Journal
ACS PHOTONICS
Volume 8, Issue 3, Pages 709-715Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acsphotonics.0c01877
Keywords
oxyhydrides; photochromic; anions; oxide; hydride; positron annihilation; lanthanides; diffusion
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Funding
- Mat4Sus Research Program - Netherlands Organisation for Scientific Research (NWO) [680.M4SF.034]
- Open Technology research program - Netherlands Organisation for Scientific Research (NWO) [13282]
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Rare-earth oxyhydride REOxH3-2x thin films exhibit a reversible photochromic effect at ambient conditions, with the extent of optical change and bleaching speed largely tunable by the O/H anion ratio and cation choice. Data suggests that oxyhydrides formed by REs with larger ionic radius have greater optical contrast and faster bleaching speed, indicating a possible dependency of the photochromic mechanism on anion site-hopping.
Rare-earth oxyhydride REOxH3-2x thin films prepared by air-oxidation of reactively sputtered REH2 dihydrides show a color-neutral, reversible photochromic effect at ambient conditions. The present work shows that the O/H anion ratio, as well as the choice of the cation, allow to largely tune the extent of the optical change and its speed. The bleaching time, in particular, can be reduced by an order of magnitude by increasing the O/H ratio, indirectly defined by the deposition pressure of the parent REH2. The influence of the cation (RE = Sc, Y, Gd) under comparable deposition conditions is discussed. Our data suggest that REs of a larger ionic radius form oxyhydrides with a larger optical contrast and faster bleaching speed, hinting to a dependency of the photochromic mechanism on the anion site-hopping.
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