Bi3+-Doped BaYF5:Yb,Er Upconversion Nanoparticles with Enhanced Luminescence and Application Case for X‑ray Computed Tomography Imaging

In this work, BaYF5:20%Yb3+/2%Er3+/x%Bi3+ (abbreviated as BaYF5:Yb,Er,Bi x , where x = 0–3.0) upconversion nanoparticles (UCNPs) with various doping concentrations of Bi3+ were synthesized through a simple hydrothermal method. The influence of the doping amount of Bi3+ on the microstructures and upc...

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Veröffentlicht in:Inorganic chemistry 2020-12, Vol.59 (24), p.17906-17915
Hauptverfasser: Luo, Ran, Chen, Lei, Li, Qinyu, Zhou, Jie, Mei, Linqiang, Ning, Zhanglei, Zhao, Yan, Liu, Mengjiao, Lai, Xin, Bi, Jian, Yin, Wenyan, Gao, Daojiang
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Sprache:eng
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Zusammenfassung:In this work, BaYF5:20%Yb3+/2%Er3+/x%Bi3+ (abbreviated as BaYF5:Yb,Er,Bi x , where x = 0–3.0) upconversion nanoparticles (UCNPs) with various doping concentrations of Bi3+ were synthesized through a simple hydrothermal method. The influence of the doping amount of Bi3+ on the microstructures and upconversion luminescence (UCL) properties of the BaYF5:Yb,Er,Bi x UCNPs was studied in detail. The doping concentration of Bi3+ has little influence on the microstructures of the UCNPs but significantly impacts their UCL intensities. Under excitation of a 980 nm near-IR laser, the observed UCL intensities for the BaYF5:Yb,Er,Bi x UCNPs display first an increasing trend and then a decreasing trend with an increase in the ratio x, giving a maximum at x = 2.5. A possible energy-transfer process and simplified energy levels of the BaYF5:Yb,Er,Bi x UCNPs were proposed. The potential of the BaYF5:Yb,Er,Bi x UCNPs as contrast agents for computerized tomography (CT) imaging was successfully demonstrated. An obvious accumulation of BaYF5:Yb,Er,Bi x in tumor sites was achieved because of high passive targeting by the enhanced permeability and retention effect and relatively low uptake by a reticuloendothelial system such as liver and spleen. This work paves a new route for the design of luminescence-enhanced UNCPs as promising bioimaging agents for cancer theranostics.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.0c01818