Emission Intensity Ratio Research Articles

Application of RET Approach for Ratiometric Response Enhancement of ICT Fluorescent Hg2+ Probe based on Crown-containing Styrylpyridinium Dye.

Styrylpyridinium dye bearing azadithia-15-crown-5 ether receptor group SP and 4-alkoxy-1,8-naphthalimide fluorophore were linked using copper-catalyzed azide-alkyne cycloaddition click reaction to afford dyad compound NI-SP. Chemosensor NI-SP exhibited selective ratiometric fluorescent response to the presence of Hg2+ in aqueous solution due to the interplay between resonance energy transfer (RET) and intramolecular charge transfer (ICT) processes occurred upon excitation. The observed switching of the ratio of emission intensities in the blue and red channels R was higher than in the case of monochromophoric styrylpyridine derivative SP showing ratiometric response based on ICT mechanism only. Biological studies revealed that NI-SP penetrates into human lung adenocarcinoma A549 cells and accumulates in cytoplasm and lysosomes. When cells were pre-incubated with mercury (II) perchlorate, the ratio R was increased 2.6 times, which enables detection of intracellular Hg2+ ions and their quantitative analysis in the 0.7-6.0 μM concentration range.

Spectroscopic analysis of single and multiphase electrical discharge for clean energy conversion

Abstract In this study, we examined non-thermal atmospheric pressure plasma processes operating under varying conditions using different liquid and gaseous hydrocarbon materials. The light emission from the discharges were analyzed through optical emission spectroscopy to comprehend the products generated in different parameter space. The gaseous products from each of these analyses were also collected and analyzed through gas chromatography. Analysis of the optical emission from the discharge and concentration of the gaseous products show a linear trend between emission intensity ratio H α /C2 and gas concentration ratio H2/C2H x . Gas temperature and electronic excitation temperature of different experimental conditions were also compared and indicates that spark discharge relates to higher electronic excitation temperature compared to glow discharge of similar medium. Higher electronic excitation temperature leads to generation of different products from spark discharge compared to glow discharge. Glow discharge generates more of the intermediate products. Whereas spark discharge, because of its higher electronic excitation temperature, leads to higher rate of dissociation and therefore generates more of the dissociated products. Glow discharge, for example generates more of OH and H from the moisture present in the carrier gas as impurity, whereas spark discharge would generate more of H α and O particles further breaking down the OH bonds. Finally, UV–Vis analysis was performed on the liquid products of the discharge and reveals that the photo-centers and the newly generated soot nano particles absorb the UV range lights and some of the visible range light emission mostly up to ∼600 nm.

Electron temperature characterization of H2 processing plasma by optical emission spectroscopy

Optical emission spectroscopy of hydrogen (H2) plasma is performed to characterize the electron temperature, T e . The H2 Fulcher band emission and radiative dissociation continuum are measured, where the Fulcher band emission is recognized to be T e -sensitive, compared with the dissociation continuum. With this T e -sensitive nature, a simple way of determining T e is proposed, specifically using the intensity ratio of the Fulcher band emission to dissociation continuum. The T e determination is demonstrated for H2 processing plasmas generated by capacitively coupled discharges at different gas pressures.

Comparative Anslysis of Carbon Emission Reduction Policies in China’s Manufacturing and Transportation Sectors

This study evaluates China’s environmental policies, specifically the increase of carbon emission tax rates and the reduction of carbon emission intensity, by developing a New Keynesian Dynamic Stochastic General Equilibrium (NK-DSGE) model that incorporates energy consumption and carbon emissions. The production sector is segmented into manufacturing, non-manufacturing, and transportation, with transportation services acting as inputs for both manufacturing and non-manufacturing firms. We construct four cases within two scenarios, each characterized by distinct targets and policies. After calibrating and estimating the relevant parameters, we compare carbon reduction outcomes and economic fluctuations across the two scenarios. Our findings indicate that when targeting the same carbon emission tax rate increase or carbon emission intensity ratio reduction, policies that increase the carbon emission tax rate or reduce carbon emission intensity implemented in the manufacturing sector achieve greater carbon emission reductions compared to the same polices implemented in the transportation sector. Meanwhile, compared to the latter case, output experienced a greater decline, and inflation exhibited a more substantial increase in the former case. However, when the quantities of carbon emission reductions are approximately the same in the first quarter, policies that increase the carbon emission tax rate or reduce carbon emission intensity enacted in the transportation sector demonstrate superior performance relative to the same polices implemented in the manufacturing sector. This leads to smaller final output reductions and milder inflation increases. In summary, for equivalent levels of carbon emission reductions, policies implemented in the transportation sector yield more favorable economic outcomes than those applied in the manufacturing sector.

