Emission Spectra Research Articles

Xuanfei Formula inhibited RSV infection by normalizing the SREBP2-mediated cholesterol synthesis process.

Respiratory syncytial virus (RSV) is the major cause of lower respiratory tract infections in children and the elderly, often progressing to pneumonia and severe sequelae. However, there are currently no feasible and cost-effective interventions with proven efficacy for children, making medications with anti-RSV activity urgently needed. Traditional Chinese medicine has shown promising therapeutic efficacy in alleviating viral infection symptoms. Therefore, we aimed to develop effective strategies for RSV treatment based on traditional Chinese medicine. The infection status was assessed in BALB/c mice with or without Xuanfei Formula (XFF) treatment over a one-week period using H&E staining, cytokine assays and RSV titer testing after RSV challenge. Remarkably, on the first day of XFF intervention, both the pro-inflammation cytokine levels in the serum and RSV-N gene copies in the lung of mice were plummeted, compared to the RSV-infected group. This implied that XFF might possess the immune-independent anti-RSV capability. To elucidate the underlying mechanism, we employed transcriptome analysis followed by k-means analysis. The reversal effects of XFF against RSV primarily focused on the processes of innate and adaptive immunity. Additionally, we found that XFF administration corrected the disordered fatty acid and cholesterol metabolism processes during RSV infection. Lipidomics profiling indicated consistent cholesterol abundance with transcriptional changes but not fatty acids. Cholesterol synthesis-related genes mRNA levels and cholesterol synthesis intermediates detection supported XFF's repression upon cholesterol biosynthesis. Aberrantly increased cholesterol production has been reported as necessary for RSV infection. To mimic that, we observed lovastatin treatment inhibited RSV replication and pro-inflammation cytokine expression in vitro. Transcription factor prediction of differentially expressed genes (DEGs) involved in cholesterol synthesis implicated SREBP2. Through network pharmacology, stigmasterol and β-sitosterol were identified as the effective active ingredients within the XFF, with the help of further molecular docking and mass spectrum detection. In vitro experiments demonstrated β-sitosterol and stigmasterol reinforced the bonding between SREBP cleavage-activation protein (SCAP) and insulin-induced gene proteins (INSIGs) to inhibit SREBP2 cleavage maturation and consequent RSV infection. Xuanfei Formula (XFF) exhibits excellent anti-RSV efficacy by inhibiting SREBP2-mediated cholesterol synthesis to reduce RSV replication and ameliorate inflammation in the lung of infected mice.

Pt-S Bond-Enabled Temperature-Dependent Phosphorescence in S-Heteroaryl Tetradentate Pt(S^C^N^O) Complexes.

This study presents the rare examples of S-heteroaryl tetradentate Pt(S^C^N^O) luminescent complexes (PtSZ and PtSZtBu) containing a Pt-S bond. The presence of the Pt-S bond allows the novel Pt(S^C^N^O) complexes to exhibit temperature-dependent phosphorescent emission behavior. The PtSZtBu exhibits dual-emission phenomena and biexponential transient decay spectra above 250 K, indicating the presence of two minimal excited states in the potential energy surface (PES) of the T1 state. Through complementary experimental and computational studies, we have identified changes in orbital composition between Pt(dxy)-S(px) and Pt(dyz)-S(pz) in excited states with increasing temperature. This results in two energy minima, enabling the excited states to decay selectively and radiatively at different temperatures. Consequently, this leads to remarkable steady-state and transient emission spectra changes. Our work not only provides valuable insights for the development of novel Pt-S bond-based tetradentate Pt(II) complexes but also enhances our understanding of the distinctive properties governed by the Pt-S bond.

A novel cryogenic VUV spectrofluorometer for the characterization of wavelength shifters

