Reduction Of Lifetime Research Articles

Preparation of fluorescent carbon dots by flow-assisted melt polymerization for tetracycline detection in medical wastewater

Tetracycline (TC) is one of the most important therapeutic drugs that is widely used in hospitals. However, its harmful effects on human health and various ecosystems cannot be ignored. Owing to its poor metabolic activity and low biodegradability, TC commonly discharges as the parent compound and accumulates readily in sludges and soils by precipitation from wastewater, which can induce the evolution of antibiotic-resistant bacteria; therefore, it has been listed as one of the new pollutants with potential ecotoxicological risk. The control measures and environmental management of TC pollutants in environmental water samples require precise determination of TC pollutant concentrations. Carbon dots (CDs) are an emerging type of fluorescent material with numerous advantages such as easy preparation, low cost, low toxicity, and good biocompatibility. Consequently, they have attracted widespread attention in the field of TC detection. Herein, we synthesized TE-CDs with good blue-fluorescence performance via flow-assisted melt polymerization using tricarboxylic acid and ethylenediamine as raw precursors. The morphology and structure of the prepared TE-CDs were characterized. The transmission electron microscopy (TEM) results showed that the prepared TE-CDs were well dispersed, with an average diameter of (2.43±0.48) nm. The X-ray diffraction (XRD) results showed that the TE-CDs had an amorphous carbon structure. Infrared spectroscopy and X-ray photoelectron spectroscopy (XPS) characterizations showed that the surface of the TE-CDs was rich in hydrophilic groups, such as amino, hydroxyl, and carboxyl groups, which indicated that TE-CDs had good water solubility and were advantageous for detecting TC in medical wastewater. Subsequently, the optical properties of the TE-CDs were investigated. The fluorescence emission spectra of the TE-CDs were recorded at various excitation wavelengths. The emission spectra of the TE-CDs exhibited excitation wavelength dependence and when the excitation wavelength changes from 300 nm to 400 nm, their fluorescence intensity decreased to varying degrees. The TE-CDs exhibited optimal fluorescence intensity at an excitation wavelength of 368 nm, while the emission wavelength was 448 nm. TC could effectively quench the blue fluorescence of the CDs, and by utilizing this property, the detection of TC concentration could be achieved. After the addition of TC, the fluorescence of the system immediately reached an extreme value, and no significant change was observed within 10 min. An incubation time of 20 s was selected to obtain precise results. Additionally, the TE-CDs exhibited stable fluorescence intensity over a wide pH range. The fluorescence stability of the TE-CDs was investigated, and no significant change in fluorescence intensity was observed after standing for 10 d, indicating that the prepared TE-CDs had excellent fluorescence stability. The fluorescence intensity of the TE-CDs decreased to varying degrees within the range of 2-200 mg/L TC until complete quenching occurred. TC mass concentration in the range of 4-20 mg/L showed a good linear relationship (R2=0.9978) with the fluorescence quenching intensity of the TE-CDs. The limit of detection was 0.2 mg/L. A preliminary investigation was undertaken to explore the quenching mechanism of the TE-CDs fluorescence by TC. Upon addition of TC, a significant reduction in the fluorescence lifetime of the TE-CDs was observed. During the quenching process, no new substances were observed by UV absorption spectroscopy. Additionally, no significant changes in the 1H NMR spectra of the TE-CDs were noted before and after the addition of TC, indicating the absence of an interaction between the TE-CDs and TC. Therefore, the quenching mechanism may involve dynamic quenching. The selectivity and anti-interference ability of the developed method were evaluated; in the presence of interfering substances, TC quenched the fluorescence of the TE-CDs, indicating that the TE-CDs had good selectivity and anti-interference performance towards TC. The method was applied to the quantitative detection of TC in medical wastewater, with recoveries of 96.5%-119.8% and relative standard deviations of 0.8%-2.6%. In conclusion, the analytical performance of the proposed method is comparable with that of previously reported detection methods; moreover, the method has the advantages of low operational cost, simple preparation process, time-saving, and good repeatability. Therefore, the TE-CDs can be used as chemical sensors for the detection of TC in medical wastewater and have good practical applications.

