Double Emission Research Articles

Tunable double emission of Sb3+/Mn2+ doping stabilized organic-inorganic hybrid zinc-based halides

Low-dimensional organic-inorganic hybrid metal halides (OIHMHs) have attracted much attention lately in contrast to all-inorganic metal halides because of their excellent photophysical properties and tunable emission wavelengths. Zn-based metal halides have the following advantages: simplicity of synthesis, wide bandgap, and excellent chemical stability. Therefore, they are well-suited as host materials for photoluminescence by cation ion doping. We have successfully synthesized intrinsically non-emissive 0D (PPZ)ZnCl4 [PPZ (1-phenylpiperazine) = C10H14N2], and by mono/co-doping with Mn2+ and Sb3+, interesting luminescence phenomena have been produced. Single-doped Mn2+ / Sb3+ shows distinctive green and single orange emission, respectively. However, the co-doped Mn2+ and Sb3+ appeared as dynamic double emission peaks at 530 nm and 670 nm. Therefore, the co-doped crystals showed luminescence from two different luminescence centers ([MnCl4]2- and [SbCl4]-). We used DFT to calculate the DOS (density of states) of co-doped crystals, which results in energy transfer between Mn2+ and Sb3+. All of the above samples showed high stability after being left for two months. In addition, two different luminescence centers can be produced by the adjustment of the excitation of the co-doped (PPZ)ZnCl4: Sb0.12Mn0.08 samples, which is a distinguishable and obvious photoluminescence phenomenon having great potential preparation of advanced anti-counterfeiting materials in the future.

Self-assembly of S,N-codoped Ce/Cu bimetallic nanoparticles for fluorescence and visual detection of hexavalent chromium.

Ce2(SO4)3 was doped into 4,6-diamino-2-mercaptopyrimidine (DAMP)-encapsulated copper nanoclusters (CuNCs) via a facile, rapid, low-temperature, and green self-assembly synthesis method to obtain fluorescent S,N-codoped Cu/Ce-DAMP nanoparticles (S,N-codoped Cu/CeNPs) for the detection of Cr(VI). The prepared Cu/CeNPs exhibit double emission peaks at 470nm and 610nm. Thefluorescence emission at 610nm is significantly enhanced due to the aggregation-induced emission (AIE) effect, and the quantum yield is as high as 20.19%. The fluorescence emission at 610nm can be selectively quenched by Cr(VI) due to the internal filter effect (IFE) and dynamic quenching, whereas the weak fluorescence at 470nm remains almost stable. On this basis, a fluorescence assay method for Cr(VI) was established, with good linearity in the concentration range 0.5-120µM and a detection limit (LOD) of 134nM. Using a smartphone to take photos of the fluorescence signals changes caused by Cr(VI) rapid visual detectionis achieved with a linear range of 10-130 μM and a LOD of 2.35 μM. The proposed method was successfully applied to the detection of Cr(VI) in actual water samples.

Ratiometric fluorescence probe based on boric acid-modified carbon dots and alizarin red for sensitive and rapid detection of glyphosate.

Bycombining boric acid-modified carbon dots (p-CDs) and alizarin red (ARS), a double emission probe p-CDs@ARS with fluorescence at 410nm and 600nm is designed for the detection of glyphosate. When Cu2+ is added, it binds with ARS to cause ARSreleasefrom p-CDs@ARS, which decreases the fluorescence at 600nm. However, in the presence of glyphosate, glyphosate competes to thebinding ofCu2+, releasing ARS to bind with p-CDs again. Therefore, the fluorescence of 600nm recovers. Based on this, the fluorescence of 410nm and 600nm act as the reference and response signal, respectively,achieving the ratiometric fluorescence detection of glyphosate. The linear range of glyphosate detection is 0.5-50µM with a limit of detection at 0.37µM which is well below the maximum residue limit for glyphosate in food. When the probe is used to detect the glyphosate residue in Pearl River water and cucumber, the detection results are well consistent with those detected by HPLC. The established method based on p-CDs@ARS has the advantages that the assembly of ratiometric fluorescence probe is simple, and the detection speed is fast. Additionally, a typical INHIBIT logical system has been successfully constructed based on glyphosate, Cu2+, and the fluorescence signal of p-CDs@ARS.

