Room Temperature Research Articles

A novel red-emitting InScW3O12:Eu3+ phosphor with anti-thermal-quenching performance for high-power WLED applications

A series of red-emitting InScW3O12:Eu3+ (ISWO:Eu3+) phosphors with anti-thermal-quenching performance were successfully synthesized by conventional solid-state reaction. The phase structure and luminescent properties of ISWO:Eu3+ were systematically studied. The photoluminescence excitation (PLE) spectrum showed that ISWO:Eu3+ phosphor can be effectively matched with commercial ultraviolet (UV), violet and blue light chips. The main emission peak of the phosphor was located at 613 nm, which was attributed to the electric dipole transition 5D0 → 7F2. Under the optimal excitation, the prepared ISWO:0.08Eu3+ phosphor showed excellent anti-thermal-quenching performance, its photoluminescence (PL) intensity at 180 °C reached 157.4 % of initial intensity at room temperature. At 465 nm excitation, it also exhibited the anti-thermal-quenching property and the PL intensity remained 115.1 % at 150 °C of that at room temperature. In situ XRD analysis revealed that the lattice contraction resulting in an increase in structural rigidity as the temperature rising, which caused the change of Eu3+ local environment and improved the PL intensity. Finally, a series of warm white LED devices under varying power density conditions with stable output were prepared using the red ISWO:0.08Eu3+ phosphor, indicating that the ISWO:Eu3+ phosphor with excellent anti-thermal-quenching performance has potential application prospects in high-power white light-emitting diodes (WLEDs).

Structural characterization of an acid-extracted polysaccharide from Suillus luteus and the regulatory effects on intestinal flora metabolism in tumor-bearing mice

Suillus luteus is an excellent edible fungus that has been applied in soil remediation and environmental pollution control, while the development of bioactive polysaccharide component including structural performance and intestinal flora regulation is still insufficient. In this study, a S. luteus acid-extracted polysaccharide (SLAP) was prepared under room temperature, then the structural characteristics and regulatory effects on gut microbiota metabolism in tumor-bearing mice were investigated. Results showed that SLAP was a kind of gulcomannan (average molecular weight of 1.76 × 107 Da) comprised of Xyl, Man, Glc, Gal (molar ratio of 0.19:1.00:0.72:0.53), which took β-(1 → 4)-Manp and β-(1 → 4)-Glcp as the backbone with β-(1 → 6)-Glcp and α-(1 → 6)-Galp as branches. The animal experiment results demonstrated that SLAP could effectively enhance the immunoregulatory activities of CD4+ and CD8+ T cells in tumor-bearing mice via improving intestinal lactobacillaceae contents and promoting primary bile acids biosynthesis, finally leading to the suppression of solid tumors growth with an inhibitory rate of 61.14 % (100 mg/kg·d). These results would provide certain data support and research basis for further applications of SLAP as an immunomodulatory adjuvant in food and medicine fields.

Evaluate the potential adsorption of graphynes (perfect and doped) for nitrogen mustard gas: A first principles study

Density functional theory (DFT) calculations are used to thoroughly examine the reactivity and electronic sensitivity of pristine and BN-doped graphyne (BNG) toward nitrogen mustard (NM). Graphyne’s electrical conductivity is unaffected by the weak adsorption of NM, which occurs via the Cl atom on the material with an adsorption energy of roughly −3.1 kcal.mol−1. In addition to decreasing graphyne’s reactivity and work function, substituting isoelectronic BN linkages for CC linkages enhances the HOMO-LUMO energy gap (Eg). BNG’s electrical conductivity increases when Eg drops from 2.99 to 1.82 eV due to the adsorption of NM. Additionally, a significant change in BNG’s work function results in a variation in the field electron emission current. Lastly, it is anticipated that the desorption of NM from the BNG surface will take a brief recovery time of roughly 0.05 s at room temperature. It has also been demonstrated that NM concentration affects changes in electrical conductivity. The findings also suggest that BNG could be a promising NM sensor.

