Controlling MoO2 and MoO3 phases in MoOx/CNTs nanocomposites and their application to anode materials for lithium-ion batteries and capacitors

Daseul Han, Sooyeon Hwang, Seong Min Bak, Kyung Wan Nam

Research output: Contribution to journalArticlepeer-review

36 Scopus citations

Abstract

Molybdenum oxides (MoO2 and MoO3) are attractive anode materials for Li- and Na- ion batteries. Although there have been extensive studies on them individually, systematic and comparative studies are still lacking. In this work, we demonstrate a facile and straightforward synthesis method to control the phase and oxidation state in the MoOx/CNTs nanocomposites via hydrothermal reaction followed by heat-treatment. By changing the gas atmosphere during the annealing process, well-dispersed MoO2/CNTs and MoO3/CNTs nanocomposites are formed without altering their overall morphology. This strategy enables us to investigate the true structure-property correlation of MoOx/CNTs nanocomposites by comparing the structure and electrochemical properties of MoO2/CNTs and MoO3/CNTs. When tested as anode materials for lithium-ion batteries, both HT-MoO2&3/CNTs electrodes show much-improved cycling stability and rate performance compared to the rod-shaped bulk MoO3 electrode. In situ Mo K-edge x-ray absorption spectroscopy (XAS) has been further employed to compare and elucidate Li+ storage mechanisms of both electrodes. When employed to the negative electrode of a high-power lithium-ion capacitor (LIC), the LIC full-cell composed of HT-MoO3/CNTs negative and activated carbon positive electrodes demonstrates impressive energy and power densities (~ 90 Wh kg−1 with 2000 W kg−1) and excellent cycling stability (96.8 % capacity retention after 300 cycles), revealing the versatility of the MoOx/CNTs electrodes in energy applications.

Original languageEnglish
Article number138635
JournalElectrochimica Acta
Volume388
DOIs
StatePublished - 20 Aug 2021

Keywords

  • Li-ion capacitor
  • Molybdenum oxide
  • MoO
  • MoO
  • X-ray absorption spectroscopy

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