Vibrational Bands Research Articles

On a Nonlinear Locally Resonant Metamaterial With Resistance-Inductance Shunt

Abstract Numerous recent works have established the potential of various types of metamaterials for simultaneous vibration control and energy harvesting. In this paper, we investigate a weakly nonlinear metamaterial with electromechanical (EM) local resonators coupled to a resistance-inductance shunt circuit, a system with no previous examination in the literature. An analytical solution is developed for the system, using the perturbation method of multiple scales, and validated through direct numerical integration. The resulting linear and nonlinear band structures are used for parametric analysis of the system, focusing on the effect of resonator and shunt circuit parameters on band gap formation and vibration attenuation. This band structure analysis informs further study of the system through wavepacket excitation as well as spectro-spatial analysis. The voltage response of the system is studied through spatial profiles and spectrograms to observe the effects of shunt inductance, nonlinearity, and their interactions. Results describe the impact of adding a shunted inductor, including significant changes to the band structure; multiple methods of tuning band gaps and pass bands of the system; and changes to wave propagation and voltage response. The results demonstrate the flexibility of the proposed metamaterial and its potential for both vibration control and energy harvesting, specifically compared to a previously studied system with resistance-only shunt.

Moiré Pattern Controlled Phonon Polarizer Based on Twisted Graphene.

Twisted van der Waals materials featuring Moiré patterns present new design possibilities and demonstrate unconventional behaviors in electrical, optical, spintronic, and superconducting properties. However, experimental exploration of thermal transport across Moiré patterns has not been as extensive, despite its critical role in nanoelectronics, thermal management, and energy technologies. Here, thefirst experimental study is conducted on thermal transport across twisted graphene, demonstrating a phonon polarizer concept from the rotational misalignment between stacked layers. The direct thermal and acoustic measurements,structural characterizations, and atomistic modeling, reveal a modulation up to 631% in thermal conductance with various Moiré angles, while maintaining a high acoustic transmission. By comparing experiments with density functional theory and molecular dynamics simulations, mode-dependent phonon transmissions are quantified based on the angle alignment of graphene band structures and attributed to the coupling among flexural phonon modes. The agreement confirms the dominant tuning mechanisms in adjusting phonon transmission from high-frequency thermal modes while having negligible effects on low-frequency acoustic modes near Brillouin zone center. This study offers crucial insights into the fundamental thermal transport in Moiré structures, opening avenues for the invention of quantum thermal devices and new design methodologies based on manipulations of vibrational band structures and phonon spectra.

Effect of Iron Ore and Copper Ore Tailings on Engineering Properties and Hydration Products of Sustainable Cement Mortar

Abstract The prohibition of river sand mining has drawn the attention of researchers in finding practicable alternatives. In the approach of finding these alternatives, it is essential to ensure minimal or zero impairment to the ecological balance, which can be mainly attained by making use of industrial waste/byproducts. The wastes from the mining industry are the major contributors in causing impairment to the environment, and their influence on the stability of mortars on using as fine aggregates needs to be systematically investigated with the view of long-term performance concerns. Thus, the present study explores the applicability of mine tailings and finding the optimum dosage in cement mortars by investigating the engineering properties and microstructure development with the aid of qualitative and quantitative analysis associated with hydration products. The studies confirm that the increased consumption of portlandite for secondary hydration reactions followed by the additional formation of calcium silicate hydrate (CSH) and calcium aluminum silicate hydrate (CASH) phases in mine tailing-based mortars helped in achieving a quality microstructure. These additional formations of CSH and CASH phases are also confirmed through Fourier transform infrared spectroscopy by identifying the shift of Si-O-Si stretching vibration bands toward a lower wavenumber. The lowering of calcium/silicate atomic ratio and increased formation of mineralogical compounds related to CSH and CASH in x-ray diffraction patterns also confirms the same. Gismondine, chabazite, and hillebrandite are the additional phases formed and found to take part in refining the pore structure. This enhanced performance of mine tailing mortars was also verified with the aid of a modified Andreasen and Andersen particle packing model. The formation of high-quality microstructure is reflected in the hardened properties of optimized cement mortar in the proportion of 20 % for iron ore tailing and 30 % for copper ore tailing.

