Near-infrared two-photon excited photoluminescence from Yb-doped CsPbClBr perovskite nanocrystals embedded into amphiphilic silica microspheres
Nonlinear absorption of metal-halide perovskite nanocrystals (NCs) makes them an ideal candidate for applications which require multiphoton-excited photoluminescence. By doping perovskite NCs with lanthanides, their emission can be extended into the near-infrared (NIR) spectral region. We demonstrat...
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Veröffentlicht in: | Nanoscale 2024-05, Vol.16 (18), p.911-92 |
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Zusammenfassung: | Nonlinear absorption of metal-halide perovskite nanocrystals (NCs) makes them an ideal candidate for applications which require multiphoton-excited photoluminescence. By doping perovskite NCs with lanthanides, their emission can be extended into the near-infrared (NIR) spectral region. We demonstrate how the combination of Yb
3+
doping and bandgap engineering of cesium lead halide perovskite NCs performed by anion exchange (from Cl
−
to Br
−
) leads to efficient and tunable emitters that operate under two-photon excitation in the NIR spectral region. By optimizing the anion composition, Yb
3+
-doped CsPbCl
x
Br
3−
x
NCs exhibited high values of two-photon absorption cross-section reaching 2.3 × 10
5
GM, and displayed dual-band emission located both in the visible (407-493 nm) and NIR (985 nm). With a view of practical applications of bio-visualisation in the NIR spectral range, these NCs were embedded into silica microspheres which were further wrapped with amphiphilic polymer shells to ensure their water-compatibility. The resulting microspheres with embedded NCs could be easily dispersed in both toluene and water, while still exhibiting a dual-band emission in visible and NIR under both one- and two-photon excitation conditions.
Yb
3+
-CsPbCl
x
Br
3−
x
perovskite nanocrystals with a high two-photon absorption cross-section of 2.3 × 10
5
GM embedded into amphiphilic silica microspheres emit visible and near-infrared light under two-photon infrared excitation in toluene and water. |
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ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/d4nr00892h |