Zinc-iodine batteries have the potential to offer high energy-density aqueous energy storage, but their lifetime is limited by the rampant dendrite growth and the concurrent parasite side reactions on the Zn anode, as well as the shuttling of polyiodides. Herein, a cation-conduction dominated hydrogel electrolyte is designed to holistically enhance the stability of both zinc anode and iodine cathode. In this hydrogel electrolyte, anions are covalently anchored on hydrogel chains, and the major mobile ions in the electrolyte are restricted to be Zn. Specifically, such a cation-conductive electrolyte results in a high zinc ion transference number (0.81) within the hydrogel and guides epitaxial Zn nucleation. Furthermore, the optimized Zn solvation structure and the reconstructed hydrogen bond networks on hydrogel chains contribute to the reduced desolvation barrier and suppressed corrosion side reactions. On the iodine cathode side, the electrostatic repulsion between negative sulfonate groups and polyiodides hinders the loss of the iodine active material. This all-round electrolyte design renders zinc-iodine batteries with high reversibility, low self-discharge, and long lifespan.
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http://dx.doi.org/10.1002/adma.202313610 | DOI Listing |
Angew Chem Int Ed Engl
January 2025
Northeast Normal University, Department of Chemistry, Renmin Street 5268, 130024, Changchun, CHINA.
Aqueous zinc-iodine batteries (AZIBs) are gaining attention as next-generation energy storage systems due to their high theoretical capacity, enhanced safety, and cost-effectiveness. However, their practical application is hindered by challenges such as slow reaction kinetics and the persistent polyiodide shuttle effect. To address these limitations, we developed a novel class of covalent organic frameworks (COFs) featuring electron-rich nitrogen sites with varied density and distribution (N1-N4) along the pore walls.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Key Laboratory for Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China.
For rechargeable zinc-iodine batteries, the low electrical conductivity of iodine and the easy dissolution of polyiodide in the electrolyte need to be carefully managed to ensure efficient operation. Herein, we introduce an organic iodized salt, formamidinium iodide (CHNI), to modulate the solvation structure of iodide ion, aimed to improve the reaction kinetics of iodine for reversible redox conversion. The participation of formamidinium ion (FA) into solvation structure leads to the formation of the favorable FAIZn(HO) complex, facilitating easier desolvation for redox conversion with iodine.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Materials Science and Engineering, City University of Hong Kong, 83 Tat Chee Avenue, Kowloon, Hong Kong 999077, China.
While many cathode materials have been developed for mild electrolyte-based Zn batteries, the lack of cathode materials hinders the progress of alkaline zinc batteries. Halide iodine, with its copious valence nature and redox possibilities, is considered a promising candidate. However, energetic alkaline iodine redox chemistry is impeded by an alkali-unadapted I element cathode and thermodynamically unstable reaction products.
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January 2025
Department of Mechanical Engineering, Research Institute for Smart Energy, The Hong Kong Polytechnic University, Hong Kong, China.
The multielectron conversion electrochemistry of I/I/I enables high specific capacity and voltage in zinc-iodine batteries. Unfortunately, the I ions are thermodynamically unstable and are highly susceptible to hydrolysis. Current endeavors primarily focus on exploring interhalogen chemistry to activate the I/I couple.
View Article and Find Full Text PDFSci Bull (Beijing)
November 2024
Key Laboratory for Colloid and Interface Chemistry, Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan 250100, China. Electronic address:
The challenges posed by the non-conductive nature of iodine, coupled with the easy formation of soluble polyiodides in water, impede its integration with zinc for the development of advanced rechargeable batteries. Here we demonstrate the in-situ loading of molybdenum carbide nanoclusters (MoC) and zinc single atoms (Zn-SA) into porous carbon fibers to invoke electrocatalytic conversion of iodine at the interface. The electronic interactions between MoC and Zn-SA lead to an upshift in the d-band center of Mo relative to the Fermi level, thus promoting the interfacial interactions with iodine species to suppress shuttle effects.
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