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Evaluates ultrahigh-rate lithium-ion battery anodes, suggesting innovative design for enhanced performance.
The development of advanced anode materials is critical for high-energy and high-power lithium-ion batteries (LIBs). Conventional conversion-type anodes, such as transition metal molybdates, suffer from poor conductivity, severe volume expansion, and structural degradation, leading to rapid capacity fading. To overcome these limitations, we propose a synergistic design strategy that integrates heterojunction engineering with fluorine doping. A fluorine-doped, heterojunction-structured F-FexMn1−xMoO4/graphene (F-FMMO/G) was successfully synthesized via a facile solvothermal route. Structural characterizations confirm the formation of a well-defined FeMoO4/Mn2Mo3O8 heterojunction with effective fluorine incorporation. When evaluated as an anode for LIBs, the F-FMMO/G composite exhibits an ultrahigh initial specific capacity of 1158 mAh g− 1 at 0.1 C and maintains 780 mAh g− 1 after 150 cycles, substantially outperforming the undoped counterpart. Notably, it delivers excellent rate performance, sustaining ~ 100 mAh g− 1 at 10 C and rapidly recovering to > 900 mAh g− 1 when cycled back to 0.1 C. The enhanced electrochemical performance is attributed to the synergistic effects of the built-in electric field at the heterojunction interface, which promotes rapid charge transfer, and fluorine doping, which optimizes the electronic structure and stabilizes the electrode–electrolyte interface. This study offers a rational design framework combining interfacial and bulk modifications for next-generation high-rate LIB anodes. The facile solvothermal synthesis, utilizing low-cost precursors and scalable reaction conditions, suggests good potential for commercial translation.
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Liu et al. (2026) studied this question.
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