Enabling highly stable quasi-solid-state zinc ion battery by a dual-network wood-based hydrogel electrolyte
Aqueous zinc-ion batteries have received much attention due to its low-cost, high safety and environmental-friendliness, however, the zinc anode is suffered from water-induced parasitic reactions and zinc dendrites. Herein, a wood-based hydrogel electrolyte is developed to reduce the water activity and guide the zinc ions deposition, which is mainly attributed to the formed dual-network between the polyacrylamide chain and the oriented wood fibers. The obtained hydrogel electrolyte exhibits a high ionic conductivity (10.9 mS·cm −1 ) with an outstanding tensile strength of 250 kPa. By taking advantages of these unique characteristics, the assembled Zn symmetric battery shows stable cycling lifespan for 2000 h at the current density of 1 mA·cm −2 with a fixed capacity of 1 mAh·cm −2 . Even at a high current density of 5 mA·cm −2 , the symmetric battery still works stably for over 400 h. Moreover, the Zn//Cu asymmetric battery with the hydrogel electrolyte delivers a high average Coulombic Efficiency of 98.7% for over 200 cycles. Besides, the full battery with the hydrogel electrolyte exhibits a long cycling lifespan of 1000 cycles at 4 A·g −1 , further confirming its functions of stabilizing zinc anode. This design of the dual-network structure in the wood-based hydrogel electrolyte provides an innovative approach for developing high-performance and dendrite-free quasi-solid-state zinc ion battery.
Authors
- Yiying Ling
- Chaozheng Liu (ORCID: https://orcid.org/0000-0003-4168-8289)
- Lei Ye (ORCID: https://orcid.org/0000-0003-2272-677X)
- Genmiao Wan
- Jihua Bai
- Bo Lin
- Changtong Mei
- Cheng Yong
- Weimin Chen
Institutions
- Nanjing Forestry University (CN)
- Jiangsu Academy of Agricultural Sciences (CN)
Publication Details
- Journal
- Journal of Energy Storage
- Published
- 2026-09-15
- DOI
- https://doi.org/10.1016/j.est.2026.124566
- Primary Topic
- Advanced battery technologies research
- Type
- article
- Field-Weighted Citation Impact
- 0.00