Decay Time Research Articles

A comparative study of microwave assisted and conventional melting techniques to glass properties

The present work focuses on the investigation of the properties of 33TeO2: 30B2O3: 30ZnO: 5BaO: 2Eu2O3 glass prepared using microwave and conventional techniques. The prepared glasses were characterized by TGA/DSC analysis, density, refractive index, FTIR, XPS, absorption spectra, photoluminescence, lifetime, quantum efficiency, and X-ray-induced luminescence properties. The photoluminescence of the samples exhibited the strongest luminescence intensity of the Eu3+ ion at 614 nm (7F2) under 394 nm excitation, resulting in a relatively high photoluminescence quantum yield of 39.64%. The luminescence decay time from the 5D0 to 7F2 level of glass prepared by the microwave technique is lower than that of a sample prepared by the conventional technique, with a luminescence decay time of 1.269 and 1.425 ms, respectively. X-ray-excited luminescence spectroscopy identified an emission peak at 614 nm in the samples, which can be attributed to 5D0-7F2 transitions in the Eu3+ ion. These high-intensity samples were compared with bismuth germanate oxide (BGO) crystals used in radiation detection applications. From the various results examined, it is clear that the 33TeO2: 30B2O3: 30ZnO: 5BaO: 2Eu2O3 glass prepared using the microwave technique is suitable for use as a scintillation material.

Tb3+ doped silicoborate glass scintillator for high resolution synchrotron X-rays imaging application

This research aims to develop a combination of SiO2 and B2O3 glass former (called, silicoborate glass) to be used as a scintillation material for digital radiography application. The silicoborate glass doped with different concentration of Tb2O3, xTb2O3–7.5Gd2O3–40Na2O–5SiO2– (47.5-x)B2O3, where x = 0, 1, 2, and 3 mol% (xTb:7.5Gd) were prepared by melting and then rapid quenching in graphite mold. The density of the prepared glasses was high with Tb2O3 concentration, indicating that the glass became denser and could strongly interact with X-rays. The molar volume increased with Tb2O3 concentration, suggesting the increase of Non-Bridging Oxygen (NBOs) in glass matrix. The xTb:7.5Gd glasses absorbed photons in visible and near-infrared regions and was observed that the absorption bands increased with Tb2O3 concentration, which was the result of the 4f6-4f6 transitions behavior of Tb3+ ions. The photoluminescence and radioluminescence results revealed the distinct emission occurring at 544 nm (5D4→7F5). The photoluminescence quantum yield (PLQY) of glass had the maximum efficiency at 30.85%. The luminescence peak area under X-rays excitation glass was maximum at 109% of BGO crystal. CIE 1931 chromaticity of the xTb:7.5Gd glasses showed the color coordinates in yellowish-green area. The decay time of the xTb:7.5Gd glasses were in the millisecond range for different excitations. The probability of energy transfer was investigated between Gd3+ and Tb3+ ions in glass and may occur mainly between the 6P7/2 level of Gd3+ and 5H7 level of Tb3+. The X-rays imaging using the developed glass as a scintillator was performed by Synchrotron X-rays and the spatial resolution 6 lp/mm was achieved. These results demonstrate that the 3 mol% of Tb2O3 doped silicoborate glass can be used as a scintillator and can be applied for a high-resolution Synchrotron X-rays imaging system.

Free boundary regularity and support propagation in mean field games and optimal transport

We study the behavior of solutions to the first-order mean field games system with a local coupling, when the initial density is a compactly supported function on the real line. Our results show that the solution is smooth in regions where the density is strictly positive, and that the density itself is globally continuous. Additionally, the speed of propagation is determined by the behavior of the cost function near small values of the density. When the coupling is entropic, we demonstrate that the support of the density propagates with infinite speed. On the other hand, for a power-type coupling, we establish finite speed of propagation, leading to the formation of a free boundary. We prove that under a natural non-degeneracy assumption, the free boundary is strictly convex and enjoys C1,1 regularity. We also establish sharp estimates on the speed of support propagation and the rate of long time decay for the density. Moreover, the density and the gradient of the value function are both shown to be Hölder continuous up to the free boundary. Our methods are based on the analysis of a new elliptic equation satisfied by the flow of optimal trajectories. The results also apply to mean field planning problems, characterizing the structure of minimizers of a class of optimal transport problems with congestion.

