ABSTRACT
Multicolor tuning of persistent luminescence has been extensively studied by deliberately integrating various luminescent units, known as activators or chromophores, into certain host compounds. However, it remains a formidable challenge to fine-tune the persistent luminescence spectra either in organic materials, such as small molecules, polymers, metal-organic complexes and carbon dots, or in doped inorganic crystals. Herein, we present a strategy to delicately control the persistent luminescence wavelength by engineering sub-bandgap donor-acceptor states in a series of single-phase Ca(Sr)ZnOS crystals. The persistent luminescence emission peak can be quasi-linearly tuned across a broad wavelength range (500-630 nm) as a function of Sr/Ca ratio, achieving a precision down to ~5 nm. Theoretical calculations reveal that the persistent luminescence wavelength fine-tuning stems from constantly lowered donor levels accompanying the modified band structure by Sr alloying. Besides, our experimental results show that these crystals exhibit a high initial luminance of 5.36 cd m-2 at 5 sec after charging and a maximum persistent luminescence duration of 6 h. The superior, color-tunable persistent luminescence enables a rapid, programable patterning technique for high-throughput optical encryption.
ABSTRACT
This study aimed to develop complex coacervates utilizing lactoferrin (LF) and chia seed mucilage (CSM) for promoting intestinal delivery of quercetin (Q) and fortification of set yogurt. Three cross-linkers, including calcium chloride (CC), transglutaminase (TG), and polyphenolic complex (HP), were used to further reinforce the coacervate network. Cross-linked coacervates had higher values of coacervate yield, encapsulation efficiency, and loading capacity. They efficiently preserved Q under gastric condition (â87%-99%), with CSM-TG-Q-LF being most effective for intestinal delivery of Q. Moreover, digested pellets of the cross-linked coacervates displayed better antioxidant activity than the uncross-linked coacervates with CSM-TG-Q-LF pellets showing maximum bioactivity. The Q-loaded coacervates demonstrated superior assembly in the yogurt matrix compared to the unencapsulated Q. Moreover, the coacervate systems, especially CSM-TG-Q-LF significantly improved the textural properties of yogurt and the stability of Q in it. Therefore, CSM-TG-LF is a promising carrier to promote intestinal delivery and food application of hydrophobic molecules.
Subject(s)
Lactoferrin , Quercetin , Seeds , Yogurt , Seeds/chemistry , Yogurt/analysis , Lactoferrin/chemistry , Lactoferrin/metabolism , Quercetin/chemistry , Plant Mucilage/chemistry , Humans , Chenopodium quinoa/chemistry , Food, Fortified/analysis , Intestinal Mucosa/metabolism , Drug Delivery Systems/instrumentationABSTRACT
Broadband near-infrared (NIR) phosphor-converted light-emitting diodes (pc-LEDs) hold promising potential as next-generation compact, portable, and intelligent NIR light sources. Nonetheless, the lack of high-performance broadband NIR phosphors with an emission peak beyond 900 nm has severely hindered the development and widespread application of NIR pc-LEDs. This study presents a strategy for precise control of energy-state coupling in spinel solid solutions composed of MgxZn1-xGa2O4 to tune the NIR emissions of Cr3+ activators. By combining crystal field engineering and heavy doping, the Cr3+-Cr3+ ion pair emission from the 4T2 state is unlocked, giving rise to unusual broadband NIR emission spanning 650 and 1400 nm with an emission maximum of 913 nm and a full width at half-maximum (fwhm) of 213 nm. Under an optimal Mg/Zn ratio of 4:1, the sample achieves record-breaking performance, including high internal and external quantum efficiency (IQE = 83.9% and EQE = 35.7%) and excellent thermal stability (I423 K/I298 K = 75.8%). Encapsulating the as-obtained phosphors into prototype pc-LEDs yields an overwhelming NIR output power of 124.2 mW at a driving current of 840 mA and a photoelectric conversion efficiency (PCE) of 10.5% at 30 mA, rendering high performance in NIR imaging applications.
