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Herein, a scheme of Sr2+/Ca2+ ion substitution was employed to simultaneously regulate the defect and intervalence charge transfer (IVCT) state of Sr2−xCaxNb2O7:Pr3+ phosphors, resulting in a dual-modulation strategy for enhancing phosphor thermal stability. [ABSTRACT FROM AUTHOR]

In our work, a totally anomalous thermal quenching phenomenon of red-shifted and enhanced charge transfer state (CTS) absorption is found for the first time in LiTaO3:xPr3+ phosphors. The crystal structure, luminescent properties and the mechanism of abnormal thermal quenching were investigated in detail. [ABSTRACT FROM AUTHOR]

Praseodymium (Pr3+) ion and the transition metal vanadium (V5+) ion with d0 electronic configuration can form an intervalence charge transfer (IVCT) band, which can function both as a compensatory channel for its red emission and as a quenching channel, thus affecting the luminescence thermal stability of the phosphors. Research studies reveal that the emission of Pr3+ in the YVO4 matrix can be quenched by the IVCT mechanism, thereby limiting the application of phosphors. As such, the present contribution is based on the solid solution replacement strategy to inhibit the constitutent of the IVCT quenching channel and thus improve thermal stability. Therefore, phosphonium (P5+) with a valence state matching V5+ and a similar ion radius was selected for the V/P substitution. It lacks a d0 electron configuration, preventing the formation of an IVCT band with Pr3+ and thereby inhibiting the construction of the quenching channels to enhance thermal stability. While the empirical formula of IVCT indicates a decrease in the IVCT energy level from 3.32438 to 3.06251 eV upon the introduction of P5+, the PLE spectra demonstrate a sharp reduction in IVCT intensity, i.e., weakening of the quenching channel. The thermal stability of the phosphors at different excitation locations was enhanced with the rise of P5+ concentration. When excited at the 3P2 level, the Y0.995PO4:0.5%Pr3+ phosphor demonstrated highly stable red emission from 303 to 523 K, with a luminescence integrated intensity ranging from 95.5% to 105.3% compared to that at 303 K. This research provides a novel approach for inhibiting the IVCT quenching channel and broadens the commercial value of YVO4:Pr3+ phosphor for various applications. [ABSTRACT FROM AUTHOR]

Currently, the unique 5D 4 energy level of terbium (Tb3+) can contribute to narrow-band green light emission, which has high application prospects. However, due to its poor thermal stability at high temperatures, how to enhance the antithermal-quenching properties of Tb-doped phosphors has become a research difficulty in the field of solid-state lighting and temperature sensing. In this contribution, the antithermal-quenching green-emitting of terbium was achieved by Nb/Ta substitution to form GdNb 1-x Ta x O 4 :Tb3+ phosphors with various components. Photoluminescence analyses reveal an increasing trend in both the optical band gap and the intervalence charge transfer (IVCT) energy level positions with substitution. Variable-temperature spectrums observed that the phosphors under different compositions presented a large discrepancy in thermal quenching performance. It is elucidated that the elevated position of the IVCT energy level (IVCT-EL) predominantly influences thermal quenching, bolstering its role as a compensatory luminescence channel of 5D 3 →5D 4 far more than functioning as a quenching luminescence channel for Tb3+5D 3 /5D 4. Delving into the perspective of IVCT-EL positioning unveils the intrinsic mechanism through which IVCT-EL positions modulate the thermal quenching properties of phosphors with varying compositions due to the substitution of Ta for Nb. This insight facilitates the realization of enhanced thermal quenching resistance in phosphors. Furthermore, the antithermal-quenching property of Tb3+ in single-phase phosphors can be effectively modulated by excitation at different wavelengths. This tuning scheme not only advances the exploration of terbium-doped antithermal-quenching phosphors but also provides a novel strategy and reference for designing green-emitting phosphors in the fields of lighting and sensing. [Display omitted] [ABSTRACT FROM AUTHOR]

Raw materials and synthesis strategies have great influence on the morphologies and optical properties of materials. In this study, ultrasonic synthesis of controllable thin sheet-like BiPO 4 with an excessive visible-light response was synthesized, using Bi-based metal-organic frameworks (CAU-17) and ionic liquid [Omim]H 2 PO 4 as raw materials. Compared with BiPO 4 -H (hydrothermal, solid rod shape) synthesized using inorganic salt, BiPO 4 -A (agitation, thin rod-like) and BiPO 4 -U (ultrasonic, thin sheet-like) have better visible-light absorption capacity and narrower band gap. Under visible-light, they could degrade 27.7 % (BiPO 4 -H), 73.0 % (BiPO 4 -A), and 76.3 % (BiPO 4 -U) tetracycline hydrochloride at 30 min, respectively. The speedy charge transfer at the photogenerated carrier interface, large specific surface areas, and improved light adsorption greatly enhance the photocatalytic performance. Cyclic experiments exhibit that the material has good photostability and repeatability. Finally, the feasible degradation mechanism of the material was proposed via a capture experiment. This paper provides a new technique for synthesizing BiPO 4 or other photocatalysts, which can be used for high-efficiency wastewater purification under visible-light. [Display omitted] • A novel ultrasonic synthesis method for BiPO 4 with excellent visible-light response is presented. • [Bi-MOF(CAU-17)] and [Omim]H 2 PO 4 were used as raw materials instead of traditional inorganic salts. • The linear average photocatalytic rate of BiPO 4 -U is 16.1 times of BiPO 4 -H synthesized by traditional methods. • Possible photocatalytic mechanism was proposed based on photo-electrochemical characterization and free radical tests. [ABSTRACT FROM AUTHOR]