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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]

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]

The synthesis conditions of most phosphors doped with lanthanide ions with d–f transition require a reducing atmosphere. The doping Bi3+ ions selected in this study perfectly avoid this requirement, and they are environmentally friendly and safe. Nevertheless, the spectral tuning of Bi3+ is a great challenge that limits its application. Herein, by regulating the value of x in the new solid solution Sr2+xLa1−xGaO5−xFx, the luminescence of Bi3+ is well promoted. Through an excitation-driven strategy, the emission peak position of Bi3+ is redshifted, and the luminescence of trivalent bismuth is successfully adjusted, which can also be applied to anti-blue lighting. In addition, we constructed a Bi3+–Eu3+ dual luminescence system, and, regardless of changes in the Bi3+/Eu3+ concentration or excitation wavelength, a single matrix white light phosphor was realized. Through calculations, the activation energy of the phosphor doped with 2.5%Eu3+ was found to be 0.257 eV, which is higher than the activation energy of some common compounds. This indicates that the phosphor has good application prospects in the field of solid-state lighting. It is worth noting that based on the different thermal response behaviors of Bi3+ and Eu3+, when the Eu3+ content is fixed at 1%, the maximum relative sensitivity of the optical thermometer based on its fluorescence intensity ratio is about 1.46% K−1 at 383 K, which is higher than that of Bi3+ and Eu3+ co-doped phosphors previously reported. We also obtained a high absolute sensitivity of 0.00139 K−1 at 403 K. Therefore, we also studied the thermal sensitivity of Bi3+ and Er3+ co-doped solid solutions. The results show that this solid-solution phosphor has far-reaching application prospects in the temperature sensing field. [ABSTRACT FROM AUTHOR]

Most praseodymium-doped red-emitting phosphors need high-temperature synthesis conditions with a reducing atmosphere. The niobate matrix selected in this work provides a sufficient electron-rich-site environment for praseodymium through charge migration, and praseodymium can be self-reduced in air atmosphere, which is safe and environmentally friendly. By building the [NbO6] group → Pr3+ energy transfer and finely modifying the doping concentration of Pr3+ ions, we constructed a dual-luminescence-system of the [NbO6] group and Pr3+. Thereby, optical temperature measurement based on fluorescence intensity ratio (FIR) technology of Pr3+ ions and [NbO6] groups was carried out using non-thermal coupling pairs, through the Boltzmann fitting and integral calculation, the maximum Sr and Sa values were 2.25% K−1 and 0.0049 K−1 at 403 K and 443 K, respectively, the Sr value is four times that obtained from the thermal coupling of Pr3+ ions, which exceeded most values previously reported for the fluorescence powder. Accordingly, we also studied the thermal sensitivity of Er3+ ions and Eu3+ ions mono-doped CaNb2O6 substrates. Results reveal that CaNb2O6:Pr3+/Er3+/Eu3+ phosphors have splendid temperature sensitivity and have far-reaching application prospects in the field of temperature measurements. [ABSTRACT FROM AUTHOR]

In2S3/BiOI composites were synthesized at room temperature which significantly improved the photocatalytic degradation of tetracycline hydrochloride (TC) under visible light irradiation. Structure and morphology characterization techniques have been performed by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction measurements (XRD) and X-ray photoelectron spectra (XPS). The separation ability of photogenerated carriers is enhanced due to the formation of heterojunctions of the composites. The best performance is obtained when the content of In2S3 is 7 wt%. Compared with In2S3 and BiOI alone, 7-In2S3/BiOI has the highest specific surface area and can provide more active sites. Based on the photo-electrochemical characterization and free radical tests, a photocatalytic mechanism of In2S3/BiOI composites in the presence of superoxide radicals (˙O2−) and holes (h+) is reasonably proposed. [ABSTRACT FROM AUTHOR]

In this communication, we report the first demonstration of an efficient photoelectrochemical aptasensor based on sputtering Au nanoparticle-modified nanoporous BiVO4 for the excellent sensitive and selective detection of thrombin with a low detection limit of 0.5 pM and a large linear range. [ABSTRACT FROM AUTHOR]

In this communication, we report for the first time the demonstration of a lithium ion intercalation strategy to significantly enhance the photoelectrochemical water splitting performance on 3-dimensional vertical hierarchical top-porous-bottom-tubular TiO2 nanotubes on a fabricable titanium mesh. [ABSTRACT FROM AUTHOR]

In this communication, a new photoelectrochemical aptasensor with Au nanoparticle functionalized self-doped TiO2 nanotube arrays (Au/SD-TiO2 NTs) as the core sensing unit and aptamers as the recognition unit was set up to accomplish the sensitive and selective detection of kanamycin with the lowest detection limit of 0.1 nM. [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 LiTaO 3 : x Pr 3+ phosphors. The crystal structure, luminescent properties and the mechanism of abnormal thermal quenching were investigated in detail.