ABSTRACT
In response to the ongoing quest for new, highly sensitive upconverting luminescent thermometers, this article introduces, for the first time, upconverting luminescent thermometers based on thermally induced structured phase transitions. As demonstrated, the transition from the low-temperature monoclinic to the high-temperature tetragonal structures of LiYO2:Yb3+,Er3+ induces multifaceted modification in the spectroscopic properties of the examined material, influencing the spectral positions of luminescence bands, energy gap values between thermally coupled energy levels, and the red-to-green emission intensities ratio. Moreover, as illustrated, both the color of the emitted light and the phase transition temperature (from 265 K, for LiYO2:Er3+, 1%Yb3+, to 180 K, for 10%Yb3+), and consequently, the thermometric parameters of the luminescent thermometer can be modulated by the concentration of Yb3+ sensitizer ions. Establishing a correlation between the phase transition temperature and the mismatch of ion radii between the host material and dopant ions allows for smooth adjustment of the thermometric performance of such a thermometer following specific application requirements. Three different thermometric approaches were investigated using thermally coupled levels (SR = 1.8%/K at 180 K for 1%Yb3+), green to red emission intensities ratio (SR = 1.5%/K at 305 K for 2%Yb3+), and single band ratiometric approach (SR = 2.5%/K at 240 K for 10%Yb3+). The thermally induced structural phase transition in LiYO2:Er3+,Yb3+ has enabled the development of multiple upconverting luminescent thermometers. This innovative approach opens avenues for advancing the field of luminescence thermometry, offering enhanced relative thermal sensitivity and adaptability for various applications.
ABSTRACT
In this study, a new fermented food was developed using pineapple by-products and whey protein (2.6%) as raw materials through the co-fermentation of autochthonous lactic acid bacteria and yeast. To better understand the fermentation mechanism and the impact of microorganisms on the entire fermentation system, we tracked the changes in carbohydrate and amino acid profiles, organoleptic quality and microbial community during the fermentation process. Compared with unfermented samples, dietary fiber and free amino acids increased significantly as fermentation proceeded. The fermented samples were significantly lower in astringency and bitterness and significantly higher in sourness, umami and richness. The fermented products were richer in volatile compounds with floral, cheesy, fruity and other flavors. Relevant analyses showed that the core microbial community was highly correlated with the quality attributes of the fermented products. Microorganisms such as Lactococcus, Weissella, Hanseniaspora, Saccharomyces and Lachancea contributed significantly to the fermented products.
ABSTRACT
Optical ratiometric thermometry techniques have gained much attention in recent years due to their reliable and noncontact temperature sensing capability for industrial and biorelated applications. Herein, we exploited the temperature dependence of the absorption band of BaTiO3 (BTO) for novel excitation intensity ratio (EIR) thermometry. Photoluminescence and excitation properties of Eu3+-doped BTO powders were studied as a function of Eu3+ doping concentration. The excitation peak intensities at 397 and 468 nm, corresponding to the 7F0 â 5L6 and 5D2 transitions of Eu3+, were used as EIR parameters. The temperature dependence of the EIR can be explained by the competitive absorption between Eu3+ and the BTO host. The EIR properties were studied in relation to the doping concentration, registering a maximum relative sensitivity (Sr) of 4.89% K-1 in BTO:Eu3+ (0.5%) at 303 K. An amphoteric Eu3+ occupation mode at both Ba2+ and Ti4+ sites was found to interpret the doping concentration dependence of the Sr. The reduced Ba2+ site occupation ratio proved to be responsible for the low Sr values at high Eu3+ doping concentrations. Accordingly, an Eu3+/Ti3+ codoping method was further proposed to improve the Sr by increasing the Ba2+ site occupation ratio. Our result showed that BTO:Eu3+ (0.5%) demonstrated an enhancement of Sr from 4.89 to 6.42% K-1 at 303 K after 2% Ti3+ codoping.