Luminescence Changeable CO2-Storage Cylinder: Triple-Stranded Helical Eu(III)/Tb(III) Fluorinated MOFs with Amide Linkers.

Triple-stranded helical lanthanide MOFs with CO2 adsorption properties were investigated. Lanthanide MOFs ([Eu0.1Tb0.9(hfa)3(dpa)]n) are composed of lanthanide luminophores (Eu(III) and/or Tb(III) ions), fluorinated antenna ligands (hfa: hexafluoroacetylacetonate), and polyamide-type linker ligands (dpa: 4-(diphenylphosphoryl)-N-(4-(diphenylphosphoryl)phenyl)benzamide). The cylindrical structure was characterized by single-crystal X-ray analysis, thermogravimetric analysis, and gas adsorption measurements. The inner surfaces of the cylindrical channels were covered with the fluorine atoms of the hfa ligands. The emission intensity ratio (IEu/ITb) in [Eu0.1Tb0.9(hfa)3(dpa)]n is affected by the CO2 gas adsorption behavior. The change in IEu/ITb value was caused by the intermolecular interactions between the CO2 gas molecules and the fluorinated ligands, resulting in an electronic structural change of the lowest triplet excited state in the photosensitized hfa ligands.

Self-reducing induced Eu2+/Eu3+ dual-emitting glasses for anti-counterfeiting and optical thermometry

Eu3+/Eu2+ co-doped glasses possess extensive application potential in diverse fields, including light-emitting diodes and sensors, due to their distinctive luminescent characteristics. To date, numerous strategies have been devised to facilitate the coexistence of Eu3+ and Eu2+ in materials. Among them, adjusting the composition of the glass matrix stands out as a straightforward and reproducible approach. Herein, a series of Eu2+/Eu3+ co-doped borosilicate aluminate glasses were successfully synthesized via a high-temperature melting method. By elevating the ratios of B2O3/MgO and Al2O3/BaO in the matrix, a remarkable self-reduction of Eu3+ in ambient air was achieved because of the structural weakness and lower optical basicity for the designed glass matrix. The reduction of Eu3+ is also related to the formation of EuZn• and VΖn′′ defects. Furthermore, by fine-tuning the melting duration and Eu content, we achieved comparable violet and red emission intensities for both Eu2+ and Eu3+ ions. Under UV irradiation with various wavelengths, anti-counterfeiting patterns fabricated from glass powder exhibited precise and pronounced color changes. Notably, the emission intensity ratio of Eu2+/Eu3+ exhibited a consistent decrease as temperature increased, enabling precise temperature determination with exceptional absolute sensitivity (1.22 % K−1) producibility, and discrimination. These findings hold significant implications for the design of Eu3+/Eu2+ co-doped inorganic multifunctional glasses.

Copper‐Mediated C–H Cyclization of Heterocycles: Facile Access to Multiple Resonance Thermally Activated Delayed Fluorescence Materials

AbstractReported herein is the first example of a copper‐mediated C─H cyclization of heterocycles to construct structurally diverse carbonyl‐bridged triphenylamine compounds with multiple resonance thermally activated delayed fluorescence (TADF) characteristics. The one‐pot synthesis method exhibits a broad substrate scope and opens a new avenue for rapidly screening high‐performance organic TADF luminescent materials. Novel organic TADF single‐molecule white‐light material 5g with anti‐Kasha dual‐emission character is the first time developed herein and shows a Commission Internationale de l’Eclairage (CIE) coordinate of (0.33, 0.35) in the thin film, and can be used to fabricate robust and low cost organic white light‐emitting diodes (LED). Furthermore, the anti‐Kasha dual‐emission material 5g is fabricated as water‐dispersed nanoparticles (NPs)NPs, which can be efficiently endocytosed into the HeLa cells and dual emission imaging in living cells, and be used in two‐channel emission intensity ratio imaging to observe the intercellular structure.