Crystal structure and spectral tuning of Eu2+/Eu3+ co-activated Na2Ba1-xSrxCa(PO4)2 phosphors with high thermal stability

The coupling of UV LED chips with phosphors to produce white or color-tunable light is still a challenge. In this work, we propose a simple rare earth occupation site engineering method to adjust the valence of doped Eu ions. Based on the Ba2+ substituted by Sr2+, new Eu2+/Eu3+ co-activated Na2Ba1-xSrxCa(PO4)2 (NB1-xSxCP) phosphors were designed and successfully synthesized. In NB1-xSxCP, the Ba2+/Sr2+ site is occupied by Eu2+, while the Ca2+ site is occupied by Eu3+. The coupled broad blue 448 nm and sharp red 619 nm luminescence under 321 nm excitation has demonstrated the coexistence of Eu2+ and Eu3+. This double emission phenomenon is studied in terms of the fluorescence lifetime as well as lattice distortion induced by the substitution ions. With the increased substitution of Sr, the luminescence of NB1-xSxCP:0.03Eu2+/3+ can be tuned from blue to red crossing the warm-white region. When x = 0.3, the chromaticity coordinates is located at (0.3779, 0.2495). The integrated intensity of Na2Ba0.7Sr0.3Ca(PO4)2:0.03Eu2+/3+ at 150℃ remains 90.9 % of that at room temperature, while the chromaticity shift (ΔE) can be calculated as 15 ×10−3. The Eu2+/Eu3+ co-activated NB1-xSxCP is a potential candidate for single-phase color-tunable phosphors used for light-tunable applications due to the combining contributions from both Eu3+ and Eu2+ ions.

Dual-Template-Directed Zero-Dimensional Bismuth Chlorides: Structures, Luminescence, Photoinduced Chromism, and Enhanced Proton Conductivity.

Zero-dimensional (0D) hybrid organic-inorganic bismuth halides have attracted immense scientific interest as promising candidates for lead-free materials. Here, by using a typical solvothermal method, two mixed-cation-phase 0D hybrid bismuth chlorides of [HPDA][H2PDA]BiCl6 (1) and [Hbzim][H2PA]BiCl6 (2) (PDA = bis(4-pyridyl)amine, bzim = benzimidazole, PA = 2-picolylamine) have been assembled based on a series of organic amine guests. Both compounds exhibit interesting photoluminescence phenomena, in which compound 1 exhibits a double emission property of blue fluorescence and yellow-green phosphorescence simultaneously, while compound 2 exhibits wide-band yellow-green emission under visible light excitation. The luminescence mechanism is explained by experiments and theoretical calculations. In view of the fact that halometallate units and the conjugated nitrogen heterocyclic systems can act as electron donors and electron acceptors, respectively, both compounds exhibit free radical-driven photochromism induced by electron transfer under xenon lamp irradiation at room temperature. In addition, benefiting from abundant hydrogen bond networks in structures, the two compounds show significant temperature-dependent proton conduction behavior in the range of 298-343 K, and the proton conductivity of both compounds is significantly improved after light irradiation. Our study demonstrates two novel hybrid mixed-cation-phase 0D hybrid bismuth halides with photoluminescence, photochromism, and photomodulated proton conduction properties, which enriches the dual-template-directed metal halide system and provides a feasible scheme for the synthesis of photoresponsive smart materials.

Preparation of carbon dots of double emission polymer and its application in the detection of tetracycline, water content in edible oil, and information anti-counterfeiting

Preparation of carbon dots of double emission polymer and its application in the detection of tetracycline, water content in edible oil, and information anti-counterfeiting

External electric field induced emission behavior for ESIPT-based 2-(benzo[d]thiazol-2-yl)-4-(pyren-1-yl)phenol towards near-infrared region