We present a novel cryogenic VUV spectrofluorometer designed to characterize wavelength shifters (WLS) crucial for experiments based on liquid argon (LAr) scintillation light detection. Wavelength shifters like 1,1,4,4-tetraphenyl-1,3-butadiene (TPB) or polyethylene naphthalate (PEN) are used in these experiments to shift the VUV scintillation light to the visible region. Precise knowledge of the optical properties of the WLS at liquid argon's temperature (87 K) and LAr scintillation wavelength (128 nm) is necessary to model and understand the detector response. The cryogenic VUV spectrofluorometer was commissioned to measure the emission spectra and relative wavelength shifting efficiency (WLSE) of samples between 300 K to 87 K for VUV (120 nm to 190 nm) and UV (310 nm) excitation. New mitigation techniques for surface effects on cold WLS were established. As part of this work, the TPB-based wavelength shifting reflector (WLSR) featured in the neutrinoless double-beta decay experiment LEGEND-200 was characterized. The WLSE was observed to increase by (54 ± 5) % from room temperature (RT) to 87 K. PEN installed in LEGEND-200 was also characterized, and a first measurement of the relative WLSE and emission spectrum at RT and 87 K is presented. The WLSE of amorphous PEN was found to be enhanced by at least (37 ± 4) % for excitation with 128 nm and by (52 ± 3) % for UV excitation at 87 K compared to RT.

Growth, thermal, spectroscopy and ∼2.7 μm multiwavelength laser output of Er:GYAP crystal

We demonstrate the growth, thermal, spectroscopy and laser performance of a Er3+ doped Gd0.1Y0.9AlO3 (Er:GYAP) disorder crystal grown by Czochralski method. The crystal with space group Pbnm and lattice parameters of =0.5185 nm, =0.5327 nm, =0.7378 nm, α=β=γ=90° and =0.203784 nm3 are obtained by fitting powder X-ray diffraction data. The Mohr’s hardnesses along three axes are 6.94, 7.27, and 7.44. The thermal expansion coefficient of axis is 4.20 × 10–6 K–1 and the density is 5.88 g/cm3. The thermal conductivities are characterized as =6.24, =5.57, and =6.83 W/(m·K). Meanwhile, the refractive index, absorption and emission spectra in triaxial directions are determined. Besides, level lifetimes of 4I11/2 and 4I13/2 are 0.86 and 2.83 ms. Finally, the ∼2.7 μm multiwavelength laser outputs are observed with maximum average power of 628 mW and beam quality factors / of 1.42/1.45. The results prove that the Er:GYAP crystal is a promising gain medium for generating mid-infrared lasers.

Incineration-source fingerprints and emission spectrums of dioxins with diagnostic application

Despite increasing waste-to-energy (WtE) capacities, there remain deficiencies in comprehension of 136 kinds of tetra- through octa-chlorinated dibenzo-p-dioxin and dibenzofurans (136 PCDD/Fs) originating from incineration sources. Samples from twenty typical WtE plants, encompassing coal-fired power plants (CPP), grate incinerators (GI), fluidized bed incinerators (FBI), and rotary kilns (RK), yielded extensive PCDD/F datasets. Research was conducted on fingerprint mapping, formation pathways, emission profiles, and diagnostic analysis of PCDD/Fs in WtE plants. Fingerprints revealed a prevalence of TCDF, followed by PeCDF, while CPP and RK respectively generated more PCDD and HxCDD. De novo synthesis was the predominant formation pathway except one plant, where CP-route dominated. DD/DF chlorination also facilitated PCDD/F formation, showing general trends of FBI > GI > CPP > RK. The PCDD/F emission intensities emitted in air pollution control system inlet (APCSI) and outlet (APCSO) followed the statistical sequence of RK > FBI > GI > CPP, with the average I-TEQ concentrations in APCSO reaching 0.18, 0.08, 0.11, and 0.04 ng I-TEQ·Nm−3. Emission spectrum were accordingly formed. Four clusters were segmented for diagnosis analysis, where PCDD/Fs in GI and FBI were similar, grouped as a single cluster. PCDD/Fs in CPP and RK demonstrated distinctive features in TCDD, HxCDD, and HxCDF. The WtE plants exceeding the limit value tended to generate and retain fewer TCDD and TCDF yet had higher fractions of HxCDD and HxCDF. The failure of APCS coupled with the intrinsic source strength of PCDD/Fs directly led to exceedance, highlighting safe operational practices. This study motivated source tracing and precise evaluation of 136 PCDD/Fs based on the revealed fingerprint profiles for WtE processes.

Luminescence and energy transfer properties of color-tunable Dy3+, Eu3+ co-activated NaGdSiO4 phosphor for WLED with great thermo-stability.

