材料科学
纳米颗粒
发光
纳米晶
六角相
光子上转换
兴奋剂
纳米技术
相(物质)
镧系元素
配体(生物化学)
化学工程
离子
化学
有机化学
光电子学
工程类
生物化学
受体
作者
Debashrita Sarkar,Brahmaiah Meesaragandla,Tuhin Samanta,Venkataramanan Mahalingam
标识
DOI:10.1002/slct.201600699
摘要
Abstract Lanthanide (Ln 3+ )‐doped NaYF 4 nanoparticles (NPs) are generally prepared using high temperature methods which generally restricts the choice of capping ligands as well as lead to the release of toxic fluorinated and oxyfluorinated carbon species during synthesis. In this work, we report the synthesis of highly crystalline Ln 3+ ‐doped NaYF 4 nanoparticles (NPs) at room temperature using a wide variety of ligands. Interestingly, the phase of the NPs could be controlled using suitable capping ligands. Formation of pure cubic phase NaYF 4 NPs is achieved using dicarboxylic acid as capping ligands, whereas diamine ligands promote formation of hexagonal phase NPs. Time‐dependent XRD analysis clearly indicates the phase evolution of the nanocrystals. Both cubic and hexagonal phase NaYF 4 NPs exhibit intense Stokes‐shifted emission when doped with Eu 3+ ions. Whereas doping Yb 3+ /Er 3+ ions led to strong luminescence in the visible region via the upconversion process. In addition, the Yb 3+ /Er 3+ ‐doped NaYF 4 nanocrystals display strong emission in the optical telecommunication window (∼1550 nm) which are generally difficult to observe in colloidal nanocrystals. We believe that with appropriate selection of capping ligands NPs with good morphology and size can be achieved. In addition to the greener approach of the synthesis route which is important for energy minimization, we strongly believe that the synthetic strategy might pave way to the fundamental understanding of the growth of NPs.
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