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Journal of Materials Science: Materials in Electronics

, Volume 29, Issue 18, pp 15486–15495 | Cite as

Chromogenic MoO3 thin films: thermo-, photo-, and electrochromic response to working pressure variation in rf reactive magnetron sputtering

  • V. Cruz-San Martín
  • M. Morales-Luna
  • P. E. García-Tinoco
  • M. Pérez-González
  • M. A. Arvizu
  • H. Crotte-Ledesma
  • M. Ponce-Mosso
  • S. A. Tomás
Article

Abstract

The thermochromic, photochromic, and electrochromic properties of molybdenum trioxide (MoO3) thin films were studied. MoO3 thin films were deposited by rf reactive magnetron sputtering and the influence of deposition parameters, i.e. O2/Ar gas ratio and working pressure, on the chromogenic properties was investigated. Thermochromism was induced by annealing the samples in either air or argon in the range 23–300 °C for 2 h. We found that the highest response was obtained for samples grown at 5.3 × 10−1 Pa, although films annealed in air showed a maximum coloration around 250 °C that became bleached above this temperature. As for the annealing in argon, the thermochromic effect increased even at 300 °C. By exposing samples to UV irradiation in air, photochromism could be induced for different intervals ranging from 0 to 3 h. The highest photochromic response was obtained for samples deposited at 1.3 Pa. Cyclic voltammetry for 20 cycles in a 1 M LiClO4 in propylene carbonate solution, inside a glovebox filled with argon, was used to evaluate the electrochromic response. Samples that showed optimum electrochromic response were deposited at 1.6 Pa. These results are explained in terms of the optical, structural, surface chemical composition, and vibrational modes.

Notes

Acknowledgements

This work was supported by CONACyT (Mexico) under projects No.168605 and 205733. One of us (M.P.-M.) is thankful to SNI-CONACyT for a SNI-III grant. We are grateful to G. Niklasson and C.-G. Granqvist (Uppsala University), and J. Santoyo-Salazar for enlightening discussions. M.M.-L. thanks the postdoctoral fellowship from CONACYT-SENER No. 2138. The technical assistance of E. Ayala, A. García-Sotelo, and M. Guerrero is acknowledged.

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Copyright information

© Springer Science+Business Media, LLC, part of Springer Nature 2018

Authors and Affiliations

  • V. Cruz-San Martín
    • 1
  • M. Morales-Luna
    • 2
  • P. E. García-Tinoco
    • 3
  • M. Pérez-González
    • 3
  • M. A. Arvizu
    • 3
  • H. Crotte-Ledesma
    • 3
  • M. Ponce-Mosso
    • 4
  • S. A. Tomás
    • 3
  1. 1.Bristol Centre for Functional Nanomaterials, School of PhysicsUniversity of BristolBristolUK
  2. 2.Facultad de Química, MaterialesUniversidad Autónoma de QuerétaroQuerétaroMexico
  3. 3.Departamento de FísicaCentro de Investigación y de Estudios Avanzados del I.P.N.Mexico CityMexico
  4. 4.Departamento de Ingeniería AeronáuticaESIME-Ticomán del I.P.N.Mexico CityMexico

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