4.8 Article

Unravelling Li+ Intercalation Mechanism and Cathode Electrolyte Interphase of Na3V2(PO4)3 and Na3(VOPO4)2F Cathode as Robust Framework Towards High-Performance Lithium-Ion Batteries

期刊

CHEMSUSCHEM
卷 15, 期 15, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cssc.202200817

关键词

batteries; electrode materials; electrolytes; energy storage; hybrid-ion intercalation

资金

  1. National Natural Science Foundation of China [21905058]
  2. Guangdong University of Technology Hundred Talents Program [220418136]
  3. Guang-dong Basic and Applied Basic Research Foundation [2021A1515110361]

向作者/读者索取更多资源

This study systematically investigated the electrochemical performances of NVP and NVOPF as cathodes for LIBs. The results showed that the NVP electrode delivered a higher discharge capacity and better capacity retention compared to the NVOPF electrode. The mechanisms and morphological changes were revealed through techniques such as transmission X-ray diffraction and scanning electron microscopy.
Although lithium-ion batteries (LIBs) are promising towards high energy density and superior safety energy storage systems (ESS), severe depletion of Li reserve cannot meet the ever-growing demand for LIBs due to the uneven distribution and limited amount of Li resource. Li-free polyanionic cathodes, such as Na3V2(PO4)(3) (NVP) and Na-3(VOPO4)(2)F (NVOPF), show intriguing electrochemical performances with prospective future for LIBs due to their appropriate crystallographic sites, robust host structure, and abundant Na resource. In this work, NVP and NVOPF were systematically investigated as cathodes for LIBs using different voltage windows of 2.5-4.3, 2.0-4.3, and 1.5-4.8 V, along with their electrochemical mechanisms, cathode electrolyte interphase properties, and electrode morphologies for comparison. Ex-situ X-ray diffraction, ex-situ X-ray photoelectron spectroscopy, and post-mortem scanning electron microscopy revealed that their mechanisms shifted from a predominant Na+ intercalation/deintercalation in the first charging/discharging to a mixed Li+/Na+ intercalation/deintercalation at the subsequent cycling. Due to the residual Na+ acting as pillar in the structure, NVP and NVPF could serve as robust host framework, providing appropriate crystallographic sites for repeated Li+/Na+ intercalation/deintercalation. NVP electrode delivered a higher discharge capacity of 107.6 mAh g(-1) with superior capacity retention of 84.3 % after 1000 cycles (2.5-4.3 V, 100 mA g(-1)) than NVOPF electrode (97.3 mAh g(-1), 68.8 %). Electrode polarization and kinetic analysis manifested one energetically similar and two energetically nonequivalent crystallographic Na sites within the R3? c and I4/mmm polyanionic structure of NVP and NVOPF. This work comprehensively demonstrates the feasibility and prospect of sodium-based NVP and NVOPF polyanions serving as advanced Li-free cathodes for LIBs, which provides novel insights into seeking Li-free candidates as prospective cathodes for LIBs towards a more sustainable society and a cost-effective battery manufacturing system.

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