Improved optical characteristics in BaBi2Nb2O9 ferroelectric ceramic infused with transition metal ion (W6+) and rare earth ions (Er3+/Yb3+)

In this paper, a detailed study of the Er/Yb/W tri-doped BaBi2-x-yNb2-zErxYbyWzO9 (BBN) system and a comparison of undoped, Er-doped, Er/Yb co-doped and Er/Yb/W tri-doped BBN systems are presented. All the BBN ceramics are prepared using the solid-state approach. The XRD spectra demonstrated that each BBN composition has an orthorhombic geometry. The UCL spectra are traced at 980 nm and exhibit two distinctive green bands and one red band at 535 nm, 556 nm, and 673 nm, respectively. The UCL intensity improves with W6+ concentration and reaches a maximum at (z = 0.02); after this concentration, the quenching effect occurs. The pump power variation on UCL spectra confirmed the involvement of two photons. The time-resolved fluorescence analysis was done for green and red emissions, and it was observed that the time decay increased for higher dopant concentrations, suggesting a non-radiative transition at higher dopant concentrations. The FIR technique measured the absolute sensitivity and had a value of 0.91% K-1 at 573 K. These improvements suggest that the prepared material may help develop advanced electronic equipment for multifunctional applications.

Synergistic Enhancement of Electron Dynamics and Optical Properties in Zeolitic Imidazolate Framework-8-Derived Zinc Oxide via Surface Plasmon Resonance Effects of Silver Nanoparticles under UV Irradiation.

This study investigates the surface plasmon resonance (SPR)-induced UV photoresponse of zinc oxide (ZnO) derived from zeolitic imidazolate framework-8 (ZIF-8) to assess the influence of silver nanoparticles (Ag NPs) on the photoresponse behavior of metal-organic framework (MOF)-derived ZnO. The initial synthesis involved a thermal treatment in air to convert ZIF-8 into ZnO. We noted enhanced optical absorption both in the UV and visible spectra with the deposition of Ag NPs onto the ZIF-8-derived ZnO. Additionally, the presence of Ag NPs in the ZnO resulted in a substantial increase in current, even without any light exposure. This increase is attributed to the transfer of electrons from the Ag NPs to the ZnO. Photocurrent measurements under UV illumination revealed that the photocurrent with Ag NPs was significantly higher-by two orders of magnitude-compared with that without Ag NPs. This demonstrates that SPR-induced absorption markedly boosted the photocurrent, although the current rise and decay time constants remained comparable to those observed with ZnO alone. Although Ag NPs contribute electrons to ZnO, creating a "pre-doping" effect that heightens baseline conductivity (even in the absence of light), this does not necessarily alter the recombination dynamics of the photogenerated carriers, as indicated by the similar rise and decay time constants. The electron transfer from Ag to ZnO increases the density of charge carriers but does not significantly influence their recombination.

PMUs data based detection of oscillatory events and identification of their associated variable: Estimation of information measures approach