The contribution of transport emissions to ozone mixing ratios and methane lifetime in 2015 and 2050 in the Shared Socioeconomic Pathways (SSPs)

Abstract. We quantify the contributions of emissions from the transport sector to tropospheric ozone and the hydroxyl radical (OH) by means of model simulations with a global chemistry-climate model equipped with a source attribution method. For the first time we applied a method which also allows for quantifying contributions to OH which is invariant upon disaggregation or recombination and additive. Based on these quantified contributions, we analyse the ozone radiative forcing (RF) and methane lifetime reductions attributable to emissions from the transport sectors. The contributions were analysed for each transport sector separately and for 2015 as well as for 2050 under the Shared Socioeconomic Pathways (SSPs) SSP1-1.9, SSP2-4.5, and SSP3-7.0. In line with previous publications using the source attribution approach, we quantify ozone RF attributable to emissions from land transport, shipping, and aviation for the year 2015 of 121, 60, and 31 mW m−2, respectively. At the same time, we diagnose a relative reduction in methane lifetime due to transport emissions of 14.3 % (land transport), 8.5 % (shipping), and 3.8 % (aviation). These reductions are significantly larger than reported by previous studies due to the application of the source attribution method. Compared to 2015, only SSP1-1.9 shows a strong decrease in ozone RF and methane lifetime reduction attributable to the entire transport sector in 2050. For the projections of SSP2-4.5, we find similar effects of the total transport sector as for 2015, while the effects in SSP3-7.0 increase compared to 2015. This small change in the effects for the two projections compared to 2015 is caused by two main factors. Firstly, aviation emissions are projected to increase in SSP2-4.5 (increase of 107 %) and SSP3-7.0 (+86 %) compared to 2015, resulting in projected ozone RF of 55 mW m−2 (+78 %) and 50 mW m−2 (+61 %) for the year 2050 from aviation emissions. Secondly, the non-linear effects of atmospheric chemistry in polluted regions such as Europe and North America lead to rather small reductions in ozone and OH in response to emission reductions, especially from land transport emissions. In addition, the increase in emissions from land transport in other parts of the world, particularly in South Asia, leads to an increased contribution of ozone and OH. In particular, ozone formed by land transport emissions from South Asia causes strong RF that partially offsets the reductions in Europe and North America. Moreover, our results show that besides the non-linear response, lack of international cooperation, as in the SSP3-7.0 projection, hinders mitigation of ground-level ozone.

Coherent Coupling of a Diamond Tin-Vacancy Center to a Tunable Open Microcavity

Efficient coupling of optically active qubits to optical cavities is a key challenge for solid-state-based quantum optics experiments and future quantum technologies. Here we present a quantum photonic interface based on a single tin-vacancy center in a micrometer-thin diamond membrane coupled to a tunable open microcavity. We use the full tunability of the microcavity to selectively address individual tin-vacancy centers within the cavity mode volume. Purcell enhancement of the tin-vacancy center optical transition is evidenced both by optical excited state lifetime reduction and by optical linewidth broadening. As the emitter selectively reflects the single-photon component of the incident light, the coupled emitter-cavity system exhibits strong quantum nonlinear behavior. On resonance, we observe a transmission dip of 50% for low incident photon number per Purcell-reduced excited state lifetime, while the dip disappears as the emitter is saturated with higher photon number. Moreover, we demonstrate that the emitter strongly modifies the photon statistics of the transmitted light by observing photon bunching. This work establishes a versatile and tunable platform for advanced quantum optics experiments and proof-of-principle demonstrations on quantum networking with solid-state qubits. Published by the American Physical Society 2024

PLPR: Joint Perpetual Lifetime and Path Reduction for Energy Recharging Using Multiple Mobile Chargers in WRSNs

PLPR: Joint Perpetual Lifetime and Path Reduction for Energy Recharging Using Multiple Mobile Chargers in WRSNs

Purcell gain equalized zero-mode waveguide

We refresh the design of zero-mode waveguides (ZMWs) by introducing metamaterials that makes the zeroth order resonant mode existence. Of particular importance, the resulting electromagnetic field exhibits nearly constant distribution but not a trivial solution of Maxwell’s equation, showing great advantage to equalize the excitation rate of molecules throughout the waveguides. A closed form expression for the wave impedance is derived which is verified by the finite-difference time-domain simulations. Benefitted from the cavity Purcell effect which is lacking in existing ZMWs, fluorescence amplification and lifetime reduction are simultaneously enhanced. A practical design where the excitation volume reduced down to sub-zeptoliter and the fluorescence lifetime shortened to picosecond scale is illustrated. This result makes single molecule real time (SMRT) sensing of biochemical reactions at biophysically relevant concentrations (~ μM) possible, combining off-the-shelf ultrafast lasers.