Doping of Mn2+ ion into boron quantum dots with enhanced fluorescence properties for sensing of L-thyroxine biomarker and bioimaging applications

L-thyroxine serves as a primary biomarker for diagnosing hypothyroidism and it is also utilized in hormone replacement therapy. Regular assessment of thyroxine levels is crucial for preventing health issues in hypothyroid patients, suggesting the requirement of a facile analytical tool for the detection of L-thyroxine. In this work, a straightforward and efficient synthetic method is introduced for in-situ preparation of Mn2+-doped boron quantum dots (Mn2+@B-QDs) derived from boron powder through a solvothermal reaction. The introduction of Mn2+ ion into B-QDs not only enhances fluorescence efficiency but also provides favorable sites within the QDs, expanding their potential applications in analytical chemistry. The blue fluorescent Mn2+ @B-QDs exhibited excellent performance for the selective recognition of L-thyroxine via a dynamic quenching mechanism. Under ideal conditions, a good linear relation was observed between the fluorescence emission intensity ratio of Mn2+@B-QDs and the concentration of L-thyroxine in the range of 0.125–5 μM, with a lower detection limit of 59.86 nM. The Mn2+@B-QDs exhibited the negligible cytotoxicity against A549 lung cancer cell lines and demonstrated good biocompatibility toward Saccharomyces cerevisiae cells.

A ratiometric fluorescent sensor based on dual-emitting carbon dots for the rapid detection of sulfite

Sulfur dioxide (SO2) derivatives are typically employed as antioxidants in food and pharmaceutical processing. However, excessive sulfite intake could trigger serious health problems. Hence, it is urgent to establish a rapid and effective system for monitoring SO2. This study adopted a one-step hydrothermal method to synthesize dual-emitting nitrogen-doped carbon quantum dots (CECDs) and developed a ratiometric sensor for sulfite using CECDs-Cr (VI) composites. The emission intensity ratio (I440/I500) of the CECDs-Cr (VI) composites increased considerably with the addition of HSO3−. A method based on the ratiometric sensor was established for SO2 derivatives with advanced efficiency and excellent linearity over a broad concentration range of 0–500 μM (R2 = 0.9946). Four medicine-food homology materials (MFHMs) fumigated with sulfur have been accurately detected using this approach. Furthermore, a portable test tube was prepared to achieve rapid and semi-quantitative detection of SO2 residues and applied to real samples. This work presents an effective approach to develop a rapid on-site detection platform for sulfite residues in food and pharmaceuticals.

Multimodal laser opto-ultrasonic spectroscopy (LOUS) Approach to investigate the impact of elemental composition on the engineering properties of high-density tungsten alloys'

The impact of elemental composition on the engineering properties of high-density tungsten alloy is crucial, particularly in relation to grain size, hardness, elastic modulus, and surface degradation. This study introduces a new multimodal laser opto-ultrasonic spectroscopy (LOUS) technique, which simultaneously integrates the benefits of laser-induced breakdown spectroscopy (LIBS) and laser ultrasonic testing to evaluate the engineering properties of tungsten alloys. The findings indicate that the increasing tungsten concentration significantly enhances the samples' hardness, grain size and elastic modulus. The composition of elements and hardness were assessed using a calibration curve derived from the emission intensity ratio (W-II/W-I) and plasma electron temperature (Te) in optical emission. The correlation results of (W-II/W-I) and Te showed significant enhancement with the increase of hardness with a regression coefficient (R2 ≥ 0.996), validating the Saha-Eggert relation and underscoring model effectiveness. Additionally, the correlation of the laser ultrasonic testing parameters (attenuation coefficient and velocities) in assessing grain size and elastic modulus showed good reliability (R2≥0.993) when compared to the results obtained from conventional optical microscopy and tensile testing. The results underscore the accuracy and predictive ability of the LOUS method for in-situ characterization.

