Guanying Chen

Upconversion Emission Enhancement in Yb3+/Er3+-Codoped Y2O3 Nanocrystals by Tridoping with Li+ Ions

We demonstrate that tridoping with Li + ions enhances the visible green and red upconversion (UC) emissions in Er 3+ /Yb 3+ -codoped Y 2 O 3 nanocrystals by up to half of the bulk counterpart, i.e., about 2 orders of magnitude higher than previous results. X-ray diffraction and decay time investigations give evidence that tridoping with Li + ions can tailor the local crystal field of the Y 2 O 3 host lattice. Theoretical calculations illustrate well that a significant UC intensity enhancement arises from the synthesized tailoring effect induced by the Li + ions, which increase lifetimes in the intermediate 4 I 11/2 (Er) and 2 F 5/2 (Yb) states, increase optically active sites in the Y 2 O 3 host lattice, and dissociate the Yb 3+ and Er 3+ ion clusters in the nanocrytals. The general theoretical description of the visible UC radiations shows that the Yb 3+ ion sensitization and the tailoring effect induced by the Li + ions are two independent enhancement mechanisms, which is expected to lead to an increasing number of photonic and biomedical applications in the future.

Upconversion emission tuning from green to red in Yb3+/Ho3+-codoped NaYF4 nanocrystals by tridoping with Ce3+ ions.

Upconversion (UC) emission tuning from green to red in monodisperse NaYF(4):Yb(3+)/Ho(3+) nanocrystals was successfully achieved by tridoping with Ce(3+) ions under diode laser excitation of 970 nm. It is proposed that two efficient cross-relaxation processes, 5S2/5F4(Ho) + 2F(5/2)(Ce) --> 5F5(Ho) + 2F(7/2)(Ce) and 5I6(Ho) + 2F(5/2)(Ce) --> 5I7(Ho) + 2F(7/2)(Ce)between Ho(3+) and Ce(3+) ions, have been employed to select UC pathways to tune the UC radiation. Theoretical investigations based on steady-state equations demonstrate the proposed UC mechanisms and explain well the observed linear increase of the UC red-to-green intensity ratio with the increment of Ce(3+) ion concentrations.

Two-color upconversion in rare-earth-ion-doped ZrO2 nanocrystals

To develop fluorescent labels for multicolor imaging, rare-earth-ion-doped ZrO2 nanocrystals were prepared by a complex precursor method. Laser excitation of 976nm induced single fluorescent bands of green and red upconversion (UC) in ZrO2:Er3+ and ZrO2:Er3++Yb3+ nanocrystals, respectively. A suppression ratio (SR) parameter was introduced, defined as the UC intensity ratio of the main band to all the other detected impurity bands, and SR values in the order of 10–100 were experimentally obtained, demonstrating the excellent monochromaticity of the UC labels. Thus, the two-color UC labels obtained are potentially ideal to be used for biological multicolor imaging.

Autofluorescence insensitive imaging using upconverting nanocrystals in scattering media

Autofluorescence is a nuisance in the field of fluorescence imaging and tomography of exogenous molecular markers in tissue, degrading the quality of the collected data. In this letter, we report autofluorescence insensitive imaging using highly efficient upconverting nanocrystals (NaYF4:Yb3+∕Tm3+) in a tissue phantom illuminated with near-infrared radiation of 85mW∕cm2. It was found that imaging with such nanocrystals leads to an exceptionally high contrast compared to traditional downconverting fluorophores due to the absence of autofluorescence. Upconverting nanocrystals may be envisaged as important biological markers for tissue imaging purposes.

Ultraviolet upconversion fluorescence in rare-earth-ion-doped Y2O3 induced by infrared diode laser excitation.

Room-temperature ultraviolet emission of Tm(3+) ions at 298 ((1)I(6)-->(3)H(6)), 364 ((1)D(2)-->(3)H(6)), and 391 nm ((1)I(6)-->(3)H(5)) was obtained in Y(2)O(3):Yb(3+)-Tm(3+) by continuous-wave diode laser excitation of 980 nm. Power dependence analysis demonstrates that five- and six-photon upconversion processes populate the (1)D(2) and (1)I(6) states, respectively. We believe that the (1)D(2) population originates from the cross relaxation (1)G(4)+(3)F(4)-->(3)H(4)+(1)D(2) of the Tm(3+) ions, while subsequent energy transfer from Yb(3+) to Tm(3+) excites the (1)D(2) state to the upper (1)I(6) state. High multiphoton-induced ultraviolet emission is also expected for other trivalent rare-earth ions similar to Tm(3+).

Near vacuum ultraviolet luminescence of Gd3+ and Er3+ ions generated by super saturation upconversion processes

Near vacuum ultraviolet (UV) upconversion (UC) emissions with a spectral resolution of 1 nm, from the (6)G(J), (6)D(J), (6)I(J), (6)P(J) levels of Gd(3+) and the (2)L(17/2), (4)D(7/2), (2)H(2)(9/2), (2)D(5/2), (4)G(7/2), (2)K(13/2), (2)P(3/2) levels of Er(3+), were observed under 974 nm laser excitation. Mechanism analyses illustrate that successive energy transfers (ETs) from Yb(3+) to Er(3+) generate UV UC radiations in Er(3+), while two resonant ETs from Er(3+) to Gd(3+) lead to UV UC radiations in Gd(3+). Power dependence analyses indicate that the expected inefficient four- and five-photon processes have been switched into efficient two-photon processes due to a super saturation UC phenomenon that employs consecutive saturations at the intermediate states.

ULTRAVIOLET AND BLUE UPCONVERSION EMISSIONS OF NaYF4:La3+(Er3+, Tb3+) NANOCRYSTALS UNDER 532 NM LASER EXCITATION

The upconversion (UC) fluorescences from 300 nm to 500 nm of NaYF4:La3+(Er3+, Tb3+) nanocrystals under 532 nm laser excitation were investigated at room temperature. These UC luminescences have potential applications in UC lasers.