Information theory can be a useful tool for quantifying the perturbations in the associated state variables at the time of disturbance occurrence. The study introduces a framework for the spectral decomposition of multivariate information measures to detect initiation of low frequency oscillations (LFOs), caused due to physical events in the power grid. A frequency-specific quantification of the information is shared between a target variable and two source variables from their time series data. Initially, the approach is applied on different synthetic test signals having different oscillatory frequency modes and decay time constant. Then, approach is extended on PMUs signals. The combination of cross-spectral and information-theoretic approaches is applied for the multi-variable analysis of PMUs signals from the same bus. The interdependence among the frequency, voltage angle and voltage magnitude, corresponding to specific oscillations, manifested due to cause-effect relationships obtained in terms of statistics is estimated. The dynamics in terms of unique (interaction), redundant and synergetic information is determined with the contribution from two of these three signals as source variables to target variable (frequency/voltage angle). This provides a direct coupling to identify driver-response relationships between source variables and target variable to indicate the onset of LFOs, following physical events in power network. The extension of approach among the variables from different buses aids to identify the responsible area of event occurrence.

Convergence rate toward shock wave under periodic perturbation for generalized Korteweg–de Vries–Burgers equation

In this paper, a viscous shock wave under space-periodic perturbation of generalized Korteweg–de Vries–Burgers equation is investigated. It is shown that if the initial periodic perturbation around the viscous shock wave is small, then the solution time asymptotically tends to a viscous shock wave with a shift partially determined by the periodic oscillations. Moreover the exponential time decay rate toward the viscous shock wave is also obtained for some certain perturbations.

First determination of the angular dependence of rise and decay times of solar radio bursts using multi-spacecraft observations

A large arsenal of space-based and ground-based instruments is dedicated to the observation of radio emissions, whether they originate within our solar system or not. Radio photons interact with anisotropic density fluctuations in the heliosphere which can alter their trajectory and influence the properties that are deduced from observations. This is particularly evident in solar radio observations, where anisotropic scattering leads to highly directional radio emissions. Consequently, observers at varying locations will measure different properties, including different source sizes, source positions, and intensities. However, it is not known whether the measurements of the decay time of solar radio bursts are also affected by the observer’s position. Decay times are dominated by scattering effects, and so are frequently used as proxies of the level of density fluctuations in the heliosphere, making the identification of any location-related dependence crucial. We combine multi-vantage observations of interplanetary Type III bursts from four non-collinear, angularly separated spacecraft with simulations to investigate the dependence of the decay- and rise-time measurements on the separation of the observer from the source. We propose a function to characterise the entire time profile of radio signals, allowing for the simultaneous estimation of the peak flux, decay time, and rise time, while demonstrating that the rise phase of radio bursts is non-exponential, having a non-constant growth rate. We determine that the decay and rise times are independent of the observer's position, identifying them as the only properties that remain unaffected and thus do not require corrections for the observer's location. Moreover, we examine the ratio between the rise and decay times and find that it does not depend on the frequency. Therefore, we provide the first evidence that the rise phase is also significantly impacted by scattering effects, adding to our understanding of the plasma emission process.

Exploring the structural, photophysical, and electrical properties of Dopant-Free hole transporting material based on 2, 7-carbazole from experimental to simulation

This paper presents the development of a dopant-free HTM as a thin film, utilizing carbazole (2,7) as a central building block. The deposition of homogeneous thin films of HTM2 was successfully achieved through Physical Vapor Deposition. The morphological, optical, and electrical properties of the fabricated samples were extensively studied using techniques such as Atomic Force Microscopy (AFM), Scanning Electron Microscopy (SEM), UV–visible spectroscopy, and Photoluminescence Technique. The AFM and SEM analyses demonstrated the uniformity and flatness of the thin film surfaces. The UV spectra results indicated that the maximum absorption spectra did not exhibit significant shifts when measured in chlorobenzene solvent, with an estimated band gap of approximately 2.96 eV. Photoluminescence spectroscopy and decay time measurements were conducted on HTM2 thin films, which revealed emission in the green-yellow region. The photoluminescence spectra of the thin films exhibited red-shifted emission bands compared to the solution, attributable to stronger π-π intermolecular interactions resulting in the closeness of the molecules in the solid state. This work finally couples the theoretical and experimental results to validate our obtained results and to get an idea about the efficiency of the cell-based HTM2. The obtained results confirmed that the investigated material can find applications in perovskite solar cells.

