Chemical Engineering,Key Laboratory for Water Quality and Conservation of the Pearl River Delta of Ministry of Education,Guangzhou University,Guangzhou 510006,China)
基金
supported by the National Natural Science Foundation of China(91963118 and 52173246)
Science Technology Program of Jilin Province(20200201066JC)
the 111 Project(B13013)。