Preparation of 3D flexible SERS substrates by mixing gold nanorods in hydrogels for the detection of malachite green and crystal violet.

A simple and cost-effective fabrication method of gold nanorods (AuNRs) nanoparticles hybridized with polyvinyl alcohol hydrogel (AuNR/PVA) for SERS substrate is described. The AuNR/PVA achieves the control of inter-particle nanogap by modulating the density of gold nanorods, and inter-particle nanogap by the spatial deformation of the hydrogel, and the reduction of the gap between the AuNRs deposited on hydrogel makes the SERS enhancement. In addition, the AuNR/PVA substrate maintains high SERS activity after more than 100 cycles of bending and storage in air for 30 days, and the substrate possesses high sensitivity and high reproducibility. Combining a flexible and transparent surface-enhanced Raman spectroscopy (SERS) substrate for in situ detection with a small portable Raman can be applied to scenarios such as environmental detection and hazardous materials detection. The substrate showed excellent SERS activity against malachite green (MG) and crystal violet (CV) with limits of detection of 1.18 × 10-13 M and 7.17 × 10-12 M, respectively. The usability of the proposed SERS substrate was demonstrated by detecting the above contaminants in aquatic water. This work not only utilizes a cost-effective method for mass production but also provides a reliable and convenient platform for the preparation of other noble metal flexible substrates.

The conductivity of Nb2O5 enhanced by the triple effect of fluorine doping, oxygen vacancy, and carbon modification for improving the lithium storage performance.

In view of the inherent pseudocapacitance, rich redox pairs (Nb5+/Nb4+ and Nb4+/Nb3+), and high lithiation potential (1.0-3.0 V vs Li/Li+), Nb2O5 is considered a promising anode material. However, the inherent low electronic conductivity of Nb2O5 limits its lithium storage performance, and the rate performance after carbon modification is still unsatisfactory because the intrinsic conductivity of Nb2O5 has not been substantially improved. In this experiment, taking the improvement of the intrinsic electrical conductivity of Nb2O5 as the guiding ideology, we prepared F-doped Nb2O5@fluorocarbon composites (F-Nb2O5@FC) with a large number of oxygen vacancies by one-step annealing. As the anode electrode of lithium-ion batteries, the reversible specific capacity of F-Nb2O5@FC reaches 150 mA g-1 at 5 A g-1 after 1100 cycles, and the rate performance is particularly outstanding, with a capacity up to 130 mA g-1 at 16 A g-1, which is far superior to other Nb2O5@carbon-based anode electrodes. Compared with other single conductivity sources of Nb2O5@carbon-based composites, the electrical conductivity of F-Nb2O5@FC composites is greatly improved in many aspects, including the introduction of free electrons by F- doping, the generation of oxygen vacancies, and the provision of a three-dimensional conductive network by FC. Through analytical chemistry (work function, UV-Vis diffuse reflectance spectroscopy, and EIS) and theoretical calculations, it is proved that F-Nb2O5@FC has high electrical conductivity and realizes rapid electron transfer.

Monitoring grey water footprint and associated environmental controls in agricultural watershed.

The grey water footprint (GWF) is an advanced index linking pollution load and water resources. However, the existing agriculture-related GWF was developed based on hydrological processes, which limits its role in watershed water pollution level (WPL) measurements. The main scope of this study is to calculate GWF and WPL based on runoff, total nitrogen (TN), and total phosphorus (TP) observations in the Hujiashan Watershed of China's Yangtze River Basin. Partial least squares structural equation modeling (PLS-SEM) was utilized to explore the impact pathways of environmental features on GWF and WPL. On this basis, propose measures for the management of this agricultural watershed. The results showed that the TN concentration had a V-shaped trend in 2008-2015, while the TP gradually decreased. The GWF calculations for the TN and TP were compatible with the temporal trends for the concentrations, which were higher in the wet season (0.45 m3/m2 for TN, 0.10 m3/m2 for TP) than in the dry season (0.11 m3/m2 for TN, 0.02 m3/m2 for TP) and increased from upstream to downstream. The WPLs of TN exceeded 2.0 in the midstream and downstream areas, whereas those for TP were inconspicuous. According to PLS-SEM, the GWF is primarily influenced by topographical variables and hydrological features, whereas the WPL is mainly controlled by hydrological features and landscape composition. Fertilizer reduction and efficiency measures should be implemented on farmland and appropriately reducing farming activities on slopes to relieve the GWF and WPL in the watershed.

Ultra-sensitive detection of tumor necrosis factor alpha based on silver-coated gold core shell and magnetically separated recognition of SERS aptamer sensors.