A series of NaGd1-x-ySiO4: y Dy3+ - x Eu3+ phosphors were synthesized by a high-temperature solid-phase method. The optimal doping ion concentration of Dy3+ ions for this phosphor was determined to be 1% from the emission spectra. The energy transfer between Dy3+ and Eu3+ ions at 351 nm was investigated by photoluminescence spectra and fluorescence decay curves. At the excitation wavelengths of 275 nm, 351 nm, 366 nm, and 394 nm, a change from yellow to white to red light can be realized by adjusting the doping concentration of Eu/Dy ions. Particularly, by testing the temperature-dependent fluorescence spectrum of the phosphor, it can be found that the luminous intensity of the phosphor is as high as 96% when 394 nm excitation is employed at 413 K. It was the maximum at this temperature comparing with other phosphors as far as we know. The color coordinate values show that the NaGd1-x-ySiO4: x Dy3+ - y Eu3+ phosphors are very close to the white light color coordinates (x = 0.33, y = 0.33) under 351 nm excitation. Meanwhile, the correlated color temperature is between 5062 - 7104 K. These results indicate that this phosphor is a promising candidate for high-quality WLED.

Crystal growth and spectroscopic performances of Dy3+:YPO4 and Dy3+/Tb3+:YPO4 crystal as potential yellow laser gain mediums

Exploring new Dy3+-doped laser gain medium is still a challenge for constructing efficient yellow solid-state laser at current stage. In this paper, high quality Dy3+:YPO4 and Dy3+/Tb3+:YPO4 crystals were grown by the high temperature solution method. The crystal structure, chemical composition, phonon energy, polarized absorption and emission spectra, fluorescence lifetime were investigated. The obtained large FWHMs (6nm) and absorption cross-sections (3.87×10-21 cm2) of Dy3+:YPO4 and Dy3+/Tb3+:YPO4 crystals at 454nm indicate that they can be efficiently pumped by the commercial blue laser diodes. J-O intensity (Ω2, Ω4, Ω6), fluorescence branching rate and radiative lifetime of Dy3+ ions were calculated by J-O theory. Benefiting from the appropriate phonon energy, the emission cross-section of Dy3+: YPO4 crystal at 575nm can reach 5.04×10-21 cm2. Moreover, after co-doping Tb3+ as deactivating ion, the emission cross-section of Dy3+/Tb3+: YPO4 crystal at 575nm was promoted to 5.98×10-21 cm2 by a resonance energy transfer process between the Dy3+-6H13/2 and Tb3+-7F4. Therefore, both Dy3+:YPO4 and Dy3+/Tb3+:YPO4 crystals are potential candidates for yellow laser gain mediums.

High-resolution Pan-STARRS and SMA Observations of IRAS 23077+6707: A Giant Edge-on Protoplanetary Disk

We present resolved images of IRAS 23077+6707 (“Dracula’s Chivito”) in 1.3 mm/225 GHz thermal dust and CO gas emission with the Submillimeter Array (SMA) and optical (0.5–0.8 μm) scattered light with the Panoramic Survey Telescope and Rapid Response System (Pan-STARRS). The Pan-STARRS data show a bipolar distribution of optically scattering dust that is characteristic for disks observed at high inclinations. Its scattered light emission spans ∼14″, with two highly asymmetric filaments extending along the upper bounds of each nebula by ∼9″. The SMA data measure 1.3 mm continuum dust as well as 12CO, 13CO, and C18O J = 2 − 1 line emission over 12″–14″ extents, with the gas presenting the typical morphology of a disk in Keplerian rotation, in both position–velocity space and in each CO line spectrum. IRAS 23077+6707 has no reported distance estimate, but if it is located in the Cepheus star-forming region (180–800 pc), it would have a radius spanning thousands of astronomical units. Taken together, we infer IRAS 23077+6707 to be a giant and gas-rich edge-on protoplanetary disk, which to our knowledge is the largest in extent so far discovered.

Molecular spectra and docking simulations investigated the binding mechanisms of tetracycline onto E. coli extracellular polymeric substances

