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All-inorganic perovskite quantum dots (PeQDs) have aroused great research interest in white light-emitting diodes (WLED) due to their excellent optoelectronic properties, but the poor stability, caused by dynamically binding long-chain capping ligands, hinders their future practical applications. To address this issue, here, we exploit short-chain butyric acid (BA) to replace long-chain oleic acid (OA) as capping ligand of CsPbX3 PeQDs by a hot-injection method. The addition of BA not only makes the morphology of CsPbBr3 PeQDs uniform and improves the crystallinity but also effectively suppresses nonradiative recombination, achieving a near unit photoluminescence quantum yield of 96%. The BA capped CsPbBr3 PeQDs exhibit high stability up to 180 d stored in ambient environment and also significantly improved resistance against polar solvent, ultra-violet lamp irradiation, and heat, which is rationalized by the strong binding capacity and shortened distance of BA to the PeQDs through ab initio calculations. Furthermore, by combining green-emission CsPbBr3 and red-emission CsPbBr0.8I2.2 PeQDs with blue GaN chip, we achieved WLEDs with excellent luminous properties, showing their great potential in practical application of wide-color-gamut display and lighting. [ABSTRACT FROM AUTHOR]

Enrofloxacin (ENR) is one of the most common drugs used in poultry production to treat bacterial diseases, and there is a high risk of drug interactions (DDIs) between polyether anticoccidial drugs added to poultry feed over time. This may affect the efficacy of antibiotics or lead to toxicity, posing a potential risk to the environment and food safety. This study aimed to investigate the DDI of ENR and salinomycin (SAL) in broilers and the mechanism of their DDI. We found that SAL increased the area under the curve and elimination half-life of ENR and ciprofloxacin (CIP) by 1.3 and 2.4 times, 1.2 and 2.5 times, respectively. Cytochrome 3A4 (CYP3A4), p-glycoprotein (P-gp) and breast cancer resistance protein (BCRP) were important factors for the DDI between ENR and SAL in broilers. ENR and SAL are substrates of CYP3A4, P-gp and BCRP in broilers; ENR and SAL inhibited the expression of CYP3A4 activity in a time- and concentration-dependent. Meanwhile, ENR downregulated the expression of P-gp and BCRP in a time- and concentration-dependent manner. A single oral administration of SAL inhibited CYP3A4, P-gp, and BCRP, but long-term mixed feeding upregulated the expression of CYP3A4, P-gp, and BCRP. Molecular docking revealed that ENR and SAL compete with each other for CYP3A4 to affect hepatic metabolism, and compete with ATP for P-gp and BCRP binding sites to inhibit efflux. ENR and SAL in broilers can lead to severe DDI. Drug residues and resistance following co-administration of ENR and SAL and other SAL-based drug-feed interactions warrant further study. [ABSTRACT FROM AUTHOR]

Transformer oil-based nanofluid-impregnated pressboard (NIP) with TiO 2 nanoparticles has been previously shown to exhibit substantially higher AC breakdown strength than that of pure oil-impregnated pressboard (OIP). In this study, OIP and NIP with TiO 2 nanoparticles were prepared and experiments on DC breakdown strength of were performed. It was found that NIP possesses higher resistance to DC breakdown strength than that of OIP. To reveal the working mechanism, a pulsed electro acoustic (PEA) device was used to measure the space charge accumulation and dissipation characteristics in OIP and NIP. The results show that the density of deep level traps in NIP is visibly reduced owing to the addition of TiO 2 nanoparticles and homopolar space charge accumulation on both sides of NIP is suppressed. Moreover, the charges injected from electrodes into NIP under DC voltage is also restrained owing to the increase of the Schottky potential barrier. Thus, the DC breakdown performance of NIP is considerably improved. [ABSTRACT FROM AUTHOR]

Nanoparticles have exhibited great potential in improving insulating property of liquid and solid dielectrics. To explore their modification mechanism on transformer oil-impregnated pressboards, TiO2 nanoparticles with different diameters of 5nm, 10nm, and 15nm were synthesized and used to prepare transformer oil-based nanofluids. The creeping flashover characteristics of both pure oil-impregnated paperboards (OPs) and nanofluid-impregnated pressboards (NPs) were examined under lightning impulse and AC voltages. It was found that the creeping flashover property of NPs is significantly improved with the decreasing of nanoparticle size. Especially, it is enhanced by 2.44 times under positive lighting impulse as nanoparticle size reduced from 15 nm to 5 nm. The results of space charge decay and trap characteristics reveal the decrease of nanoparticle size can lower trap depth and greatly enhance the space charge dissipation rate, leading to more uniform electric field distribution at the interface between nanofluid and pressboards and higher creeping flashover property. [ABSTRACT FROM AUTHOR]

