Hydrothermal Synthesis of Monoclinic VO2 Microparticles without Use of Hazardous Reagents: A Key Role for the W‑Dopant

  • Kimberly Timmers
  • , Alisha Chote
  • , Luc Leufkens
  • , Roberto Habets
  • , Ken Elen
  • , Marcel A. Verheijen
  • , Marlies K. van Bael
  • , Daniel Mann (Corresponding author)
  • , Pascal J.P. Buskens (Corresponding author)

Research output: Contribution to journalArticleAcademicpeer-review

1 Citation (Scopus)
223 Downloads (Pure)

Abstract

Monoclinic vanadium dioxide (VO2 (M)) is a promising material for various applications ranging from sensing to signature management and smart windows. Most applications rely on its reversible structural phase transition to rutile VO2 (VO2 (R)), which is accompanied by a metal-to-insulator transition. Bottom-up hydrothermal synthesis has proven to yield high quality monoclinic VO2 but requires toxic and highly reactive reducing agents that cannot be used outside of a research lab. Here, we present a new hydrothermal synthesis method using nontoxic and safe-to-use oxalic acid as a reducing agent for V2O5 to produce VO2 (M). In early stages of the process, polymorphs VO2 (A) and VO2 (B) were formed, which subsequently recrystallized to VO2 (M). Without the presence of W6+, this recrystallization did not occur. After a reaction time of 96 h at 230 °C in the presence of (NH4)6H2W12O40 in Teflon-lined rotated autoclaves, we realized highly crystalline, phase pure W-doped VO2 (M) microparticles of uniform size and asterisk shape (ΔH = 28.30 J·g–1, arm length = 6.7 ± 0.4 μm, arm width = 0.46 ± 0.06 μm). We extensively investigated the role of W6+ in the kinetics of formation of VO2 (M) and the thermodynamics of its structural phase transition.
Original languageEnglish
Pages (from-to)5400-5413
Number of pages14
JournalInorganic Chemistry
Volume63
Issue number12
Early online date15 Mar 2024
DOIs
Publication statusPublished - 25 Mar 2024

Funding

K.T., A.C., L.L., R.H., D.M., and P.B. acknowledge funding by the TKI Sustainable Chemistry and Circularity (project THERPA). M.A.V. acknowledges Solliance and the Dutch province of Noord-Brabant for funding the TEM facilities. All authors thank the Analytical Chemistry group of Hasselt University for ICP-AES analyses.

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