Chen Jiewei, Luo Bi, Chen Qiushui, Li Fei, Guo Yanjiao, Wu Tom, Peng Peng, Qin Xian, Wu Gaoxiang, Cui Mengqi, Liu Lehao, Chu Lihua, Jiang Bing, Li Yingfeng, Gong Xueqing, Chai Yang, Yang Yongping, Chen Yonghua, Huang Wei, Liu Xiaogang, Li Meicheng
State Key Laboratory of Alternate Electrical Power System with Renewable Energy Sources, North China Electric Power University, Beijing, 102206, China.
Department of Chemistry, National University of Singapore, Singapore, 117543, Singapore.
Adv Mater. 2020 Apr;32(14):e1905578. doi: 10.1002/adma.201905578. Epub 2020 Feb 26.
The rate-determining process for electrochemical energy storage is largely determined by ion transport occurring in the electrode materials. Apart from decreasing the distance of ion diffusion, the enhancement of ionic mobility is crucial for ion transport. Here, a localized electron enhanced ion transport mechanism to promote ion mobility for ultrafast energy storage is proposed. Theoretical calculations and analysis reveal that highly localized electrons can be induced by intrinsic defects, and the migration barrier of ions can be obviously reduced. Consistently, experiment results reveal that this mechanism leads to an enhancement of Li/Na ion diffusivity by two orders of magnitude. At high mass loading of 10 mg cm and high rate of 10C, a reversible energy storage capacity up to 190 mAh g is achieved, which is ten times greater than achievable by commercial crystals with comparable dimensions.
电化学储能的速率决定过程很大程度上由电极材料中发生的离子传输决定。除了缩短离子扩散距离外,提高离子迁移率对于离子传输至关重要。在此,提出了一种局部电子增强离子传输机制,以促进超快储能中的离子迁移率。理论计算和分析表明,固有缺陷可诱导产生高度局域化的电子,并且离子的迁移势垒可明显降低。实验结果一致表明,该机制使锂/钠离子扩散率提高了两个数量级。在10 mg cm的高质量负载和10C的高倍率下,实现了高达190 mAh g的可逆储能容量,这比具有可比尺寸的商业晶体所能达到的容量大十倍。