Creeping flashover of mineral-oil-impregnated pressboard under impulse stress is a common insulating failure in oil-immersed transformers, arousing increasing attention. Recent studies have shown that the breakdown strength of transformer oil under positive lightning impulse voltage can be significantly improved through nanoparticles-based modification, and Fe3O4 has shown the best improvement in breakdown strength compared to other nanoparticles that have been used. This paper presents the creeping flashover characteristics of pure oil-impregnated pressboard (OIP) and nanofluid-impregnated pressboard (NIP) based on Fe3O4 nanoparticles under positive and negative lightning impulse voltages, respectively. It was found that NIP possessed higher resistance to creeping flashover than OIP. The relative permittivities of oil and oil-impregnated pressboard before and after nanoparticles-based modification were measured, and the results revealed that the addition of nanoparticles led to a better match in relative permittivity between oil and oil-impregnated pressboard, and a more uniform electric field distribution. Furthermore, the shallow trap density in NIP was obviously increased compared to that of OIP through the thermally stimulated depolarization current (TSDC), which promoted the dissipation of surface charges and weakened the distortion of the electric field. Therefore, the creeping flashover characteristics of oil-impregnated pressboard were greatly improved with Fe3O4 nanoparticles. [ABSTRACT FROM AUTHOR]

Polarization and traps determine the electrical property of oil-paper insulation, but most attention has been paid to the modification of insulating oil with nanoparticles, so there are is little research about oil-impregnated paper, and the origin for performance variation is not understood yet. In this paper, spherical nanoscale titanium dioxide was prepared by the hydrolysis method and nanofluid-impregnated paper (NP) was fabricated through oil-impregnation. The frequency domain spectrum was measured for polarization analysis, and both thermally stimulated depolarization current (TSDC) and isothermal surface potential decay (ISPD) methods were used to reveal trap parameters. Results show that NP's low frequency permittivity is much larger, and another peak appears in the spectrum even though the content of nanoparticles is very low. With the addition of TiO2 nanoparticles, TSDC's amplitude and peak temperature increase, and the trap energy becomes shallower. TiO2 nanoparticles' strong polarization and high activation energy contribute to NP's larger interface polarization intensity and activation energy. Furthermore, because of oxygen vacancies, TiO2 nanoparticles offer a transfer site for holes and electrons to escape from deep traps; thus, the trap energy is greatly reduced. [ABSTRACT FROM AUTHOR]

Sulfur quantum dots (SQDs), as a novel metal-free fluorescent material, are getting increasingly tremendous attention in metal ion detection, especially for Fe3+, due to the merits of antimicrobial potential, low toxicity, and exciting optoelectronic properties. However, sensing mechanism of SQD based fluorescent probe for Fe3+ is not clear yet, and high sensitivity and large detection range remain a challenge. Here, we report the synthesis of hydrophilic SQDs as a fluorescent nanoprobe for Fe3+ via a fluorescent turn-off mode. We systematically studied the quenching mechanism by ultraviolet–visible absorption spectra, steady-state and time-resolved photoluminescent spectra, and temperature-dependent quenching constants. Results unclearly evidenced the quenching behavior to both inner filter effect and static quenching. Furthermore, the nanoprobe presents a large detection range from 2.5 to 700 μM and a limit of detection low to 53.6 nM, both of which are the record performance to our knowledge. At last, it shows high selectivity toward Fe3+ and presents no ionic strength effect in the range of investigation, which enables surprising results for Fe3+ detection in deionized water with interference ion and real water samples. [Display omitted] • A novel fluorescent nanoprobe based on sulfur quantum dots for Fe3+ was reported. • The nanoprobe delivers a record detection range and limit of detection. • The sensing mechanism is systematically studied and uncovered. • The nanoprobe shows high selectivity and results for Fe3+ in real water samples. [ABSTRACT FROM AUTHOR]