ABSTRACT
Thus far, little is known about whether jackfruit flake, a byproduct of jackfruit, can be used as a fermentation substrate to obtain value-added products through microbial fermentation. Here, jackfruit flake puree was fermented by three different ways: spontaneous fermentation (JF), inoculated with LAB (JFL), inoculated co-fermentation with LAB and yeast (JFC). In contrast to JF, the total polyphenol and flavonoid content and syndrome-associated enzyme inhibition are significantly increased in JFC at the end of fermentation. Electronic tongue analysis revealed that the JFC was significantly lower in astringency and higher in bitterness. 41 volatile compounds were identified during fermentation by HS-SPME-GC-MS, and JFC was richer in honey, rose, and fruity flavors. A total of 290 compounds were screened for discriminative pre- and post-fermentation differential metabolites by non-target metabolomics analysis. These results provide a potential reference for the conversion of jackfruit waste into functional products using fermentation.
ABSTRACT
In recent years, Bi3+ activated phosphors have received a lot of attention from researchers; however, the performance and application areas of phosphors are yet to be developed. In this work, a series of CaScBO4(CSBO):xBi3+ phosphors were successfully prepared using a high-temperature solid-state method. Under UV excitation, blue light emission was achieved at 430 nm with a quantum yield of 91%, and at 423 K, the emission intensity retained 82.8% of the original intensity at 298 K. By crystal field engineering, the substitution of Sr2+ at the Ca2+ site enhances the temperature stability of the material, and at 423 K, 473 K and 573 K, the samples maintain 104%, 103% and 85% of the emission intensity at room temperature, respectively. It indicates that the cation substitution causes the increase in the oxygen vacancy concentration, and the oxygen vacancy defect compensates the energy lost in electrons at high temperature, producing resistance to anti-TQ performance. Finally, a blue-violet LED was fabricated by using the phosphor and an ultraviolet LED chip, and white LEDs (CCT = 4683 K, Ra = 89.7) were obtained by co-packaging this phosphor with commercial phosphors and a UV chip. Importantly, the great potential of this phosphor in the field of plant lighting and biocontrol can be demonstrated.
ABSTRACT
Luminescent materials that display quick spectral responses to thermal stimuli have attracted pervasive attention in sensing technologies. Herein, a programmable luminescence color switching in lanthanide-doped LiYO2 under thermal stimuli, based on deliberate control of the monoclinic (ß) to tetragonal (α) phase transition in the crystal lattice, is reported. Specifically, a lanthanide-doping (Ln3+ ) approach to fine-tune the phase-transition temperature in a wide range from 294 to 359 K is developed. Accordingly, an array of Ln3+ -doped LiYO2 crystals that exhibit progressive phase transition, and thus sequential color switching at gradually increasing temperatures, is constructed. The tunable optical response to thermal stimuli is harnessed for colorimetric temperature indication and quantitative detection, demonstrating superior sensitivity and temperature resolution (Sr = 26.1% K-1 , δT = 0.008 K). The advances in controlling the phase-transition behavior of luminescent materials also offer exciting opportunities for high-performance personalized health monitoring.
ABSTRACT
Red wine polyphenolic complexes have attracted increasing attention as potential modulators of human metabolic disease risk. Our previous study discovered that red wine high-molecular-weight polymeric polyphenolic complexes (HPPCs) could inhibit key metabolic syndrome-associated enzymes and favorably modulate human gut microbiota (GM) in simulated colonic fermentation assay in vitro. In this work, the efficacy of HPPC supplementation (150 and 300 mg/kg/day, respectively) against high-fat diet (HFD)-induced metabolic disturbance in mice was investigated. HPPCs effectively attenuated HFD-induced obesity, insulin resistance, and lipid and glucose metabolic dysregulation and ameliorated inflammatory response and hepatic and colonic damage. It also improved the relative abundance of Bacteroidetes and Firmicutes, consistent with an anti-obesity phenotype. The favorable modulation of GM was further supported by improvement in the profile of fecal short-chain fatty acids. The higher dosage generally had a better performance in these effects than the low dosage. Moreover, serum metabolite profiling and pathway enrichment analysis revealed that HPPCs significantly modulated vitamin B metabolism-associated pathways and identified N-acetylneuraminic acid and 2-methylbutyroylcarnitine as potential biomarkers of the favorable effect on HFD-induced metabolic dysregulation. These findings highlight that dietary supplementation with red wine HPPCs is a promising strategy for the management of weight gain and metabolic dysregulation associated with HFD.