Organic light-emitting diodes (OLEDs) for low energy transfer and double emission, but the current methods for regulating ESIPT processes are mostly solvent and substituent effects. Here, utilizing the density theory functional (DFT) and time-dependent density functional theory (TD-DFT) methods, the ESIPT process controlled by an external electric field (EEF) is proposed, and the changes in photophysical properties of 2-(benzo[d]thiazol-2-yl)-4-(pyren-1-yl)phenol (PyHBT) are investigated. Structural parameter variations and IR vibrational spectra measure the prerequisite for the ESIPT process, namely, intramolecular hydrogen bond (IHB) strength, and the scanned potential energy curves (PECs) demonstrate that the ESIPT process of PyHBT is harder to execute as the positive EEF increases, and the opposite is true for the negative EEF. The absorption and fluorescence spectra show shifts under the distinct EEFs, and even the emission wavelength reaches the short-wave near-infrared (SW-NIR) region (780–1100 nm), such as 815.2 nm for a positive EEF of + 30 × 10-4 a.u. in the keto form. Additionally, the fluorescence intensity of PyHBT is strongly influenced by the positive EEF, especially in the enol form, and the investigation of the mechanism by hole-electron analysis demonstrates that under the positive EEF, the twisted intramolecular charge transfer (TICT) process is induced, which triggers the weakening of the fluorescence intensity. In summary, our work not only complements the theoretical approach to modulate the ESIPT process, but also reveals that the photophysical properties of materials affected by the external electric field are even expected to reach the NIR region.

Discrimination of doubled acoustic emission events using neural networks

In observatory seismology, the effective automatic processing of seismograms is a time-consuming task. A contemporary approach for seismogram processing is based on the Deep Neural Network formalism, which has been successfully applied in many fields. Here, we present a 4D network, based on U-net architecture, that simultaneously processes seismograms from an entire network. We also interpret Acoustic Emission data based on a laboratory loading experiment. The obtained data was a very good testing set, similar to real seismograms. Our Neural network is designed to detect multiple events. Input data are created by augmentation from previously interpreted single events. The advantage of the approach is that the positions of (multiple) events are exactly known, thus, the efficiency of detection can be evaluated. Even if the method reaches an average efficiency of only around 30% for the onset of individual tracks, average efficiency for the detection of double events was approximately 97% for a maximum target, with a prediction difference of 20 samples. Such is the main benefit of simultaneous network signal processing.

Dual-template molecularly imprinted double emission proportional fluorescence sensor based on CsPbBr3 and CsPb(Br/I)3 perovskite quantum dots for visual, selective and sensitive detection of methyl eugenol and aristolochic acid A

Phenolic acids with extensive pharmacological activity often coexist with harmful impurities in traditional Chinese medicine (TCM). Therefore, it is imperative to meticulously scrutinize the presence of harmful components while assessing the efficacy of TCM. Here, we present a dual-template molecularly imprinted double emission ratio fluorescence sensor to selectively and sensitively detect methyl eugenol (ME) and aristolochic acid A (AAs). The sensor consists of CsPbBr3 and CsPb(Br/I)3 perovskite quantum dots molecularly imprinted polymer with dual emission peaks at 515 nm and 650 nm. Surprisingly, ME can only quench the emission peak at 650 nm, while AAs can quench both the two emission peaks. When ME and AAs coexist, their effect on the peak at 515 nm is similar to that of AAs, but the peak at 650 nm is quenched more. Therefore, it is possible to qualitatively identified whether the presence of ME, AAs or both of them based on the different colors of the sensors. In addition, the ratio of fluorescence intensity at 650 nm and 515 nm exhibits good linear relationships with both the concentrations of ME and AAs with the limit of detection of 8.3 nM for ME and 9.6 nM for AAs. Meanwhile, different concentrations of target molecules cause significant color changes, making it possible to visually semi-quantitatively detect AAs, ME and both of them. Moreover, the quenching mechanisms induced by ME and AAs are also investigated. Finally, the sensors have been successfully used to the determination of ME and AAs in Asarum of TCM.

Spatiotemporal dynamic of rice production and its carbon footprint in Hainan, China: Implications for food security and environmental sustainability.

Rice (Oryza sativa L.) feeds more than half of the global population and faces the critical issues related to food security and environmental sustainability. This study analyzed double rice production data from 2010 to 2020 to assess its spatiotemporal dynamic in food production and carbon (C) footprint in Hainan province, China. The results revealed a 29.5% reduction in rice planting area, leading to a significantly decreased rice self-sufficiency rate from 38% to 33% from 2010 to 2020. During this period, the carbon footprint per unit area (CFa) for early, late, and double rice showed a fluctuating upward trend ranging from 8.1 to 8.4, 8.9 to 9.2, and 17.0 to 17.4 t CO2-eq ha-1, respectively. The total greenhouse gas (GHG) emissions of rice production decreased to around 2 million t CO2-eq, primarily due to reduced planting area. The C sequestration initially increased before decreasing to 1.2 million t C in 2020 at a temporal scale. Spatially, the northeast and southwest regions exhibited ∼70% of the total GHG emissions and ∼80% of C sequestration. The regional C footprint per unit yield displayed less favorable outcomes, with some areas (e.g., Wenchang and Haikou) experiencing emission hotspots in recent years. Higher yield and smaller CFa for Lingao and Tunchang were observed compared to the average between 2010 and 2020. This study provides insights into the spatiotemporal dynamics of double rice production and GHG emissions in Hainan, offering a scientific reference for regional food security and environmental sustainability.