Effect of thickness on properties of La-doped Zinc Blende/Wurtzite ZnO thin films prepared by spray pyrolysis

Thin films of ZnO doped with 3 wt% Lanthanum were deposited on glass substrates using spray pyrolysis for varying thicknesses. The impact of thickness on the physical properties of the films was investigated using various techniques. XRD results revealed the formation of a mixture of two phases, cubic Zinc Blende (ZB) and hexagonal Wurtzite (WU), with their ratios changing based on film thickness. Crystallite size measurements indicated that the cubic phase granules remained stable at 14.6 nm up to a thickness of 719 nm, decreasing to 14 nm at 846 nm, while the crystallite size of the hexagonal phase increased to 18 nm at 846 nm. FE-SEM images showed changes in surface morphology with increasing thickness, and EDX analysis demonstrated a consistent La/Zn ratio across all film thicknesses. The refractive index exhibited a shift from normal to abnormal dispersion when the thickness exceeded 719 nm, and the high-frequency dielectric constant decreased from 3.2 to 2.91 as the thickness increased. Additionally, optical band gaps ranged from a minimum of 3.19 eV at 719 nm thickness to a maximum of 3.23 eV at 846 nm thickness. The study examined the effectiveness of the deposited films in blocking UV light with a wavelength of 365 nm. It was discovered that the decay time significantly decreased to 143 s at a thickness of 661 nm, compared to longer times observed at other thicknesses.

Hydrothermally Synthesized Bi-Doped CdTe Nanoparticles with Tunable Optical and Photoresponse Properties for Visible Photodetectors.

The remarkable applicability and unique properties of CdTe nanoparticles make them vital in various applications such as optoelectronics and photovoltaics. It has been demonstrated that adding a metal dopant to a nanomaterial matrix significantly improves its characteristics, increasing its potential for a variety of applications. In this work, a simple hydrothermal synthesis process for bidoped CdTe nanoparticles is reported, wherein four distinct samples are generated by adjusting the concentration of Bi doping. Structural analysis using X-ray diffraction (XRD) confirmed the presence of the CdTe cubic phase in the material with observable phase shifts due to Bi incorporation. Rietveld refinement of the XRD results further enabled a detailed structural analysis. Raman spectroscopy provided insights into the different vibrational modes of CdTe, while transmission electron microscopy analysis further elucidated the CdTe phase and determined interplanar spacing values. Morphological examination via field emission scanning electron microscopy revealed a consistent nanoparticle-like morphology, unaffected even by increased Bi concentration. Elemental analysis conducted through inductively coupled plasma mass spectrometry offered valuable insights into the composition of the material. Furthermore, UV-vis analysis revealed a decrease in the bandgap, indicating potential shifts in the material's optical properties. Notably, the photoresponse study demonstrated an increase in current value, as well as alterations in the rise and decay times of the material. These properties highlight its potential for various optical and electrical applications. Overall, these findings underscore the promising prospects of bidoped CdTe nanoparticles in various advancements.

One-Dimensional Copper-Doped Rb2AgI3 with Efficient Sky-Blue Emission as a High-Performance X-ray Scintillator.

Scintillators have garnered heightened attention for their diverse applications in medical imaging and security inspection. Nonetheless, commercial scintillators encounter challenges with costly rare-earth metals and toxic elements like thallium (Tl), driving the need for sustainable, cost-effective, and eco-friendly alternatives to meet contemporary X-ray detection demands. This study focuses on exploring the potential of Cu+-doped Rb2AgI3 as an effective metal halide (MH) scintillator. One-dimensional (1D) Rb2AgI3 and Cu+-doped Rb2AgI3 single crystals (SCs) were synthesized by using the conventional temperature-lowering crystallization method. When excited by UV light, Cu+-doped SCs emitted a broad sky-blue light at 490 nm with a high photoluminescence (PL) quantum yield (PLQY) of 76.48%. Remarkably, under X-ray excitation, these Cu+-doped SCs demonstrated an outstanding light yield of 36,293 photons MeV-1, a relatively low detection threshold of 1.022 μGyair s-1, and a rapid scintillation decay time of 465 ns. The prepared translucent scintillation film has good uniformity and flexibility, with a high spatial resolution of 10.2 lp mm-1. These results position Cu+-doped Rb2AgI3 as a leading candidate among promising X-ray scintillators, offering superior scintillation light yield, excellent stability, and nontoxicity.

