ACS Energy Letters · 2020 · 232 citations · 45 references
Natural SciencesChemistryMaterials ScienceElectrochemistryInorganic ChemistryMaterials ChemistryBattery Cell ChemistryBattery MaterialsElectrochemical CellsElectrochemical Energy StorageElectrode MaterialsMetal OxidesAqueous BatteriesBattery ChemistryBattery Electrode MaterialsElectrochemical CharacterizationElectrochemical IntercalationElectrolyte ChemistryElectrolytesZinc-ion Battery Materials
Vanadium oxides have been recognized to be among the most promising positive electrode materials for aqueous zinc metal batteries (AZMBs). However, their underlying intercalation mechanisms are still vigorously debated. To shed light on the intercalation mechanisms, high-performance δ-V2O5 is investigated as a model compound. Its structural and electrochemical behaviors in the designed cells with three different electrolytes, i.e., 3 m Zn(CF3SO3)2/water, 0.01 M H2SO4/water, and 1 M Zn(CF3SO3)2/acetonitrile, demonstrate that the conventional structural and elemental characterization methods cannot adequately clarify the separate roles of H+ and Zn2+ intercalations in the Zn(CF3SO3)2/water electrolyte. Thus, an operando pH determination method is developed and used toward Zn/δ-V2O5 AZMBs. This method indicates the intercalation of both H+ and Zn2+ into δ-V2O5 and uncovers an unusual H+/Zn2+-exchange intercalation–deintercalation mechanism. Density functional theory calculations further reveal that the H+/Zn2+ intercalation chemistry is a consequence of the variation of the electrochemical potential of Zn2+ and H+ during the electrochemical intercalation/release.
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Recent Advances in Aqueous Zinc-Ion Batteries
Guozhao Fang, Jiang Zhou, Anqiang Pan et al. · ACS Energy Letters · 2018 · 2.2K citations