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Photochromism in Isotopically Labeled Oxygen‐Containing Yttrium−Hydride and Deuteride Thin‐Film Systems
Author(s) -
Moro Marcos V.,
Aðalsteinsson Sigurbjörn M.,
Moldarev Dmitrii,
Wolff Max,
Primetzhofer Daniel
Publication year - 2022
Publication title -
physica status solidi (rrl) – rapid research letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.786
H-Index - 68
eISSN - 1862-6270
pISSN - 1862-6254
DOI - 10.1002/pssr.202100508
Subject(s) - photochromism , hydride , yttrium , deuterium , hydrogen , materials science , thin film , diffusion , oxygen , analytical chemistry (journal) , sputtering , photochemistry , chemistry , nanotechnology , metallurgy , organic chemistry , atomic physics , oxide , physics , thermodynamics
Photochromic mono‐ and bilayered thin films of oxygen‐containing isotope‐labeled yttrium−hydride (i.e., protium and deuterium) are synthesized via reactive Ar sputtering. Selected samples are encapsulated with transparent diffusion barriers. Combining depth‐resolved nondestructive ion beam‐based techniques for composition and optical spectrophotometry, material mobility in the samples during illumination and over time is investigated. The results reveal that deuteride thin films exhibit a strong photochromic response equivalent to hydrogenated systems. No evidence of long‐distance light‐induced hydrogen mobility or thermal diffusion is found. The findings thus show that photochromism is not connected to long‐distance material transport. The observations for encapsulated samples also exclude direct material exchange with the environment and any environmental influence on material mobility.