Strongly-ordered infrared counterterms from factorisation

In the context of infrared subtraction algorithms beyond next-to-leading order, it becomes necessary to consider multiple infrared limits of scattering amplitudes, in which several particles become soft or collinear in a strongly-ordered sequence. We study these limits from the point of view of infrared factorisation, and we provide general definitions of strongly-ordered soft and collinear kernels in terms of gauge-invariant operator matrix elements. With these definitions in hand, it is possible to construct local subtraction counterterms for strongly-ordered configurations. Because of their factorised structure, these counterterms cancel infrared poles of real-virtual contributions by construction. We test these ideas at tree level for multiple emissions, and at one loop for single and double emissions, contributing to NNLO and N3LO distributions, respectively.

Ratiometric luminescent simultaneous sensing of aristolochic acids (I-IV) by a novel metal-organic framework and its nanowire.

Aristolochic acids(AAs), which are a group of nitrophenanthrene carboxylic acids formed by Aristolochia plant, have become an increasing serious threat to humans due to their nephrotoxicity and carcinogenicity. Fast and accurate approaches capable of simultaneous sensing of aristolochic acids (I-IV) are vital to avoid intake of such compounds. In this research, the novel ratiometric fluorescence zinc metal-organic framework and its nanowire have been prepared. The two different coordination modes (tetrahedral configuration and twisted triangular bipyramidal configuration) within zinc metal-organic framework lead to the significant double emissions. The ratiometric fluorescence approach based on nanowire provides a broader concentration range (3.00 × 10-7~1.00 × 10-4 M) and lower limit of detection (3.70 × 10-8 M) than that based on zinc metal-organic framework (1.00 × 10-6~1.00 × 10-4 M, 5.91 × 10-7 M). The RSDs of the results are in the range 1.4-3.5% (nanowire). The density functional theory calculations and UV-Vis absorption verify that the sensing mechanism is due to charge transfer and energy transfer. Excellent spiked recoveries for AAs(I-IV) in soil and water support that nanowire is competent to simultaneously detect these targets in real samples, and the proposed approach has potential as a fluorescence sensing platform for the simultaneous detection of AAs (I-IV) in complex systems.

A single excitation dual emission semi-salamo type multi-functional probe for sensitive pH and Cu2+ detection

pH and Cu2+ ion concentration changes are linked to disorders like Alzheimer's and cancer. Rapid detection of pH and Cu2+ ions is critical for public health and environmental concerns. The semi-salamo-type probe (E)-2-hydroxy-1-naphthaldehyde O-(2-(aminooxy)ethyl) oxime (NSS) demonstrated substantial dual-functional performance, sensing pH change and Cu2+ ions. A single excitation and double emission characteristic on the probe NSS made it distinctive. Probe NSS exhibits pH-dependent excited state intramolecular proton transfer (ESIPT), and its optical properties vary based on the pH environment. Probe NSS detects pH changes from 2 to 11 by changing the “off-on-off” of the excited state intra-molecular proton transfer (ESIPT) mechanism, exhibiting rapid, reversible, and selective responses. In addition, the luminescent salamo-like naphthalene-based probe NSS can coordinate with Cu2+ ions, achieving great selectivity and sensitivity to identify Cu2+ ions with a detection limit of 0.84 ppb (13.2 nM) Probe NSS can detect Cu2+ ions in actual water samples such as tap water and yellow river water. The test strip loaded with probe NSS enabled quick and accurate detection of Cu2+ ions in water samples. Consequently, the versatile salamo-type probe NSS lays the foundation for developing high sensitivity and fast-response dual-mode pH meters as well as Cu2+ sensing.

