Sukjune Choi , Daseul Ham , Sae Hyun Kang , Su Yong Lee , Do Young Noh , Hyon Chol Kang
{"title":"Polymorphic solid phase epitaxy of amorphous SnO2 thin films deposited on sapphire(0001) substrates","authors":"Sukjune Choi , Daseul Ham , Sae Hyun Kang , Su Yong Lee , Do Young Noh , Hyon Chol Kang","doi":"10.1016/j.ceramint.2025.02.217","DOIUrl":null,"url":null,"abstract":"<div><div>The polymorphic solid phase epitaxy of amorphous tin oxide (SnO<sub>2</sub>) thin films deposited on sapphire(0001) substrates through radio-frequency powder sputtering was investigated. A multimodal X-ray probe station was utilized to simultaneously investigate the crystallization and electronic conductivity changes during the <em>in situ</em> annealing of amorphous SnO<sub>2</sub> thin films under vacuum conditions. Crystallization was initiated at 200 °C, and most of the amorphous phase was converted to the crystalline phase upon annealing to 500 °C. This trend was consistent with the temperature-dependent electrical conductance variation, demonstrating metal-like behavior. Off-specular X-ray diffraction results confirmed the polymorphism of the SnO<sub>2</sub> thin films, i.e., the coexistence of orthorhombic columbite (C–SnO<sub>2</sub>) and tetragonal rutile (R–SnO<sub>2</sub>) phases and their epitaxial relationship with the sapphire(0001) substrate. In the 35-nm-thick sample, both C–SnO<sub>2</sub> and R–SnO<sub>2</sub> phases were formed epitaxially, while an additional polycrystalline R–SnO<sub>2</sub> phase was observed with increasing film thickness. This indicated that the formation of the metastable C–SnO<sub>2</sub> phase is determined by the strain field induced by the sapphire(0001) substrate. The result also revealed that the volume effect in the absence of interfacial strain favors the formation of a polycrystalline R–SnO<sub>2</sub> phase in the bulk region of amorphous thin films.</div></div>","PeriodicalId":267,"journal":{"name":"Ceramics International","volume":"51 15","pages":"Pages 20475-20481"},"PeriodicalIF":5.1000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ceramics International","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0272884225009009","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, CERAMICS","Score":null,"Total":0}
引用次数: 0
Abstract
The polymorphic solid phase epitaxy of amorphous tin oxide (SnO2) thin films deposited on sapphire(0001) substrates through radio-frequency powder sputtering was investigated. A multimodal X-ray probe station was utilized to simultaneously investigate the crystallization and electronic conductivity changes during the in situ annealing of amorphous SnO2 thin films under vacuum conditions. Crystallization was initiated at 200 °C, and most of the amorphous phase was converted to the crystalline phase upon annealing to 500 °C. This trend was consistent with the temperature-dependent electrical conductance variation, demonstrating metal-like behavior. Off-specular X-ray diffraction results confirmed the polymorphism of the SnO2 thin films, i.e., the coexistence of orthorhombic columbite (C–SnO2) and tetragonal rutile (R–SnO2) phases and their epitaxial relationship with the sapphire(0001) substrate. In the 35-nm-thick sample, both C–SnO2 and R–SnO2 phases were formed epitaxially, while an additional polycrystalline R–SnO2 phase was observed with increasing film thickness. This indicated that the formation of the metastable C–SnO2 phase is determined by the strain field induced by the sapphire(0001) substrate. The result also revealed that the volume effect in the absence of interfacial strain favors the formation of a polycrystalline R–SnO2 phase in the bulk region of amorphous thin films.
期刊介绍:
Ceramics International covers the science of advanced ceramic materials. The journal encourages contributions that demonstrate how an understanding of the basic chemical and physical phenomena may direct materials design and stimulate ideas for new or improved processing techniques, in order to obtain materials with desired structural features and properties.
Ceramics International covers oxide and non-oxide ceramics, functional glasses, glass ceramics, amorphous inorganic non-metallic materials (and their combinations with metal and organic materials), in the form of particulates, dense or porous bodies, thin/thick films and laminated, graded and composite structures. Process related topics such as ceramic-ceramic joints or joining ceramics with dissimilar materials, as well as surface finishing and conditioning are also covered. Besides traditional processing techniques, manufacturing routes of interest include innovative procedures benefiting from externally applied stresses, electromagnetic fields and energetic beams, as well as top-down and self-assembly nanotechnology approaches. In addition, the journal welcomes submissions on bio-inspired and bio-enabled materials designs, experimentally validated multi scale modelling and simulation for materials design, and the use of the most advanced chemical and physical characterization techniques of structure, properties and behaviour.
Technologically relevant low-dimensional systems are a particular focus of Ceramics International. These include 0, 1 and 2-D nanomaterials (also covering CNTs, graphene and related materials, and diamond-like carbons), their nanocomposites, as well as nano-hybrids and hierarchical multifunctional nanostructures that might integrate molecular, biological and electronic components.