Infrared emission of specific polycyclic aromatic hydrocarbon molecules: indene

ABSTRACT Polycyclic aromatic hydrocarbon (PAH) molecules have long been suggested to be present in the interstellar medium (ISM). Nevertheless, despite their expected ubiquity and sustained searching efforts, identifying specific interstellar PAH molecules from their infrared (IR) spectroscopy has so far been unsuccessful. However, due to its unprecedented sensitivity, the advent of the JWST may change this. Meanwhile, recent years have witnessed breakthroughs in detecting specific PAH molecules (e.g. indene, cyanoindene, and cyanonaphthalene) through their rotational lines in the radio frequencies. As JWST holds great promise for identifying specific PAH molecules in the ISM based on their vibrational spectra in the IR, in this work, we model the vibrational excitation of indene, a molecule composed of a six-membered benzene ring fused with a five-membered cyclopentene ring, and calculate its IR emission spectra for a number of representative astrophysical regions. This will facilitate JWST to search for and identify indene in space through its vibrational bands and to quantitatively determine or place an upper limit on its abundance.

Metro Monolithic Track Bed Vibration Characterization

With the rapid development of cities, metro transportation has also developed rapidly to solve the congestion problems caused by urban development. However, with the continuous development of metro transportation, the vibration problems caused by it have become increasingly obvious. Based on the phonon crystal theory, this paper investigates the vibration characteristics of the metro track structure. It analyzes the influence of the track structure parameters on the band gap characteristics to regulate the metro vibration band gap range. To study the band gap characteristics of metro monolithic bed track structure, establish the double-layer Euler beam model and use the plane wave expansion method (PWE) to calculate its energy band structure; use the finite element method (FEM) to calculate to get its band structure, frequency response function, and time domain analysis. The calculation of PWE shows that there is a band gap in the range of 0–300[Formula: see text]Hz for the metro monolithic track bed, which is 0–194.5[Formula: see text]Hz; the calculation of FEM shows that the range of band gap is 0–193.7[Formula: see text]Hz. Fastening spacing, stiffness, and sub-slab support stiffness will have an impact on the band gap, so appropriate fastening and spacing need to be selected for effective vibration damping of the track structure. The results show that the band gap characteristics of the metro monolithic track bed can be calculated effectively and accurately by using the phononic crystal theory.

Rovibrational Energies of 13C16O2 Determined with Kilohertz Accuracy.

Accurate spectroscopic data of carbon dioxide are widely used in many important applications, such as carbon monitoring missions. Here, we present comb-locked cavity ring-down saturation spectroscopy of the second most abundant isotopologue of CO2, 13C16O2. We determined the positions of 88 lines in three vibrational bands in the 1.6 μm region, 30011e/30012e/30013e-00001e, with an accuracy of a few kHz. Based on the analysis of combination differences, we obtained for the first time the ground-state rotational energies with kHz accuracy. We also provide a set of hybrid line positions for 150 13C16O2 transitions. The rotational energies (J < 50) in the 30013e vibrational state can be fitted by a set of rotational and centrifugal constants with deviations within a few kHz, indicating that the 30013e state is free of perturbations. These precise isotopic line positions will be utilized to improve the Hamiltonian model and quantitative remote sensing of carbon dioxide. Moreover, they will help to track changes in the carbon source and sink through isotopic analysis.