Mixed-halide CsPb(Br/Cl) 3 perovskite quantum dots (PeQDs) have attracted extensive attention in light-emitting diodes (LEDs), but their low photoluminescent efficiency and especially poor stability impede their practical applications. Here, we employ bifunctional didodecyldimethylammonium thiocyanide (DDASCN) with a pseudohalogen SCN - and branched DDA + to obtain blue-emitting CsPbBr 2 Cl PeQDs. DDASCN significantly boosts the photoluminescence quantum yield to 92% by inhibiting nonradiative recombination. Importantly, DDASCN PeQDs show excellent stabilities against air, UV light, heat, and polar solvents. These improved performances were explained by density functional theory calculation, which shows that SCN - fills the Cl - vacancy by simultaneously binding with undercoordinated Pb 2+ and Cs + , while DDA + connects undercoordinated Br - and lies parallel to the PeQD core, leading to efficient passivation and a strong binding capacity. Finally, we achieved high-performance white LEDs by integrating our PeQDs, resulting in a color-rendering index of 92.9, a color gamut of 119.61%, and chromaticity coordinates of (0.33, 0.33). This provides an effective method to obtain efficient and stable CsPb(Br/Cl) 3 PeQDs for practical applications.

Inorganic CsPbX 3 perovskite quantum dots (PeQDs) show great potential in white light-emitting diodes (WLEDs) due to excellent optoelectronic properties, but their practical application is hampered by low photoluminescence quantum yield (PLQY) and especially poor stability. Herein,  we developed an in-situ and general multidentate ligand passivation strategy that allows for CsPbX 3 PeQDs not only near-unit PLQY, but significantly improved stability against storage, heat, and polar solvent. The enhanced optical property arises from high effectiveness of the multidentate ligand, diethylenetriaminepentaacetic acid (DTPA) with five carboxyl groups, in passivating uncoordinated Pb 2+ defects and suppressing nonradiative recombination. First-principles calculations reveal that the excellent stability is attributed to tridentate binding mode of DTPA that remarkably boosts the adsorption capacity to PeQD core. Finally, combining the green and red PeQDs with blue chip,  we demonstrated highly luminous WLEDs with distinctly enhanced operation stability, a wide color gamut of 121.3% of national television system committee, standard white light of (0.33,0.33) in CIE 1931, and tunable color temperatures from warm to cold white light readily by emitters' ratio. This study provides an operando yet general approach to achieve efficient and stable PeQDs for WLEDs and accelerates their progress to commercialization., (© 2023 Wiley-VCH GmbH.)

All-inorganic perovskite quantum dots (PeQDs) have sparked extensive research focus on white-light-emitting diodes (WLEDs), but stability and photoluminescence efficiency issues are still remain obstacles impeding their practical application. Here, we reported a facile one-step method to synthesize CsPbBr 3 PeQDs at room temperature using branched didodecyldimethylammonium fluoride (DDAF) and short-chain-length octanoic acid as capping ligands. The obtained CsPbBr 3 PeQDs have a near-unity photoluminescence quantum yield of 97% due to the effective passivation of DDAF. More importantly, they exhibit much improved stability against air, heat, and polar solvents, maintaining >70% of initial PL intensity. Making use of these excellent optoelectronic properties, WLEDs based on CsPbBr 3 PeQDs, CsPbBr 1.2 I 1.8 PeQDs, and blue LEDs were fabricated, which show a color gamut of 122.7% of the National Television System Committee standard, a luminous efficacy of 17.1 lm/W, with a color temperature of 5890 K, and CIE coordinates of (0.32, 0.35). These results indicate that the CsPbBr 3 PeQDs have great practical potential in wide-color-gamut displays.

As a novel strategy for in vivo visualization tracking and monitoring, carbon dots (CDs) emitting long wavelengths (LW, 600-950 nm) have received tremendous attention due to their deep tissue penetration, low photon scattering, satisfactory contrast resolution and high signal-to-background ratios. Although, the mechanism of CDs emitting LW remains controversial and what properties are best for in vivo visualization have not been specifically elucidated, it is more conducive to the in vivo application of LW-CDs through rational design and ingenious synthesis based on the appreciation of the luminescence mechanism. Therefore, this review analyzes the current tracer technologies applied in vivo and their advantages and disadvantages, with emphasis on the physical mechanism of emitting LW fluorescence for in vivo imaging. Subsequently, the general properties and merits of LW-CDs for tracking and imaging are summarized. More importantly, the factors affecting the synthesis of LW-CDs and its luminescence mechanism are highlighted. Simultaneously, the application of LW-CDs for disease diagnosis, integration of diagnosis and therapy are summarized. Finally, the bottlenecks and possible future directions of LW-CDs in visualization tracking and imaging in vivo are detailly discussed., Competing Interests: Competing Interests: The authors have declared that no competing interest exists., (© The author(s).)