Extracellular polymeric substances (EPS), which were an important fraction of natural organic matter (NOM), played an important role in various environmental processes. However, the heterogeneity, complexity, and dynamics of EPS make their interactions with antibiotics elusive. Using advanced multispectral technology, this study examined how EPS interacts with different concentrations of tetracycline (TC) in the soil system. Our results demonstrated that protein-like (C1), fulvic-like (C2), and humic-like (C3) fractions were identified from EPS. Two-dimensional synchronous correlation spectroscopy (2D-SF-COS) indicated that the protein-like fraction gave faster responses than the fulvic-like fraction during the TC binding process. The sequence of structural changes in EPS due to TC binding was revealed by two-dimensional Fourier Transformation Infrared correlation spectroscopy (2D-FTIR-COS) as follows: 1550 > 1660 > 1395 > 1240 > 1087 cm−1. It is noteworthy that the sensitivity of the amide group to TC has been preserved, with its intensity gradually increasing to become the primary binding site for TC. The integration of hetero-2DCOS maps with moving window 2D correlation spectroscopy (MW2DCOS) provided a unique insight into understanding the correlation between EPS fractions and functional groups during the TC binding process. Moreover, molecular docking (MD) discovered that the extracellular proteins would provide plenty of binding sites with TC through salt bridges, hydrogen bonds, and π-π base-stacking forces. With these results, systematic investigations of the dynamic changes in EPS components under different concentrations of antibiotic exposure demonstrated the advanced capabilities of multispectral technology in examining intricate interactions with EPS in the soil environment.

Risk prediction for hydrogen sulfide emission based on sulfate-reducing bacteria in the water flooding oilfield

The water quality of the injection–production systems deteriorates as the water flooding oilfields are developed more deeply, and the content of sulfate-reducing bacteria (SRB) increases. Accordingly, hydrogen sulfide (H2S) emission related to SRB is intensified, which will arise safety and health problems. In order to investigate the effect of SRB on H2S emission in the water flooding oilfield, the contents of SRB and sulfide of the different nodes of a typical injection–production system of Daqing Oilfield were measured first, and then, H2S emission from water was simulated under different conditions. Consequently, a H2S emission prediction model was established based on Henry coefficient and the correlation between sulfide content and SRB content in the water. The measured sulfide contents were ranging from 0.25 to 6.34 mg/l, and the SRB contents were from 2.5 to 25 000 pcs/ml, and the highest SRB and sulfide contents were found in the settling tank. The correlation between sulfide content and SRB content was much remarkable, and the R2 value of the correlation analysis was 0.94. Henry coefficient of H2S emission was obtained from the simulated experiments under varied conditions such as sulfate content, oil content, and temperature. The established H2S emission prediction model was much reliable for predicting H2S emission for water flooding injection–production system, and the accuracy of the predicted H2S emission of four nodes of the injection–production system was larger than 95% compared to the measured results. This study provides theoretical guidance for predicting H2S emission risks in water flooding injection–production systems.

Carbon-free hydrogen production via plasma-catalytic ammonia decomposition over transition metal-based catalysts: In situ probing by DRIFTS and SVUV-PIMS

The lack of comprehensive understanding of the reaction mechanism hinders the development of plasma-catalytic ammonia (NH3) decomposition as a potential route for producing carbon-free hydrogen. Herein, we investigated the reaction process over transition metal-based catalysts in a dielectric barrier discharge (DBD) reactor. For the first time, a combination of an integrated in situ diffuse reflectance infrared Fourier transform spectroscopy-DBD (in situ DRIFTS-DBD) and Optical Emission Spectra (OES) were applied to reveal that as for Ni/Al2O3, less NH3* was observed in the gas phase and more NH3 adsorbed on the surface. Combined with online synchrotron vacuum ultraviolet-photoionization mass spectrometry (SVUV-PIMS) it was further illustrated that N2 desorbed more quickly from Ni/Al2O3 than other tested catalysts. Additionally, compared with thermal catalysis, plasma further enhanced the adsorption of NH3 on Lewis acid sites and facilitated the desorption of N2. This study provided a better understanding of the plasma-catalytic NH3 decomposition reaction.

Tunable optoelectronic performances of fluorinated benzene-EDOT based hybrid electrochromic polymers

