光子上转换
材料科学
光致发光
镱
纳米晶
镧系元素
猝灭(荧光)
光化学
纳米颗粒
分子
化学物理
配体(生物化学)
纳米技术
光电子学
物理
兴奋剂
发光
荧光
化学
光学
离子
受体
有机化学
生物化学
作者
Hui Xu,Sanyang Han,Renren Deng,Qianqian Su,Ying Wei,Yongan Tang,Xian Qin,Xiaogang Liu
出处
期刊:Nature Photonics
[Springer Nature]
日期:2021-09-09
卷期号:15 (10): 732-737
被引量:93
标识
DOI:10.1038/s41566-021-00862-3
摘要
Upconversion nanocrystals have been extensively investigated for optical imaging and biomedical applications1,2. However, their photoluminescence is strongly attenuated by surface quenching as the nanocrystal size diminishes3. Despite considerable efforts4,5, the quenching mechanism remains poorly understood. Here we report that surface coordination of bidentate picolinic acid molecules to NaGdF4:Yb/Tm nanoparticles enhances four-photon upconversion by 11,000-fold. Mechanistic studies indicate that surface ligand coordination reconstructs orbital hybridization and crystal-field splitting, minimizing the energy difference between the 4f orbitals of surface and inner lanthanide sensitizers. The 4f-orbital energy resonance facilitates energy migration within the ytterbium sublattice, impeding energy diffusion to surface defects and ultimately enhancing energy transfer to the emitters. Moreover, ligand coordination can exert energy-level reconstruction with a ligand–sensitizer separation of over 2 nm. These findings offer insights into the development of highly emissive nanohybrids and provide a platform for constructing optical interrogation systems at single-particle levels. Strong lanthanide-doped upconversion luminescence enhancement is achieved by the use of surface molecules which enhance four-photon upconversion emission. The results may lead to new, highly emissive, nanohybrid systems.
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