Subject(s)
Gastrointestinal Microbiome , Wine , Humans , Animals , Mice , Diet, High-Fat/adverse effects , Obesity/drug therapy , Obesity/etiology , Weight Gain , Mice, Inbred C57BLABSTRACT
Seed mucilages are potential sources of natural polysaccharides. They are biodegradable, biocompatible, sustainable, renewable, and safe for human consumption. Due to the desirable physicochemical and functional properties (e.g. gelling, thickening, stabilizing, and emulsifying), seed mucilages have attracted extensive attention from researchers for utilization as a promising material for the development of advanced carrier systems. Seed mucilages have been utilized as natural polymers to improve the properties of various carrier systems (e.g. complex coacervates, beads, nanofibers, and gels) and for the delivery of diverse hydrophilic and lipophilic compounds (e.g. vitamins, essential oils, antioxidants, probiotics, and antimicrobial agents) to achieve enhanced stability, bioavailability, bioactivity of the encapsulated molecules, and improved quality attributes of food products. This review highlights the recent progress in seed mucilage-based carrier systems for food and nutraceutical applications. The main contents include (1) sources, extraction methods, and physicochemical and functional characteristics of seed mucilages, (2) application of seed mucilages for the development of advanced carrier systems, (3) major issues associated with carrier fabrication, and (4) mechanisms of carrier development, latest improvements in carrier formulation, carrier efficiency in the delivery of bioactive agents, and application in food and nutraceuticals. Furthermore, major challenges and future perspectives of seed mucilage-based carriers for a commercial application are discussed.
ABSTRACT
Owing to some special superiority, luminescence ratiometric thermometry, mainly including dual excitations single emission and single excitation dual emissions, has gained popularity over the past few years. However, developing novel ratiometric thermometry that can work in multi-mode is still a challenge. Here we report a temperature measurement method based on the photoinduced luminescence of Tb3+ in the low-cost and easy to prepare calcium tungstate. Both the conventional luminescence intensity ratio (LIR) and recently developed single-band ratiometric (SBR) strategies have been achieved in our materials. On the one hand, upon excitation of the charge transfer state, the emissions from the excited 5D4 and 5D3 states present different responses to temperature. A thermometry depending on the LIR between these two emissions has thus been developed, with adjustable relative sensitivity that is sensitive to the excitation wavelength. On the other hand, both the emissions from the excited 5D4 and 5D3 states respond dissimilarly to the temperature variation. A SBR thermometer has thus been constructed with two excitation modes, reaching the maximum relative sensitivity of 1.83% K-1 at 573 K. The present work is expected to inspire other researchers to exploit more multi-mode optical ratiometric thermometries.
ABSTRACT
The present study aimed to investigate the effects of five emulsifiers, including DATEM, DMG, PL, SDS, and SPP, on HA formation in chemical models and roasted chicken patties. UPLC-MS analysis showed that DMG and SPP were the most promising among them. In particular, at 0.15-0.9% (w/w) in roasted chicken patties, they effectively reduced the contents of PhIP (21-43%), MeIQx (26-50%) and 4,8-DiMeIQx (16-43%) relative to the control, whereas DATEM, PL and SDS promoted their formation. Low-Field Nuclear Magnetic Resonance and Magnetic Resonance Imaging analysis revealed that the inhibitory effect of SPP and DMG was partly mediated through their capability to help retain water in the macromolecular structures of the muscle tissue. This favorable effect was also supported by the significantly improved adhesiveness of the SPP and DMG samples relative to other samples. These findings suggest that SPP and DMG are effective additives for attenuation of HA contents in meat-based products.
