Unraveling the Complex Role of Iodide Additives in Li-O2 Batteries

被引:102
|
作者
Qiao, Yu [1 ,4 ]
Wu, Shichao [1 ]
Sun, Yang [1 ]
Guo, Shaohua [1 ,2 ,3 ]
Yi, Jin [1 ]
He, Ping [2 ,3 ]
Zhou, Haoshen [1 ,2 ,3 ,4 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Energy Technol Res Inst, 1-1-1 Umezono, Tsukuba, Ibaraki 3058568, Japan
[2] Nanjing Univ, Natl Lab Solid State Microstruct, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Dept Energy Sci & Engn, Nanjing 210093, Jiangsu, Peoples R China
[4] Univ Tsukuba, Grad Sch Syst & Informat Engn, 1-1-1 Tennoudai, Tsukuba, Ibaraki 3058573, Japan
来源
ACS ENERGY LETTERS | 2017年 / 2卷 / 08期
基金
日本科学技术振兴机构;
关键词
REDOX MEDIATOR; OXYGEN REDUCTION; LIOH FORMATION; RECHARGEABILITY; DISCHARGE; WATER; GROWTH; LI2O2; ELECTROLYTE; LIMITATIONS;
D O I
10.1021/acsenergylett.7b00462
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Lithium iodide (LiI) has garnered considerable attention in aprotic Li-O-2 batteries. However, the reaction mechanism is still under hot debate and is attracting increasing controversy due to contrasting observations. Herein, on the basis of thorough evidence, a relevant mechanism has been systematically illustrated. LiI has been revealed to promote the superoxide-related nucleophilic attack toward electrolyte by catalyzing the decomposition of peroxide intermediate, resulting in the accumulation of LiOH and other parasitic products. Also, they refuse to be oxidized by not only triiodide (I-3(-)) but also iodine (I-2), resulting in inevitable degradation. However, as a proton-donor, water can buffer the superoxide-related nucleophilic attack by reducing it to moderate hydroperoxide (HO2-). More importantly, the catalysis of iodide toward speroxide is restrained with the increase of alkalinity in water-contained electrolyte, resulting in the formation of Li2O2. Turning LiOH into Li2O2, the newly proposed mechanism leads to revolutionary reunderstanding toward the role of iodide and water in Li-O-2 battery systems.
引用
收藏
页码:1869 / 1878
页数:10
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