Regulating thermometric properties of single-band ratiometric luminescent thermometers based on Eu3+-activated Y2W3O12·3H2O nanoparticles via controlling doping content and excitation model

Series of Eu3+-activated Y2W3O12·3H2O nanoparticles were designed to realize high-sensitive optical thermometry. The resultant nanoparticles can emit bright visible emission from Eu3+ upon the excitation of 296 nm (charge-transfer state (CTS) of O2- → W6+), 394 nm (ground state absorption (GSA)) and 536 nm (excitation state absorption (ESA)), of which the fluorescence intensities were influenced by dopant content. The negative thermal expansion properties of studied nanoparticles were clarified via temperature-dependent X-ray diffraction patterns. Moreover, the thermal quenching behaviors of final products were also investigated through temperature-related emission spectra. Specifically, upon the CTS and GSA processes, the developed nanoparticles underwent significant thermal quenching effect, whereas the thermally enhanced luminescence was observed under ESA process. Herein, through using the single-band ratiometric (SBR) method to investigate the fluorescence intensity ratio of the red emission from 5D0 → 7F2 transition of Eu3+ at high temperature, the thermometric properties of prepared nanoparticles were studied. It was found that maximum absolute and relative sensitivities of Eu3+-activated Y2W3O12·3H2O nanoparticles reached up to 0.061 and 4.944 % K−1, respectively, and they can be regulated by changing Eu3+ dopant and SBR models (i.e., ESA+CTS and ESA+GSA combinations), realizing high-sensitive optical thermometry. Our findings may provide some guidelines for manipulating the thermometric properties of rare-earth ions activated materials and developing new SBR luminescence thermometers.

Highly Sensitive and Selective Fluorescence and Smartphone-Based Sensor for Detection of Rutin Using Boron Nitrogen Co-doped Graphene Quantum Dots.

This research explores the fluorescence properties and photostability of boron nitrogen co-doped graphene quantum dots (BN-GQDs), evaluating their effectiveness as sensors for rutin (RU). BN-GQDs are biocompatible and exhibit notable absorbance and fluorescence characteristics, making them suitable for sensing applications. The study utilized various analytical techniques to investigate the chemical composition, structure, morphology, optical attributes, elemental composition, and particle size of BN-GQDs. Techniques included X-ray diffraction (XRD), energy-dispersive X-ray spectroscopy (EDS), transmission electron microscopy (TEM), scanning electron microscopy (SEM), and atomic force microscopy (AFM). The average particle size of the BN-GQDs was determined to be approximately 3.5 ± 0.3nm. A clear correlation between the emission intensity ratio and RU concentration was identified across the range of 0.42 to 4.1μM, featuring an impressively low detection limit (LOD) of 1.23nM. The application of BN-GQDs as fluorescent probes has facilitated the development of a highly sensitive and selective RU detection method based on Förster resonance energy transfer (FRET) principles. This technique leverages emission at 465nm. Density Functional Theory (DFT) analyses confirm that FRET is the primary mechanism behind fluorescence quenching, as indicated by the energy levels of the lowest unoccupied molecular orbitals (LUMOs) of BN-GQDs and RU. The method's effectiveness has been validated by measuring RU concentrations in human serum samples, showing a recovery range between 97.8% and 103.31%. Additionally, a smartphone-based detection method utilizing BN-GQDs has been successfully implemented, achieving a detection limit (LOD) of 49nM.

Tailoring optical properties and humidity sensing response of multilayered Tb(Sal)3Phen and Eu(DBM)3Phen complex nanofibres

In this work, we investigate the opto-humidity sensing and colour tuning in polyvinyl alcohol (PVA) polymeric electrospun nanofibres dispersed with Tb(Sal)3Phen (TSP) and Eu(DBM)3Phen (EDP) complexes. Fourier transform infrared spectroscopy, scanning electron microscopy, and photoluminescence analysis were used to thoroughly analyse the structural, morphological, and spectroscopic features of the synthesised nanofibres in single and stacked multilayer nanofibres. A spectroscopic analysis was performed on all configuration schemes. Under UV excitations, the synthesised TSP complex and EDP complex inhibited nanofibres yield green and red emission corresponding to 5D4→7Fj (j = 4, 5, 6) and 5D0→7Fj (j = 0, 1, 2, 3) transitions attributed to Tb3+ and Eu3+ ions, respectively. The EDP nanofibres presented better UV radiation absorption than TSP, which was attributed to higher absorptivity of DBM than Sal. Additionally, the photoluminescence intensity ratio of characteristic emission peaks i.e. 544 nm (5D4→7F5)/615 nm (5D0→7F2) is function of humidity exposure and excitation wavelength. The stacked multilayer nanofibres exhibit good response and recovery times, 35 and 52 s, negligible hysteresis, and cyclic stability.

