The exponentiated generalized power Lindley distribution: Properties and applications

In this paper, we introduce a new extension of the power Lindley distribution, called the exponentiated generalized power Lindley distribution. Several mathematical properties of the new model such as the shapes of the density and hazard rate functions, the quantile function, moments, mean deviations, Bonferroni and Lorenz curves and order statistics are derived.Moreover, we discuss the parameter estimation of the new distribution using the maximum likelihood and diagonally weighted least squares methods. A simulation study is performed to evaluate the estimators. We use two real data sets to illustrate the applicability of the new model. Empirical findings show that the proposed model provides better fits than some other well-known extensions of Lindley distributions.     

SMFs-supported Pd nanocatalysts in selective acetylene hydrogenation:Pore structure-dependent deactivation mechanism

In the present study,CNFs,ZnO and Al2O3 were deposited on the SMFs panels to investigate the deactivation mechanism of Pd-based catalysts in selective acetylene hydrogenation reaction.The examined supports were characterized by SEM,NH3-TPD and N2adsorption-desorption isotherms to indicate their intrinsic characteristics.Furthermore,in order to understand the mechanism of deactivation,the resulted green oil was characterized using FTIR and SIM DIS.FTIR results confirmed the presence of more unsaturated constituents and then,more branched hydrocarbons formed upon the reaction over alumina-supported catalyst in comparison with the ones supported on CNFs and ZnO,which in turn,could block the pores mouths.Besides the limited hydrogen transfer,N2 adsorption-desorption isotherms results supported that the lowest pore diameters of Al2O3/SMFs close to the surface led to fast deactivation,compared with the other catalysts,especially at higher temperatures.     

SMFs-supported Pd nanocatalysts in selective acetylene hydrogenation: Pore structure-dependent deactivation mechanism

In the present study, CNFs, ZnO and Al₂O₃ were deposited on the SMFs panels to investigate the deactivation mechanism of Pd-based catalysts in selective acetylene hydrogenation reaction. The examined supports were characterized by SEM, NH₃-TPD and N₂ adsorption-desorption isotherms to indicate their intrinsic characteristics. Furthermore, in order to understand the mechanism of deactivation, the resulted green oil was characterized using FTIR and SIM DIS. FTIR results confirmed the presence of more unsaturated constituents and then, more branched hydrocarbons formed upon the reaction over alumina-supported catalyst in comparison with the ones supported on CNFs and ZnO, which in turn, could block the pores mouths. Besides the limited hydrogen transfer, N₂ adsorption-desorption isotherms results supported that the lowest pore diameters of Al₂O₃/SMFs close to the surface led to fast deactivation, compared with the other catalysts, especially at higher temperatures.     

White CsPbBr3: Characterizing the One-Dimensional Cesium Lead Bromide Polymorph

Inorganic lead halide perovskites have gained immense scientific interest for optoelectronic applications. In this work, we present a one-dimensional polymorph of cesium lead bromide (δ-CsPbBr₃) synthesized through a simple anion-exchange reaction, wherein distorted edge-sharing PbBr₆ octahedra form 1D chains isolated by Cs ions. δ-CsPbBr₃ was characterized by Raman spectroscopy, X-ray diffraction, ²⁰⁷Pb and ¹³³Cs solid-state NMR, and by optical emission and absorption spectroscopies. This non-perovskite material irreversibly transforms into the well-known three-dimensional perovskite phase (γ-CsPbBr₃) upon heating to above 151 °C. The indirect bandgap was determined by absorption measurements and calculation to be 2.9 eV. δ-CsPbBr₃ exhibits broadband yellow photoluminescence with a quantum yield of 3.2 %±0.2 % at room temperature and 95 %±5 % at 77 K, and this emission is attributed to the recombination of self-trapped excitons. This study emphasizes that the metastable δ-CsPbBr₃ may be a persistent, concomitant phase in Cs−Pb-Br-containing materials systems, such as those used in solar cells and LEDs, and it showcases the characterization tools used for its detection.     

