4.5 Article

Excellent electrochemical performance of lithium manganese composite decorated with poly(ethylene glycol) and carbon nanotube

期刊

JOURNAL OF POROUS MATERIALS
卷 28, 期 5, 页码 1619-1626

出版社

SPRINGER
DOI: 10.1007/s10934-021-01135-8

关键词

Lithium manganate oxide; Poly(ethylene glycol); Carbon nanotube; Surface modification; Synergistic effect

资金

  1. Natural Science Foundation of Henan Province [202300410163]
  2. Program for Innovative Research Team (in Science and Technology) in University of Henan Province [20IRTSTHN016]
  3. Young Key Teachers Projects in Henan Higher Education Institutions [2018GGJS113]
  4. Preferential Scientific Research Projects for Talents Studying Abroad, High-Level Talents Introduction Project of Henan Institute of Science and Technology [203010617011]
  5. University Students' Innovation and Pioneering Project [2021CY002]

向作者/读者索取更多资源

The electrochemical performance of LiMn2O4 was significantly improved by a co-modification approach based on the synergistic effect of PEG and CNT. The CNT@PEG@LMO composite showed higher initial discharge capacity and better cycling stability, attributed to the close association with the synergistic effect of PEG and CNT.
To significantly improve the electrochemical performance of LiMn2O4, we proposed a simple and low-cost co-modification approach based on the synergistic effect of poly(ethylene glycol) (PEG) and carbon nanotubes (CNT). The CNT@PEG@LiMn2O4 (CNT@PEG@LMO) composite was prepared by ultrasound assisted wet-coating method. PEG is a highly conductive ionic conductor, which can improve the transport efficiency of lithium ions, and CNT is a good electronic conductor, which possesses excellent electrical conductivity. Moreover, the combination of PEG and CNT can effectively inhibit the dissolution of manganese and promote the uniform distribution of LiMn2O4 octahedra. The structure and surface morphology of the CNT@PEG@LMO composite were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The electrochemical test result showed that the initial discharge capacity of the CNT@PEG@LMO composite could reach up to 123.8 mAh g(-1) at 1.0 C with capacity retention of 95.2 % after 100 cycles, which is higher than that of the unmodified LiMn2O4 sample. The high-rate capability of the CNT@PEG@LMO composite was significantly improved. When cycled at 55 degrees C, the CNT@PEG@LMO composite could show good cycling stability and rate performance. Such excellent electrochemical performance is due to close association with the synergistic effect of PEG and CNT.

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