A highly sensitive tumor necrosis factor α (TNF-α) detection method based on a surface-enhanced Raman scattering (SERS) magnetic patch sensor is reported. Magnetic beads (MNPs) and core shells were used as the capture matrix and signaling probe, respectively. For this purpose, antibodies were immobilized on the surface of magnetic beads, and then Au@4-MBN@Ag core-shell structures coupled with aptamers and TNF-α antigen were added sequentially to form a sandwich immune complex. Quantitative analysis was performed by monitoring changes in the characteristic SERS signal intensity of the Raman reporter molecule 4-MBN. The results showed that the limit of detection (LOD) of the proposed method was 4.37 × 10-15 mg·mL-1 with good linearity (R2 = 0.9918) over the concentration range 10-12 to 10-5 mg·mL-1. Excellent assay accuracy was also demonstrated, with recoveries in the range 102% to 114%. Since all reactions occur in solution and are separated by magnetic adsorption of magnetic beads, this SERS-based immunoassay technique solves the kinetic problems of limited diffusion and difficult separation on solid substrates. The method is therefore expected to be a good clinical tool for the diagnosis of the inflammatory biomarker THF-α and in vivo inflammation screening.

Investigation of the luminescence properties and energy transfer mechanisms in Gd3TaO7:Bi3+,Eu3+ phosphors for their potential application in full-spectrum WLEDs.

In recent years, there has been increasing effort devoted to the development of single-phase white phosphors due to drawbacks such as severe reabsorption and color deviation in traditional white light-emitting diodes (WLEDs). A new feasible strategy has emerged for achieving white light emission through the Bi3+-Eu3+ energy transfer in suitable single-phase phosphors. Therefore, a series of Gd3TaO7:xBi3+ and Gd3TaO7:0.01Bi3+,yEu3+ phosphors were synthesized via a high-temperature solid-state method, and their properties were systematically characterized. In Gd3TaO7, Bi3+ occupies two kinds of Gd3+ site, resulting in two broad emission bands peaking at 427 nm and 500 nm respectively under ultraviolet (UV) excitation, which arise from 3P1 → 1S0 transitions. By adjusting the concentration of Eu3+ in Gd3TaO7:0.01Bi3+,yEu3+, effective energy transfer can occur between Bi3+ and Eu3+, thus enabling the regulation of green-white-red luminescence under 332 nm excitation and blue-white-red luminescence under 365 nm UV light irradiation. Upon stimulation with a 365 nm UV chip, Gd3TaO7:0.01Bi3+,0.02Eu3+ emits white light with CIE coordinates of (0.3509, 0.3202), a color temperature of 4629 K, and an impressive color rendering index of 87.96. The above results indicate the potential of Gd3TaO7:0.01Bi3+,yEu3+ phosphor as a viable candidate for WLED applications.

Effectiveness of multiple eHealth-delivered lifestyle strategies for preventing or intervening overweight/obesity among children and adolescents: A systematic review and meta-analysis.

Objective: To investigate the effect of multiple eHealth-delivered lifestyle interventions on obesity-related anthropometric outcomes in children and adolescents. Methods: The Medline (via PubMed), Embase, Cochrane Library, Web of Science, CBM, VIP, CNKI, and Wanfang electronic databases were systematically searched from their inception to March 18, 2022, for randomized controlled trials (RCTs). Meta-analyses were performed to investigate the effect of multiple eHealth-delivered lifestyle interventions on obesity-related anthropometric outcomes (body mass index [BMI], BMI Z-score, waist circumference, body weight, and body fat%). Two independent investigators reviewed the studies for accuracy and completeness. All included studies were evaluated using the Cochrane Risk-of-Bias (ROB) Tool. Results: Forty trials comprising 6,403 patients were selected for the meta-analysis. The eligible trials were published from 2006 to 2022. Compared with the control group, the eHealth-intervention group was more effective in reducing BMI (weighted mean difference [WMD] = -0.32, 95% confidence interval [CI]: -0.50 to -0.13, I2 = 85.9%), BMI Z-score (WMD = -0.08, 95% CI: -0.14 to -0.03, I2 = 89.1%), waist circumference (WMD = -0.87, 95% CI: -1.70 to -0.04, I2 = 43.3%), body weight (WMD = -0.96, 95% CI: -1.55 to -0.37, I2 = 0.0%), and body fat% (WMD = -0.59, 95% CI: -1.08 to -0.10, I2 = 0.0%). The subgroup analysis showed that parental or school involvement (WMD = -0.66, 95% CI: -0.98 to -0.34), eHealth-intervention duration of >12 weeks (WMD = -0.67, 95% CI: -0.96 to -0.38), and mobile-based interventions (WMD = -0.78, 95% CI: -1.13 to -0.43) had a significantly greater intervention effect size on BMI. Conclusions: This review recommends that multiple eHealth-delivered lifestyle strategies may be useful for preventing or treating overweight and obesity among children and adolescents. However, our results should be cautiously interpreted due to certain limitations in our study.