Thickness-dependent exciton behavior in two-dimensional indium selenide

A comprehensive investigation into the exciton behaviors in indium selenide (InSe) is yet to be conducted. Here, the power factor K, which can characterize the excitonic behaviors, was determined for InSe with varying thicknesses. The photoluminescence results suggest that defects play a dominant role in the recombination of excitons with varying thicknesses. Consequently, the free exciton peak at 931 nm, which is linked to the double exciton emission behavior, becomes obscured by the presence of a bound exciton peak at 980 nm resulting from defect-induced recombination. However, at specific thicknesses and power levels, the enhancement of quantum confinement effect coupled with a reduction in defect proportion enables the observation of the peak corresponding to free exciton. Furthermore, the extracted K values from the InSe photodetectors corroborated the aforementioned findings. The results presented here provide an in-depth understanding of exciton behavior in InSe and provide theoretical underpinning for the development of InSe-based optoelectronics.

Dual-mode optical thermometers via the thermochromic Bi3+, Eu3+ co-doped La2LiSbO6 phosphors for real-time chip temperature monitoring

In recent years, with the increasing demand for non-contact temperature measurement, it is urgent to develop a new type of phosphor with double emission centers, high sensitivity and good reliability. A series of Bi3+and Eu3+ co-doped La2LiSbO6 double emission center phosphors were successfully prepared. The response characteristics of Bi3+and Eu3+ at different temperatures in the range of 293–473k were calculated by fluorescence intensity ratio (FIR) technique. The optimal relative sensitivity Sr and absolute sensitivity Sa were 1.13 % K−1 and 1.27 % K−1, respectively. Hence, La2LiSbO6:Bi3+, Eu3+ phosphors have the capability of non-contact optical temperature measurement and are a promising material for application. The phosphor is combined with the optical fiber temperature sensor to monitor the real-time temperature of the computer central processing unit. The optical fiber temperature sensor system breaks through the limitations of traditional temperature measurement, and can be used in special environments such as small size and strong electromagnetic interference. It has become an ideal choice to replace the traditional temperature sensor.

Wavelength-interval switchable Brillouin–Raman random fiber laser through Brillouin pump manipulation

Abstract A wavelength-interval switchable Brillouin–Raman random fiber laser (BRRFL) based on Brillouin pump (BP) manipulation is proposed in this paper. The proposed wavelength-interval switchable BRRFL has a full-open cavity configuration, featuring multiwavelength output with wavelength interval of double Brillouin frequency shifts. Through simultaneously injecting the BP light and its first-order stimulated Brillouin-scattered light into the cavity, the laser output exhibits a wavelength interval of single Brillouin frequency shift. The wavelength-interval switching effect can be manipulated by controlling the power of the first-order stimulated Brillouin scattering light. The experimental results show the multiwavelength output can be switched between double Brillouin frequency shift multiwavelength emission with a broad bandwidth of approximately 60 nm and single Brillouin frequency shift multiwavelength emission of 44 nm. The flexible optically controlled random fiber laser with switchable wavelength interval makes it useful for a wide range of applications and holds significant potential in the field of wavelength-division multiplexing optical communication.

Chinese organic rice transition spatial econometrics empirical analysis.

Based on the integrated model of Super-SBM model, spatial Durbin model (SDM) and Grey neural network model, this paper analyzes the panel data of various provinces in China from multiple angles and dimensions. It was found that there were significant differences in eco-efficiency between organic rice production and conventional rice production. The response of organic rice to climate change, the spatial distribution of ecological and economic benefits and the impact on carbon emission were analyzed. The results showed that organic rice planting not only had higher economic benefits, but also showed a rising trend of ecological benefits and a positive feedback effect. This finding highlights the importance of organic rice farming in reducing carbon emissions. Organic rice farming effectively reduces greenhouse gas emissions, especially carbon dioxide and methane, by improving soil management and reducing the use of fertilizers and pesticides. This has important implications for mitigating climate change and promoting soil health and biodiversity. With the acceleration of urbanization, the increase of organic rice planting area shows the trend of organic rice gradually replacing traditional rice cultivation, further highlighting the potential of organic agriculture in emission reduction, environmental protection and sustainable agricultural production. To this end, it is recommended that the Government implement a diversified support strategy to encourage technological innovation, provide guidance and training, and raise public awareness and demand for organic products. At the same time, private sector participation is stimulated to support the development of organic rice cultivation through a public-private partnership model. Through these measures, further promote organic rice cultivation, achieve the dual goals of economic benefits and environmental benefits, and effectively promote the realization of double carbon emission reduction targets.