Subject(s)
Chickens , Heterocyclic Compounds , Animals , Cooking/methods , Chromatography, Liquid , Water , Tandem Mass Spectrometry/methods , Heterocyclic Compounds/analysis , Meat/analysis , Amines/chemistry , Emulsifying Agents/analysisABSTRACT
Halide perovskites have gained tremendous attention in the past decade owing to their excellent properties in optoelectronics. Recently, a fascinating property, ferroelectricity, has been discovered in halide perovskites and quickly attracted widespread interest. Compared with traditional perovskite oxide ferroelectrics, halide perovskites display natural advantages such as structural softness, low weight, and easy processing, which are highly desirable in applications pursuing miniaturization and flexibility. This review focuses on the current research progress in halide perovskite ferroelectrics, encompassing the emerging materials systems and their potential applications in ferroelectric photovoltaics, self-powered photodetection, and X-ray detection. The main challenges and possible solutions in the future development of halide perovskite ferroelectric materials are also attempted to be pointed out.
ABSTRACT
Ultra-broadband near-infrared (NIR) spectroscopy has unparalleled application prospects in intelligent detection and phosphor-converted light-emitting diodes (pc-LED), which are most likely to become the next generation of NIR light sources, has become a hot spot for research nowadays. To cope with the demand for more NIR spectroscopy applications, more efficient NIR phosphors need to be developed. Here, by screening the subject with a smaller band gap and by screening the suitable ion electronegativity of the lattice position where the Cr3+ is located, and then through the energy transfer, a series of Gd3Zn2GaGe2O12:xCr3+, yYb3+ (GZGG:Cr3+/Yb3+) NIR broadband garnet phosphors were found for the first time. By controlling the energy transfer process, the internal quantum yield (IQY) (54.9%), external quantum yield (EQY) (24.65%), bandwidth (260â nm), and thermal stability (60% at 150 °C) of NIR emission were substantially improved. The obtained phosphors are packaged with blue light chips into pc-LED, which can be applied in different fields such as vascular visualization and night vision.
ABSTRACT
In this work, a new NIR phosphor Ca2GeO4:xCr was developed, whose emission range (1000-1700 nm) is well within NIR-II, with a full width at half maximum (FWHM) of 215 nm. Interestingly, by sintering under an air atmosphere, the Cr3+ ions in the raw material are oxidized to Cr4+, and the near-infrared light emitted by the material is not the usual luminescence of Cr3+ ions located in NIR-I, which can be attributed to the dominant substitution of Cr4+ ions doped into the lattice sites. A pc-LED fabricated with this phosphor can detect different concentrations of ethanol, which demonstrates its good potential for non-destructive testing applications.
ABSTRACT
Stubborn resistant bacteria, bacterial biofilms and severe inflammation are challenging issues in refractory keratitis treatment. Herein, we design a multifunctional near-infrared light-responsive nanoplatform for efficient therapy of refractory keratitis based on a "three-birds-with-one-stone" strategy, which integrates the bacteria targeting photodynamic therapy, nitric oxide (NO) sterilization, and NO-mediated anti-inflammatory property into one system. This nanoplatform (UCNANs) is constructed using the dual-emissive upconversion nanoparticles (UCNPs) as cores coated with mesoporous silica for the loading of photosensitizers with aggregation-induced emission (AIE) property and the grafting of NO donors and bacteria targeting molecules. Upon irradiation of 808 nm light, UCNPs simultaneously produce UV emission and visible emission to trigger NO release and reactive oxygen species (ROS) such as superoxide radical (O2â¢-) generation. Furthermore, O2â¢- resulting from PDT can react with NO to yield powerful oxidizing and nitrating agent peroxynitrite (ONOO-). The three components work synergistically to enhance the antibacterial outcome confirmed by in vitro and in vivo tests. The short-distance light excitation and excitation light absorption are important reasons for reducing the toxicity of materials, especially ultraviolet light damage. Moreover, bacteria elimination reduced endotoxin secretion and the released NO simultaneously inhibit the NF-κB pathways by regulating the expression of toll-like receptor 2 (TRL2) and tumor necrosis factor-α (TNF-α), which significantly relieves the inflammation of cornea. Given its excellent antibacterial and anti-inflammatory properties, UCNANs provides a competitive strategy for refractory keratitis therapy.