Heavy Ion Radiolysis of the Chiral Terpene α-pinene

ABSTRACT Radiolysis of α-pinene by 61.3 MeV 84Kr15 + ions was analysed with the scope to simulate the effects of heavy ion cosmic ray bombardment on chiral molecules in the interstellar medium. The α-pinene ice samples were irradiated at 10 K and their chemical evolution was monitored by mid-infrared Fourier transform (FTIR) spectroscopy to characterize the reaction products and to determine the extent of racemization. The integrated band strengths have been obtained for all the neutral α-pinene vibrational bands using the experimental band integrated absorbances and the theoretical absolute intensities calculated along the column densities. In the current heavy ion bombardment experiments, small molecules were formed and the precursor, α-pinene, was destroyed instead of being racemized. Twelve hydrocarbons were produced (final fluence of 2.0 × 1012 ions cm−2): methane (CH4), acetylene (C2H2), ethylene (C2H4), propylene (C3H6), propane (C3H8), n-butane (C4H10), butene (C4H8), propyne (C3H4), benzene (C6H6), ethane (C2H6), vinylacetylene (C4H4), and 2-methyl-1,3-butadiene or isoprene (C5H8). The highest formation cross-section (∼ 40 × 10−15 cm2) was observed for the C3H4 and the lowest was for C3H8 (∼ 3 × 10−15 cm2). The radiochemical yields for these molecules follow the same trends as those of their cross-sections. The atom budget calculation confirms that all the expected products have been generated during the radiolysis and supports the conclusion that the proposed A values are accurate. The α-pinene sputtering yield for this ion beam was found to be Y0 = 1.84 × 106 molecules per impact.

Two-photon excitation two-dimensional fluorescence spectroscopy (2PE-2DFS) of the fluorescent nucleobase 6-MI.

Base stacking is fundamentally important to the stability of double-stranded DNA. However, few experiments can directly probe the local conformations and conformational fluctuations of the DNA bases. Here we report a new spectroscopic approach to study the local conformations of DNA bases using the UV-absorbing fluorescent guanine analogue, 6-methyl isoxanthopterin (6-MI), which can be used as a site-specific probe to label DNA. In these experiments, we apply a two-photon excitation (2PE) approach to two-dimensional fluorescence spectroscopy (2DFS), which is a fluorescence-detected nonlinear Fourier transform spectroscopy. In 2DFS, a repeating sequence of four collinear laser pulses (with center wavelength ~ 675 nm and relative phases swept at radio frequencies) is used to excite the lowest energy electronic-vibrational (vibronic) transitions of 6-MI (with center wavelength ~ 340 nm). The ensuing low flux fluorescence is phase-synchronously detected at the level of individual photons and as a function of inter-pulse delay. The 2PE transition pathways that give rise to electronically excited state populations include optical coherences between electronic ground and excited states and non-resonant (one-photon-excited) virtual states. Our results indicate that 2PE-2DFS experiments can provide information about the electronic-vibrational spectrum of the 6-MI monomer, in addition to the conformation-dependent exciton coupling between adjacent 6-MI monomers within a (6-MI)2 dimer. In principle, this approach can be used to determine the local base-stacking conformations of (6-MI)2 dimer-substituted DNA constructs.

Exploring the non-covalent interactions, vibrational and electronic properties of 2-methyl-4-hydro-1,3,4-triazol-thione-5 in different solutions

In this study, the optimal geometry and vibrational assignments of 2-methyl-4-hydro-1,3,4-triazol-thione-5, one of the triazole derivatives, were analysed by the DFT approach and vibrational spectroscopy. PED values were calculated, and vibrational assignments were determined. Experimental results showed that interactions between 2-methyl-4-hydro-1,3,4-triazol-thione-5 and solvent (acetone, acetonitrile, dioxane, and DMF) molecules lead to a red shift of the N-H stretching vibrational band. The computations were performed at the B3LYP/6-311++G(d,p) functional set. The molecular electrostatic potential surface was used to distinguish between electrophilic and nucleophilic regions. The reactivity of the molecular complexes was determined by examining their frontier molecular orbitals. Topological investigations revealed the existence of N-H…N and N-H…O-type hydrogen bonds between 2-methyl-4-hydro-1,3,4-triazole-thiol-5 and solvent molecules. The red-shift of the N-H stretching band and H-bond strength between solute–solvent molecules are in the order of acetonitrile, acetone, dioxane, and DMF.

