What question did this study set out to answer?

This research aims to enhance the cycling stability of lithium metal anodes by regulating lithium plating and stripping processes effectively.

Regulating Li Plating/Stripping by Synergistic Dual‐Alloy Modification and Robust LiF‐Rich Interface for High‐Performance Li Metal Batteries

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Randomized trial showcases enhanced cycling stability in lithium metal batteries, suggesting improvements for energy density.

This research aims to enhance the cycling stability of lithium metal anodes by regulating lithium plating and stripping processes effectively.
Developed a lithium metal anode with a LiF-rich solid electrolyte interphase using alloy modifications and a carbon host.
Applied density functional theory (DFT) calculations to understand the electronic structure of alloys.
Tested cycling performance in symmetric cells and full cells with various cathode materials.
Symmetric cells maintained high cyclability for over 1200 hours with a low overpotential of 23 mV at 2 mA cm−2.
Full cells with LiFePO4 and LiNi0.8Co0.1Mn0.1O2 cathodes achieved 131.5 mAh g−1 after 400 cycles at 1 C rate.
Pouch cells showed 90.3% capacity retention after 90 cycles, indicating strong cycling stability.

Chen et al. (2026) studied this question.

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View Full Paper

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Authors

Randomized trial showcases enhanced cycling stability in lithium metal batteries, suggesting improvements for energy density.

This research aims to enhance the cycling stability of lithium metal anodes by regulating lithium plating and stripping processes effectively.
Developed a lithium metal anode with a LiF-rich solid electrolyte interphase using alloy modifications and a carbon host.
Applied density functional theory (DFT) calculations to understand the electronic structure of alloys.
Tested cycling performance in symmetric cells and full cells with various cathode materials.
Symmetric cells maintained high cyclability for over 1200 hours with a low overpotential of 23 mV at 2 mA cm−2.
Full cells with LiFePO4 and LiNi0.8Co0.1Mn0.1O2 cathodes achieved 131.5 mAh g−1 after 400 cycles at 1 C rate.
Pouch cells showed 90.3% capacity retention after 90 cycles, indicating strong cycling stability.

Chen et al. (2026) studied this question.

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