<p>Manganese oxides have emerged as promising cathode materials for aqueous zinc-ion batteries (ZIBs) owing to their low cost, high safety, and environmental benignity. However, the practical application is hindered by poor cycling stability and low electronic conductivity. This study proposes a Cu-Li co-doping strategy to enhance Mn<sub>3</sub>O<sub>4</sub>’s electrochemical performance, producing the co-doped material (CLMO) using a facile one-step solution combustion method. Experimental results revealed Cu<sup>2+</sup> substitution at Mn<sup>2+</sup> sites triggered lattice contraction, shortening Zn<sup>2+</sup> diffusion pathways, while Li<sup>+</sup> enhanced cycling stability by suppressing Mn dissolution and stabilizing the lattice. Synergistic co-doping significantly increased oxygen vacancy concentration, improving electronic conductivity. The CLMO cathode exhibited a remarkable capacity of 270 mAh g<sup>−1</sup> at 0.1 A g<sup>−1</sup> and retained 98% capacity after 800 cycles at 0.5 A g<sup>−1</sup>, outperforming single-doped and undoped counterparts. EIS analysis further validated the reduced charge transfer resistance (13.17 Ω vs. 75.59 Ω) and accelerated Zn<sup>2+</sup> diffusion kinetics. These findings elucidate the synergistic mechanisms of bimetallic co-doping and offer a theoretical and technical foundation for developing high-stability ZIBs cathodes.</p>

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Cu-Li Co-Doped Mn3O4 cathode materials employed in aqueous zinc-ion batteries

  • Jidong Ma,
  • Zhizhu Tang,
  • Wenjun Zhou,
  • Xinya Gu,
  • Kai Du,
  • YiChen Wu,
  • Siyong Gu,
  • Houan Zhang

摘要

Manganese oxides have emerged as promising cathode materials for aqueous zinc-ion batteries (ZIBs) owing to their low cost, high safety, and environmental benignity. However, the practical application is hindered by poor cycling stability and low electronic conductivity. This study proposes a Cu-Li co-doping strategy to enhance Mn3O4’s electrochemical performance, producing the co-doped material (CLMO) using a facile one-step solution combustion method. Experimental results revealed Cu2+ substitution at Mn2+ sites triggered lattice contraction, shortening Zn2+ diffusion pathways, while Li+ enhanced cycling stability by suppressing Mn dissolution and stabilizing the lattice. Synergistic co-doping significantly increased oxygen vacancy concentration, improving electronic conductivity. The CLMO cathode exhibited a remarkable capacity of 270 mAh g−1 at 0.1 A g−1 and retained 98% capacity after 800 cycles at 0.5 A g−1, outperforming single-doped and undoped counterparts. EIS analysis further validated the reduced charge transfer resistance (13.17 Ω vs. 75.59 Ω) and accelerated Zn2+ diffusion kinetics. These findings elucidate the synergistic mechanisms of bimetallic co-doping and offer a theoretical and technical foundation for developing high-stability ZIBs cathodes.