A sustainable bioprocess to produce bacterial cellulose (BC) using waste streams from wine distilleries and the biodiesel industry: evaluation of BC for adsorption of phenolic compounds, dyes and metals

BackgroundThe main challenge for large-scale production of bacterial cellulose (BC) includes high production costs interlinked with raw materials, and low production rates. The valorization of renewable nutrient sources could improve the economic effectiveness of BC fermentation while their direct bioconversion into sustainable biopolymers addresses environmental pollution and/or resource depletion challenges. Herein a green bioprocess was developed to produce BC in high amounts with the rather unexplored bacterial strain Komagataeibacter rhaeticus, using waste streams such as wine distillery effluents (WDE) and biodiesel-derived glycerol. Also, BC was evaluated as a bio-adsorbent for phenolics, dyes and metals removal to enlarge its market diversification.ResultsBC production was significantly affected by the WDE mixing ratio (0–100%), glycerol concentration (20–45 g/L), type of glycerol and media-sterilization method. A maximum BC concentration of 9.0 g/L, with a productivity of 0.90 g/L/day and a water holding capacity of 60.1 g water/g dry BC, was achieved at 100% WDE and ≈30 g/L crude glycerol. BC samples showed typical cellulose vibration bands and average fiber diameters between 37.2 and 89.6 nm. The BC capacity to dephenolize WDE and adsorb phenolics during fermentation reached respectively, up to 50.7% and 26.96 mg gallic acid equivalents/g dry BC (in-situ process). The produced BC was also investigated for dye and metal removal. The highest removal of dye acid yellow 17 (54.3%) was recorded when 5% of BC was applied as the bio-adsorbent. Experiments performed in a multi-metal synthetic wastewater showed that BC could remove up to 96% of Zn and 97% of Cd.ConclusionsThis work demonstrated a low-carbon approach to produce low-cost, green and biodegradable BC-based bio-adsorbents, without any chemical modification. Their potential in wastewater-treatment-applications was highlighted, promoting closed-loop systems within the circular economy era. This study may serve as an orientation for future research towards competitive or targeted adsorption technologies for wastewater treatment or resources recovery.

Coordination complexes of reduced organic dye isoviolanthrone with transition metals and lanthanides [Mn(II), Dy(III), Gd(III), Nd(III)

The reduction of a vat dye isoviolanthrone to the dianion state in the presence of metal-containing compounds yields binuclear coordination complexes. Two manganese(II) acetylacetonate units coordinate to isoviolanthrone2− (L) in {(K+)cryptand}2{[MnII(acac)2]2⋅L}2– (1) with an average Mn–O bond length of 2.022(2) Å. Dysprosium(III)- or gadolinium(III)-2,2,6,6-tetramethyl-3,5-heptanedionate (TMHD) units form {(K+)cryptand}2{[MIII(TMHD)3]2⋅L}2− (M = DyIII for 2 and GdIII for 3) with the length of the M−O bonds of 2.193(3) and 2.254(4) Å, respectively. Tris(cyclopentadienyl)neodymium(III) forms {(Cs+)cryptand}2{[Cp3NdIII]2⋅L}2–⋅C6H4Cl2 (4) with the Nd–O bonds of 2.264(2) and 2.308(2) Å length. The formation of isoviolanthrone2− is supported by their optical spectra, disappearance of the bands of the CO vibrations in the IR-spectra as well as elongation of the CO bonds in 1–4. High-spin (S = 5/2) MnII atoms in 1 have exchange interaction of J = − 0.122 cm−1 at g = 1.98. Lanthanides have weaker coupling through isoviolanthrone2− in 2 and 3 with J = − 0.029 and D = − 0.004 cm−1 for DyIII and J = 0.0019 cm−1 for GdIII. Complex 4 with two Cp3NdIII species demonstrates the χMT value of 2.33 emu⋅K/mol at 300 K, and this value is lower than the theoretically calculated value of 3.39 emu⋅K/mol. The decrease of χMT is observed in the whole 300–1.9 K range providing negative Weiss temperatures of –32 K. That is explained by magnetic behavior of Cp3NdIII similar to pristine Cp3NdIII. Complexes comprising MnII, GdIII, and NdIII show electron paramagnetic resonance (EPR) signals. Zero-field splitting (ZFS) is observed from MnII and GdIII allowing the estimation of zero-field splitting parameter D as − 0.047 and E close to 0 cm−1 for 1 and − 0.033 and − 0.020 cm−1 for 3. Complex 4 with NdIII manifests an asymmetric two-component EPR signal without ZFS. Weak antiferromagnetic couplings are explained by diamagnetism of isoviolanthrone2− and rather long distances between the metal centers of 15.47–16.25 Å. This study shows that the dianions of organic dyes are promising bidentate ligands for preparation of coordination complexes with d- and f-block metal ions.

