4.6 Article

Achieving in-situ hybridization of NaTi2(PO4)3 and N-doped carbon through a one-pot solid state reaction for high performance sodium-ion batteries

期刊

JOURNAL OF SOLID STATE CHEMISTRY
卷 310, 期 -, 页码 -

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jssc.2022.123036

关键词

NaTi2(PO4)(3); Heteroatom-doped carbon; Nanocomposite; Cathode material; Sodium-ion batteries; Ethylenediamine tetramethylene phosphonic acid

资金

  1. National Natural Science Foundation of China [22004070, 52072181]
  2. Natural Science Foundation of the Jiangsu Higher Ed-ucation Institutions of China [20KJB150023]
  3. Natural Science Foundation of Jiangsu Province [BK20191365]

向作者/读者索取更多资源

The NTP@NC composite, prepared by hybridizing NTP with a N-doped carbon matrix through a one-pot solid state reaction, exhibits improved electrical conductivity and mitigated particle agglomeration. It shows outstanding sodium storage behavior with high specific charge capacity, excellent cycle performance, and outstanding rate capabilities.
The development of green, sustainable and low-cost energy storage materials through simple and environmental friendly routes is of great significance for futural large-scale energy storage systems. Due to its unique sodium super ionic conductor (NASICON) structure, polyanion-type NaTi2(PO4)(3) (NTP) is regarded as one of the promising potential cathode materials for sodium-ion batteries (SIBs). However, its practical application has been impeded by its intrinsic poor conductivity for unmodified NTP. To resolve this issue, this work hybridizes the NTP with a N-doped carbon matrix (NC) through a facile one-pot solid state reaction, taking an organophosphonic acid (ethylenediamine tetramethylene phosphonic acid, EDTMPA) as source material providing carbon, nitrogen and phosphorous element at the same time. The as-prepared NTP@NC composite not only possesses improved elec-trical conductivity, but also mitigates particle agglomeration during prolonged charge-discharge cycles. As a result, the NTP@NC composite exhibits an outstanding sodium storage behavior, in terms of a high specific charge capacity (105.6 mA h g(-1) at 0.2 C with 87.3% initial coulombic efficiency), an excellent cycle performance (101.2 mA h g(-1) charge capacity after 100 cycles at 0.2 C with a charge capacity retention of 95.8%) and outstanding rate capabilities (103.6 mA h g(-1) charge capacity at 1 C and 71.5 mA h g(-1) at 5 ?C, respectively).

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