Towards Sustainable Energy Storage: Evaluating Polymer Electrolytes for Zinc Ion Batteries
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arXiv
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| Format: | Preprint |
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2025
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| _version_ | 1866910927338602496 |
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| author | Rajabi, Roya Sun, Shichen Wu, Booker Khan, Jamil Huang, Kevin |
| author_facet | Rajabi, Roya Sun, Shichen Wu, Booker Khan, Jamil Huang, Kevin |
| contents | Polymer electrolytes present a promising solution to the challenges posed by aqueous electrolytes in energy storage systems, offering the flexibility needed for wearable electronics. Despite the increasing interest in polymer electrolyte-based zinc ion batteries (ZIBs), their development is still in its early stages due to various challenges. In this study, we fabricated three promising polymer electrolytes: CSAM (carboxyl methyl chitosan with acrylamide monomer), PAM (polyacrylamide monomer hydrogel electrolyte), and p-PBI (Phosphoric acid (PA)-doped polybenzimidazole) with Zn(ClO4)2 and Zn(OTf)2, for their application in zinc ion batteries. Our results demonstrated that PAM hydrogel electrolyte exhibited very low LDH formation after a long cycle, demonstrating effective protection for zinc foil, and the high mechanical stability of the p-PBI membrane provided prolonged durability against short circuits through the formation of LDH. The presence of carboxyl groups in CSAM and the formation of O-H bonding facilitated ion movement, resulting in enhanced ionic conductivity, and preventing dendrite formation. Incorporating these hydrogels with high-performance zinc salts, such as zinc triflate (Zn(OTf)2), resulted in impressive stability, with the symmetric cell demonstrating over 4000 hours of uniform and stable voltage profile under 1 mA/cm2 and low overpotential of around 53 mV cycling with CSAM. The full-cell battery with PBI-T membrane showed the highest durability and capacity compared to CSAM-T and PAM-T, due to the greater availability of free protons for storing zinc in the cathode. |
| format | Preprint |
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arxiv_https___arxiv_org_abs_2505_01890 |
| institution | arXiv |
| publishDate | 2025 |
| record_format | arxiv |
| spellingShingle | Towards Sustainable Energy Storage: Evaluating Polymer Electrolytes for Zinc Ion Batteries Rajabi, Roya Sun, Shichen Wu, Booker Khan, Jamil Huang, Kevin Materials Science Systems and Control Polymer electrolytes present a promising solution to the challenges posed by aqueous electrolytes in energy storage systems, offering the flexibility needed for wearable electronics. Despite the increasing interest in polymer electrolyte-based zinc ion batteries (ZIBs), their development is still in its early stages due to various challenges. In this study, we fabricated three promising polymer electrolytes: CSAM (carboxyl methyl chitosan with acrylamide monomer), PAM (polyacrylamide monomer hydrogel electrolyte), and p-PBI (Phosphoric acid (PA)-doped polybenzimidazole) with Zn(ClO4)2 and Zn(OTf)2, for their application in zinc ion batteries. Our results demonstrated that PAM hydrogel electrolyte exhibited very low LDH formation after a long cycle, demonstrating effective protection for zinc foil, and the high mechanical stability of the p-PBI membrane provided prolonged durability against short circuits through the formation of LDH. The presence of carboxyl groups in CSAM and the formation of O-H bonding facilitated ion movement, resulting in enhanced ionic conductivity, and preventing dendrite formation. Incorporating these hydrogels with high-performance zinc salts, such as zinc triflate (Zn(OTf)2), resulted in impressive stability, with the symmetric cell demonstrating over 4000 hours of uniform and stable voltage profile under 1 mA/cm2 and low overpotential of around 53 mV cycling with CSAM. The full-cell battery with PBI-T membrane showed the highest durability and capacity compared to CSAM-T and PAM-T, due to the greater availability of free protons for storing zinc in the cathode. |
| title | Towards Sustainable Energy Storage: Evaluating Polymer Electrolytes for Zinc Ion Batteries |
| topic | Materials Science Systems and Control |
| url | https://arxiv.org/abs/2505.01890 |