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Ultrahigh Density Array of Vertically Aligned Small-molecular Organic Nanowires on Arbitrary Substrates
Published on: June 18, 2013
Enabling Ultrahigh-Power-Density LiMn0.6Fe0.4PO4 Cathodes via Kinetics Limitation Breakthrough and Jahn-Teller
Pengxu Wang1, Haifeng Yu2, Ling Chen1
1Shanghai Engineering Research Center of Hierarchical Nanomaterials, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China.
Abstract:
Development of high-power LiMnxFe1-xPO4 (LMFP) cathodes is fundamentally challenged by the interplay between sluggish one-dimensional Li+ diffusion and severe Jahn-Teller distortion. Herein, we propose a synergistic substitution strategy to concurrently tackle these issues. Partial replacement of PO4 tetrahedra by planar BO3 groups creates three-dimensional interconnected Li-ion diffusion networks, while doping Nb5+ into transition-metal sites widens the diffusion channels. This tailored microstructure not only overcomes the intrinsic Li+ diffusion kinetics limitation but also dissipates the mechanical stress arising from high-rate operating conditions, suppressing the Jahn-Teller distortion in MnO6 octahedra by 36%. The optimized LMFP cathode delivers an ultrahigh reversible capacity of 126 mAh g-1 at 10C (about a 3.6-fold improvement over the pristine LMFP) and retains 80.2% of its initial capacity after 2000 cycles at 3C in pouch-type full cells. This work elucidates the critical link between Li+ diffusion kinetics and structural stability, providing an available paradigm for designing high-power, long-life Mn-based cathode materials.
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