Large and reversible elastocaloric effect induced by low stress in a Ga-doped Ni-Mn-Ti alloy

The Solid-state cooling based on caloric effects is considered a potential alternative to conventional refrigeration technology, which uses ozone-depleting gases. Several shape memory alloys have attracted attention for solid-state cooling since they present a high reversibility of the caloric effect, which depends mainly on thermal hysteresis and sensitivity to the applied field. In the present work, a study substitution of Mn by Ga in the Ni50Mn34Ti16 alloy led to diminished thermal hysteresis in the martensitic transformation by 6 K. The elastocaloric effect, thermal and microstructure properties of a polycrystalline Ni50Mn32Ti16Ga2 alloy have been characterized. The elastocaloric effect was obtained indirectly from the length change as a function of temperature at constant stress. An isothermal entropy change (ΔSISO) of 23.0 J kg−1 K−1 during heating and 22.0 J kg−1 K−1 during cooling was observed for applied stress of 160 MPa. In addition, the ΔSISO is reversible for a temperature span between 287 and 319 K, reaching a maximum of 20.5 J kg−1 K−1 at 299 K. The thermal hysteresis changed slightly while the applied stress increased up to 160 MPa since the sensitivity of the martensitic transformation temperatures to stress was 0.150 K M/MPa during cooling and 0.160 K/MPa during heating. The X-ray diffraction analysis revealed a mixture of B2-type cubic austenite, 5 M modulated martensite, and a second intermetallic phase identified as Ni3Ti. All these results were obtained around room temperature.

Optimal carbofuran degradation via CWPO in NOM-doped water by a framework Cu-doped aluminate perovskite catalyst derived from aluminum saline slags

This study is the first to propose the synthesis of LayAl1–xCuxO3–δ perovskite catalysts using Al recovered from acid leaching of saline slags. The effect of parameters such as the La/Al molar ratio was explored during the synthetic process. A suite of characterization techniques—including XRF, XRD, N2 adsorption, H2-TPR, FTIR, TGA-DTA, TEM, SEM, EDX, and XPS—confirmed the successful synthesis of high-purity (up to 90 %) perovskites with La and O vacancies, and a high concentration of Cu(I) active sites dispersed within the perovskite lattice. The best catalyst was used to optimize the degradation of carbofuran (CBF) in water doped with synthetic dissolved natural organic matter (NOM) using the Fenton-like catalytic wet peroxide oxidation (CWPO) approach. The effects of catalyst concentration, H2O2 dose, and pH on catalytic performance were investigated. Degradation, mineralization (COD removal), and H2O2 consumption were maximized, while Cu leaching was minimized using a statistical desirability function for multiple responses. Optimal conditions were found to be a catalyst concentration (mg Cu/mg H2O2) of 0.234 (2.0 g L–1), an H2O2 dose of 73.3 % (0.73 times the stoichiometric dose for full COD mineralization), and a remarkable circumneutral pH of 6.2. Under these conditions, degradation reached 94.1 %, and COD mineralization was 51 % under room temperature. Notably, the perovskite catalyst exhibited remarkable stability during reuse in up to three cycles, as demonstrated by the low Cu leaching (<1.30 mg L–1).

Robust, transparent, self-healable, recyclable all-starch-based gel with thermoelectric capability for wearable sensor

Conventional all-starch-based (ASB) gels are weak and lack ductility. The preparation of a robust ASB gel with multi-functionalities e.g., self-healing, anti-freezing, conductivity, and so forth, is highly desirable but challenging. Herein, a new kind of ASB gel was prepared by gelatinizing starch in urea and choline chloride solution (UC) with the aid of water. Its tensile strength was up to 1.08 MPa with a tensile strain of 313 %, and this value hardly changed after 10 days ageing. A high healing efficiency of 98 % can be achieved after 1 h of healing at room temperature, and the healed tensile strength reaches up to ca. 1.06 MPa, which is almost the highest value for ASB gel. The resultant ASB gel can surfer from bending and twisting at −80 °C. Moreover, ASB gel also exhibits excellent biocompatibility and biodegradability. In addition, UC endowed the ASB gel with ion conductivity, allowing it to be used as a flexible strain sensor to monitor human movement. The ion-conductive ASB gel also exhibited thermoelectric ability with a Seebeck coefficient of 2.5 mV K−1, which can be further improved to 5 mV K−1 with a maximum output voltage of 252 mV by introducing a gradient of ionic concentration.

