发光
材料科学
结晶度
纳米颗粒
退火(玻璃)
化学工程
氧化物
胶体
热处理
纳米技术
量子产额
纳米晶
矿物学
光电子学
化学
光学
复合材料
冶金
荧光
工程类
物理
作者
Rafael V. Perrella,Rabei Mohammedi,Robin Kuhner,Christophe Cardone,Éric Larquet,Antigoni Alexandrou,Paulo C. de Sousa Filho,Thierry Gacoin
标识
DOI:10.1021/acs.cgd.3c00308
摘要
Optical applications of colloidal oxide nanoparticles are often limited by low luminescence efficiencies caused by poor crystallinity and surface quenching. Bulk oxides prepared via conventional high-temperature annealing offer intense luminescence but commonly fail to yield stable colloidal dispersions. Coupling the best of these two situations to afford highly crystalline, dispersible nanoparticles with luminescence performance exceeding that of bulk solids is still challenging, thus requiring new, safe, scalable, and reproducible methodologies. Herein, we report a silicate-coating strategy followed by aggregate elimination to recover stable colloids of 40–150 nm single crystalline rare earth vanadates after unprotected annealing (800–1000 °C). Eu3+-doped nanoparticles showed enhanced photostability and ∼50% emission quantum yields in water (λexc = 280 nm), while Dy3+-, Tm3+-, and Yb3+/Er3+-doped vanadates provided remarkably intense multicolor emissions via downshift or upconversion luminescence. We correlated the spectroscopic properties of pristine and annealed solids to microstructural characteristics to explain the superior emission features, opening new perspectives for sensing applications.
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