4.0 V Aqueous Li-Ion Batteries

被引:486
作者
Yang, Chongyin [1 ]
Chen, Ji [1 ]
Qing, Tingting [1 ]
Fan, Xiulin [1 ]
Sun, Wei [1 ]
von Cresce, Arthur [2 ]
Ding, Michael S. [2 ]
Borodin, Oleg [2 ]
Vatamanu, Jenel [2 ]
Schroeder, Marshall A. [1 ]
Eidson, Nico [1 ,2 ]
Wang, Chunsheng [1 ]
Xu, Kang [2 ]
机构
[1] Univ Maryland, Dept Chem & Biomol Engn, College Pk, MD 20740 USA
[2] US Army Res Lab, Electrochem Branch, Sensor & Electron Devices Directorate, Power & Energy Div, Adelphi, MD 20783 USA
关键词
IN-SALT ELECTROLYTE;
D O I
10.1016/j.joule.2017.08.009
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
Although recent efforts have expanded the stability window of aqueous electrolytes from 1.23 V to > 3 V, intrinsically safe aqueous batteries still deliver lower energy densities (200 Wh/kg) compared with state-of-the-art Li-ion batteries (similar to 400 Wh/ kg). The essential origin for this gap comes from their cathodic stability limit, excluding the use of themost ideal anodematerials (graphite, Limetal). Here, we resolved this ''cathodic challenge'' by adopting an ''inhomogeneous additive'' approach, in which a fluorinated additive immiscible with aqueous electrolyte can be applied on anode surfaces as an interphase precursor coating. The strong hydrophobicity of the precursor minimizes the competitive water reduction during interphase formation, while its own reductive decomposition forms a unique composite interphase consisting of both organic and inorganic fluorides. Such effective protection allows these high-capacity/low-potential anode materials to couple with different cathode materials, leading to 4.0 V aqueous Li-ion batteries with high efficiency and reversibility.
引用
收藏
页码:122 / 132
页数:11
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