Microfluidics-Driven Dripping Technique for Fabricating Polymer Microspheres Doped with AgInS2/ZnS Quantum Dots.

Fluorescent microspheres are at the forefront of biosensing technologies. They can be used for a wide range of biomedical applications. They consist of organic dyes and polymers, which are relatively immune to photobleaching and other environmental factors. However, recently developed AgInS2/ZnS quantum dots are a water-soluble, low-toxicity class of semiconductor nanocrystals with enhanced stability as fluorescent materials. Here, we propose a simple way for making microspheres: a microfluidic dripping technique for acrylamide polymer spheres doped with quantum dots. Analyses of their spectra show that the emission of quantum dots, dispersed in water, is saturated with an increasing pump intensity, while quantum dots embedded into polymer microspheres exhibit a more sustained emission. Moreover, our study unveils a remarkable reduction in the luminescence lifetime of quantum dots embedded in microspheres: the mean value of the decay time for quantum dots in solutions was 91 and 3.5 ns for similar quantum dots incorporated into polymer microspheres.

Comparison of fatigue characteristics and failure analysis of Ni-based superalloy subjected to thermomechanical fatigue under different phase conditions

In this research, the thermomechanical fatigue (TMF) characteristics of a second-generation Ni-based single-crystal superalloy were investigated. The combined effects of temperature cycling and mechanical stress were examined using a strain-controlled approach under different TMF testing conditions. The results indicated that cyclic softening occurred during the early stages during in-phase (IP) loading. In contrast, out-of-phase (OP) tests exhibited cyclic hardening, as evidenced by an increase in the stress range, which intensified at higher mechanical strain amplitudes. This resulted in a shorter fatigue life compared to the IP TMF case. The crack distribution patterns and damage mechanisms on the cross-sectional and fracture surfaces of the failed specimens were analyzed. In the OP TMF tests, oxidation-assisted cracking was identified as the primary damage mechanism. The dominance of oxide layers was a key distinguishing feature. Additionally, twinning-related deformation and topologically close-packed (TCP) phase particles were observed in specimens subjected to a higher mechanical strain of 0.6%, where they ran parallel to the main crack, contributing to a reduction in lifetime. Conversely, the IP TMF cases were mainly dominated by creep damage mechanisms, with some signs of oxidation penetration observed during testing. The application of the Ostergren model to the fatigue life prediction of a Ni-based single-crystal superalloy under both conditions was evaluated. As this model was insufficient, a modified Ostergren model was proposed by incorporating the maximum and amplitude stresses in the power law forms.

Enhancement of photodetector performance of aluminum-doped zinc oxide thin films fabricated via SILAR method: Structural, optical, and electrical analysis

This study presents a comprehensive analysis of the structural, optical, electrical, and photosensing characteristics of aluminum-doped zinc oxide (Al:ZnO) thin films, fabricated via successive ionic layer adsorption and reaction (SILAR) techniques. The Raman and X-ray diffraction (XRD) analyses validated the hexagonal wurtzite structure and revealed that Al doping enhances crystallinity and crystal growth of ZnO. The average crystallite size increased from 21.6 nm in undoped sample to 23.8 nm in 5.0 wt% Al-doped sample, while strain effects decreased from 4.67 × 10-3 to 4.36 × 10-3. Scanning electron microscopy (SEM) images revealed improved film morphology and more defined geometries with increased Al doping, while energy-dispersive X-ray analysis (EDAX) confirmed successful Al integration into the ZnO lattice. Optical analyses indicate a narrowing of the ZnO bandgap to 2.81 eV in 5.0 wt% Al:ZnO from 3.02 eV in the undoped variant, while photoluminescence (PL) peak positions remains unchanged. Time-resolved fluorescence (TRF) indicated a reduction in electron lifetime with higher Al doping. Furthermore, Hall effect assessments reveal a decrease in carrier mobility and electrical resistivity, alongside a rise in carrier concentration with higher Al content. The photodetection efficacy was substantially improved with Al doping, particularly at 2.5 wt% Al, achieving a responsivity of 42.5 × 10-2 A/W, external quantum efficiency of 99.3 %, and detectivity of 1.8 × 1011 Jones. These findings exhibit that Al-doping substantially enhances the photodetection properties of ZnO thin films.

