{"title":"通过位点裁剪扩大环境不对称性以增强(Gd,Na)3(Ga,In)2(Ga,Ge)3O12石榴石中 Sm3+ 的发光特性","authors":"Jiajun Feng, Yongxin Yu, Hongji Song, Zibo Chen, Yingxiang Zhu, Jiahui Liu, Jingtian Xie, Lianfen Chen, Junhao Li","doi":"10.1021/acs.inorgchem.5c00549","DOIUrl":null,"url":null,"abstract":"A structural design strategy was employed to develop NaGd<sub>2</sub>Ga<sub>2</sub>InGe<sub>2</sub>O<sub>12</sub>:Sm<sup>3+</sup> (NGGIG:Sm<sup>3+</sup>) garnet phosphors, optimizing the local coordination environment to enhance luminescence performance. By tailoring site occupation, Sm<sup>3+</sup> ions were incorporated into an asymmetric crystal field, where a statistical probability model confirmed that ∼97% of Sm<sup>3+</sup> ions reside in distorted coordination environments, promoting electric dipole(ED) transitions. The phosphors exhibit a high red-to-orange (<i>R</i>/<i>O</i>) intensity ratio of 2.97, contributing to enhanced red emission. CIE chromaticity coordinates of (0.61, 0.39) indicate a significant shift toward the red region, and the phosphors retain over 70% of their luminescence intensity at 400 K, demonstrating good thermal stability. These characteristics make NGGIG:Sm<sup>3+</sup> a promising candidate for high-performance red phosphors in solid-state lighting applications, highlighting the effectiveness of site engineering in garnet structures for optimizing luminescence efficiency and stability.","PeriodicalId":40,"journal":{"name":"Inorganic Chemistry","volume":"23 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-04-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enlarging Environmental Asymmetry by the Site Tailoring to Enhance Luminescence Properties of Sm3+ in the (Gd,Na)3(Ga,In)2(Ga,Ge)3O12 Garnet\",\"authors\":\"Jiajun Feng, Yongxin Yu, Hongji Song, Zibo Chen, Yingxiang Zhu, Jiahui Liu, Jingtian Xie, Lianfen Chen, Junhao Li\",\"doi\":\"10.1021/acs.inorgchem.5c00549\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A structural design strategy was employed to develop NaGd<sub>2</sub>Ga<sub>2</sub>InGe<sub>2</sub>O<sub>12</sub>:Sm<sup>3+</sup> (NGGIG:Sm<sup>3+</sup>) garnet phosphors, optimizing the local coordination environment to enhance luminescence performance. By tailoring site occupation, Sm<sup>3+</sup> ions were incorporated into an asymmetric crystal field, where a statistical probability model confirmed that ∼97% of Sm<sup>3+</sup> ions reside in distorted coordination environments, promoting electric dipole(ED) transitions. The phosphors exhibit a high red-to-orange (<i>R</i>/<i>O</i>) intensity ratio of 2.97, contributing to enhanced red emission. CIE chromaticity coordinates of (0.61, 0.39) indicate a significant shift toward the red region, and the phosphors retain over 70% of their luminescence intensity at 400 K, demonstrating good thermal stability. These characteristics make NGGIG:Sm<sup>3+</sup> a promising candidate for high-performance red phosphors in solid-state lighting applications, highlighting the effectiveness of site engineering in garnet structures for optimizing luminescence efficiency and stability.\",\"PeriodicalId\":40,\"journal\":{\"name\":\"Inorganic Chemistry\",\"volume\":\"23 1\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-04-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Inorganic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.inorgchem.5c00549\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.inorgchem.5c00549","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Enlarging Environmental Asymmetry by the Site Tailoring to Enhance Luminescence Properties of Sm3+ in the (Gd,Na)3(Ga,In)2(Ga,Ge)3O12 Garnet
A structural design strategy was employed to develop NaGd2Ga2InGe2O12:Sm3+ (NGGIG:Sm3+) garnet phosphors, optimizing the local coordination environment to enhance luminescence performance. By tailoring site occupation, Sm3+ ions were incorporated into an asymmetric crystal field, where a statistical probability model confirmed that ∼97% of Sm3+ ions reside in distorted coordination environments, promoting electric dipole(ED) transitions. The phosphors exhibit a high red-to-orange (R/O) intensity ratio of 2.97, contributing to enhanced red emission. CIE chromaticity coordinates of (0.61, 0.39) indicate a significant shift toward the red region, and the phosphors retain over 70% of their luminescence intensity at 400 K, demonstrating good thermal stability. These characteristics make NGGIG:Sm3+ a promising candidate for high-performance red phosphors in solid-state lighting applications, highlighting the effectiveness of site engineering in garnet structures for optimizing luminescence efficiency and stability.
期刊介绍:
Inorganic Chemistry publishes fundamental studies in all phases of inorganic chemistry. Coverage includes experimental and theoretical reports on quantitative studies of structure and thermodynamics, kinetics, mechanisms of inorganic reactions, bioinorganic chemistry, and relevant aspects of organometallic chemistry, solid-state phenomena, and chemical bonding theory. Emphasis is placed on the synthesis, structure, thermodynamics, reactivity, spectroscopy, and bonding properties of significant new and known compounds.