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The commercialization trajectory of aqueous zinc-ion batteries (AZIBs) faces critical challenges, including zinc dendrites, parasitic side reactions, and inadequate cycling stability. The electrode-electrolyte interface (EEI), serving as the nexus between macroscopic device performance and microscopic electrochemical processes, fundamentally dictates reaction pathways through solvation structure modulation. A comprehensive understanding of both cathode and anode interfacial chemistries is imperative, as expanding and stabilizing reactive interfaces can significantly enhance depth of discharge (DOD). With this in mind, this review synthesizes recent advancements in electrolyte additive-mediated interface engineering for high-energy-density AZIBs. The fundamental principles and practical evaluation methodologies governing additive implementation are systematically examined, while remaining challenges and future research directions are delineating. The review further catalogs cutting-edge characterization techniques and discusses performance assessment protocols spanning laboratory-scale experiments to pilot-scale standardization efforts. Through comparative analysis of diverse additive categories, the critical importance of establishing scientifically grounded screening paradigms and standardized evaluation metrics to accelerate technology maturation from fundamental research to industrial implementation is emphasized. Finally, a critical analysis is presented of the remaining obstacles that must be overcome for AZIB deployment under diverse practical conditions, and prospects are provided for advancing durable, high-energy AZIB energy storage systems toward commercialization.
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http://dx.doi.org/10.1002/smll.202507546 | DOI Listing |
Nano Lett
September 2025
School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan, Hubei 430070, China.
Aqueous zinc-ion batteries (AZIBs) represent an environmentally benign energy storage alternative. However, the VO cathode suffers from limited cycling stability and rate capability due to structural instability, vanadium dissolution, and high desolvation energy caused by the large size of [Zn(HO)] deintercalation. Address these issues, we introduce a VO/VOPO (VOP) heterostructure that that reinforces the crystal structure to suppress vanadium dissolution and establishes a hydrophilic interface reducing the desolvation energy of Zn.
View Article and Find Full Text PDFChem Commun (Camb)
September 2025
Department of Applied Chemistry, School of Chemistry and Chemical Engineering, Chongqing University, Chongqing 401331, China.
In this work, a series of potassium ion (K) pre-intercalated sodium hydrogen vanadates (K-HNVO) are prepared through a facile route. The introduction of K modulates the microstructure of the pristine sodium metavanadate and increases the interlayer spacing, thereby resulting in improved charge transport kinetics. Moreover, the pillaring effect of K enhances the structural stability of the pristine material.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
State Key Laboratory of Electrical Insulation and Power Equipment, Xi'an Jiaotong University, Xi'an 710049, China.
Economically viable and biologically compatible amino acids demonstrate significant potential as electrolyte microstructure modifiers in aqueous zinc-ion batteries (AZIBs). Compared to polar amino acids, nonpolar amino acids simultaneously own zincophilicity and hydrophobicity, showing great potential in the industrial application of AZIBs. However, nonpolar amino acids have been comparatively understudied in existing research investigations.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
September 2025
Department of Materials Science and Engineering, City University of Hong Kong, Kowloon, Hong Kong 999077, China.
Solid-state electrolytes (SSEs) are being extensively researched as replacements for liquid electrolytes in future batteries. Despite significant advancements, there are still challenges in using SSEs, particularly in extreme conditions. This study presents a hydrated metal-organic ionic cocrystal (HMIC) solid-state ion conductor with a solvent-assisted ion transport mechanism suitable for extreme operating conditions.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
Department of Materials Science and Engineering, University of Washington, Seattle, WA 98195, USA. Electronic address:
Pre-intercalation has emerged as a highly effective strategy to enhance structural integrity and ion transport kinetics in cathodes for aqueous Zn-ion batteries. Here, we report a zinc-ion pre-intercalated hydrate vanadium oxide cathode, in which the initial insertion of Zn induces a significant expansion of the interplanar spacing, followed by contraction at higher Zn concentrations owing to strong electrostatic interactions with the VO framework. Such competing expansion and contraction of interplanar spacing enhances the overall electrochemical properties.
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