Superior bendability enabled by inherent in-plane elasticity in Bi2Te3 thermoelectrics

With the rapid development of modern wearable electronics, powerful and deformable thermoelectric generators have become an urgent need as the power units that convert environmental or body heat into electricity. Existing efforts mostly focused on the assistance for deformability by substrates/additives, the resultant devices usually output much less power and showed very poor power retainment. Elasticity is inherent to all solids, which therefore offers an intrinsic solution for making thermoelectrics deformable without compromise in power output because of its full recoverability. This work demonstrates this in best-performing (Bi, Sb)2(Te, Se)3 thermoelectrics near room temperature, ending up in the film devices with both extraordinary power density and robust recoverable bendability. This originates from the inherent large elasticity for the in-plane orientation, which is enabled by an easy tape stripping approach for the Van der Waals layered structure, allowing the realization of both powerfulness and bendability that are equally important for wearable thermoelectrics.

Failure criterion and damage evolution of high-strength geopolymer concrete under compression-shear composite loading after high temperatures

Geopolymer concrete (GPC) holds significant potential for building fire safety design due to its green, low-carbon, and high-temperature resistant properties. In practical applications, concrete structures often face multiaxial composite loads. Therefore, investigating the composite stress performance of high-strength geopolymer concrete (HGPC) after exposure to high temperatures is crucial for assessing structural damage and enhancing fire prevention measures. This paper examines the compressive shear performance of HGPC at various temperatures T (20°C, 200°C, 400°C, 600°C) and stress ratios k (0.15, 0.3, 0.45, 0.6). The study analyzes failure patterns, shear load-displacement curves, shear strengths and their components, and peak shear deformation. Failure criteria are proposed to describe the damage patterns of HGPC under compressive shear loading after high temperatures. Additionally, the damage evolution process is evaluated using the energy method. The results show that HGPC damage surfaces penetrate the coarse aggregate at room temperature under compression-shear composite loading but shift to the aggregate-mortar interface at 600°C. Shear stiffness, peak shear strength, and residual strength increase with higher stress ratios but decrease with rising temperatures. Temperature affects peak shear strength by over 95 %, significantly more than the stress ratio. The shear strength decreases more slowly than compressive strength up to 400°C but more rapidly beyond 400°C. The cohesive strength of HGPC decreases with increasing stress ratio under different temperatures, while contact friction strength exceeds 50 % of peak shear strength. Shear dilation strength generally increases, then decreases, peaking at k = 0.45. The failure criterion based on the modified twin shear unified strength theory aligns best with experimental results. Furthermore, an increased stress ratio retarded the development of damage evolution, which was first accelerated and then slowed with rising temperature.

A Comprehensive Review on Imperative Role of Ionic Liquids in Pharmaceutical Sciences.

