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Aqueous Li-ion battery enabled by halogen conversion-intercalation chemistry in graphite.
Yang, Chongyin; Chen, Ji; Ji, Xiao; Pollard, Travis P; Lü, Xujie; Sun, Cheng-Jun; Hou, Singyuk; Liu, Qi; Liu, Cunming; Qing, Tingting; Wang, Yingqi; Borodin, Oleg; Ren, Yang; Xu, Kang; Wang, Chunsheng.
Afiliação
  • Yang C; Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, USA.
  • Chen J; Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, USA.
  • Ji X; Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, USA.
  • Pollard TP; Electrochemistry Branch, Power and Energy Division, Sensor and Electron Devices Directorate, US Army Research Laboratory, Adelphi, MD, USA.
  • Lü X; Center for High Pressure Science and Technology Advanced Research, Shanghai, China.
  • Sun CJ; X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, IL, USA.
  • Hou S; Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, USA.
  • Liu Q; X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, IL, USA.
  • Liu C; Department of Physics, City University of Hong Kong, Hong Kong, China.
  • Qing T; X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, IL, USA.
  • Wang Y; Department of Chemical and Biomolecular Engineering, University of Maryland, College Park, MD, USA.
  • Borodin O; Center for High Pressure Science and Technology Advanced Research, Shanghai, China.
  • Ren Y; Electrochemistry Branch, Power and Energy Division, Sensor and Electron Devices Directorate, US Army Research Laboratory, Adelphi, MD, USA.
  • Xu K; X-ray Science Division, Advanced Photon Source, Argonne National Laboratory, Argonne, IL, USA.
  • Wang C; Electrochemistry Branch, Power and Energy Division, Sensor and Electron Devices Directorate, US Army Research Laboratory, Adelphi, MD, USA.
Nature ; 569(7755): 245-250, 2019 05.
Article em En | MEDLINE | ID: mdl-31068723
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.

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Nature Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Bases de dados: MEDLINE Idioma: En Revista: Nature Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Estados Unidos