Optimizing geometry and metal-dependent performance of Si-based Schottky plasmonic photodetectors

In this study, different Schottky photodetectors with a plasmonic assist which receives Near-infrared (NIR) light at room temperature were demonstrated. We achieved remarkable detection over a wide range of wavelengths through a comparative study of Schottky plasmonic photodetectors employing Au, Ti, Mo, and Cr as a Schottky metal, a diffusion barrier, an adhesion promoter, and to suppress the formation of intermetallic compounds and plasmonic resonance shifts. The device structure is determined by extensive experimental and modeling results, ensuring a wavelength-specific plasmonic photodetection and a near one-to-one correspondence between incident angles and wavelengths within the NIR region. The combination of different metals in the plasmonic structure efficiently broadened the SPR response, due to the variation of junction barrier height and enhanced interface properties. It exhibited exceptional photocurrent response under room temperature and zero biasing conditions, characterized by high linearity and sensitivity. Light acquisition for longer NIR wavelengths became possible, and applicable in gas sensing, particularly within the vibrational absorption bands of alkane groups. These findings provide valuable design guidelines for optimizing device structures and insights into their application for various scenarios.

Ion core switching during photodissociation dynamics via the Rydberg states of XeAr

The heterodimer, XeAr, is a classic example of a weakly bound van der Waals molecule, which has a variety of accessible bound excited states that exhibit complex interactions. In this study, XeAr has been investigated in the 77,500–81,500 cm−1 region using a combination of Resonance Enhanced Multi-Photon Ionization (REMPI) spectroscopy and Velocity Map Imaging (VMI). By monitoring REMPI and photodissociative product channels across the spectrum, several novel excited states, product channels, excited state symmetries and lifetimes, as well as highly localized perturbations were observed and characterized, including the first VMI study of Ar* dissociating from XeAr Rydberg states accessed by two-photon excitation. In this work we have analyzed 38 vibronic bands representing nine different electronic transitions, and we provide new assignments for two 0+←0+ electronic transitions dissociating to the Xe* 5d [3/2]02 (ca. 80,323 cm−1) and Xe* 5d [7/2]03 (ca. 80,970 cm−1) limits. Several new predissociation product channels were identified at the two- and three-photon levels, including production of Xe* 5p[5/2]3, Xe* 6s'[1/2]o1, Xe* 6p[1/2]1, Ar* 4p[1/2]0, Ar* 4p'[3/2]1, Ar* 4p'[1/2]1, and Ar* 4p[5/2]3. Using the multidimensional analysis offered by VMI, we explore interesting photophysics whereby a resonant state that is reached after absorbing two photons can predissociate to yield Xe*, but which also can absorb a 3rd photon, yielding super-excited Ar*Xe that predissociates to Ar* limits. The ground state dissociation energy for XeAr was determined to be D0 = 114.4 ± 2.7 cm−1, in excellent agreement with previous measurements.

Dipolar Coupling as a Mechanism for Fine Control of Magnetic States in ErCOT-Alkyl Molecular Magnets.

The design of molecular magnets has progressed greatly by taking advantage of the ability to impart successive perturbations and control vibronic transitions in 4fn systems through the careful manipulation of the crystal field. Herein, we control the orientation and rigidity of two dinuclear ErCOT-based molecular magnets: the inversion-symmetric bridged [ErCOT(μ-Me)(THF)]2 (2) and the nearly linear Li[(ErCOT)2(μ-Me)3] (3). The conserved anisotropy of the ErCOT synthetic unit facilitates the direction of the arrangement of its magnetic anisotropy for the purposes of generating controlled internal magnetic fields, improving control of the energetics and transition probabilities of the electronic angular momentum states with exchange biasing via dipolar coupling. This control is evidenced through the introduction of a second thermal barrier to relaxation operant at low temperatures that is twice as large in 3 as in 2. This barrier acts to suppress through-barrier relaxation by protecting the ground state from interacting with stray local fields while operating at an energy scale an order of magnitude smaller than the crystal field term. These properties are highlighted when contrasted against the mononuclear structure ErCOT(Bn)(THF)2 (1), in which quantum tunneling of the magnetization processes dominate, as demonstrated by magnetometry and ab initio computational methods. Furthermore, far-infrared magnetospectroscopy measurements reveal that the increased rigidity imparted by successive removal of solvent ligands when adding bridging methyl groups, along with the increased excited state purity, severely limits local spin-vibrational interactions that facilitate magnetic relaxation, manifesting as longer relaxation times in 3 relative to those in 2 as temperature is increased.