Benefit to Harm (B2H) Ratio for Bulk Vehicle to Grid (V2G) Services Using Lifetime Degradation Digital Twin: Emulating Various Dominant Degradation Mechanism

Vehicle-to-grid (V2G) services, utilizing electric vehicle (EV) batteries for grid support, enhance reliability and reduce peak energy demand. We present a physics-based model tuned for three different cell chemistry families and examine the influence of bulk V2G services on EV battery life. We consider various duty cycles, cell chemistries with nickel content (NMCxyz and various anode graphites), and associated dominant degradation mechanisms. To quantify the impact of offering V2G services, we introduce the V2G benefit-to-harm ratio (B2H). We define the benefit as the Ah gained with V2G and the harm as the life lost in days due to V2G, both compared to the baseline noV2G.B2H=(normalized Ah gained by 70% capacity fade) divided by (time in days reduction by the time that capacity fade has reached 70%). Note that the 70% capacity fade can be changed for various vehicle models depending on the warranty definition of the % capacity or usable battery energy (UBE) at the end of the warranty.Our findings indicate that the dominant degradation mechanism plays a crucial role in the benefit-to-harm (B2H) ratio of V2G or vehicle-to-building (V2B) [1]. Specifically, we clarify that the relative contribution of calendar aging to overall capacity loss is pivotal in determining the degradation due to V2G and possible associated benefits.Our model takes into account four degradation mechanisms based on a single-particle model. SEI growth and cathode transition metal dissolution are part of the calendar aging loss of lithium inventory (LLICal). The remaining LLI is attributed to Li-plating and mechanical degradation caused by particle cracking.We calibrate the model for three families of cell chemistries and conditions. The primary degradation mechanism for one cell family is anode mechanical degradation (LAMNeg). The second family of cells predominantly ages due to SEI layer growth, and the third family is degrading due to both mechanisms [2].We show that, in cases with a higher contribution of calendar aging to degradation (LLICal/LLI), V2G can be potentially more beneficial (in Ah gained by 70% capacity fade) than harmful (lifetime reduction in days by the time that capacity fade has reached 70%). Furthermore, we have evidence that the V2G charging pattern can have a secondary effect on the B2H ratio. For example, being a risk taker and charging the battery late or being cautious and charging it as soon as possible can lead to different degrees of degradation depending on the chemistry and conditions of the battery [3].With our multiphysics reduced order model of battery lifetime degradation, we fully explain why previous studies [4] have shown that the impact on EV battery degradation varies from inconsequential [5] to projecting a need for early battery replacement [6]. Our results clarify that battery chemistry and usage patterns are important factors in determining whether or not to utilize a vehicle for grid support, as well as the overall financial impact on the owner and OEM warranty.

(Invited) Photoluminescence Dynamics in PbS/CdS Core/Shell Nanocrystal Films: Carrier Recombination and Energy Transfer

Colloidal semiconductor nanocrystals (NCs) exhibit highly controllable size-dependent optical properties due to the quantum confinement effect. Among other semiconductor NCs, the lead chalcogenides, especially PbS, are one of the most studied and promising NC systems. They are the material of choice for studies of fundamental phenomena as well as for the development of solution processed infrared optoelectronic devices including LEDs, lasers, solar cells, and photodetectors. Compared to organically passivated NCs, the core-shell approach (more specifically PbS/CdS core-shell NCs) offers not only the improved stability and higher photoluminescence (PL) quantum efficiency but also an opportunity of the core/shell interface nano-engineering resulting in suppression of Auger recombination, reduction of the exciton radiative lifetime and an improved lasing threshold. However, despite more than a decade of detailed studies there are conflicting reports on PL dynamics in PbS/CdS core-shell NCs, and there is no accepted model explaining the observed PL lifetimes ranging from hundred nanoseconds to tens of microseconds. In this work we use time-resolved PL measurements and demonstrate that low-temperature PL dynamics in PbS/CdS core shell NCs show strong dependence on the PL detection wavelengths. The presented experimental results allow us to distinguish between processes of energy transfer and exciton recombination. We propose a model, which considers energy transfer between NCs and various mechanisms of exciton recombination (non-radiative, radiative, spin-flip, diffusion limited, etc.).

