<p>In this work, a novel Zn<sub>2</sub>GeO<sub>4</sub>/VS<sub>2</sub> composite electrode was synthesized via a simple hydrothermal method to enhance the electrochemical performance of lithium-ion batteries (LIBs). Comprehensive structural and morphological analyses were carried out using XRD, BET, SEM, TEM, XPS, and FTIR, confirming the successful formation of a well-integrated composite structure. The Zn<sub>2</sub>GeO<sub>4</sub> electrode delivers an initial discharge capacity of 578.62 mAh g<sup>−1</sup> and retains about 127 mAh g<sup>−1</sup> after 400 cycles at a current density of 0.1 A g<sup>−1</sup>, whereas the Zn<sub>2</sub>GeO<sub>4</sub>/VS<sub>2</sub> electrode shows an initial discharge capacity of 340 mAh g⁻<sup>1</sup> and maintains nearly the same capacity (340 mAh g<sup>−1</sup>) at 0.1 A g<sup>−1</sup> with enhanced cycling stability over 400 cycles. The electrode exhibited a first-cycle irreversible capacity loss (ICL) of approximately 39%, primarily attributed to solid electrolyte interphase (SEI) formation and initial structural rearrangements. The enhanced performance is attributed to the synergistic interaction between Zn<sub>2</sub>GeO<sub>4</sub> and VS<sub>2</sub>, which improves lithium-ion diffusion, structural integrity, and electrical conductivity during repeated charge–discharge cycles. This study demonstrates that integrating Zn<sub>2</sub>GeO<sub>4</sub> with a 2D layered material like VS<sub>2</sub> is a promising strategy for developing high-performance LIB anodes. Thus, the VS<sub>2</sub>-modified Zn<sub>2</sub>GeO<sub>4</sub> provides a practical pathway for designing next-generation electrode materials with enhanced capacity and long-term stability Zn<sub>2</sub>GeO<sub>4</sub> by incorporating VS<sub>2</sub> nanosheets.</p> Graphical Abstract <p></p>

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Improving the lithium storage capacity of Zn2GeO4 by incorporating VS2 nanosheets

  • B. R. Anusha,
  • S. Appu,
  • Udayabhanu,
  • Alexis Maurel,
  • K. Prashantha

摘要

In this work, a novel Zn2GeO4/VS2 composite electrode was synthesized via a simple hydrothermal method to enhance the electrochemical performance of lithium-ion batteries (LIBs). Comprehensive structural and morphological analyses were carried out using XRD, BET, SEM, TEM, XPS, and FTIR, confirming the successful formation of a well-integrated composite structure. The Zn2GeO4 electrode delivers an initial discharge capacity of 578.62 mAh g−1 and retains about 127 mAh g−1 after 400 cycles at a current density of 0.1 A g−1, whereas the Zn2GeO4/VS2 electrode shows an initial discharge capacity of 340 mAh g⁻1 and maintains nearly the same capacity (340 mAh g−1) at 0.1 A g−1 with enhanced cycling stability over 400 cycles. The electrode exhibited a first-cycle irreversible capacity loss (ICL) of approximately 39%, primarily attributed to solid electrolyte interphase (SEI) formation and initial structural rearrangements. The enhanced performance is attributed to the synergistic interaction between Zn2GeO4 and VS2, which improves lithium-ion diffusion, structural integrity, and electrical conductivity during repeated charge–discharge cycles. This study demonstrates that integrating Zn2GeO4 with a 2D layered material like VS2 is a promising strategy for developing high-performance LIB anodes. Thus, the VS2-modified Zn2GeO4 provides a practical pathway for designing next-generation electrode materials with enhanced capacity and long-term stability Zn2GeO4 by incorporating VS2 nanosheets.

Graphical Abstract