Subject(s)
Keratitis , Nanoparticles , Photochemotherapy , Anti-Bacterial Agents/pharmacology , Anti-Bacterial Agents/therapeutic use , Anti-Inflammatory Agents/therapeutic use , Humans , Inflammation/drug therapy , Infrared Rays , Keratitis/drug therapy , Nitric Oxide , Photochemotherapy/methods , Photosensitizing Agents/therapeutic useABSTRACT
The exploration of efficient broadband near-infrared (NIR) emitting materials is essential to establishing new NIR applications. In this work, an excellent NIR phosphor Mg7Ga2GeO12:Cr3+, with an emission band of 650-1350 nm and a full width at half maximum of 266 nm, was successfully prepared. When Ga3+ ions were replaced by In3+ ions, its emission intensity increased 4 times, and the internal and external quantum efficiency reached 86 and 37%, respectively. A NIR phosphor-converted light-emitting diode (pc-LED) component was made by combining a synthetic Mg7Ga1.84In0.07GeO12:0.09Cr3+ phosphor with a 450 nm blue luminescent chip. The vascular and skeletal distribution on human fingers and the back of the hand can be seen under the display of a commercial NIR camera, indicating that Mg7Ga1.84In0.07GeO12:0.09Cr3+ phosphors have promising applications in the field of the blood vessel and bone visualization.
Subject(s)
Chromium , Luminescence , Humans , OccupationsABSTRACT
Recently, single-band ratiometric (SBR) thermometry becomes a hot-spot in the research field of optical thermometry. Here we propose a new SBR thermometry by combining the temperature-induced red shift of charge transfer state (CTS) of W-O and Eu-O with the ground state absorption (GSA) and excited state absorption (ESA) of Eu3+. The emitting intensity of the 5D0-7F2 transition of Eu3+ is monitored under CTS, GSA and ESA excitations at different temperatures. It is found that the SBR thermometry, depending on the combination of [GSA + CTS] of Eu3+ doped calcium tungstate, has the highest relative sensitivity of 1.25% K-1 at 573â K, higher than conventional luminescent ratiometric thermometry such as the 2H11/2 and 4S3/2 thermally coupled states of Er3+.
ABSTRACT
Graphene/silicon Schottky junctions have been proven efficient for photodetection, but the existing high dark current seriously restricts applications such as weak signal detection. In this paper, a thin layer of gadolinium iron garnet (Gd3Fe5O12, GdIG) film is introduced to engineer the interface of a graphene/silicon Schottky photodetector. The novel structure shows a significant decrease in dark current by 54 times at a -2 V bias. It also exhibits high performance in a self-powered mode in terms of an Ilight/Idark ratio up to 8.2 × 106 and a specific detectivity of 1.35 × 1013 Jones at 633 nm, showing appealing potential for weak-light detection. Practical suitability characterizations reveal a broadband absorption covering ultraviolet to near-infrared light and a large linear response with a wide range of light intensities. The device holds an operation speed of 0.15 ms, a stable response for 500 continuous working cycles, and long-term environmental stability after several months. Theoretical analysis shows that the interlayer increases the barrier height and passivates the contact surface so that the dark current is suppressed. This work demonstrates the good capacity of GdIG thin films as interlayer materials and provides a new solution for high-performance photodetectors.