Blasting Vibration Control and Signal Analysis of Adjacent Existing Deterioration Tunnels

Building a new tunnel adjacent to an existing tunnel has become a common means of transformation in engineering. Existing tunnels are prone to some deterioration, such as cavities and cracks under long-term traffic load. This kind of deterioration tunnel is prone to collapsing under the action of blasting. Therefore, the vibration caused by blasting should be strictly controlled. Based on the reconstruction project of the Bo Jiling Tunnel, this paper puts forward the method of mechanical cutting in a central position combined with an ordinary detonator to reduce blasting vibrations. ANSYS/LS-DYNA version 19.2, was used to simulate two conditions of full-section blasting and central mechanical cutting blasting. By comparing the stress and velocity of the existing tunnel, the damping effect of mechanical cutting blasting is analyzed. Via field experiments, the superiority of the mechanical cutting method in reducing blasting vibration is further discussed. At the same time, the relationship between the main vibration frequency and the peak velocity of the existing deterioration tunnel is obtained by wavelet packet analysis of the field experimental data. The frequency band energy distribution in each direction of vibration velocity is also obtained. The results show that the central mechanical cutting increases the blasting free surface, and the mechanical cutting method reduces the vibration velocity by 36.3%. The third frequency band (31.25~46.875 Hz) is the most concentrated, which is the dominant frequency band of the signal. The novelty of this paper is to propose mechanical cutting of the central hole instead of traditional blasting for existing deterioration tunnels. The feasibility of this method is verified by numerical simulation and field tests. The relationship between peak vibration velocity, band energy, and tunnel frequency is clarified, which can better control blasting vibration and ensure the safety of existing deterioration tunnels.

Optical spectroscopy of comets using Hanle Echelle Spectrograph (HESP)

ABSTRACT Observing the vibrational/rotational lines in a comet’s optical spectrum requires high-resolution spectroscopy, as they are otherwise seen as a blended feature. To achieve this, we have obtained medium and high-resolution (R (λ/Δλ) = 30 000 and 60 000) spectra of several comets, including C/2015 V2 (Johnson), 46P/Wirtanen, 41P/Tuttle–Giacobini–Kresák, and 38P/Stephan–Oterma, using the Hanle Echelle Spectrograph (HESP) mounted on the 2-m Himalayan Chandra Telescope (HCT) in India. The spectra effectively cover the wavelength range 3700–10 000 Å, allowing us to probe the various vibrational bands and band sequences to identify the rotational lines in the cometary molecular emission. We were also able to separate the cometary Oxygen lines from the telluric lines and analyse the green-to-red (G/R) forbidden oxygen [O i] ratios in a few comets. For comets C/2015 V2, 46P, and 41P, the computed G/R ratios, 0.04 ± 0.01, 0.04 ± 0.01, and 0.08 ± 0.02, respectively, point to H2O being a major source of Oxygen emissions. Notably, in the second fibre pointing at a location 1000 km away from the photocentre of comet 46P, the G/R ratio reduced by more than half the value observed in the first fibre, indicating the effects of quenching within the inner coma. We also measured the NH2 ortho-to-para ratio of comet 46P to be about 3.41 ± 0.05 and derived an ammonia ratio of 1.21 ± 0.03 corresponding to a spin temperature of ∼26 K. With these, we present the results of the study of four comets from different cometary reservoirs using medium and high-resolution optical spectroscopy, emphasizing the capabilities of the instrument for future cometary studies.

