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Ultra-small two dimensional MXene nanosheets for selective and sensitive fluorescence detection of Ag+ and Mn2+ ions
摘要： The present work offers a new exploration for the selective sensing of metal ions (Ag+ and Mn2+) via fluorescence quenching of Ti3C2 MXene nanosheets (NSs). Monolayer MXene Ti3C2 NSs exhibited excellent ability to sense Ag+ and Mn2+ ions because of their good hydrophilicity and distinctive surface functionality. The as-synthesised Ti3C2 NSs exhibited highest emission fluorescence peak at 461 nm upon the excitation wavelength of 384 nm. The fluorescence emission peak of Ti3C2 NSs was remarkably quenched only upon the addition of Ag+ and Mn2+ ions, exhibiting good linear response between I0/I and concentration in the range of 0.1–40 μM and 0.5–60 μM for Ag+ and Mn2+ ions. The proposed sensor shows lower detection limits of 9.7 and 102 nM for Ag+ and Mn2+ ions with good selectivity. Additionally, the method is effectively applied to detect Ag+ and Mn2+ ions in food and real water samples with excellent recoveries.
关键词： FT-IR,MXene nanosheets,Florescence and UV–vis spectroscopic techniques,Ag+ and Mn2+ ions
更新于2025-09-23 15:23:52
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Detecting Water in the Atmosphere of HR 8799 c with <i>L</i> -band High-dispersion Spectroscopy Aided by Adaptive Optics
摘要： High-dispersion spectroscopy of brown dwarfs and exoplanets enables exciting science cases, e.g., mapping surface inhomogeneity and measuring spin rate. Here, we present L-band observations of HR 8799 c using Keck NIRSPEC (R = 15,000) in adaptive optics (AO) mode (NIRSPAO). We search for molecular species (H2O and CH4) in the atmosphere of HR 8799 c with a template-matching method, which involves cross-correlation between reduced spectra and a template spectrum. We detect H2O but not CH4, which suggests disequilibrium chemistry in the atmosphere of HR 8799 c, and this is consistent with previous findings. We conduct planet signal injection simulations to estimate the sensitivity of our AO-aided high-dispersion spectroscopy observations. We conclude that 10?4 contrast can be reached in the L band. The sensitivity is mainly limited by the accuracy of line list used in modeling spectra and detector noise. The latter will be alleviated by the NIRSPEC upgrade.
关键词： planets and satellites: atmospheres,planetary systems,methods: observational,planets and satellites: composition,techniques: spectroscopic,techniques: high angular resolution
更新于2025-09-23 15:21:21
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Spectroscopic Studies of M??ssbauer, Infrared, and Laser-Induced Luminescence for Classifying Rare-Earth Minerals Enriched in Iron-Rich Deposits
摘要： Rare-earth (RE) phosphates often appear as an accessory phase in igneous or metamorphic rocks; however, these rocks are composed of myriad chemical elements and nuclides that interfere with the qualitative or quantitative analyses of the RE phosphates over a range of concentrations in the absence of a pretreatment. In addition, the limit of each analytical methodology constrains the approach as well as the usefulness of the results in geoscience applications. Here, we report the specific mineral characterization of RE-containing ores from Yen Phu mine, Vietnam, using a range of state-of-the-art spectroscopic techniques in conjunction with microscopy: M?ssbauer spectroscopy, infrared microspectroscopy, time-resolved laser-induced fluorescence spectroscopy (TRLFS), and scanning electron microscopy with energy-dispersive X-ray spectroscopy. Because the distribution of each element in the deposit differs, such combinatorial works are necessary and could lead to more plausible answers to questions surrounding the point of origin of RE elements. The results of our M?ssbauer spectroscopic analysis indicate that the three ores sampled at different locations all contain magnetite-like, hematite-like, and iron(III) salts other than hematite. In addition, we confirmed the presence of phosphate around the grain boundary in the magnetite-like mineral phase by infrared microspectroscopic analysis. The present analytical findings of trace amounts of europium(III) using TRLFS suggest that the europium ions generate identical luminescence spectra despite being embedded in three different matrices of iron minerals. This demonstration highlights the benefits of combinatorial spectroscopic analyses to gain insights into the effects of the environment of REs on their solid-state chemistry and shows the potential utility of TRLFS as a resource mining tool. Further applications of this approach in the analytical screening of rocks and minerals are feasible.
关键词： energy-dispersive X-ray spectroscopy,spectroscopic techniques,rare-earth phosphates,Yen Phu mine,infrared microspectroscopy,scanning electron microscopy,time-resolved laser-induced fluorescence spectroscopy,M?ssbauer spectroscopy,Vietnam
更新于2025-09-23 15:21:01
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Understanding the Microscopic Behavior of Binary Mixtures of Ionic Liquids Through Various Spectroscopic Techniques
摘要： In recent times it has been shown that certain binary mixture of pure ionic liquids having appropriate chemical composition can behave like a new chemical entity. However, current knowledge about the microscopic behavior of these interesting systems is rather limited. The present study is undertaken with an objective to understand the microscopic behavior in terms of intermolecular interaction, structure and dynamics of these systems. In the present study, few (IL+IL) mixtures are chosen with a common cation and a variation of anion. The investigations are also carried out by taking individual pure ILs so that the difference in behavior between pure IL and (IL+IL) mixtures are understood. Initially the systems have been investigated by studying the thermophysical properties of the concerned mixtures. Synergistic effect between combining pure ILs through photochromism has also been studied. These mixtures have been investigated further through steady state and time resolved fluorescence spectroscopy, electron paramagnetic resonance (EPR), nuclear magnetic resonance (NMR) and fluorescence correlation spectroscopy (FCS). Interestingly, time-resolved fluorescence data also pointed out that (IL+IL) mixtures are not only spatially heterogeneous but they are dynamically heterogeneous too. EPR measurements have suggested that the micro-polarity (ET(30)) of (IL+IL) mixture is close to aliphatic polyalcohol. Measurements of translational diffusion coefficients of the diffusing species through NMR and FCS studies have provided idea about the nano-structural organization within (IL+IL) binary mixtures. The analysis of data essentially reveals that the mixtures of ILs that are used in the current study do not behave like a non-ideal solution. The behavior of the IL mixtures is observed to be more like quasi-ideal type.
