The electrolyte-electrode interface plays a crucial role in aqueous Zn/I battery and is largely determined by the properties of electrolyte and separator. Here, the synergistic effect of sulfonic acid-rich electrolyte additive and separator impacts the interface stability of Zn/I batteries is comprehensively investigated using operando synchrotron-based Fourier-transform infrared spectroscopy, cryo-electron microscopy, and in situ spectroscopy. As a case study, a cost-effective additive known as lignosulfonic acid sodium (LAS) and a flexible sulfonated polyether sulfone membrane are employed to facilitate the formation of a stable solid electrolyte interface (SEI) on the Zn anode and effectively suppress the shuttle effect. The chemisorption of LAS on Zn, its interaction with Zn, and the impact on the Zn desolvation process are systematically investigated through both theoretical simulations and operando measurements. Furthermore, the formation of an in situ SEI consisting of ZnS and ZnF is identified, which facilitates the uniform nucleation and planar plating of Zn(002), while effectively suppressing detrimental side reactions. Additionally, visualization experiments and in situ spectroscopy confirm that R-SO- groups effectively impede the shuttle process of I/I anions through electrostatic repulsion. This work provides valuable insights for designing robust electrolyte interfaces for high-performance aqueous Zn/I batteries.
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http://dx.doi.org/10.1002/adma.202419502 | DOI Listing |
Adv Mater
March 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.
The electrolyte-electrode interface plays a crucial role in aqueous Zn/I battery and is largely determined by the properties of electrolyte and separator. Here, the synergistic effect of sulfonic acid-rich electrolyte additive and separator impacts the interface stability of Zn/I batteries is comprehensively investigated using operando synchrotron-based Fourier-transform infrared spectroscopy, cryo-electron microscopy, and in situ spectroscopy. As a case study, a cost-effective additive known as lignosulfonic acid sodium (LAS) and a flexible sulfonated polyether sulfone membrane are employed to facilitate the formation of a stable solid electrolyte interface (SEI) on the Zn anode and effectively suppress the shuttle effect.
View Article and Find Full Text PDFJ Colloid Interface Sci
February 2025
Faculty of Chemistry, Northeast Normal University, 5268 Renmin Street, Changchun, Jilin 130024, PR China. Electronic address:
Zinc-iodide (Zn-I) batteries have attracted widespread attention owing to the advantages of low cost, high specific capacity, and integrated safety. However, challenges involving the dissolution and shuttle of polyiodides and sluggish iodine redox kinetics constrain their practical applications. Herein, we designed a freestanding carbon nanofibers (CNFs) membrane embedded with ultrafine Sn nanoparticles (uSn-CNFs) as an efficient interlayer for Zn-I batteries.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
February 2025
Department of Chemistry and Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, Institute of New Energy, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), Fudan University, Shanghai, 200433, China.
Aqueous zinc-ion batteries (AZIBs) offer notable advantages in safety and cost-efficiency, but Zn dendrite growth and unstable interfacial reactions hinder their commercial viability. A crucial factor in addressing these challenges lies in optimizing the separator to regulate ion transport and stabilize electrode interfaces. Herein, we propose a covalent organic framework (COF)-based separator with quasi-single-ion conduction, specifically a Zn-substituted sulfonate COF (COF-Zn) membrane, designed to tackle these issues.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
February 2025
State Key Laboratory of Chem/Bio-Sensing and Chemometrics, Joint International Research Laboratory of Energy Electrochemistry, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, China.
The diverse valences of iodine enable it with multi-electron transfer capability for energy dense batteries. However, previous studies indicate that the primary I/I redox couple exhibits distinct behaviors depending on electrolyte choice, with the mechanistic basis of aqueous versus nonaqueous systems remaining unclear. Here, we elucidated the solvent effect on iodine redox, particularly focusing on polyiodide formation and their molecular interaction correlations.
View Article and Find Full Text PDFAdv Mater
February 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.
The practical development of aqueous zinc-iodine (Zn-I) batteries is greatly hindered by the low energy density resulting from conventional I/I conversion and the limited temperature tolerance. Here, a temperature-insensitive polycationic hydrogel electrolyte borax-bacterial cellulose / p(AM-co-VBIMBr) (denoted as BAVBr) for achieving an energy-dense cascade aqueous Zn-I battery over a wide temperature range from -50 to 50 °C is designed. A comprehensive investigation, combining advanced spectroscopic investigation and DFT calculations, has revealed that the presence of Br species in the gel electrolyte facilitates the conversion reaction of Br/Br.
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