Surface iron concentration gradient: A strategy to suppress Mn3+ Jahn-Teller effect in lithium manganese iron phosphate

[Display omitted] •Single-particle LMFP with iron-enriched, manganese-depleted surface prepared for enhanced stability.•Phosphate layer on surface is 1-2 nm with a high iron gradient, boosting performance.•The modified material plays a crucial role in suppressing Jahn-Teller distortion.•Experiments...

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Veröffentlicht in:Applied surface science 2025-02, Vol.682, p.161689, Article 161689
Hauptverfasser: Li, Zhen, You, Yang, Zhu, Zhiqi, Wang, Lianghua, Ou, Shengwen, Xu, Jingyue, Yuan, Mingliang
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Sprache:eng
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Zusammenfassung:[Display omitted] •Single-particle LMFP with iron-enriched, manganese-depleted surface prepared for enhanced stability.•Phosphate layer on surface is 1-2 nm with a high iron gradient, boosting performance.•The modified material plays a crucial role in suppressing Jahn-Teller distortion.•Experiments and DFT provide insights into performance enhancement mechanisms. To address the low energy density of LiFePO4 (LFP) for electric vehicles and high-voltage energy storage, LiMn0.5Fe0.5PO4 (LMFP) provides a potential solution but faces performance degradation due to Mn3+-induced Jahn-Teller distortion and Mn ion dissolution during cycling. This study proposes a surface engineering strategy to enhance LMFP’s electrochemical performance by increasing surface iron concentration and reducing manganese content, based on the electronic differences between Mn3+ and Fe3+ in MO6 octahedra. Density Functional Theory (DFT) calculations confirmed the viability of this approach by analyzing volume changes and binding energies with HF during charging. Guided by DFT, an LMFP@LFP/C material was synthesized with a high-iron-concentration surface layer (∼2 nm), as observed through AC-STEM. Post-cycling TEM analysis and corrosion simulations demonstrated that LMFP@LFP/C suppresses Mn ion dissolution and stabilizes the crystal lattice compared to unmodified LMFP/C. Electrochemical tests showed that LMFP@LFP/C has superior electronic conductivity and faster lithium-ion diffusion. It delivered an initial discharge capacity of 150.82 mAh g−1 at 0.1C, surpassing LMFP/C (147.65 mAh g−1). At 1C, LMFP@LFP/C retained 95.85 % of its capacity after 500 cycles, significantly outperforming LMFP/C (74.18 %). This surface modification strategy advances phosphate-based cathode materials for electric vehicles and renewable energy applications.
ISSN:0169-4332
DOI:10.1016/j.apsusc.2024.161689