4.8 Article

Ultrahigh rate capability of manganese based olivine cathodes enabled by interfacial electron transport enhancement

Journal

NANO ENERGY
Volume 104, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.nanoen.2022.107895

Keywords

Lithium manganese iron phosphate; Lithium vanadium phosphate; Interfacial transport; Affinitive conductor; Rate performance

Funding

  1. National Natural Science Foundation of China [U21A20170, 22175106, 52007099]
  2. Ministry of Science and Technology of China [2021YFB2501900, 2019YFE0100200, 2019YFA0705703]
  3. Tsinghua University Initiative Scientific Research Program [2021THFS0216, 2019Z02UTY06, 2019THFS0104]
  4. U.S. Department of Energy (DOE), Vehicle Technologies Office
  5. Joint Work Plan for Research Projects under the Clean Vehicles Consortium at U.S. and China-Clean Energy Research Center [CERC-CVC2.0]
  6. US Department of Energy by U Chicago Argonne, LLC [DE-AC02-06CH11357]

Ask authors/readers for more resources

This study achieves ultrahigh rate performance by introducing an affinitive conductor, Li3V2(PO4)(3), to enhance the interfacial electron transport of LiMn0.7Fe0.3PO4 as the cathode material for lithium-ion batteries. The results reveal the synergistic effect between LiMn0.7Fe0.3PO4 and Li3V2(PO4)(3) through in situ X-ray diffraction and conductive-atomic force microscopy.
Manganese-based Olivine is a promising cathode candidate with high energy and low cost for Li-ion batteries (LIBs). Its rate capability and cyclability challenges still remain even with nano-size and carbon coating. Herein, an ultrahigh rate performance is achieved by introducing an affinitive conductor to enhance the interfacial electron transport of LiMn0.7Fe0.3PO4 via Li3V2(PO4)(3). It is found that the Li3V2(PO4)(3) facilitates sp(2) hybridization to form a highly conductive carbon coating during the carbonized process. The composite 0.9LiMn(0.7)-Fe0.3PO4.0.1Li(3)V(2)(PO4)(3) can deliver a capacity of 90.9 mAh g(-1) and power density of 11444 W kg(-1) at 50 C-rate. Both in situ X-ray diffraction and conductive-atomic force microscopy are conducted to understand the synergetic effect between LiMn0.7Fe0.3PO4 and Li3V2(PO4)(3). The results suggest that the interfacial electron transfer between LiMn0.2Fe0.3PO4 particles and the electron conducting medium, such as binder/carbon black composite, is greatly improved so that the highly Li+ conductive nature of olivine materials can be fully unleashed. This work demonstrates the importance of efficient interfacial electron transfer to the active cathode particles, and opens up a new venue for the rational design of high-energy and high-power batteries.

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