| Literature DB >> 31068723 |
Chongyin Yang1, Ji Chen1, Xiao Ji1, Travis P Pollard2, Xujie Lü3, Cheng-Jun Sun4, Singyuk Hou1, Qi Liu4,5, Cunming Liu4, Tingting Qing1, Yingqi Wang3, Oleg Borodin2, Yang Ren4, Kang Xu2, Chunsheng Wang6,7.
Abstract
The use of 'water-in-salt' electrolytes has considerably expanded the electrochemical window of aqueous lithium-ion batteries to 3 to 4 volts, making it possible to couple high-voltage cathodes with low-potential graphite anodes1-4. However, the limited lithium intercalation capacities (less than 200 milliampere-hours per gram) of typical transition-metal-oxide cathodes5,6 preclude higher energy densities. Partial7,8 or exclusive9 anionic redox reactions may achieve higher capacity, but at the expense of reversibility. Here we report a halogen conversion-intercalation chemistry in graphite that produces composite electrodes with a capacity of 243 milliampere-hours per gram (for the total weight of the electrode) at an average potential of 4.2 volts versus Li/Li+. Experimental characterization and modelling attribute this high specific capacity to a densely packed stage-I graphite intercalation compound, C3.5[Br0.5Cl0.5], which can form reversibly in water-in-bisalt electrolyte. By coupling this cathode with a passivated graphite anode, we create a 4-volt-class aqueous Li-ion full cell with an energy density of 460 watt-hours per kilogram of total composite electrode and about 100 per cent Coulombic efficiency. This anion conversion-intercalation mechanism combines the high energy densities of the conversion reactions, the excellent reversibility of the intercalation mechanism and the improved safety of aqueous batteries.Entities:
Year: 2019 PMID: 31068723 DOI: 10.1038/s41586-019-1175-6
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962