E. Strods , M. Zubkins , V. Vibornijs , D. Moldarev , A. Sarakovskis , K. Kundzins , E. Letko , D. Primetzhofer , J. Purans
{"title":"Role of hydrogen dynamics and deposition conditions in photochromic YHO/MoO3 bilayer films","authors":"E. Strods , M. Zubkins , V. Vibornijs , D. Moldarev , A. Sarakovskis , K. Kundzins , E. Letko , D. Primetzhofer , J. Purans","doi":"10.1016/j.solmat.2025.113789","DOIUrl":null,"url":null,"abstract":"<div><div>Oxygen-containing yttrium hydride (YHO) and molybdenum trioxide (MoO<sub>3</sub>) bilayer films (YHO/MoO<sub>3</sub>) are produced using reactive magnetron sputtering, and their photochromic properties are investigated in relation to the thickness and density of the MoO<sub>3</sub> layer. Compared to single YHO films, the YHO/MoO<sub>3</sub> films exhibit faster coloration and larger contrast, with both parameters adjustable by varying the thickness or deposition pressure of the MoO<sub>3</sub> layer. Transparent YHO/MoO<sub>3</sub> films (∼75 % at 550 nm) demonstrate a photochromic contrast of up to 60 %, significantly higher than the 25–30 % contrast observed for single YHO films after 20 h of UVA-violet light exposure. This enhancement arises from hydrogen intercalation from the (200)-textured polycrystalline YHO film into the X-ray amorphous MoO<sub>3</sub>, leading to the formation of molybdenum bronze (H<sub><em>x</em></sub>MoO<sub>3</sub>), as confirmed by X-ray photoelectron and optical spectroscopies. However, the darkened YHO/MoO<sub>3</sub> films do not fully recover to their initial transparency after illumination due to the irreversible nature of the coloured MoO<sub>3</sub> layer. Most of the hydrogen intercalated into MoO<sub>3</sub> originates from the YHO layer during the initial darkening process. Furthermore, the bilayer films are chemically unstable, exhibiting gradual darkening over time even without intentional UV illumination, as confirmed by nuclear reaction analysis.</div></div>","PeriodicalId":429,"journal":{"name":"Solar Energy Materials and Solar Cells","volume":"292 ","pages":"Article 113789"},"PeriodicalIF":6.3000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Solar Energy Materials and Solar Cells","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927024825003903","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENERGY & FUELS","Score":null,"Total":0}
引用次数: 0
Abstract
Oxygen-containing yttrium hydride (YHO) and molybdenum trioxide (MoO3) bilayer films (YHO/MoO3) are produced using reactive magnetron sputtering, and their photochromic properties are investigated in relation to the thickness and density of the MoO3 layer. Compared to single YHO films, the YHO/MoO3 films exhibit faster coloration and larger contrast, with both parameters adjustable by varying the thickness or deposition pressure of the MoO3 layer. Transparent YHO/MoO3 films (∼75 % at 550 nm) demonstrate a photochromic contrast of up to 60 %, significantly higher than the 25–30 % contrast observed for single YHO films after 20 h of UVA-violet light exposure. This enhancement arises from hydrogen intercalation from the (200)-textured polycrystalline YHO film into the X-ray amorphous MoO3, leading to the formation of molybdenum bronze (HxMoO3), as confirmed by X-ray photoelectron and optical spectroscopies. However, the darkened YHO/MoO3 films do not fully recover to their initial transparency after illumination due to the irreversible nature of the coloured MoO3 layer. Most of the hydrogen intercalated into MoO3 originates from the YHO layer during the initial darkening process. Furthermore, the bilayer films are chemically unstable, exhibiting gradual darkening over time even without intentional UV illumination, as confirmed by nuclear reaction analysis.
期刊介绍:
Solar Energy Materials & Solar Cells is intended as a vehicle for the dissemination of research results on materials science and technology related to photovoltaic, photothermal and photoelectrochemical solar energy conversion. Materials science is taken in the broadest possible sense and encompasses physics, chemistry, optics, materials fabrication and analysis for all types of materials.