Nanoparticle ZnS:Ag/6LiF—a new high count rate neutron scintillator with pulse shape discrimination

A neutron sensitive scintillator employing nanoparticles of ZnS:Ag has been developed for the first time. Pulse shape differences between neutron and gamma signals were observed in this material and neutron-gamma discrimination was applied. With initial signal processing parameters, gamma sensitivities of 8.5×10−6 to 60Co gammas were achieved. The average primary decay of neutron scintillation in nanoparticle ZnS:Ag/6LiF was measured to be 18ns, and afterglow was significantly suppressed in comparison to standard ZnS:Ag/6LiF scintillators that employ micron sized ZnS:Ag. Fast decay times and minimal afterglow indicate potential for use in high count rate capability applications. Prospective count rate capabilities were investigated here as proof of concept, with rates of 1.12Mcps measured for a single readout channel with less than 3.5% count loss. This is approximately 70 times greater than the count rate capability of the current standard ZnS:Ag/6LiF scintillation detectors. With improvements to signal processing and scintillator composition, nanoparticle ZnS:Ag/6LiF could be a promising candidate for future high rate capability neutron detectors.

Machine learning elucidates electrophysiological properties predictive of multi- and single-firing human and mouse dorsal root ganglia neurons.

Human and mouse dorsal root ganglia (hDRG and mDRG) neurons are important tools in understanding the molecular and electrophysiological mechanisms that underlie nociception and drive pain behaviors. One of the simplest differences in firing phenotypes is that neurons are single-firing (exhibit only one action potential) or multi-firing (exhibit 2 or more action potentials). To determine if single- and multi-firing hDRG exhibit differences in intrinsic properties, firing phenotypes, and AP waveform properties, and if these properties could be used to predict multi-firing, we measured 22 electrophysiological properties by whole-cell patch-clamp electrophysiology of 94 hDRG neurons from 6 male and 4 female donors. We then analyzed the data using several machine learning models to determine if these properties could be used to predict multi-firing. We used 1000 iterations of Monte Carlo Cross Validation to split the data into different train and test sets and tested the Logistic Regression, k-Nearest Neighbors, Random Forest, Supported Vector Classification, and XGBoost machine learning models. All models tested had a greater than 80% accuracy on average, with Supported Vector Classification and XGBoost performing the best. We found that several properties correlated with multi-firing hDRG neurons and together could be used to predict multi-firing neurons in hDRG including a long decay time, a low rheobase, and long first spike latency. We also found that the hDRG models were able to predict multi-firing with 90% accuracy in mDRG. Targeting the neuronal properties that lead to multi-firing could elucidate better targets for treatment of chronic pain.

Estimation of sound absorption coefficient at modal frequencies using decay time measurements and eigenvalue model in a small room

Measuring the sound absorption coefficient in a small reverberation room below the Schroeder frequency is a challenging task and the results are subject to a high degree of uncertainty. Recent research shows that the low-frequency acoustic properties of the enclosure and the test sample should be characterized by quantities that describe the modal sound field. The aim of this paper is to present a method for estimating the absorption coefficient of a test sample at modal frequencies in the low frequency range and to demonstrate its applicability in a small room. The hybrid inverse approach is based on eigenvalue measurement data coupled with a finite element model to estimate the sound-absorbing properties of a small room and the test sample. The method was tested experimentally and the results were consistent with those of the long impedance tube method. The applicability of the proposed method was further demonstrated by the in-situ characterization of different acoustic samples in the low frequency range.