Enhanced luminescence and tunable color in [Eu2+, Si4+]/Mn2+ doped K2BaCa(PO4)2 based on charge compensation and energy transfer.

Recently, using the Eu2+ → Mn2+ energy transfer strategy to explore new single-phase phosphors suitable for the near-ultraviolet (n-UV) region has become one of the major strategies in solid-state lighting applications. Therefore, a novel color-tunable K2BaCa(PO4)2 (KBCPO):[Eu2+,Si4+],Mn2+ phosphor was developed because of the preeminent thermal stability of luminescence of Eu2+-activated KBCPO. In this study, we first designed a [Eu2+, Si4+] → [K+, P5+] charge compensation strategy to optimize the luminescence properties of Eu2+ in the KBCPO matrix. In terms of the obtained KBCPO:[Eu2+,Si4+] phosphor, this charge compensation method on the one hand strengthens the emission of Eu2+, and on the other hand, it dramatically improves the thermal stability of luminescence. In particular, the emission intensity of the KBCPO:0.03[Eu2+,Si4+] sample at 548 K can reach 103% relative to that at the initial temperature of 298 K. Based on this charge compensation strategy, we finally obtained a new dual emission KBCPO:[Eu2+,Si4+],Mn2+ phosphor. The analysis of the luminescence properties indicates that the emission enhancement of Mn2+ in KBCPO:[Eu2+,Si4+],Mn2+ stems from the energy transfer of Eu2+ → Mn2+ with the mechanism of the electric dipole-dipole interaction when excited at 365 nm. In addition, KBCPO:[Eu2+,Si4+],Mn2+ also has excellent thermal stability and the emission color could be easily tuned from cyan to orange only by adjusting the Eu2+ doping level. These results confirm that the KBCPO:[Eu2+,Si4+],Mn2+ phosphor is a viable candidate for n-UV white light emitting diodes.

LiYF4-nanocrystal-embedded glass ceramics for upconversion: glass crystallization, optical thermometry and spectral conversion.

Glass ceramics (GCs) can perfectly integrate nanocrystals (NCs) into bulk materials. Herein, GCs containing LiYF4 NCs were fabricated via a traditional melt-quenching method and subsequent glass crystallization. Structural characterization was carried out via X-ray diffraction (XRD), transmission electron microscopy (TEM), selected area electron diffraction (SAED), and scanning transmission electron microscopy high-angle annular dark-field (STEM-HAADF) analysis, suggesting the precipitation of LiYF4 NCs from a glass matrix. Taking Eu3+ as a structural probe, the spectrographic features provide compelling evidence for the partition of dopants. In particular, intense upconversion (UC) emission was achieved when co-doped with Yb3+ and Er3+. Temperature-dependent UC emission behaviour was also established based on the fluorescence intensity ratio (FIR) of Er3+, to study its properties for optical thermometry. Furthermore, spectral conversion was attained through cross relaxation (CR) between Ce3+ and Ho3+, tuning from green to red with various Ce3+ doping concentrations. There is evidence that LiYF4 NC-embedded GCs were favorable for UC, which may be extremely promising for optical thermometry and spectral conversion applications. This work may open up new avenues for the exploration of GC materials for expansive applications.

A study on temperature sensing performance based on the luminescence of Eu3+ and Er3+ co-doped YNbO4.

Eu3+ and Er3+ co-doped YNbO4 powder phosphors were synthesized by a traditional high-temperature solid-state reaction method. A laser of 487.6 nm wavelength was selected to be the excitation source which can pump Eu3+ ions from its thermally populated low-lying 7F2 ground state to the excited state 5D2 and lift the Er3+ ions from their 4I15/2 to 4F7/2 states. Fluorescence intensity ratio (FIR) between the 5D0 → 7FJ emissions of Eu3+ and 4S3/2 → 4I15/2 emissions of Er3+ ions is remarkably dependent on temperature because of the dramatic increase of Eu3+ luminescence against a slight quenching of Er3+ luminescence with the rise of temperature. This temperature sensitive FIR can be favorably employed for temperature sensing, owing to this novel scheme of 5D2 excitation, instead of 5D0, from 7F2 and utilizing Er3+ luminescence as a reference for FIR measurements. This sample is also prominent for its excellent signal-to-noise ratio and is a promising candidate for an optical temperature sensor.