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Phase Transformations in TiS2 during K Intercalation

  • Bingbing Tian
  • , Wei Tang
  • , Kai Leng
  • , Zhongxin Chen
  • , Sherman Jun Rong Tan
  • , Chengxin Peng
  • , Guo Hong Ning
  • , Wei Fu
  • , Chenliang Su
  • , Guangyuan Wesley Zheng
  • , Kian Ping Loh
  • Shenzhen University
  • National University of Singapore
  • Agency for Science, Technology and Research, Singapore

Research output: Contribution to journalArticlepeer-review

116 Scopus citations

Abstract

The electrochemical performances of TiS2 in potassium ion batteries (KIBs) are poor due to the large size of K ions, which induces irreversible structural changes and poor kinetics. To obtain detailed insights into the kinetics of phase changes, we investigated the electrochemical properties, phase transformations, and stability of potassium-intercalated TiS2 (KxTiS2, 0 ≤ x ≤ 0.88). In situ XRD reveals staged transitions corresponding to distinct crystalline phases during K ion intercalation, which are distinct from those of Li and Na ions. Electrochemical (cyclic voltammetry and galvanostatic charge/discharge) studies show that the phase transitions among various intercalated stages slow down the kinetics of the discharge/charge in bulk TiS2 hosts. By chemically prepotassiating the bulk TiS2 (K0.25TiS2) to reduce the domain size of the crystal, these phase transitions are bypassed and more facile ion insertion kinetics can be obtained, which leads to improved Coulombic efficiency, rate capability, and cycling stability.

Original languageEnglish
Pages (from-to)1835-1840
Number of pages6
JournalACS Energy Letters
Volume2
Issue number8
DOIs
StatePublished - 11 Aug 2017
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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