Ratiometric fluorescence sensor for protamine and heparin based on N,P‐doped carbon dots and Eosin Y

AbstractA novel ratiometric fluorescent assay was proposed for protamine and heparin based on blue‐emitting N,P‐doped carbon dots (N,P‐CDs) and green‐emitting Eosin Y. The N,P‐CDs were prepared using arginine as carbon and nitrogen sources according to hydrothermal method with favorable luminescence intensity, photostability, and good reproducibility. And the N,P‐CDs were used as internal reference fluorescence molecules. The anionic Eosin Y was used as fluorescence signal molecule. Protamine with positive group could interact with Eosin Y through electrostatic effect, leading to the fluorescence quenching of Eosin Y. Upon the addition of heparin, heparin was combined with protamine with stronger affinity through electrostatic interactions and hydrogen bonds, which preventing the bonding of protamine with Eosin Y and obvious fluorescence emissions of Eosin Y at 538 nm could be observed. Meanwhile, the fluorescence signal of N,P‐CDs at 420 nm remained stable during the whole process. A good linear range between the fluorescence emission intensity ratio of I538/I420 was obtained for protamine from 0.01 to 40 μg/mL with a low detection limit of 5.6 ng/mL, and heparin from 0 to 35 μg/mL with a low detection limit of 2.5 ng/mL. Moreover, the method was further applied to detection of heparin with satisfactory results in fetal bovine serum samples.

Enhancement of Excimer Formation Ability by Modulating the Length of Side-Chains in Polyhedral Oligomeric Silsesquioxane (POSS) and Application for Fluorescence Sensors for Metal Cations

Abstract Polyhedral oligomeric silsesquioxane (POSS) is a molecule with an inorganic cubic structure and organic side-chains and has attracted great attention for its application to luminescent materials by modifying luminophores. In this study, pyrenes-integrated POSSs with various lengths of side-chains were synthesized and the effect of the length on luminescent properties was evaluated. In optical measurements, highly efficient excimer emission was observed under dilute solution conditions. The higher value of the intensity ratio of the excimer emission to the monomer one was detected in the shortest side-chains. It is likely that the shorter side-chains of POSS lead to more efficient intramolecular interaction. Interestingly, we also found that the luminescence color was changed in response to metal cations in the dilute solutions. From the mechanistic study, metal cations such as Cu2+ can accelerate hydrolysis at the linker moiety. As a result, highly-sensitive luminescent sensors were obtained. These data represent that POSS can work as a reaction field where chemical reactions are accelerated through the accumulation of reactive species.

Qualitative Geochemical Analysis of the 2004 Indian Ocean Giant Tsunami Deposits Excavated at Seungko Mulat Located in Aceh Besar of Indonesia Using Laser-Induced Breakdown Spectroscopy

Laser-induced breakdown spectroscopy (LIBS) was employed to characterize the geochemical signatures layer by layer of 2004 Indian Ocean tsunami deposits in Seungko Mulat Village, Aceh Province, Indonesia. In the LIBS experimental setup, a Nd-YAG laser beam is directed towards the deposit samples, and the resulting atomic emission lines from the laser-induced plasma are captured using a spectrometer. Our analysis reveals terrestrial indicators (Fe), heavy metals (Cu, Cr, Co, Cd), and increased emission intensity of Mg, Ca, Al, K, Si, Ba, N, and O in the 2004 Indian Ocean tsunami layers. The emission intensity ratios of several elements in the 2004 Indian Ocean tsunami deposit layers, namely Ca/Ti, Si/Ti, and K/Ti, unveil notable disparities among the elements evaluated. This indicates the possibility of utilizing these ratios as reliable geochemical markers to differentiate the layer by layer of tsunami deposits. LIBS surpasses XRF in detecting nearly all elements simultaneously and identifying both light elements and specific heavy metals (Ba, Cu, Cr, Co, Cd, Pb, Ni, V, W), exceeding XRF's detection capabilities. This study emphasizes the effectiveness of LIBS as an advanced optical technique, offering speed and promise in analyzing layer-by-layer geochemical markers of the 2004 Indian Ocean tsunami deposits in Seungko Mulat Village.