Ionic liquids (ILs) are poorly-coordinated ionic salts that can exist as a liquid at room temperatures (or <100 °C). ILs are also referred to as "designer solvents" because so many of them have been created to solve particular synthetic issues. ILs are regarded as "green solvents" because they have several distinctive qualities, including better ionic conduction, recyclability, improved solvation ability, low volatility, and thermal stability. These have been at the forefront of the most innovative fields of science and technology during the past few years. ILs may be employed in new drug formulation development and drug design in the field of pharmacy for various functions such as improvement of solubility, targeted drug delivery, stabilizer, permeability enhancer, or improvement of bioavailability in the development of pharmaceutical or vaccine dosage formulations. Ionic liquids have become a key component in various areas such as synthetic and catalytic chemistry, extraction, analytics, biotechnology, etc., due to their superior abilities along with highly modifiable potential. This study concentrates on the usage of ILs in various pharmaceutical applications enlisting their numerous purposes from the delivery of drugs to pharmaceutical synthesis. To better comprehend cuttingedge technologies in IL-based drug delivery systems, highly focused mechanistic studies regarding the synthesis/preparation of ILs and their biocompatibility along with the ecotoxicological and biological effects need to be studied. The use of IL techniques can address key issues regarding pharmaceutical preparations such as lower solubility and bioavailability which plays a key role in the lack of effectiveness of significant commercially available drugs.

In-situ fabrication of defect rich Cu2+1O on electrodeposited Cu cone arrays for promoting electrocatalytic anode hydrogen production

The low-potential formaldehyde oxidation reaction (FOR) is a significant replacement for oxygen evolution reaction, as FOR can couple with the cathode hydrogen evolution reaction (HER) to obtain a bipolar H2 production system with an extra low cell voltage. Cu-based electrocatalysts offer cost advantages in FOR but suffer from poor intrinsic activity and stability. Herein, a novel defect rich CF-Cu@Cu2+1O/Cu pinecone-shaped array electrocatalyst is fabricated by in-situ solution immersion of electrodeposited Cu cone arrays on foam for efficient and stable formaldehyde selective oxidation reaction to co-produce hydrogen and valuable formate. Benefitting from the partially mixed Cu2+1O in metallic copper and concomitant production of defect rich oxygen vacancies, only 0.04 VRHE is required for electrocatalytic FOR at 100 mA·cm−2 under alkaline conditions. FOR current density of CF-Cu@Cu2+1O/Cu electrode exhibits 2.35 times than that of CF-Cu (144 mA·cm−2) and 77 times than that of copper foam (4.4 mA·cm−2) at 0.5 VRHE. Moreover, the special pinecone-shaped structure is constructed to modify Cu-based catalysts with substantially enhanced stability. A FOR-HER co-electrolysis device of CF-Cu@Cu2+1O/Cu(+)||Pt/C(−) can achieve bipolar H2 production with an approaching 200 % Faradaic efficiency, requiring an extremely low electrical energy consumption of only ∼ 0.35 kWh per m3 of H2 and potential of 0.291 V at 100 mA·cm−2 at room temperature.

Spectroscopic ellipsometry investigation of a 6H-SiC single crystal plate for potential use in graphene optoelectronic devices

At room temperature, the spectroscopic ellipsometry SE parameters Epsi (ψ) and Delta (Δ) for 6H-SiC crystal substrate were measured in the wavelength range 350-1700nm at four different angles of incidence, 60o, 65o, 70o, and 75o. An SE model was developed to extract optical consents of 6H-SiC crystal substrate from the experimentally measured SE parameters. In the wavelength range 350-1700 nm, the refractive index of the 6H-SiC crystal substrate was extracted and fitted to two terms of the Sellmeier dispersion function. In the wide spectral range (350-1700 nm), the Wemple-DiDomenico (WDD) dispersion model shows how the real refractive index changes with wavelength. The analysis of refractive index dispersion of the 6H-SiC crystal substrate using Sellmeier dispersion function and WDD optical model allows to extract oscillator strength Nfij, average oscillator energy Eo, dispersion energy of the single oscillator Ed, lattice oscillator strength El, Abbe dispersion number, energy gap Eg, density of valence electrons nv, refractive index at infinite wavelength n∞, lattice dielectric constant εL, the ratio of free carrier density to free carrier effective mass (N/m*), and plasma frequency ωp. For the 6H-SiC crystal substrate, in the desired spectral range (240–1700 nm), it does not have any depolarization effect on the reflected polarized light.

