{"title":"LaGaO3/SrTiO3混合晶体中Ti3+离子的蓝色荧光","authors":"S. Kaczmarek","doi":"10.1117/12.475317","DOIUrl":null,"url":null,"abstract":"In the absorption spectrum of the crystal there was stated the presence of Ti3+ ions at octahedral Ga positions in strong crystal field. Ti3+ ions arise due to some reducing conditions of the crystal growth. It was found that electron delocalization at higher temperature, e.g. In oxidation-reduction reaction: Ti4+ + e equals Ti3+ may appear in optical spectra as charge transfer bands in the NIR region giving rise to blue absorption. The observed fluorescence of 2T2-2E transition of Ti3+ in the LaGaO3/SrTiO3 mixed crystals shows two bands centered at about 420 and 447 nm coming from excitation at 314, 340 and 384 nm.","PeriodicalId":312884,"journal":{"name":"Feofilov Symposium on Spectropscopy of Crystals Activated by Rare-Earth and Transition Metal Ions","volume":"45 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2002-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Blue fluorescence of Ti3+ ions in LaGaO3/SrTiO3 mixed crystals\",\"authors\":\"S. Kaczmarek\",\"doi\":\"10.1117/12.475317\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In the absorption spectrum of the crystal there was stated the presence of Ti3+ ions at octahedral Ga positions in strong crystal field. Ti3+ ions arise due to some reducing conditions of the crystal growth. It was found that electron delocalization at higher temperature, e.g. In oxidation-reduction reaction: Ti4+ + e equals Ti3+ may appear in optical spectra as charge transfer bands in the NIR region giving rise to blue absorption. The observed fluorescence of 2T2-2E transition of Ti3+ in the LaGaO3/SrTiO3 mixed crystals shows two bands centered at about 420 and 447 nm coming from excitation at 314, 340 and 384 nm.\",\"PeriodicalId\":312884,\"journal\":{\"name\":\"Feofilov Symposium on Spectropscopy of Crystals Activated by Rare-Earth and Transition Metal Ions\",\"volume\":\"45 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2002-07-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Feofilov Symposium on Spectropscopy of Crystals Activated by Rare-Earth and Transition Metal Ions\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1117/12.475317\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Feofilov Symposium on Spectropscopy of Crystals Activated by Rare-Earth and Transition Metal Ions","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1117/12.475317","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
在强晶体场的吸收光谱中,在八面体Ga位置存在Ti3+离子。Ti3+离子的产生是由于晶体生长的一些还原条件。发现在较高温度下电子离域,例如在氧化还原反应中:Ti4+ + e = Ti3+可能在光谱中以近红外区电荷转移带的形式出现,引起蓝色吸收。LaGaO3/SrTiO3混合晶体中Ti3+的2T2-2E跃迁荧光显示,在314、340和384 nm激发下,Ti3+的2T2-2E跃迁有两个以420和447 nm为中心的荧光带。
Blue fluorescence of Ti3+ ions in LaGaO3/SrTiO3 mixed crystals
In the absorption spectrum of the crystal there was stated the presence of Ti3+ ions at octahedral Ga positions in strong crystal field. Ti3+ ions arise due to some reducing conditions of the crystal growth. It was found that electron delocalization at higher temperature, e.g. In oxidation-reduction reaction: Ti4+ + e equals Ti3+ may appear in optical spectra as charge transfer bands in the NIR region giving rise to blue absorption. The observed fluorescence of 2T2-2E transition of Ti3+ in the LaGaO3/SrTiO3 mixed crystals shows two bands centered at about 420 and 447 nm coming from excitation at 314, 340 and 384 nm.