Multifunctional Optical Sensing with Lanthanide-Doped Upconverting Nanomaterials: Improving Detection Performance of Temperature and Pressure in the Visible and NIR Ranges.

Temperature and pressure are fundamental physical parameters in the field of materials science, making their monitoring of utmost significance for scientists and engineers. Here, the NaSrY(MoO4)3:0.02Er3+/0.01Tm3+/0.15Yb3+ nanophosphor is developed as an optical sensor material. Under 975 nm laser excitation, the upconversion characteristics and optical detection performance of the multifunctional sensing platform of temperature and pressure (vacuum) are investigated. We have successfully developed a novel detection platform that enables optical detection of pressure (vacuum) and temperature. This platform utilizes thermally coupled levels (TCLs) and non-TCLs of Er3+ and Tm3+ to achieve ratiometric detection. The multimodal optical temperature and pressure detection based on TCLs and non-TCLs is successfully realized by using different emission bands of double emission centers, which makes it possible for self-referencing optical temperature and pressure measurement modes. These results indicate that the developed nanophosphor is a promising candidate for optical sensors, and our findings suggest potential strategies for modulating the sensor properties of luminescent materials doped with rare-earth ions.

Fine-Tuning Optoelectronic Features in Organic-Inorganic Hybrid Metal Halides: A Focus on the Phenylbutanammonium Series.

Extensive research has been dedicated to exploring the potential applications of organic-inorganic hybrid metal halides in optoelectronics. This study presents findings on three metal halides based on phenylbutanammonium (PBA). Specifically, (PBA)2MnBr4(H2O)2 and (PBA)2Sn(IV)Cl6 exhibit zero-dimensional structures with P21/c and Pnma space groups, respectively, while (PBA)2Sn(II)Br4 features a two-dimensional structure with P1̅ space group. Under UV excitation, (PBA)2MnBr4(H2O)2 exhibits double emission arising from the 4T1 → 6A1 transitions of Mn2+ in two distinct coordination environments. The emission spectrum of (PBA)2SnCl6 aligns with that of PBACl, suggesting that the luminescence originates from the organic component. The yellow emission of (PBA)2SnBr4 is attributed to the self-trapped excitons. This study introduces the PBA series of compounds, revealing that varying metal ions and halogen combinations can adjust the structural dimensions and influence optical properties. The insights gained from this work serve as a guide for the preparation of efficient white light-emitting diodes.

The individual tubular low-toxic combustion chamber

BACKGROUND: intensive works in improvement and development of microturbine power plants for energy and transport continues worldwide. These works are still relevant due to near-to-zero emissions of microturbines, as well as due to the fact that microturbines efficiency can be increased up to 50% and above, which opens the potential to compete with well-known power plants in the foreseeable future, including in terms of efficiency. Therefore, the work on the study of a low-toxic combustion chamber for a microturbine seems relevant as well. AIM: Сomputational and experimental study of an individual tubular low-toxic combustion chamber of a 50 kW microturbine with an increase in pressure at the inlet to the chamber. METHODS: The description of the experimental facility for combustion chamber testing and the results of its experimental study are given. A sufficient convergence of the experimentally obtained parameters of the combustion chamber with the parameters obtained from the simulation modeling of flow and combustion in the combustion chamber was obtained. RESULTS: In the course of the calculated and full-scale studies, hydraulic losses, nitrogen oxide emissions, and temperature unevenness at the outlet of the combustion chamber with increasing air pressure at its inlet were determined. CONCLUSIONS: The calculated study showed a significant effect of an increase in air pressure from 3 to 3.5 bar at the entrance to the combustion chamber on its main parameters. Thus, hydraulic losses have more than doubled and nitrogen oxide emissions have increased almost 1.3 times. The conducted experimental study of the combustion chamber generally confirmed the results of mathematical modeling and thereby tested the computational model used. Thus, the discrepancy in the experimentally and computationally obtained values of relative pressure losses in the combustion chamber does not exceed 15%, and in emissions of nitrogen oxides 7%.