Benchmark and Roadmap for Low Temperature Water Electrolysis for Green H2 Production and Applications

Water electrolysis has attracted world-wide attention due to its ability to produce green hydrogen when coupled with renewable electricity. Green hydrogen is a viable solution to decarbonizing a variety of industries including fertilizer, metal production, petrochemical, and synthetic fuels. There are three major low temperature water electrolysis technologies, alkaline water electrolyzer (AWE), proton exchange membrane water electrolyzer (PEMWE), and anion exchange membrane water electrolyzer (AEMWE). This work will first provide the status of these three technologies in terms of operating conditions, lifetime, and capital cost. Subsequently, the challenges and constraints for these technologies will be discussed in the scenarios of large-scale manufacturing and integration with intermittent renewables. More efforts will be made to illustrate the trajectory of the next-gen water electrolysis technologies, which feature at ultralow PGM or PGM-free catalysts, thin membranes with reduced hydrogen crossover, high-current high-power operation, long lifetime, and remarkable cost reduction. The work will also address the challenges of automated MEA fabrication and stack manufacturing at scale. Finally, a real example of renewable wind turbine integrated with water electrolyzer to produce green hydrogen and subsequently green ammonia will be demonstrated.

A Data-Driven Approach for Predicting the Lifetime of Lithium-Metal Batteries

Lithium-metal batteries (LMBs) are promising candidates for accelerating the implementation of electric vehicles in our society. LMBs comprise of a lithium-metal anode that possesses the highest theoretical specific capacity (3860 mAh/g) and the lowest redox potential (-3.04V vs standard hydrogen electrode).1 LMBs undergo repeated plating and stripping of lithium ions on the anode surface. The non-homogenous stripping process leads to the isolation of metallic lithium from the anode surface, forming dead-lithium.2 The parasitic reaction between the lithium-metal anode and the electrolyte leads to the formation of the solid electrolyte interphase (SEI) layer. These phenomena lead to the reduction of available lithium and a rise in cell impedance, causing a rapid reduction of lifetime for these batteries.3 , 4 In this talk, we present a diverse dataset collected from different LMBs of different capacities and voltage ranges, that includes features from the initial formation cycle, rest voltages and CV charging during cycling. A data-driven model from the LMB cycling data is presented to predict the remaining useful lifetime (RUL) of these cells. Insights from the model can be used to determine the bad cells in a batch, improve the designs of the cells and derive optimal charging protocols for their implementation in the BMS. References Lin, D., Liu, Y. & Cui, Y. Reviving the lithium metal anode for high-energy batteries. Nat. Nanotechnol. 12, 194 (2017).Xu, S., Chen, K.-H., Dasgupta, N. P., Siegel, J. B. & Stefanopoulou, A. G. Evolution of Dead Lithium Growth in Lithium Metal Batteries: Experimentally Validated Model of the Apparent Capacity Loss. J. Electrochem. Soc. 166, A3456–A3463 (2019).Liu, G. & Lu, W. A Model of Concurrent Lithium Dendrite Growth, SEI Growth, SEI Penetration and Regrowth. J. Electrochem. Soc. 164, A1826–A1833 (2017).Gao, N. et al. Fast Diagnosis of Failure Mechanisms and Lifetime Prediction of Li Metal Batteries. Small Methods 5, 1–11 (2021).

Suppression of stacking-fault expansion in 4H-SiC diodes by helium implantation

Abstract Bipolar degradation is a critical problem in Silicon carbide devices, caused by the expansion of single Shockley stacking faults (1SSFs) from basal plane dislocations. This paper presents the effects of helium implantation on the suppression of 1SSFs expansion. The fabricated PiN diodes were analyzed using current–voltage characteristics and electroluminescence imaging. The results show that helium implantation can effectively suppress 1SSFs expansion without significantly degrading diode performance. We consider that this suppression is due to the pinning of dislocations by point defects introduced during helium implantation, and the reduction of carrier lifetime may also play a role in suppressing 1SSFs expansion.

