Angewandte Chemie International Edition · 2019 · 111 citations · 28 references
Natural SciencesChemical EngineeringMaterials ScienceElectrochemistryEnergy MaterialsInorganic ChemistryBattery Cell ChemistryBattery MaterialsElectrochemical CellsElectrochemical Energy StorageElectrolyte SolutionsSolid ElectrolytesAlkali Metal ChemistryAqueous BatteriesAqueous ElectrolytesElectrochemical WindowElectrolytesEnergy DensityHydration ShellsSodium-ion Batteries
Abstract Aqueous Na‐ or K‐ion batteries could virtually eliminate the safety and cost concerns raised from Li‐ion batteries, but their widespread applications have generally suffered from narrow electrochemical potential window (ca. 1.23 V) of aqueous electrolytes that leads to low energy density. Herein, by exploring optimized eutectic systems of Na and K salts with asymmetric imide anions, we discovered, for the first time, room‐temperature hydrate melts for Na and K systems, which are the second and third alkali metal hydrate melts reported since the first discovery of Li hydrate melt by our group in 2016. The newly discovered Na‐ and K‐ hydrate melts could significantly extend the potential window up to 2.7 and 2.5 V (at Pt electrode), respectively, owing to the merit that almost all water molecules participate in the Na + or K + hydration shells. As a proof‐of‐concept, a prototype Na 3 V 2 (PO 4 ) 2 F 3 |NaTi 2 (PO 4 ) 3 aqueous Na‐ion full‐cell with the Na‐hydrate‐melt electrolyte delivers an average discharge voltage of 1.75 V, that is among the highest value ever reported for all aqueous Na‐ion batteries.
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