Due to its high electronegativity and small atomic radius without undesirable steric hindrance, the incorporation of fluorine atoms into the benzene unit which started from the commercially available compounds is a feasible way to tune the energy levels of polymers, and its electrochromic application is expected to achieve a new breakthrough. Herein, in this paper, benzene units with different fluorine atom numbers were selected as the core and 3,4-ethylenedioxythiophene (EDOT) as the terminal unit, three fluorinated electrochromic precursors (FPh-EDOT, 2FPh-EDOT, and 4FPh-EDOT) were designed and synthesized by Stille coupling reaction, and the corresponding fluorinated π-conjugated electrochromic polymers (P(FPh-EDOT), P(2Ph-EDOT), and P(4FPh-EDOT)) were prepared by electrochemical polymerization method. The effects of different fluorinated benzene units on the photophysics, electrochemistry, and electrochromic properties of precursors and polymers were systematically investigated, and the structure-property relationship was further revealed. All of them have low initial oxidation potentials {FPh-EDOT (0.65 V), 2FPh-EDOT (0.72 V), and 4FPh-EDOT (0.70 V)}, which makes it easy to obtain high-quality new fluorinated polymers at low polymerization potential. With the increase of the number of F atoms, the UV–vis absorption spectra and emission spectra of fluorinated monomer firstly red-shifted and then blue-shifted. The corresponding fluorinated polymers have good electrochemical activity and stability (the P(2Ph-EDOT) activity remained 82.7% after 500 cycles), making it possible to realize their electrochromic devices. All these three fluorinated polymers show obvious color change from the neutral state to the fully oxidized state (P(FPh-EDOT) changes from brown to grayish blue, P(2FPh-EDOT) changes from brown to gray, and P(4FPh-EDOT) changes from dark blue to light blue). The kinetic study further shows that all of them have distinguish electrochromic properties with good optical stability, very short response time (0.9 s for P(2FPh-EDOT) at 700 nm), and favorable coloration efficiency (130.7 cm2 C−1 for P(FPh-EDOT) at 503 nm). Overall, all these three fluorinated polymers have low optical band gap, good redox stability and electrochromic properties, are very promising electrochromic materials, which is worthy for the further research and development.

Vibration‐Dependent Dual‐Phosphorescent Cu4 Nanocluster with Remarkable Piezochromic Behavior

The dual emission (DE) characteristics of atomically precise copper nanoclusters (Cu NCs) are of significant theoretical and practical interest. Despite this, the underlying mechanism driving DE in Cu NCs remains elusive, primarily due to the complexities of excited state processes. Herein, a novel [Cu4(PPh3)4(C≡C‐p‐NH2C6H4)3]PF6 (Cu4) NC, shielded by alkynyl and exhibiting DE, was synthesized. Hydrostatic pressure was applied to Cu4, for the first time, to investigate the mechanism of DE. With increasing pressure, the higher‐energy emission peak of Cu4 gradually disappeared, leaving the lower‐energy emission peak as the dominant emission. Additionally, the Cu4 crystal exhibited notable piezochromism transitioning from cyan to orange. Angle‐dispersive synchrotron X‐ray diffraction results revealed that the reduced inter‐cluster distances under pressure brought the peripheral ligands closer, leading to the formation of new C−H···N and N−H···N hydrogen bonds in Cu4. It is proposed that these strengthened hydrogen bond interactions limit the ligands´ vibration, resulting in the vanishing of the higher‐energy peak. In situ high‐pressure Raman and vibrationally resolved emission spectra demonstrated that the benzene ring C=C stretching vibration is the structural source of the DE in Cu4.

Microwave-plasma surface modification of nanostructured-polyaniline:graphite composite counter electrode in dye-sensitized solar cells

This work demonstrates microwave plasma surface modifications of nanostructured polyaniline (NPES)-based counter electrodes (CE). Oxidative oxygen (O2) plasma and reductive hydrogen (H2) plasma were used in this study. Optical emission spectra confirm the presence of reactive species in both plasmas through the emissive species, such as O2+, O+, O•, H(nl), and H2 Fulcher-α. Microwave plasma treatment does not affect the surface morphology of NPES composite CE, which conserves its granule nanostructures, as revealed by SEM. The water contact angle measurements demonstrate how the O2 plasma treatment improves surface hydrophilicity, contrary to the H2 plasma treatment. Raman spectroscopy results show significant changes in the intrinsic-oxidation state and the number of semiquinonoid species (SQ) of NPES after plasma treatments, which are represented by the ratios of Raman intensity at 1368–1260 cm−1 and 1624–1583 cm−1, respectively. Generally, O2 plasma treatment increases the intrinsic-oxidation state and SQ number, opposite to the H2 plasma. The optimum condition of microwave plasma-assisted surface modification was attained in one minute of O2 plasma treatment, producing NPES with the highest intrinsic-oxidation state and SQ number. A power conversion efficiency of 3.17 % was obtained by a dye-sensitized solar cell fabricated with a modified CE using a one-minute O2 plasma treatment.