Wettability tuning on stainless steel LIPSS by laser oxidation and its implication on cavitation bubble dynamics

The modification of surface wettability of stainless steel is essential for many biological applications and industrial implementations. Having a hydrophobic or hydrophilic surface is ideal depending on its application. In this study, the wettability tuning of stainless steel was carried out by producing LIPSS at different laser peak energies. Results showed non-significant changes in the periodicity of the ripples, however hydrophilicity increased with greater laser energies. Raman spectroscopy and SED analysis demonstrated the presence of iron oxide peaks and increased oxygen concentration, demonstrating a chemical surface modification governed by oxidation. Transitions from hydrophilic to hydrophobic surfaces were accomplished by ethanolic triethoxyoctylsilane coated LIPSS. Hydrophobicity enhancement was achieved by the adsorption of organic species promoted by the oxide layer at the ripples. The dynamics of cavitation bubbles close to the coated LIPPS were analyzed. A reduction of the main bubble lifetime with hydrophobicity, whereas a delay of collapse time and deformation of the rebound bubble were found. This led to an experiment for erosion testing producing multiple cavitation events. An increment of surface damage area with increased hydrophobicity was observed. This was attributed to longer collapse times of the rebound bubble which led to stronger shockwaves at the samples surface. This work demonstrates a simple method to tune the surface wettability of stainless steel by laser oxidation, which is a crucial factor for applications related to cavitation phenomena.

Non-linear MHD investigations of high-confinement regimes without type-I ELMs in ASDEX Upgrade and JT-60SA

Large edge localised modes (ELMs) would cause an unacceptable reduction of material lifetime in future large tokamaks due to the significant amount of energy expelled from the magnetically confined region towards the plasma facing components. Thoroughly validated modelling of regimes devoid of large ELMs is crucial as it may then provide predictive insights prior to tokamak operation and design. This paper describes recent efforts pursued with the non-linear extended MHD code JOREK in the modelling of three scenarios without large ELMs: quiescent H-mode (QH-mode), quasi-continuous exhaust regime (QCE regime), and the enhanced D-alpha H-mode (EDA H-mode). For each of these regimes, the non-linear dynamics observed in the simulations are detailed and compared to experimental observations of the underlying instabilities of each regime (edge harmonic oscillation for QH-mode, small ELMs for QCE regime, and quasi-coherent mode for EDA H-mode). For QH-mode, the kink-peeling mode is found to govern the dynamics and a transition to a large ELM is obtained above the same density threshold as in the modelled experiment. For the QCE regime and EDA H-mode, resistive peeling–ballooning modes dominate and pedestal fluctuation frequencies correspond well to experimental observations. The dominant mechanisms for the excitation and suppression of these instabilities are presented and their influence on simulation dynamics is shown. Finally, predictive simulations of edge instabilities at different values of plasma resistivity in a 4.60 MA scenario with low edge safety factor in JT-60SA are presented.

Optical characterizations of densely doped Tm3+:KYW crystals at low temperatures

We investigate the optical lifetime, decay characteristics, spectral linewidth and energy level properties of thulium ions doped in a KY(WO 4 ) 2 crystal at 4 K temperature. High doping concentration of thulium ions with inhomogeneous broadening allow us to study nonradiative behaviors, instantaneous spectral diffusion, and spectral power broadening in this solid-state material. The theoretical consideration of ion–ion interactions is shown to accurately characterize the absorption, decay and other spectral behaviors of Tm 3+ ions. We observe more than ten-fold reduction in the decay time of 3H4 state and about three-fold reduction in the spectral-hole lifetime as we approach the center of the inhomogeneous broadening, corresponding to higher optical densities.

Lifetime Reduction of Single Germanium-Vacancy Centers in Diamond via a Tunable Open Microcavity

Coupling between a single quantum emitter and an optical cavity presents a key capability for future quantum networking applications. Here, we explore interactions between individual germanium-vacancy (GeV) defects in diamond and an open microcavity at cryogenic temperatures. Exploiting the tunability of our microcavity system to characterize and select emitters, we observe a Purcell-effect-induced lifetime reduction of up to 4.5±0.3 and extract coherent-coupling rates up to 360±20 MHz. Our results indicate that the GeV defect has favorable optical properties for cavity coupling, with a quantum efficiency of at least 0.34±0.05 and likely much higher. Published by the American Physical Society 2024

