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KYb2F7:Er3+ based nanothermometers: controlled synthesis, enhanced red emission, and improved sensitivities via crystal-site engineering
KYb2F7 nanocrystals have stimulated extensive research interest due to their unique structure and tunable upconversion (UC) properties for the development of different technological applications. Herein, the controlled synthesis of KYb2F7:Er3+ nanocrystals for precise control over the crystal phases...
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Published in: | Journal of materials chemistry. C, Materials for optical and electronic devices Materials for optical and electronic devices, 2023-02, Vol.11 (6), p.2375-2388 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | KYb2F7 nanocrystals have stimulated extensive research interest due to their unique structure and tunable upconversion (UC) properties for the development of different technological applications. Herein, the controlled synthesis of KYb2F7:Er3+ nanocrystals for precise control over the crystal phases and morphologies was realized by varying the KF dose and reaction time via a facile hydrothermal method. Upon 365 nm excitation, the downconverted red emission of the KYb2F7:Er3+ nanocrystals pre-excited with the 980 nm laser was significantly enhanced. By manipulating the KYb2F7:Er3+ host structure via substitution of cations such as Ca2+, Ti4+, Si4+, Ge4+, Y3+, and Nd3+ for Yb3+ with optimized concentrations, the thermometric properties of KYb2F7:Er3+ were greatly improved. The substitution of Ti4+, Ge4+, and Y3+ has significantly improved the SR (for Ti4+ both SA and SR are improved). The highest SA (0.0028 K−1) and SR (1158/T2 K−1) were obtained for KYb1.8Ti0.15F7:Er3+ and KYb1.8Ge0.15F7:Er3+, respectively. The mechanistic investigations revealed that the green and red UC emissions resulted from the three- and two-photon process, respectively. We believe that the substitution strategy could be a powerful tool for enhancing the thermometric properties of luminescent materials. |
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ISSN: | 2050-7526 2050-7534 |
DOI: | 10.1039/d2tc04121a |