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Rechargeable aqueous zinc-ion batteries (AZIBs) are among the most promising candidates for next-generation energy-storage devices. However, the large voltage polarisation and infamous dendrite growth hinder the practical application of AZIBs owing to their complex interfacial electrochemical environment. In this study, a hydrophobic zinc chelate-capped nano-silver (HZC-Ag) dual interphase is fabricated on the zinc anode surface using an emulsion-replacement strategy. The multifunctional HZC-Ag layer remodels the local electrochemical environment by facilitating the pre-enrichment and de-solvation of zinc ions and inducing homogeneous zinc nucleation, thus resulting in reversible dendrite-free zinc anodes. The zinc deposition mechanism on the HZC-Ag interphase is elucidated by density functional theory (DFT) calculations, dual-field simulations, and in situ synchrotron X-ray radiation imaging. The HZC-Ag@Zn anode exhibited superior dendrite-free zinc stripping/plating performance and an excellent lifespan of >2000 h with ultra-low polarisation of ≈17 mV at 0.5 mA cm . Full cells coupled with a MnO cathode showed significant self-discharge inhibition, excellent rate performance, and improved cycling stability for >1000 cycles. Therefore, this multifunctional dual interphase may contribute to the design and development of dendrite-free anodes for high-performance aqueous metal-based batteries.
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http://dx.doi.org/10.1002/smll.202303268 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Shandong Key Laboratory of Advanced Chemical Energy Storage and Intelligent Safety, Advanced Technology Research Institute, Beijing Institute of Technology, Jinan, 250300, China.
Lithium-sulfur batteries have been regarded as a promising candidate for next-generation energy storage systems owing to their high energy density and low cost. Sulfurized polyacrylonitrile (SPAN) as a cathode material has received wide interest due to the solid-solid conversion mechanism, while the Li-SPAN cell performance has been limited by the notorious issue of lithium metal anode. Developing solid-state electrolytes for lithium-sulfur batteries with favorable electrode-electrolyte compatibility is urgently desired.
View Article and Find Full Text PDFSmall
September 2025
University of Münster, Institute of Organic Chemistry, Corrensstr. 36, 48149, Münster, Germany.
The development of next-generation Lithium-ion batteries (LIBs) to meet the demands of advancing technology and energy storage requires focus on the formation of effective interphases on both the positive and negative electrodes. Different promising approaches to facilitate effective interphase formation are already known Out of these, the incorporation of film-forming electrolyte additives is a straight-forward strategy to achieve this goal. In the presented study, a bifunctional electrolyte additive, (5-methyl-2-oxo-1,3-dioxol-4-yl)methyl thiophene-3-carboxylate composed of two functional motifs, vinylene carbonate (VC) and thiophene, is reported.
View Article and Find Full Text PDFJ Colloid Interface Sci
August 2025
Hebei Key Laboratory of Flexible Functional Materials, School of Materials Science and Engineering, Hebei University of Science and Technology, Shijiazhuang 050000, China. Electronic address:
Sodium metal batteries (SMBs) are promising next-generation energy storage systems due to their exceptional theoretical capacity (1165 mAh g) and the widespread availability of sodium. However, heterogeneous sodium deposition triggers irregular solid electrolyte interphase (SEI) formation, intensifies parasitic interfacial reactions, and accelerates persistent SEI deterioration. This study introduces a molecular engineering approach for constructing a novel carbonate-derived gel polymer electrolyte (GPE) system, denoted as THEP (composed of trimethylolpropane trimethacrylate (TMPTMA), 1,6-hexanediol diacrylate (HDDA), ethyl methyl carbonate (EMC), and propylene carbonate (PC)), via in-situ thermal polymerization.
View Article and Find Full Text PDFACS Appl Energy Mater
August 2025
Department of Electrical and Computer Engineering, Kennesaw State University, Marietta, Georgia 30060, United States.
Ceramic-in-polymer composite solid electrolytes (SEs) show great potential for meeting the high-performance requirements of all-solid-state batteries (ASSBs) due to the combined benefits of easy processability, tunable Li-ion conductivity, wide electrochemical window, and facile interfacial contact with the Li-metal anode. However, their Li-ion conductivity remains lower than that of the pure ceramic phase, which can be attributed to the highly resistive ceramic/polymer interphase. In this paper, we introduced sulfur-containing functional groups through a less-explored metal/sulfur interaction strategy, enabling simultaneous modification of the polyethylene glycol diacrylate (PEGDA) polymer scaffold and the LiLaZrTaO (LLZO) ceramic surface.
View Article and Find Full Text PDFAdv Mater
August 2025
Advanced Energy Storage Technology Research Center, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, P. R. China.
Sodium-based dual-ion batteries (SDIBs) attract extensive attention in stationary energy storage for their low cost, environmental friendliness, and high working voltage. However, traditional liquid electrolytes for SDIBs undergo solvent co-intercalation and severe oxidation decomposition at high voltage, causing unstable cathode structure and low Coulombic efficiency, especially with high loading (>5 mg cm). Herein, an interfacial self-compatible quasi-solid electrolyte (ACPE) is developed via an additive-induced solvation design strategy.
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