Solid–liquid heterojunction UV photoelectrochemical photodetector based on WO3 nanosheets and acidic electrolyte

The acid-resistant tungsten trioxide photoelectrochemical solid–liquid ultraviolet (UV) photodetector uses a thin film of tungsten trioxide as the photoelectrode, forming a stable heterojunction with the electrolyte. This study employed band theory and double electron layer theory to analyze the mechanisms underlying the effect of pH on the redox potential and photocurrent, utilizing the ion product constant of water and the Nernst equation. By applying the principles of energy band theory and the two-electron layer model, the electron transfer process was analyzed and explained. These findings hold significant promise for enhancing solid–liquid heterojunction UV photodetectors. Tungsten trioxide has fast response and high sensitivity under extreme conditions. The device performance of WO3 nanosheets fabricated by annealing at 300 °C for one hour is excellent, including a rise time of 0.7 s, decay time of 6.8 s, photosensitivity of 1.90, and photoresponsivity of 2.31 mA/W. 0.5M sulfuric acid produced the highest photocurrent (5.46 μA) and sensitivity (14.07). This material has potential applications in optoelectronics, catalysis, sensing, water treatment, and air purification.

Quantification of alloy atomic composition sites in 2D ternary MoS2(1-x)Se2x and their role in persistent photoconductivity, enhanced photoresponse and photo-electrocatalysis

Engineering transition metal dichalcogenides-based semiconducting two-dimensional (2D) layered materials for photo(electro)chemical (PEC) hydrogen evolution reaction (HER) by water splitting is an enduring challenge. Here, alloy-assisted photoconductivity and photoresponse from CVD-grown MoS2(1-x)Se2x (MSSE) 2D ternary atomic layered alloy-based photodetector device is presented for the realization of PEC HER. The explicit role of ‘S–Se’ and ‘Se2’ atomic alloy sites including chalcogen-induced vacancy defects on the photoconductivity/photoresponse and PEC HER performance of MSSE 2D alloy is investigated. Alloy formation, atomic site-by-site ‘Se’ composition and atomic structure are characterized using Raman/Photoluminescence (PL) spectroscopy, high-angle annular dark field (HAADF)- scanning transmission electron microscopy (STEM) extensively and supported with Auger Electron Spectroscopy (AES) mapping. Further, the local density and concentration of S–Se, Se2 atomic sites and defects were quantitatively estimated using HAADF-STEM image analysis in correlation with AES and it is found between the range of ∼15–20 % in MSSE alloy. A 10-fold high photoresponsivity in the case of MSSE concerning as-grown MS having fast photocurrent growth time and the prolonged decay time originates from the ‘Se’ and this alloy assisted states to enhance the PEC performance of MSSE alloy. The enhanced PEC HER activity of MSSE alloy was identified in terms of overpotential and current density. In addition, increased density of states as a function of ‘Se’ alloying, shifts in a p-band centre and lowers ΔGH* according to density functional theory calculations, which makes MSSE alloy an efficient HER activity. Further, the PEC stability and presence of the ‘S–Se’ and ‘Se2’ alloying and their role towards HER have been correlated by the spectral line shape analysis of PL and Raman spectra from post-PEC HER catalysts. These experimental and theoretical findings establish the role of chalcogen, and transition metal-based 2D alloy, leading to the design of new PECs of engineered 2D atomic layer interfaces.

