| Autor: |
Zhu D; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Li J; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Zheng Z; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Ye S; Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan., Pan Y; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Wu J; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., She F; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Lai L; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Zhou Z; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Chen J; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Li H; Advanced Institute for Materials Research (WPI-AIMR), Tohoku University, Sendai 980-8577, Japan., Wei L; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia., Chen Y; School of Chemical and Biomolecular Engineering, The University of Sydney, Darlington, New South Wales 2006, Australia. |
| Abstrakt: |
Zinc-ion batteries (ZIBs) are promising energy storage devices with safe, nonflammable electrolytes and abundant, low-cost electrode materials. Their practical applications are hampered by various water-related undesirable reactions, such as the hydrogen evolution reaction (HER), corrosion of zinc metal, and water-induced decay of cathode materials. Polymer hydrogel electrolytes were used to control these reactions. However, salt, water, and polymeric backbones intervene in polymer hydrogels, and currently, there are no systematic studies on how salt and water concentrations synergistically affect polymer hydrogels' electrochemical performance. Here, we used an in situ polymerization method to synthesize polyacrylamide (PAM) hydrogels with varied Zn(ClO 4 ) 2 (0.5 to 2.0 mol kg -1 ) and water (40 to 90 wt %) concentrations. Their electrochemical performances in Zn||Ti half-cells, Zn||Zn symmetrical cells, and Zn||V 2 O 5 full cells have been comprehensively evaluated. Although the ionic conductivity of electrolytes increases with the salt concentration, a high salt concentration of 2.0 mol kg -1 with more Zn 2+ solvated H 2 O would induce more severe HER and Zn corrosion at the electrolyte/electrode interfaces. A narrow window of the water concentration at 70-80 wt % is optimal to balance needs for achieving a high ionic conductivity and restricting water-related undesirable reactions. The chemically more active water counts roughly 64.1-73.1 wt % of the total water in electrolytes. PAM hydrogel electrolyte with 1.0 mol kg -1 Zn(ClO 4 ) 2 and 80 wt % water enables 1200 h of stable cycling in a Zn||Zn symmetric cell and 99.24% of Coulombic efficiency in a Zn||Ti half-cell. Due to the water-induced decay of V 2 O 5 , the electrolyte with 70 wt % water delivers the best performance in a Zn||V 2 O 5 full cell, which can retain 73.7% of its initial capacity after 400 charge/discharge cycles. Our results show that achieving precise control of salt and water concentrations of hydrogel electrolytes in their optimal windows to reduce the fraction of chemically more active water while retaining high ionic conductivity is essential to enabling high-performance ZIBs. |
