发光
光子上转换
材料科学
激发
红外线的
镧系元素
粒子(生态学)
光漂白
光电子学
纳米颗粒
光学
纳米技术
荧光
化学
物理
离子
地质学
海洋学
有机化学
量子力学
作者
Qian Liu,Yunxiang Zhang,Chunte Sam Peng,Tianshe Yang,Lydia‐Marie Joubert,Steven Chu
出处
期刊:Nature Photonics
[Springer Nature]
日期:2018-08-06
卷期号:12 (9): 548-553
被引量:200
标识
DOI:10.1038/s41566-018-0217-1
摘要
Lanthanide-doped upconversion nanoparticles (UCNPs) are promising single-molecule probes given their non-blinking, photobleach-resistant luminescence upon infrared excitation. However, the weak luminescence of sub-50 nm UCNPs limits their single-particle detection to above 10 kWcm-2 that is impractical for live cell imaging. Here, we systematically characterize single-particle luminescence for UCNPs with various formulations over a 106 variation in incident power, down to 8 Wcm-2. A core-shell-shell (CSS) structure (NaYF4@NaYb1-xF4:Erx@NaYF4) is shown to be significantly brighter than the commonly used NaY0.78F4:Yb0.2Er0.02. At 8 Wcm-2, the 8% Er3+ CSS particles exhibit a 150-fold enhancement given their high sensitizer Yb3+ content and the presence of an inert shell to prevent energy migration to defects. Moreover, we reveal power-dependent luminescence enhancement from the inert shell, which explains the discrepancy in enhancement factors reported by ensemble and previous single-particle measurements. These brighter probes open the possibility of cellular and single-molecule tracking at low irradiance.
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