Optical and electrical properties of Al-doped ZnO thin films deposited by sol-gel method

The multilayer (10 layers) Al doped ZnO (AZO) thin films were deposited on glass substrate by sol-gel &amp; dipping method. X-Ray diffraction measurements showed that the AZO films were polycrystalline with a hexagonal wurtzite structure. The morphological properties of the films were analyzed by atomic force microscopy showing continuous and homogeneous film, completely covering the substrates. The thickness, optical constants, optical band gap (Eg) and transmittance (T) of AZO films were assessed by spectroscopic ellipsometry on UV-vis-NIR spectral range. The AZO film has high transmittance above 80% in the visible region and the optical band-gap energy around 3.7 eV. The electrical characteristics regarding conductivity, mobility and carrier concentrations, were measured by Hall Effect measurements (van der Pauw method). The bulk carrier concentration of the AZO film with 10 layers was found to be 1.16x1019 cm-3. The vibrational bands were obtained by Raman analysis. Defects due to oxygen vacancies in the prepared AZO films were evidenced by photoluminescence spectroscopy (PL). The optical and electrical properties of the AZO thin films proved the possibility to be used in optoelectronic applications.

Low-frequency broadband vibration reduction based on a square spiral beam local resonance phononic crystal

Low-frequency vibration poses a great danger to both industrial production and human health. Therefore, the development of efficient low-frequency vibration reduction structures remains a focus of academic and engineering research. In this paper, a novel low-frequency vibration reduction local resonance phononic crystal (LRPnC) plate with a square spiral beam LRPnC design is proposed. Through finite element simulation, the band structure and vibration characteristics of the LRPnC are first analyzed. On this basis, a gradient LRPnC plate with rainbow trapping effect is constructed by gradient arranging unit cells with different structural parameters to achieve broadband vibration reduction. Finally, the vibration reduction performance of the designed structure is experimentally verified. The finite element analysis results show that the designed gradient LRPnC plate can provide more than 20 dB of transmission attenuation over the full frequency range of 20–200 Hz. And the experimental results are consistent with the simulation results.

Vibrational spectroscopy of aniline cations and their H-loss cations in helium droplets

We produced aniline cations (c–C6H5NH2+) and their dehydro- (H-loss) cations inside helium droplets by electron ionization and observed their mass-selected vibrational spectra in the NH stretching region. We observed vibrational bands at m/q = 93 which were identified as aniline cations. These bands showed only a few cm−1 shifts from the symmetric and anti-symmetric NH stretching bands for the amino (NH2) group in the gas phase. For the H-loss cation at mass m/q = 92, the agreement of the observed NH band frequency with the result of DFT calculations suggests several candidate species, including a seven-membered ring structure, 4-monodehydro azepinylium (c–C6NH6+). A new reaction pathway to this cation was discussed by considering large excess energy in the ionization process.

Effect of interlayer cations on the adsorption of ionic liquid on montmorillonite clays: comparative study

Industries are the most important resource of water pollution due as a result of toxic pollutants including surfactant or ionic liquids. It becomes urgent to propose low cost and environmentally friendly involving the use of local resources. Here,one of the main ionic liquids (BMImCl) were intercalated into three alkaline-earth, Mg2+, Ca2+, and Ba2+ exchanged montmorillonites. For all samples interlayer spacing after intercalation are similar about 13 Å as measured by X-ray diffraction. These findings are compared with previous results on similar montmorillonite exchanged with every type of alkali cations, i.e. Li+, Na+, K+, Rb+, and Cs+. The basal spacing of intercalated montmorillonite increased as the ionic potential (Z/R) is increased. The FTIR is another tool to confirm the differences between modified and unmodified montmorillonite samples. More specifically, the results showed that the formation of new bands of vibrations (1400–1500 cm-1) and (2850–2900 cm-1).Thermal measurements indicate that homoionic clay display two distinct regions. ‎(I) from room temperature to 160 0C corresponding to physical adsorption and removal of water of hydration, (II) dehydroxylation of the silicate structure in the temperature range of 160-700 0C.