Some results from a transversely excited atmospheric carbon dioxide-laser induced breakdown spectroscopy investigation of tsunami deposit cored from Aceh Besar coastal region

Abstract We undertook an extensive analysis to examine the geochemical imprints encapsulated within the samples of the 2004 Indian Ocean tsunami deposits procured from the Seungko Mulat coastal region, nestled in the western section of Aceh Besar Regency, Aceh Province, Indonesia. In order to induce the formation of micro-plasma, a Transversely Excited Atmospheric Carbon Dioxide-Laser Induced Breakdown Spectroscopy (TEA CO2-LIBS) has been employed as the excitation source. Our investigation unveils distinct spectral signatures within every layer of the stratified tsunami deposit. We observed the unmistakable presence of salt elements (Ca, K, Mg, Na, Al), transition metals, heavy metals (Si, Fe, Ti, Ba, Sr, Cu, Cr, Pb, Mn, Ni, V), and also organic constituents (C, H, O, and N). The emission intensities of these elements exhibited a significant increase within the layers of the tsunami deposit, unequivocally setting them apart from their non-tsunami equivalents. In addition, we performed a vertical analysis of LIBS elemental emission intensity ratios, unveiling unique values for the Ca/Ti, and Si/Ti, ratios, which significantly distinguish them from all other ratios scrutinized in this exhaustive investigation. This research serves to highlight the effectiveness of TEA-LIBS as a promising and efficient optical technique for discerning the chemical profile associated with the renowned 2004 Indian Ocean tsunami deposits from Seungko Mulat Village in Aceh Province.

Self‐Inclusion Complexation of Electron‐Accepting Guest into Electron‐Donating Cyclic Host by Photoexcitation

AbstractSelf‐inclusion complexes consisting of host‐guest conjugates are one of the unique supramolecular structures because they form in‐state and out‐state depending on the external stimuli. Despite many reports of the stimuli‐responsive self‐inclusion complex formation, study of the structural relaxation from out‐state to in‐state by photoexcitation has been unexplored. Herein, we report that an electron‐donating host and an electron‐accepting guest conjugate exhibits the structural relaxation from out‐state to in‐state by photoexcitation. Formation of the in‐state in the excited state resulted in exciplex emission along with the locally excited emission from the out‐state. Moreover, this structural relaxation by photoexcitation was suppressed not only by temperature, but also by the presence of guest molecules, resulting in changes in the ratio of the dual emission intensities.

Self-Inclusion Complexation of Electron-Accepting Guest into Electron-Donating Cyclic Host by Photoexcitation.

Self-inclusion complexes consisting of host-guest conjugates are one of the unique supramolecular structures because they form in-state and out-state depending on the external stimuli. Despite many reports of the stimuli-responsive self-inclusion complex formation, study of the structural relaxation from out-state to in-state by photoexcitation has been unexplored. Herein, we report that an electron-donating host and an electron-accepting guest conjugate exhibits the structural relaxation from out-state to in-state by photoexcitation. Formation of the in-state in the excited state resulted in exciplex emission along with the locally excited emission from the out-state. Moreover, this structural relaxation by photoexcitation was suppressed not only by temperature, but also by the presence of guest molecules, resulting in changes in the ratio of the dual emission intensities.

Upconversion Emission and Dual-Mode Sensing Characteristics of NaYF4:Yb3+/Er3+ Microcrystals at High and Ultralow Temperatures.

In this study, we investigate micrometer-sized NaYF4 crystals double-doped with Yb3+/Er3+ lanthanide ions, designed for temperature-sensing applications. In contrast to previous studies, which focused predominantly on the high-temperature regime, our investigation spans a comprehensive range of both high and ultralow temperatures. We explore the relationship between temperature and the upconversion luminescence (UCL) spectra in both frequency and time domains. Our findings highlight the strong dependence of these spectral characteristics of lanthanide-doped NaYF4 crystals on temperature. Furthermore, we introduce a dual-mode luminescence temperature measurement technique, leveraging the upconversion emission intensity ratio for both green and red emissions. This study also examines the correlation between temperature sensing, energy level disparities, and thermal coupling in Er3+ ions across various temperature scales. Our research contributes to advancing the understanding and application of lanthanide-doped materials, setting a foundation for future innovations in temperature sensing across diverse fields.