Potential application of room temperature synthesized MIL-100(Fe) in enhancing methane production in microbial electrolysis Cells-Anaerobic digestion treating Protein-Rich wastewater

Microbial electrolysis cell-anaerobic digestion (MEC-AD) is an emerging technology for methane production. However, low substrate degradation efficiency remains a challenge when processing protein substrates. This study developed a MIL-100(Fe) carbon cloth anode to enhance methane production and substrate degradation in MEC-AD. The effects of MIL-100(Fe) prepared under hydrothermal (H-MIL-100(Fe)) and room temperature conditions (R-MIL-100(Fe)) were compared. Results indicated that H-MIL-100(Fe) and R-MIL-100(Fe) increased cumulative methane production by 16.01% and 14.99%, respectively compared to normal cloth, each influencing methane production through distinct mechanisms. Electrochemical characterization showed that H-MIL-100(Fe) enhanced the electrochemical performance more significantly due to the enrichment of Geotalea, with the oxidation current improved by 7.39-fold (R-MIL-100(Fe) increased it by only 2.95-fold) to promote growth of Methanobacterium. Metagenomic analysis revealed that R-MIL-100(Fe) tended to metabolize amino acids into methane rather than support cellular life activities, indicating its practicality under limited substrate concentration. In summary, R-MIL-100(Fe) shows greater potential for application due to its mild synthesis conditions and advantages in treating complex substrates.

Nanostructure-induced functional combination of vanishing magnetostriction and magnetic softness in ferromagnetic (GaNi)xCoCrFe (x = 0.4–1.6) high-entropy alloys

Searching for high-entropy alloys with functional properties that emerge from their multi-scale structure, we have investigated the (GaNi)xCoCrFe (x = 0.4–1.6) system. We have characterized structure, microstructure, nanostructure and chemical composition of the individual phases in the multi-phase alloys and determined their magnetic, magnetostrictive and electrical properties. We found that the alloys are ferromagnetic and exhibit functional combination of magnetic softness and vanishing magnetostriction, classifying them as energy-efficient “supersilent” materials (inaudible to a human ear) for alternating-current (AC) electromagnetic applications in the audio-frequency range. The alloys develop a two-phase structure, a face-centered cubic (fcc) and a body-centered cubic (bcc), where the fcc phase fraction decreases, while the bcc fraction increases with the increasing (GaNi)x content. Ferromagnetism of the alloys originates from the highly nanostructured bcc phase, with the ferromagnetic Curie temperatures in the range TC = 750–700 K, depending on x. The fcc phase is not nanostructured and is paramagnetic at room temperature, but undergoes a spin glass transition at Tf≈6.4 K. The magnetic softness and vanishing magnetostriction of the alloys are both nanomagnetic phenomena. The magnetic-softness and magnetostriction parameters of the x = 1.3 and 1.6 alloys make them relevant for supersilent AC applications at low frequencies.

Compressive creep damage of Ti-6Al-4V ELI alloy with bimodal structure at room temperature

The compressive creep performance of Ti alloy is critical for the application of submersibles due to the pressure hull of deep-diving equipment mainly subjected to the seawater pressure during its service. The compressive creep behaviors and the corresponding deformation mechanism of Ti-6Al-4V ELI alloy under different applied stress amplitudes were investigated. It was found that the stress threshold for Ti-6Al-4V ELI alloy produced significant compressive creep damage was 0.8 times yield strength (Rp0.2), and the primary mechanism was prismatic slip. Specifically, a large number of prismatic slips were preferentially activated in the αp grains with a relative high Schmid factor when the applied stress amplitude was greater than 0.8Rp0.2. As the applied stress amplitude increases, the prismatic slips were also activated in the αlath. Meanwhile, the Burgers relationship between αlath and βlamellae gradually destroyed due to the dislocation pile-up at the αlath/βlamellae interface. This investigation provides data support for the compressive creep performance evaluation of Ti-6Al-4V ELI pressure hull.

