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Comparison of the rate capability of nanostructured amorphous and anatase TiO2 for lithium insertion using anodic TiO2 nanotube arrays

  • Hai Tao Fang*
  • , Min Liu
  • , Da Wei Wang
  • , Tao Sun
  • , Dong Sheng Guan
  • , Feng Li
  • , Jigang Zhou
  • , Tsun Kong Sham
  • , Hui Ming Cheng
  • *Corresponding author for this work
  • Harbin Institute of Technology
  • CAS - Institute of Metal Research
  • Western University

Research output: Contribution to journalArticlepeer-review

Abstract

Nanostructured amorphous and anatase TiO2 are both considered as high rate Li-insertion/extraction electrode materials. To clarify which phase is more desirable for lithium ion batteries with both high power and high density, we compare the electrochemical properties of anatase and amorphous TiO2 by using anodic TiO2 nanotube arrays (ATNTAs) as electrodes. With the same morphological features, the rate capacity of nanostructured amorphous TiO2 is higher than that of nanostructured anatase TiO2 due to the higher Li-diffusion coefficient of amorphous TiO2 as proved by the electrochemical impedance spectra of an amorphous and an anatase ATNTA electrode. The electrochemical impedance spectra also prove that the electronic conductivity of amorphous TiO2 is lower than that of anatase TiO2. These results are helpful in the structural and componential design of all TiO2 mesoporous structures as anode material in lithium ion batteries. Moreover, all the advantages of the amorphous ATNTA electrode including high rate capacity, desirable cycling performance and the simplicity of its fabrication process indicate that amorphous ATNTA is potentially useful as the anode for lithium ion batteries with both high power and high energy density.

Original languageEnglish
Article number225701
JournalNanotechnology
Volume20
Issue number22
DOIs
StatePublished - 2009
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

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