Synthesis of eco-friendly borosilicate glass with Eu3+ dopants: harnessing recovered silica gel waste for reddish-orange emission materials

In this study, recovered silica gel waste (RSGW) is used as a key raw material to create borosilicate glass doped with Eu3+ ions in a new and environmentally friendly way. The glass compositions were fabricated using the melt quenching method, with different amounts of RSGW and a constant 1.0 mol% Eu3+ doping concentration. The study shows that increasing the doping concentration of RSGW improves the glass density and rigidity while reducing the molar volume, indicating enhanced glass stability. Photoluminescence and X-ray luminescence analyses confirm that the optimal composition with 50 mol% RSGW exhibits the strongest emission. Based on the phonon sideband analysis, the host glasses have a phonon energy of 966.53 cm− 1. An X-ray absorption near-edge structure (XANES) analysis showed that most of the europium ions were in the 3+ oxidation state. The CIE 1931 chromaticity investigation shows the x,y color coordinates at (0.645, 0.351) in the reddish-orange region. To optimize the doping concentration of Eu2O3, it was determined that a fixed concentration of 50 mol% RSGW created the most suitable mixture. Both luminescence emission spectra exhibit strong luminescence, with a peak emission wavelength of 615 nm (⁵D0→⁷F2), confirming concentration quenching in both photoluminescence and x-ray luminescence at a concentration of 1.0 mol%. The study explores potential applications of this novel material in photonics and suggests that this eco-friendly synthesis approach holds great promise for sustainable and efficient production of reddish-orange emission materials.

Harnessing the brilliance of Cr3+ doped LaAlO3–Al2O3 phosphors with exceptional responsiveness to far-red phytochrome for plant growth LEDs

Perovskite-based materials have recently gained significant attention due to their unique properties. Herein, the deep and far-red-emitting LaAlO3–Al2O3:Cr3+ perovskite-based phosphors with particle sizes of 2–5 μm have been reported for the first time, demonstrating excellent responsiveness to far-red phytochrome. The synthesized phosphors exhibited a sharply defined deep and far-red emission, peaking at 735 nm, and significant absorptions in the violet (∼410 nm) and green (∼565 nm) regions. The distinct lines at 735 nm can be attributed to the robust crystal field effect of surrounding Cr3+ ions, wherein the 3+ oxidation state substitutes smaller-sized Al3+ ions in the [AlO6] octahedral site of the LaAlO3–Al2O3 lattice. The optimized LaAlO3–Al2O3:0.6%Cr3+ phosphor, annealed at 1400 °C, demonstrated exceptional characteristics, including a color purity of 100 %, a prolonged lifetime of 32.26 ms, a high activation energy of 0.501 eV, and an impressive internal quantum efficiency of 68.1 %. Moreover, a prototype of a violet-pumped LaAlO3–Al2O3:0.6%Cr3+ phosphor-coated LED showcased a well-matched emission spectrum with the absorption spectrum of far-red phytochrome, underscoring its significant potential for applications in LED-based plant growth systems.

Vibration-Dependent Dual-Phosphorescent Cu4 Nanocluster with Remarkable Piezochromic Behavior.

The dual emission (DE) characteristics of atomically precise copper nanoclusters (Cu NCs) are of significant theoretical and practical interest. Despite this, the underlying mechanism driving DE in Cu NCs remains elusive, primarily due to the complexities of excited state processes. Herein, a novel [Cu4(PPh3)4(C≡C-p-NH2C6H4)3]PF6 (Cu4) NC, shielded by alkynyl and exhibiting DE, was synthesized. Hydrostatic pressure was applied to Cu4, for the first time, to investigate the mechanism of DE. With increasing pressure, the higher-energy emission peak of Cu4 gradually disappeared, leaving the lower-energy emission peak as the dominant emission. Additionally, the Cu4 crystal exhibited notable piezochromism transitioning from cyan to orange. Angle-dispersive synchrotron X-ray diffraction results revealed that the reduced inter-cluster distances under pressure brought the peripheral ligands closer, leading to the formation of new C-H···N and N-H···N hydrogen bonds in Cu4. It is proposed that these strengthened hydrogen bond interactions limit the ligands´ vibration, resulting in the vanishing of the higher-energy peak. In situ high-pressure Raman and vibrationally resolved emission spectra demonstrated that the benzene ring C=C stretching vibration is the structural source of the DE in Cu4.