Identification of graphite with perfect rhombohedral stacking by electronic Raman scattering

Rhombohedral graphite (RG) shows strong correlations in its topological flat band and is pivotal for exploring emergent, correlated electronic phenomena. One key advantage is the enhancement of electronic interactions with the increase in the number of rhombohedrally stacked graphene layers. Increasing thickness also leads to an exponential increase in the number of stacking configurations, necessitating a precise method to identify flawless rhombohedral stackings. Overcoming this challenge is difficult because the established technique for stacking sequence identification, based on phonon originated Raman processes (e.g. the 2D peak), fails in thick RG samples. We demonstrate that the strong layer dependence of the band structure can be harnessed to identify RG without stacking faults. For thicknesses ranging from 3 to 12 layers, we show that each perfect RG structure presents distinctive peak positions in electronic Raman scattering (ERS), directly fingerprinting the flawless stacking. This measurement can be carried out using a conventional confocal Raman spectrometer at room temperature, using visible excitation wavelengths. Consequently, this overcomes the identification challenge by providing a simple and fast optical measurement technique, thereby helping to establish RG as a platform for studying strong correlations in one of the simplest crystals possible.

Synthesis, crystal structures and antiproliferative activities of a new indole-containing dipyridylmethanone hydrazone Schiff base and its cadmium(II) complex.

In this study, we introduce a novel indole-containing pyridine-based Schiff base, (E)-2-({[bis(pyridin-2-yl)methylidene]hydrazin-1-ylidene}methyl)-1H-indole, C20H15N5 (2-DPHI), and its cadmium(II) complex poly[[2-({[bis(pyridin-2-yl)methylidene]hydrazin-1-ylidene}methyl)-1H-indole]di-μ-chlorido-cadmium(II)], [CdCl2(C20H15N5)]n (pCd2), as potential anticancer agents. The Schiff base was synthesized by reacting dipyridylmethanone hydrazone with indole-2-formaldehyde, while the cadmium complex was prepared by combining CdCl2 and 2-DPHI in methanol at room temperature. Both compounds were evaluated for their cytotoxicity against three human cancer cell lines (A375, A549 and HeLa) and a normal cell line (HFF-1). The ligand 2-DPHI exhibited notable antitumour activity, with an IC50 value of 12.22 µM against A375 and 15.17 µM against A549 after 48 h, while the pCd2 complex showed an even stronger inhibition of A375 cells, with an IC50 value of 4.88 µM, outperforming both 2-DPHI and CdCl2. Both compounds demonstrated lower toxicity towards normal cells compared to cancer cells. The structures of 2-DPHI and pCd2 were fully characterized using single-crystal X-ray diffraction, elemental analysis, high-resolution mass spectrometry and FT-IR, 1H NMR, 13C NMR and UV-Vis spectroscopy.

Magnetic injection of α-CP nanoribbons and investigation of spintronic device applications of magnetic α-CP nanoribbons based on first principles calculations

Since the successful synthesis of α-phosphorus carbide (α-CP) using carbon doping technology, α-CP has exhibited excellent carrier mobility and anisotropy at room temperature, underscoring its potential for spintronic applications. The application of CP in spintronic devices is limited due to its lack of magnetism. Effective magnetic injection in non-magnetic semiconductors can typically be achieved by doping with magnetic atoms. In this study, we calculated the electromagnetic properties of transition metal (TM) atoms adsorbed at different positions on α-CP using first principles. Notably, we found that α-CP nanoribbons adsorbed with Fe and Mn atoms of a specific width exhibit stable half-metallicity. We discovered that α-CP nanoribbons adsorbed with Fe and Mn atoms of a specific width exhibit stable half-metal properties and design magnetic tunnel junctions with half-metallic Fe_H12 and Mn_H12 adsorption structures. The results show that Mn_H12 and Fe_H12 devices exhibit a highly efficient spin filtering effect, with a TMR as high as 5521%. These findings provide theoretical guidance for the application of CP-based spintronic devices.

