Abstract
Optical thermometry as an important local temperature-sensing technique, has received increasing attention in scientific and industrial areas. However, it is still a big challenge to develop luminescent materials with self-activated dual-wavelength emissions toward high-sensitivity optical thermometers. Herein, a novel ratiometric thermometric strategy of Bi3+-activated dual-wavelength emission band was realized in the same lattice position with two local electronic states of La3Sb1-xTaxO7:Bi3+(0 ≤ x ≤ 1.0) materials based on the different temperature-dependent emission behaviors, benefiting from the highly-sensitive and regulable emission to the coordination environment of Bi3+. The structural and spectral results demonstrate that the emission tremendously shifted from green to blue with 68 nm and the intensity was enhanced 2.6 times. Especially, the visual dual-wavelength emitting from two emission centers was presented by increasing the Ta5+substitution concentration to 20% or 25%, mainly originating from the two local electronic states around the Bi3+ emission center. Significantly, the dual-wavelength with different thermal-quenching performance provided high-temperature sensitivity and good discrimination signals for optical thermometry in the range between 303 and 493 K. The maximum relative sensitivity reached 2.64%/K (La3Sb0.8Ta0.2O7:0.04Bi3+@383 K) and 1.91%/K (La3Sb0.75Ta0.25O7:0.04Bi3+@388 K). This work reveals a rational design strategy of different local electronic states around the single-doping multiple emission centers towards practical applications, such as luminescence thermometry and white LED lighting.
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