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The rapid development of energy storage technologies has led to an increasing demand for high-performance electrode materials that can enhance both the energy density and the cycling stability of batteries. In this study, polypyrrole (PPy) nanorods with partial hollow features are utilized as a conductive and flexible framework for the in situ growth of VO nanospheres via a simple hydrothermal method, forming a well-defined core-shell PPy/VO nanocomposite. This hierarchical nanostructure combines the excellent electrical conductivity and mechanical flexibility of PPy with the high theoretical capacity of VO, creating a synergistic effect that significantly enhances the electrochemical performance. The well-integrated interface between PPy and VO reduces interfacial resistance, promotes efficient electron and ion transport, and improves the overall energy conversion efficiency. Electrochemical testing reveals that the PPy/VO nanocomposite delivers a high specific capacity of 413 mAh g at 100 mA g and retains 87.2% of its initial capacity after 1200 cycles, demonstrating exceptional rate capability and long-term cycling stability. This work provides a versatile strategy for designing high-performance cathode materials and highlights the promising potential of PPy/VO nanocomposites for next-generation high-energy-density aqueous zinc-ion batteries.
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http://dx.doi.org/10.3390/mi16060705 | DOI Listing |
J 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.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
National Synchrotron Radiation Laboratory, University of Science and Technology of China, Hefei, Anhui, 230029, China.
The Jahn-Teller distortion caused by high-spin state Mn (t e ) is a major limiting factor for improving both the specific capacity and cycling stability of MnO cathodes in aqueous zinc-ion batteries. Thus, an intrinsic strategy for optimizing MnO involves the effective elimination of the high-spin state Mn (t e ) during electrochemical process. Herein, we focus on structural design that constructed NHVO-coated MnO (Mn@V) nanorods to achieve the low-spin state of Mn (t e ) and inhibit the Jahn-Teller distortion.
View Article and Find Full Text PDFChemSusChem
September 2025
School of Materials Science and Engineering, Harbin Institute of Technology, Shenzhen, 518055, China.
The mechanical degradation of cathodes during charge-discharge cycling poses a critical limitation to the cycle life of aqueous zinc-ion batteries (AZIBs). Although the degradation of MnO cathodes has been extensively investigated, the underlying reaction mechanisms have long remained a subject of debate, and the associated mechanical evolution during cycling is still poorly understood. In this work, a comprehensive investigation of electrochemical phase transitions and chemical strain evolution in δ-MnO cathode is presented using a custom-built in situ strain testing system based on digital image correlation.
View Article and Find Full Text PDFJ Colloid Interface Sci
September 2025
School of Automobile and Traffic Engineering, Jiangsu University of Technology, Changzhou, Jiangsu Province 213001, China.
Aqueous zinc ion batteries (AZBs) are characterized by high capacity, environmental friendliness and low cost. However, the dendrites and parasitic reactions (e.g.
View Article and Find Full Text PDFNanomicro Lett
September 2025
Materials Synthesis and Processing Lab, School of Fashion and Textiles, The Hong Kong Polytechnic University, Kowloon, 999077, Hong Kong SAR, People's Republic of China.
NHVO (NVO) is considered a promising cathode material for aqueous zinc-ion batteries due to its high theoretical capacity. However, its practical application is limited by irreversible deamination, structural collapse, and sluggish reaction kinetics during cycling. Herein, K and CN co-intercalated NVO (KNVO-CN) nanosheets with expanded interlayer spacing are synthesized for the first time to achieve high-rate, stable, and wide-temperature cathodes.
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