Hofmeister effect driven dynamic-bond cross-linked dialdehyde xylan hydrogels with rapid response and robust mechanical properties for expanding stent

The biomedical field urgently needs for programmable stent materials with nontoxic, autonomous self-healing, injectability, and suitable mechanical strength, especially self-expanding characteristics. However, such materials are still lacking. Herein, based on gelatin and dialdehyde-functionalized xylan, we synthesized 3D-printable, autonomous, self-healing, and mechanically robust hydrogels with a reversible Schiff base crosslink network. The hydrogels exhibited excellent mechanical properties and automatic healing properties at room temperature. The solid mechanical properties originate from the Schiff base, hydrogen bonding interactions, and xylan nanoparticle reinforcement of the polymer networks. As a proof of concept, the Hofmeister effect enabled the hydrogel to contract in highly concentrated salt solutions. In contrast, the same hydrogel expanded and relaxed in dilute salt solutions (quick response within 10 s), showing ionic stimulus-response and excellent shape memory characteristics, which demonstrated that the prepared hydrogel could be used as self-expanding artificial vascular stents. In particular, good biocompatibility was confirmed by cytotoxicity and compatibility tests, and ex vivo arterial experiments further indicated the feasibility of these artificial vascular scaffolds (the expansion force reached 1.51 N). Combined with its ionic stimuli-responsive shape memory ability, the strong mechanical, self-healing, 3D-printable, and biocompatibility properties make this hydrogel a promising material for artificial stents in various biomedical applications.

A novel Cr3+-doped MgGaBO4 phosphor: expanding the horizons in plant illumination

Near-infrared (NIR) spectroscopy technology has demonstrated unparalleled efficacy in night vision, iris authentication, plant illumination, food inspection, and various other domains. Nonetheless, the quest for novel phosphors exhibiting superior luminescent efficiency and enduring thermal stability persists as a formidable obstacle. In this study, phosphors MgGaBO4: Cr3+, Al3+ were successfully synthesized by high-temperature solid-phase reaction method. Firstly, starting from MgGaBO4: Cr3+, the crystal field environment around Cr3+ ions was modulated by replacing Ga3+ with Al3+ to further improve the luminescence performance of the phosphor. The emission peak wavelength of MgGaBO4: 0.0075Cr3+,0.005Al3+ phosphor was about 756 nm, the full width at half-maximum (FWHM) was about 174 nm under the blue light excitation of 440 nm. In addition, the luminescence intensity at 100 °C remains at 77.41% of that at room temperature. Finally, the excellent moisture resistance of this phosphor was demonstrated. This work not only introduces a novel broadband NIR phosphor with promising application potential in advanced agricultural lighting but also proposes a synergistic enhancement strategy for effectively improving the performance of broadband NIR phosphor-converted LED light sources.

Long-term stability of five atypical antipsychotics (risperidone, olanzapine, paliperidone, clozapine, quetiapine) and the antidepressant mirtazapine in human serum assessed by a validated SPE LC-MS/MS method.

Long-term sample stability of five atypical antipsychoticdrugs risperidone, paliperidone, clozapine, quetiapine and olanzapine and the antidepressant drug mirtazapine in serum was studied by use of a newly developed and validated analytical method based on solid-phase extraction and liquid chromatography-tandem mass spectrometry. Ascorbic acid was used as an antioxidative agent to stabilize olanzapine during storage and sample preparation. We assessed analyte stability on long-term storage in serum samples at 25°C, 5°C, -20°C and -80°C, and during five freeze-thaw cycles. Analytes were stable for 23 days at room temperature except for olanzapine and mirtazapine (17 days). All analytes were stable for at least 30 days at 5°C. All analytes were stable for 270 days at -20°C, except for paliperidone and mirtazapine with 60 days and 180 days, respectively. All analytes were stable for 270 days at -80°C. Furthermore, all analytes were stable for five freeze-thaw cycles. We recommend storage at -80°C when samples drawn for analysis of antipsychotic drugs are stored for more than 60 days, whereas a temperature of -20°C is sufficient for storage less than 60 days.