Fabrication of energy efficient P-i-G structure with novel dysprosium-doped yttrium calcium borate (Dy: Y2CaB10O19) phosphors: Highly efficient materials for cool white light emission conducive to green technology

Novel polycrystalline phosphor-yttrium calcium borate doped with dysprosium ions (Dy3+: Y2CaB10O19) was synthesized for the first time by solid-state reaction technique. The crystal structure was found to be monoclinic having C2 space group. SEM was performed to analyze the surface morphology of the phosphor materials and to assess the distribution of phosphor particles in the glass matrix. Fourier transform infrared (FTIR) spectroscopy of the samples was studied to know the molecules present. The emission spectra by 350 nm excitation possessed characteristic peaks at 480 nm (blue) and 577 nm (yellow). The CIE chromaticity co-ordinate and correlated color temperature (CCT) were deduced to be (x = 0.3384, y = 0.3823) and 5297 K respectively. Luminescence decay time for the optimized phosphor was determined to be 0.70 ms. The prepared phosphors were embedded in the glass matrix at an elevated temperature of 1000 °C. The transmittance spectra of the prepared glass materials were recorded to analyze its transparency in the visible region. The internal quantum yield was deduced to be 53.91 %.

Harnessing bright upconversion luminescence from PEG-coated NaGdF4:Ho3+/Yb3+ nanoparticles for contrast enhancement in dual mode OCT imaging and optical temperature sensing

In this work, authors synthesized the Polyethylene Glycol (PEG) coated NaGdF4:Ho3+/Yb3+ nanoparticles using the thermal decomposition reaction route. Our primary objective was to comprehensively evaluate their suitability for augmenting image contrast, particularly within the intricate domain of Swept Source Optical Coherence Tomography (SSOCT) and photo-thermal Optical Coherence Tomography (PTOCT) imaging modalities. Our meticulous inquiry yielded the revelation of extraordinary upconversion emissions, which emanated from the distinct transitions of Ho3+ ions, most notably the 5F4(5S2)→ 5I8 and 5F5→ 5I8 transitions. These transitions manifested as strikingly vibrant green emissions, precisely at the 539 nm and 661 nm wavelengths. Furthermore, we investigated the underlying upconversion mechanism, delving deeply into the elucidation of decay times and the nanoparticles' ability to transform incident radiation into thermal energy. Impressively, these nanoparticles exhibited a noteworthy photo-thermal conversion efficiency, specifically measured at an impressive 47.4% along with the bright green luminescence. Our study also extended to bio-compatibility, where we achieved highly encouraging outcomes. Following 24 hours of incubation with HeLa cells treated with UCNP-PEG, we ascertained a compelling cell survival rate exceeding 80%, underscoring the favorable biocompatibility of these nanoparticles. Moreover, these nanoparticles demonstrated a conspicuous thermal sensitivity, quantified at 5.1×10-3 K-1 at 380K, thus signaling their potential for precision temperature monitoring and could be applied at the cellular level.

Synaptic effects of xenon on NMDA receptor-mediated response in rat spinal neuron

To investigate the precise mechanism of xenon (Xe), pharmacologically isolated AMPA/KA and NMDA receptor-mediated spontaneous (s) and evoked (e) excitatory postsynaptic currents (s/eEPSCAMPA/KA and s/eEPSCNMDA) were recorded from mechanically isolated single spinal sacral dorsal commissural nucleus (SDCN) neurons attached with glutamatergic nerve endings (boutons) using conventional whole-cell patch-clamp technique. We analysed kinetic properties of both s/eEPSCAMPA/KA and s/eEPSCNMDA by focal single- and/or paired-pulse electrical stimulation to compare them. The s/eEPSCNMDA showed smaller amplitude, slower rise time, and slower 1/e decay time constant (τDecay) than those of s/eEPSCAMPA/KA. We previously examined how Xe modulates s/eEPSCAMPA/KA, therefore, examined the effects on s/eEPSCNMDA in the present study. Xe decreased the frequency and amplitude of sEPSCNMDA, and decreased the amplitude but increased the failure rate and paired-pulse ratio of eEPSCNMDA without affecting their τDecay. It was concluded that Xe might suppress NMDA receptor-mediated synaptic transmission via both presynaptic and postsynaptic mechanisms.