关键词： thermophysical properties,binary mixtures,EPR,FCS,fluorescence spectroscopy,NMR,Ionic liquids,photochromism,spectroscopic techniques
更新于2025-09-23 15:21:01
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Application of Spectroscopic UV-Vis and FT-IR Screening Techniques Coupled with Multivariate Statistical Analysis for Red Wine Authentication: Varietal and Vintage Year Discrimination
摘要： One of the most important issues in the wine sector and prevention of adulterations of wines are discrimination of grape varieties, geographical origin of wine, and year of vintage. In this experimental research study, UV-Vis and FT-IR spectroscopic screening analytical approaches together with chemometric pattern recognition techniques were applied and compared in addressing two wine authentication problems: discrimination of (i) varietal and (ii) year of vintage of red wines produced in the same oenological region. UV-Vis and FT-IR spectra of red wines were registered for all the samples and the principal features related to chemical composition of the samples were identi?ed. Furthermore, for the discrimination and classi?cation of red wines a multivariate data analysis was developed. Spectral UV-Vis and FT-IR data were reduced to a small number of principal components (PCs) using principal component analysis (PCA) and then partial least squares discriminant analysis (PLS-DA) and linear discriminant analysis (LDA) were performed in order to develop qualitative classi?cation and regression models. The ?rst three PCs used to build the models explained 89% of the total variance in the case of UV-Vis data and 98% of the total variance for FR-IR data. PLS-DA results show that acceptable linear regression ?ts were observed for the varietal classi?cation of wines based on FT-IR data. According to the obtained LDA classi?cation rates, it can be a?rmed that UV-Vis spectroscopy works better than FT-IR spectroscopy for the discrimination of red wines according to the grape variety, while classi?cation of wines according to year of vintage was better for the LDA based FT-IR data model. A clear discrimination of aged wines (over six years) was observed. The proposed methodologies can be used as accessible tools for the wine identity assurance without the need for costly and laborious chemical analysis, which makes them more accessible to many laboratories.
关键词： chemometrics,FT-IR,wine authentication,spectroscopic techniques,UV-Vis
更新于2025-09-11 14:15:04
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Effects of Varying the Benzannulation Site and π Conjugation of the Cyclometalating Ligand on the Photophysics and Reverse Saturable Absorption of Monocationic Iridium(III) Complexes
摘要： A series of monocationic iridium(III) complexes, [Ir(C^N)2(pqu)]+PF6? [pqu = 2-(pyridin-2-yl)quinoline, C^N = 2-phenylquinoline (1), 3-phenylisoquinoline (2), 1-phenylisoquinoline (3), benzo[h]quinoline (4), 2-(pyridin-2-yl)naphthalene (5), 1-(pyridin-2-yl)naphthalene (6), 2-(phenanthren-9-yl)pyridine (7), 2-phenylbenzo[g]quinoline (8), 2-(naphthalen-2-yl)quinoline (9), and 2-(naphthalen-2-yl)benzo[g]quinoline (10)], were synthesized in this work. These complexes bear C^N ligands with varied degrees of π conjugation and sites of benzannulation, allowing for elucidation of the effects of the benzannulation site at the C^N ligand on the photophysics of the complexes. Ultraviolet?visible (UV?vis) absorption and emission of the complexes were systematically investigated via spectroscopic techniques and time-dependent density functional theory calculations. Their triplet excited-state absorption and reverse saturable absorption (RSA) were studied by nanosecond transient absorption (TA) spectroscopy and nonlinear transmission techniques. The fusion of phenyl ring(s) to the phenyl ring or the 4 and 5 positions of the pyridyl ring of the C^N ligand resulted in red-shifted UV?vis absorption and emission spectra in complexes 2, 5?7, 9, and 10 compared to those of the parent complex 0, while their triplet lifetimes and emission quantum yields were significantly reduced. In contrast, the fusion of one phenyl ring to the other sites of the pyridyl group of the C^N ligand showed an insignificant impact on the energies of the lowest singlet (S1) and triplet (T1) excited states in complexes 1, 3, and 4 but noticeably affected their TA spectral features. The fusion of the naphthyl group to the 5 and 6 and positions at the pyridyl ring did not influence the S1 energy of complex 8 but altered the nature of the T1 states in 8 and 10 by switching them to the benzo[g]quinoline-localized 3π,π* state, which resulted in completely different emission and TA spectra in these two complexes. The site-dependent variations of the ground- and excited-state absorption induced strong but varied RSA from these complexes for 4.1-ns laser pulses at 532 nm, with the RSA strength decreasing in the trend of 3 > 7 ≈ 4 ≈ 9 ≈ 6 > 8 ≈ 1 ≈ 2 ≈ 5 > 10.
关键词： iridium(III) complexes,time-dependent density functional theory,spectroscopic techniques,photophysics,reverse saturable absorption,benzannulation
更新于2025-09-04 15:30:14