Resonance energy transfer aided detection of nitroaromatics in aqueous medium by a luminescent Mn based metal-organic framework

A light brown needle-like crystal of Mn-based metal–organic framework (MOF); [Mn2.5(µ3-OH)(DTDB)2], (DTDB = 2,2′-dithiodibenzoate), compound 1, was synthesized using hydrothermal technique. Compound 1 was systematically characterized by single-crystal X-ray diffraction (SCXRD), powder X-ray diffraction (PXRD), and infrared spectroscopy (IR). Photoluminescence study of compound 1 in an aqueous medium showed intense blue emission centred at 395 nm upon excitation at 310 nm. This emissive property of compound 1 was utilized for selective and sensitive detection of 2,4,6- trinitrophenol (TNP), 2,4- dinitrophenol (DNP) and 4-nitrophenol (NP) in the aqueous medium through luminescence quenching mechanism. As indicated by the good overlap of the absorption spectra of the analytes and the emission spectrum of the compound 1, and manifested as the reduction in luminescence lifetimes, it can be concluded that the resonance energy transfer is the most significant factor for the selective detection of aromatic nitro-phenol compounds. The resonance energy transfer requires the proximity of the donor and acceptor, which was achieved by the molecular level interactions between the ‘S’ atom of the DTDB ligand and phenolic –OH groups of the nitrophenols through non-covalent type interactions like hydrogen bonding and dipolar type interactions. Detection limits for TNP, DNP, and NP with the values of 208 ppb, 156 ppb, and 556 ppb, respectively, were obtained in an aqueous medium. The studies indicate that compound 1 could be helpful for detecting nitrophenol derivatives in water.

Electronic Transport and Interaction of Lattice Dynamics in Topological Nodalline Semimetal HfAs2 Single Crystals

AbstractTopological semimetals represent a novel class of quantum materials displaying non‐trivial topological states that host Dirac/Weyl fermions. The intersection of Dirac/Weyl points gives rise to essential properties in a wide range of innovative transport phenomena, including extreme magnetoresistance, high mobilities, weak antilocalization, electron hydrodynamics, and various electro‐optical phenomena. In this study, the electronic, transport, phonon scattering, and interrelationships are explored in single crystals of the topological semimetal HfAs2. It reveals a weak antilocalization effect at low temperatures with high carrier density, which is attributed to perfectly compensated topological bulk and surface states. The angle‐resolved photoemission spectroscopy (ARPES) results show anisotropic Fermi surfaces and surface states indicative of the topological semimetal, further confirmed by first‐principle density functional theory (DFT) calculations. Moreover, the lattice dynamics in HfAs2 are investigated both with the Raman scattering and density functional theory. The phonon dispersion, density of states, lattice thermal conductivity, and the phonon lifetimes are computed to support the experimental findings. The softening of phonons, the broadening of Raman modes, and the reduction of phonon lifetimes with temperature suggest the enhancement of phonon anharmonicity in this new topological material, which is crucial for boosting the thermoelectric performance of topological semimetals.

Experimental investigation on enhanced combustion of methanol/heavy fuel oil by droplet puffing at elevated temperatures

To achieve high-efficiency combustion of heavy fuel oil (HFO), this study investigated the combustion characteristics of methanol/HFO droplets with methanol content from 10 to 30% using the suspension method under ambient temperature from 923 to 1023 K. The combustion of methanol/HFO droplets was summarized as a two-phase process consisting of six typical stages, emphasizing liquid phase. Especially, the fluctuation evaporation stage, induced by frequent and intense puffing, was identified as prominent character. Both the ignition delay and lifetime of HFO and methanol/HFO droplets decreased with increasing ambient temperatures. For the methanol/HFO droplet, the ignition delay and droplet lifetime increased with the increasing methanol content. Prominently, compared to HFO, HM10 had the most significant reduction in droplet lifetime and TINL under the same operating conditions, which indicated that the addition of 10% methanol accelerated the combustion process and reduced soot generation. Additionally, the thermos-dynamic characteristics of methanol/HFO droplets were investigated. Puffing was primarily attributed to superheating of methanol and pyrolysis of heavy components in HFO, which resulted in active and passive rupture of bubbles. Similarity and maximum deformation were employed to qualitatively distinguish between them. The obtained findings aimed to develop a promising alternative fuel to reduce emissions and preserve energy.