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Pixel switching of epitaxial Pd/YHx/CaF2 switchable mirrors

Author

Listed:
  • J. W. J. Kerssemakers

    (Faculty of Sciences, Vrije Universiteit)

  • S. J. van der Molen

    (Faculty of Sciences, Vrije Universiteit)

  • N. J. Koeman

    (Faculty of Sciences, Vrije Universiteit)

  • R. Günther

    (Faculty of Sciences, Vrije Universiteit)

  • R. Griessen

    (Faculty of Sciences, Vrije Universiteit)

Abstract

Exposure of rare-earth films to hydrogen can induce a metal–insulator transition, accompanied by pronounced optical changes. This ‘switchable mirror’ effect1 has received considerable attention from theoretical2,3,4, experimental5 and technological6 points of view. Most systems use polycrystalline films, but the synthesis of yttrium-based epitaxial switchable mirrors7 has also been reported. The latter form an extended self-organized ridge network during initial hydrogen loading7, which results in the creation of micrometre-sized triangular domains. Here we observe homogeneous and essentially independent optical switching of individual domains in epitaxial switchable mirrors during hydrogen absorption. The optical switching is accompanied by topographical changes as the domains sequentially expand and contract; the ridges block lateral hydrogen diffusion and serve as a microscopic lubricant for the domain oscillations. We observe the correlated changes in topology and optical properties using in situ atomic force and optical microscopy. Single-domain phase switching is not observed in polycrystalline films, which are optically homogeneous8. The ability to generate a tunable, dense pattern of switchable pixels is of technological relevance for solid-state displays based on switchable mirrors.

Suggested Citation

  • J. W. J. Kerssemakers & S. J. van der Molen & N. J. Koeman & R. Günther & R. Griessen, 2000. "Pixel switching of epitaxial Pd/YHx/CaF2 switchable mirrors," Nature, Nature, vol. 406(6795), pages 489-491, August.
  • Handle: RePEc:nat:nature:v:406:y:2000:i:6795:d:10.1038_35020024
    DOI: 10.1038/35020024
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