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Abstract Under 980 nm wavelength excitation, 530 and 550 nm green upconversion emission spectra of erbium-doped gadolinium gallium garnet single-crystal were measured in the temperature range of 298–423 K for ratiometric thermometry based on fluorescence intensity ratio (FIR). The crystal shows strong emission intensity, highly efficient ratiometric thermometric performance, as well as thermally stable emission spectral structure, it is thus a promising luminescent material for ratiometric thermometry. A multiple ratiometric thermometry is proposed and demonstrated in comparison with the usually adopted ratiometric thermometry based on integrated emission intensity. The multiple ratiometric thermometry considers six FIRs involving two component peaks of the 530 nm emission band and three component peaks of the 550 nm emission band, which result from an electronic transition from one Stark sublevel of the 2H 11/2 or 4S 3/2 state to another of the ground state 4I 15/2 of Er3+. All the six FIR schemes show highly efficient sensing performances with slightly different temperature characteristics. The temperature is overall determined by the six FIR schemes, largely increasing the reliability of temperature measurement. Graphical abstract We have studied ratiometric thermometry based on six fluorescence intensity ratios (FIR) involving two component peaks of 530 nm emission band and three component peaks of 550 nm emission band of erbium-doped gadolinium gallium garnet single-crystal. All the six EIR schemes display higher, slightly different relative sensitivities and thermal resolutions. The temperature is overall and reliably determined by the six EIR schemes. In addition, the crystal shows strong green upconversion emissions and thermally stable spectral structure, it is thus a promising material for the ratiometric thermometry. The multiple ratiometric thermometry based on the material has highly efficient performance, and is thus promising for reliable temperature detection in electromagnetically and/or thermally harsh environments and some industrial processes. fx1 [ABSTRACT FROM AUTHOR]

We measured fluorescence spectra of visible and infrared electronic transitions at 530 (2H 11/2 → 4I 15/2), 560 (4S 3/2 → 4I 15/2), 670 (4F 9/2 → 4I 15/2), 980 (4I 11/2 → 4I 15/2), 1530 (4I 13/2 → 4I 15/2) and 2700 nm (4I 11/2 → 4I 13/2) of Er3+ in Gd 3 (Al 0.4 Ga 0.6) 5 O 12 garnet single-crystal excited at the wavelength 520 nm (for the 980 nm emission) or 980 nm (for other emissions). From measured fluorescence spectrum, Er3+ emission cross-section spectrum was calibrated for each transition. Absorption cross-section spectra were further derived on the basis of McCumber equation, and compared with those spectra obtained from measured absorption spectrum on the basis of the Beer-Lambert law. The comparison showed that the results given by two methods can be regarded as same within the error. The transient features of visible and infrared emissions were also studied under pulse excitation. The results showed that, while the three IR emissions at 980, 1530 and 2700 nm all follow a mono-exponential function, both green and red 980-nm-upconverted emissions at 560 and 670 nm exhibit non-mono-exponentially decaying feature, and each decaying trace can be fitted by a sum of two exponential functions. The non-mono-exponential feature is related to cross relaxation caused by non-radiative short-distance energy transfer between clustered Er3+ sites. • Cross-section spectra of Er3+ ions in Gd 3 (Al,Ga) 5 O 12 garnet crystal were studied. • Emission cross-section spectra are computed from measured fluorescence spectra. • Absorption cross-section spectra are derived by two ways and results are same. • 980-nm-upconverted visible emissions show non-mono-exponential transient feature. • It is caused by non-radiative energy transfer between clustered Er3+ sites. [ABSTRACT FROM AUTHOR]