光致变色
氢化物
钇
氘
氢
材料科学
薄膜
扩散
氧气
分析化学(期刊)
溅射
光化学
化学
纳米技术
冶金
有机化学
原子物理学
氧化物
物理
热力学
作者
Marcos V. Moro,Sigurbjörn M. Aðalsteinsson,Dmitrii Moldarev,Max Wolff,Daniel Primetzhofer
标识
DOI:10.1002/pssr.202100508
摘要
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.
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