Role of propagating slit mode in enhanced transmission through slit arrays in a metallic films

The mechanisms responsible for enhanced transmission of electromagnetic wave through an array of subwavelength slits in a metallic film are analyzed. Theoretical model of the enhanced transmission which takes into account the penetration of electromagnetic field into real metal is developed. Semi-analytical model based on Fabry–Perot formula is considered. Comparison of theoretical model, semi-analytical model and results of numerical simulation of Maxwell equations in time-dependent form (FDTD method) for silver with various geometric parameters is presented. The roles of surface plasmons and plasmon localized along slits are studied.     

Analysis of stability and Hopf bifurcation of delayed feedback spin stabilization of a rigid spacecraft

The stability and bifurcation of delayed feedback spin stabilization of a rigid spacecraft is investigated in this paper. The spin is stabilized about the principal axis of the intermediate moment of inertia using a simple delayed feedback control law. In particular, linear stability is analyzed via the exponential-polynomial characteristic equations and then the method of multiple scales is used to obtain the normal form of the Hopf bifurcation. Bifurcation diagrams and the dynamics of the delayed closed-loop system are verified using continuation software and with numerical simulations.     

Nanoporous carbons as promising novel methane adsorbents for natural gas technology

Nanoporous carbons were synthesized using furfuryl alcohol and sucrose as precursors and MCM-41 and mordenite as nanoporous templates.The produced nanoporous carbons were used as adsorbent for methane storage.The average pore diameter of the samples varied from 3.9 nm to 5.9 nm and the BET surface area varied from 320m2/g to 824m2/g.The volumetric adsorption experiments revealed that MCM-41 and sucrose had better performance compared with mordenite and furfuryl alcohol,correspondingly.Also,the effect of precursor to template ratio on the structure of nanoporous carbons and their adsorption capacities was investigated.The nanoporous carbon produced from MCM-41 mesoporous molecular sieve partially filled by sucrose shows the best methane adsorption capacity among the tested samples.     

Multivariate analyses for biomarkers hunting and validation through on-tissue bottom-up or in-source decay in MALDI-MSI: application to prostate cancer

The large amount of data generated using matrix-assisted laser desorption/ionization mass spectrometric imaging (MALDI-MSI) poses a challenge for data analysis. In fact, generally about 1.10⁸–1.10⁹ values (m/z, I) are stored after a single MALDI-MSI experiment. This imposes processing techniques using dedicated informatics tools to be used since manual data interpretation is excluded. This work proposes and summarizes an approach that utilizes a multivariable analysis of MSI data. The multivariate analysis, such as principal component analysis–symbolic discriminant analysis, can remove and highlight specific m/z from the spectra in a specific region of interest. This approach facilitates data processing and provides better reproducibility, and thus, broadband acquisition for MALDI-MSI should be considered an effective tool to highlight biomarkers of interest. Additionally, we demonstrate the importance of the hierarchical classification of biomarkers by analyzing studies of clusters obtained either from digested or undigested tissues and using bottom-up and in-source decay strategies for in-tissue protein identification. This provides the possibility for the rapid identification of specific markers from different histological samples and their direct localization in tissues. We present an example from a prostate cancer study using formalin-fixed paraffin-embedded tissue.     

Hybrid Metal Halides with Multiple Photoluminescence Centers

Very little is known about the realm of solid‐state metal halide compounds comprising two or more halometalate anions. Such compounds would be of great interest if their optical and electronic properties could be rationally designed. Herein, we report a new example of metal halide cluster‐assembled compound (C₉NH₂₀)₉[Pb₃Br₁₁](MnBr₄)₂, featuring distinctly different anionic polyhedra, namely, a rare lead halide cluster [Pb₃Br₁₁]^5? and [MnBr₄]^2?. In accordance with its multinary zero‐dimensional (0D) structure, this compound is found to contain two distinct emission centers, 565 nm and 528 nm, resulting from the formation of self‐trapped excitons and ⁴T₁‐⁶A₁ transition of Mn²⁺ ions, respectively. Based on the high durability of (C₉NH₂₀)₉[Pb₃Br₁₁](MnBr₄)₂ upon light and heat, as well as high photoluminescence quantum yield (PLQY) of 49.8 % under 450 nm blue light excitation, white light‐emitting diodes (WLEDs) are fabricated, showcasing its potential in backlight application.