98%
921
2 minutes
20
Zn-I batteries have emerged as promising next-generation energy storage systems owing to their inherent safety, environmental compatibility, rapid reaction kinetics, and small voltage hysteresis. Nevertheless, two critical challenges, i.e., zinc dendrite growth and polyiodide shuttle effect, severely impede their commercial viability. To conquer these limitations, this study develops a multifunctional separator fabricated from straw-derived carboxylated nanocellulose, with its negative charge density further reinforced by anionic polyacrylamide incorporation. This modification simultaneously improves the separator's mechanical properties, ionic conductivity, and Zn ion transfer number. Remarkably, despite its ultrathin 20 μm profile, the engineered separator demonstrates exceptional dendrite suppression and parasitic reaction inhibition, enabling Zn//Zn symmetric cells to achieve impressive cycle life (> 1800 h at 2 mA cm/2 mAh cm) while maintaining robust performance even at ultrahigh areal capacities (25 mAh cm). Additionally, the separator's anionic characteristic effectively blocks polyiodide migration through electrostatic repulsion, yielding Zn-I batteries with outstanding rate capability (120.7 mAh g at 5 A g) and excellent cyclability (94.2% capacity retention after 10,000 cycles). And superior cycling stability can still be achieved under zinc-deficient condition and pouch cell configuration. This work establishes a new paradigm for designing high-performance zinc-based energy storage systems through rational separator engineering.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1007/s40820-025-01921-y | DOI Listing |
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC12413360 | PMC |
Nanomicro Lett
September 2025
Shenzhen Research Institute of Nanjing University, Nanjing University, Shenzhen, 518057, People's Republic of China.
Zn-I batteries have emerged as promising next-generation energy storage systems owing to their inherent safety, environmental compatibility, rapid reaction kinetics, and small voltage hysteresis. Nevertheless, two critical challenges, i.e.
View Article and Find Full Text PDFChem Sci
August 2025
School of Materials Science and Engineering, Institutes of Physical Science and Information Technology, Leibniz International Joint Research Center of Materials Sciences of Anhui Province, Anhui University Hefei 230601 China
Aqueous zinc-iodine batteries (ZIBs), exploiting reversible conversion among various iodine species, have drawn significant research interest due to their fast redox kinetics and capability for multi-electron transfer. Although significant progress has been made in ZIBs based on the two-electron I/I redox pathway (2eZIBs), their inherently limited energy density impedes practical deployment. Achieving the additional reversible conversion of high-valence iodine species, particularly the I/I redox chemistry, offers substantial potential for improving energy density up to 630 Wh kg based on the mass of I.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Department of Chemistry, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong, 999077, China.
Aqueous zinc-iodine (Zn-I) batteries have emerged as a promising candidate for large-scale energy storage applications, owing to their inherent safety, cost-effectiveness, and high specific capacity. However, their commercial implementation is severely hindered by the irreversible capacity degradation and limited cycle life, which are caused by the unavoidable iodine shuttle effect resulting from the formation of soluble I species. Herein, we report the synthesis of three-dimensional hexapod-like fluorine-containing zeolitic imidazolate framework (H-F-ZIF) nanoparticles for separator modification to effectively inhibit the iodine shuttle effect.
View Article and Find Full Text PDFACS Nano
September 2025
Faculty of Materials Science and Energy Engineering, Shenzhen University of Advanced Technology, Shenzhen 518107, China.
The variable valence states of iodine(I) render Zn-I batteries an intriguing area of research. However, current Zn-I batteries are mostly based on I/I redox chemistry. Effective strategies for activating the high-voltage I/I redox couple in iodine-based cathode materials remain relatively scarce.
View Article and Find Full Text PDFACS Nano
September 2025
School of Chemical Engineering, Sungkyunkwan University (SKKU), Suwon 16419, Republic of Korea.
Despite the potential of Zn metal batteries (ZMBs) due to their low cost, environmental benefits, and favorable Zn/Zn redox potential, challenges such as low Zn utilization and parasitic reactions hinder their performance. These issues arise from the thermodynamic instability of the Zn anode and high-desolvation energy barriers. To overcome these challenges, this study investigates two zwitterionic compounds with hydrophilic and zincophilic functional groups, BES (N,N-bis(2-hydroxyethyl)-2-aminoethanesulfonic acid) and MES (2-(N-morpholino)ethanesulfonic acid), selecting BES as the optimal electrolyte additive.
View Article and Find Full Text PDF