Praseodymium (Pr 3+ ) ion and the transition metal vanadium (V 5+ ) ion with d 0 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 Pr 3+ in the YVO 4 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 (P 5+ ) with a valence state matching V 5+ and a similar ion radius was selected for the V/P substitution. It lacks a d 0 electron configuration, preventing the formation of an IVCT band with Pr 3+ 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 P 5+ , 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 P 5+ concentration. When excited at the 3 P 2 level, the Y 0.995 PO 4 :0.5%Pr 3+ 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 YVO 4 :Pr 3+ phosphor for various applications.

The synthesis conditions of most phosphors doped with lanthanide ions with d-f transition require a reducing atmosphere. The doping Bi 3+ ions selected in this study perfectly avoid this requirement, and they are environmentally friendly and safe. Nevertheless, the spectral tuning of Bi 3+ is a great challenge that limits its application. Herein, by regulating the value of x in the new solid solution Sr 2+ x La 1- x GaO 5- x F x , the luminescence of Bi 3+ is well promoted. Through an excitation-driven strategy, the emission peak position of Bi 3+ is redshifted, and the luminescence of trivalent bismuth is successfully adjusted, which can also be applied to anti-blue lighting. In addition, we constructed a Bi 3+ -Eu 3+ dual luminescence system, and, regardless of changes in the Bi 3+ /Eu 3+ concentration or excitation wavelength, a single matrix white light phosphor was realized. Through calculations, the activation energy of the phosphor doped with 2.5%Eu 3+ was found to be 0.257 eV, which is higher than the activation energy of some common compounds. This indicates that the phosphor has good application prospects in the field of solid-state lighting. It is worth noting that based on the different thermal response behaviors of Bi 3+ and Eu 3+ , when the Eu 3+ content is fixed at 1%, the maximum relative sensitivity of the optical thermometer based on its fluorescence intensity ratio is about 1.46% K -1 at 383 K, which is higher than that of Bi 3+ and Eu 3+ co-doped phosphors previously reported. We also obtained a high absolute sensitivity of 0.00139 K -1 at 403 K. Therefore, we also studied the thermal sensitivity of Bi 3+ and Er 3+ co-doped solid solutions. The results show that this solid-solution phosphor has far-reaching application prospects in the temperature sensing field.

Most praseodymium-doped red-emitting phosphors need high-temperature synthesis conditions with a reducing atmosphere. The niobate matrix selected in this work provides a sufficient electron-rich-site environment for praseodymium through charge migration, and praseodymium can be self-reduced in air atmosphere, which is safe and environmentally friendly. By building the [NbO 6 ] group → Pr 3+ energy transfer and finely modifying the doping concentration of Pr 3+ ions, we constructed a dual-luminescence-system of the [NbO 6 ] group and Pr 3+ . Thereby, optical temperature measurement based on fluorescence intensity ratio (FIR) technology of Pr 3+ ions and [NbO 6 ] groups was carried out using non-thermal coupling pairs, through the Boltzmann fitting and integral calculation, the maximum S r and S a values were 2.25% K -1 and 0.0049 K -1 at 403 K and 443 K, respectively, the S r value is four times that obtained from the thermal coupling of Pr 3+ ions, which exceeded most values previously reported for the fluorescence powder. Accordingly, we also studied the thermal sensitivity of Er 3+ ions and Eu 3+ ions mono-doped CaNb 2 O 6 substrates. Results reveal that CaNb 2 O 6 :Pr 3+ /Er 3+ /Eu 3+ phosphors have splendid temperature sensitivity and have far-reaching application prospects in the field of temperature measurements.

In this communication, we report for the first time the demonstration of a lithium ion intercalation strategy to significantly enhance the photoelectrochemical water splitting performance on 3-dimensional vertical hierarchical top-porous-bottom-tubular TiO2 nanotubes on a fabricable titanium mesh.

In this communication, a new photoelectrochemical aptasensor with Au nanoparticle functionalized self-doped TiO2 nanotube arrays (Au/SD-TiO2 NTs) as the core sensing unit and aptamers as the recognition unit was set up to accomplish the sensitive and selective detection of kanamycin with the lowest detection limit of 0.1 nM.