Luminescence studies and Judd Ofelt parameterization of Dy3+ activated La2(WO4)3 yellow phosphor

The synthesis and detailed luminescence studies of a series of La2-xDyx(WO4)3 (x = 0.02, 0.1, 0.2, 0.4, 0.6, 0.8) phosphors synthesized via microwave-assisted co-precipitation technique is reported in this paper. The XRD analysis confirmed that the phosphors were crystalized in a monoclinic structure with space group C2/c and FTIR analysis identified the characteristic vibrational modes. Morphological studies were conducted using FESEM analysis, and the EDS technique substantiated the effective incorporation of Dy3+ ions in La2(WO4)3. The photoluminescence excitation and emission spectra of varying concentrations of Dy3+ ions were recorded and an optimum concentration of 10 % exhibited the highest intensity. The emission spectra of all phosphors were dominated by peaks at 484 nm and 574 nm. The radiative properties were evaluated using Judd-Ofelt analysis and the JO intensity parameters followed the trend Ω2 > Ω6 > Ω4. The gradual decrease in the decay lifetime value of 4F9/2 excited level with an increase in doping concentration elucidates concentration quenching phenomena due to dipole – quadrupole interaction. The emission data were also analyzed by calculating CIE coordinates and concluded that Dy3+ doped La2(WO4)3 phosphors have potential applications in yellow light generation.

Experimental investigation for temperature and emissivity by flame emission spectrum in a cavity of rocket based combined cycle combustor chamber

Flame temperature and spectral emissivity were the important parameters characterizing the sufficient degree of fuel combustion and the particle radiative characteristics in the Rocket Based Combined Cycle (RBCC) combustor. To investigate the combustion characteristics of the complex supersonic flame in the RBCC combustor, a new radiation thermometry combined with Levenberg-Marquardt (LM) algorithm and the least squares method was proposed to measure the temperature, emissivity and spectral radiative properties based on the flame emission spectrum. In-situ measurements of the flame temperature, emissivity and spectral radiative properties were carried out in the RBCC direct-connected test bench with laser-induced plasma combustion enhancement (LIPCE) and without LIPCE. The flame average temperatures at fuel global equivalence ratio (α) of 1.0b and 0.6 with LIPCE were 4.51% and 2.08% higher than those without LIPCE. The flame combustion oscillation of kerosene tended to be stable in the recirculation zone of cavity with the thermal and chemical effects of laser induced plasma. The differences of flame temperature at α=1.0b and 0.6 were 503 K and 523 K with LIPCE, which were 20.07% and 42.64% lower than those without LIPCE. The flame emissivity with methane assisted ignition was 80.46% lower than that without methane assisted ignition, due to the carbon-hydrogen ratio of kerosene was higher than that of methane. The spectral emissivities at 600 nm with LIPCE were 1.25%, 22.2% and 4.22% lower than those without LIPCE at α=1.0a (with methane assisted ignition), 1.0b (without methane assisted ignition) and 0.6. The effect of concentration in the emissivity was removed by normalization to analyze the flame radiative properties in the RBCC combustor chamber. The maximum differences of flame normalized emissivity were 50.91% without LIPCE and 27.53% with LIPCE. The flame radiative properties were stabilized under the thermal and chemical effects of laser induced plasma at α=0.6.

Theoretical insights into long-range coupling of electron-hole pairs in TCTA–PO-T2T exciplex

This work reports theoretical investigations concerning long-range coupling of electron-hole pairs in spatially separated exciplex (SSE) systems via Density Functional Theory and Time-Dependent Density Functional Theory. Based on TCTA−PO-T2T parent exciplex, where 4,4′,4″-Tris(carbazol-9-yl)triphenylamine (TCTA) serves as donor (D) and 2,4,6-Tris[3-(diphenylphosphinyl)phenyl]-1,3,5-triazine (PO-T2T) as acceptor (A), SSEs are constructed by intentionally tuning the D−A distance. The calculation results demonstrate that all SSEs, even if the D−A distance is over 14 Å, exhibit the clear and strong charge transfer character in terms of DCT, qCT, and t indexes. As the D−A distance increases, the energy gap of SSEs is increased, resulting in the blueshift of emission spectra. Calculation and experiment results show a good consistency, indicating that our model could well describe SSEs. Meanwhile, the reduced energy gap between CT and 3LE and more degenerate states could boost reverse intersystem crossing via vibronic coupling and hyperfine coupling, eventually improving the electroluminescent performance of SSEs. Our study suggests that manipulation of relative energy alignment via controlling D−A distance not only promotes the properties of exciplexes, but also offers guidance for designing thermally activated delayed fluorescence emitters through-space charge transfer.