Tuning the Liquid Crystallinity and Electroluminescence via Sulfonation of S-Annulated Perylene Tetraester.

This study presents a comparative analysis of S-annulated perylene tetraester (PTE-S) and its sulfone (PTE-SO2) analogue. This sulfone modification reduced melting point and stabilized a room temperature columnar rectangular (Colr) phase in contrast to its parent PTE-S which showed a crystalline behaviour at room temperature. This molecular design also leads to red-shifted absorbance and emission in comparison to PTE-S, along with a tuning of photoluminescence from sky blue to green, achieving an impressive quantum yield of 85 %. OLED devices fabricated using PTE-SO2 as emitter material at concentrations of 0.2, 0.5, and 1 wt.% in CBP as host material. A maximum external quantum efficiency (EQE) of 2.9 % was observed with the 0.5 wt.% PTE-SO2 in CBP with CIE coordinates of (0.45, 0.35), accompanied by an orange luminance of 848 cd/m2. Notably, a device with a 0.5 wt% doping concentration of PTE-S demonstrates an EQE of 3.5 %, and cyan luminance of 2,598 cd/m2.

Detection of soybean oil adulteration in cow ghee (clarified milk fat): an ultrafast study using flash gas chromatography electronic nose coupled with multivariate chemometrics.

BACKGROUND: Cow ghee is one of the expensive edible fats in the dairy sector. Ghee is often adulterated with low-priced edible oils, like soybean oil, owing to its high market demand. The existing adulteration detection methods are time-consuming, requiring sample preparation and expertise in these fields. The possibility of detecting soybean oil adulteration (from 10% to 100%) in pure cow ghee was investigated in this study. The fingerprint information of volatile compounds was collected using a flash gas chromatography electronic nose (FGCEN) instrument. The classification results were studied using the pattern recognition chemometric models principal component analysis (PCA), soft independent modelling of class analogy (SIMCA), and discriminant function analysis (DFA). RESULTS: The most powerful fingerprint odor of all the samples identified from FGCEN analysis was acetaldehyde (Z)-4-heptenal, 2-propanol, ethyl propanoate, and pentan-2-one. The odor analysis investigation was accomplished with an average analysis time of 90 s. A clear differentiation of all the samples with an excellent classification accuracy of more than 99% was achieved with the PCA and DFA chemometric methods. However, the results of the SIMCA model showed that SIMCA could only be used to detect ghee adulteration at higher concentration levels (30% to 100%). The validation study shows good agreement between FGCEN and gas chromatography-mass spectrometry methods. CONCLUSION: The methodology demonstrated coupled with PCA and DFA methods for adulteration detection in ghee using FGCEN apparatus has been an efficient and convenient technique. This study explored the capability of the FGCEN instrument to tackle the adulteration problems in ghee. © 2022 Society of Chemical Industry.

Electronic nose for detection of food adulteration: a review.

The food products may attract unscrupulous vendors to dilute it with inexpensive alternative food sources to achieve more profit. The risk of high value food adulteration with cheaper substitutes has reached an alarming stage in recent years. Commonly available detection methods for food adulteration are costly, time consuming and requires high degree of technical expertise. However, a rapid and suitable detection method for possible adulterant is being evolved to tackle the aforesaid issues. In recent years, electronic nose (e-nose) system is being evolved for falsification detection of food products with reliable and rapid way. E-nose has the ability to artificially perceive aroma and distinguish them. The use of chemometric analysis together with gas sensor arrays have shown to be a significant procedure for quality monitoring in food. E-nose techniques with numerous provisions are reliable and favourable for food industry in food fraud detection. In the present review, the contributions of gas sensor based e-nose system are discussed extensively with a view to ascertain the adulteration of food products.

Photoinduced quasi-2D to 3D phase transformation in hybrid halide perovskite nanoplatelets.

We present a photo-induced quasi-2D to 3D phase transition of MAPbBr3 (MA = CH3NH3) perovskite nanoplatelets (NPLs). To begin with, we synthesized quasi-2D MAPbBr3 NPLs (two octahedral layers thick, n = 2). A systematic increase in the thickness of the perovskite platelets is observed as a result of continuous photon irradiation leading to a 78 nm red shift in the emission spectra through different stages. Moreover, the bandgap of the compound decreases from 2.72 eV to 2.2 eV as we move from a quasi-2D to 3D phase. The excitonic Bohr radius of the MAPbBr3 NPLs is found to be 1.8 nm, whereas the thickness of a single layer of PbBr64- octahedra is 5.9 Å. As the layer thickness increases (>4-6 layers), MAPbBr3 NPLs move out of the quantum confinement regime, governed by the red shift in the emission spectra. To complement the experimental results, density functional theory calculations were performed on MAPbBr3 of various layer thicknesses. The van der Waals interaction and a more accurate Heyd-Scuseria-Ernzerhof functional were used to calculate the optical bandgap for MAPbBr3 platelets of different layer thicknesses, which matches exceptionally well with the experimental results. Our findings disclose an interesting and meaningful phenomenon in the emerging hybrid perovskite NPLs and are beneficial for any future development of perovskite-based devices.

Composition-Controlled Synthesis of Hybrid Perovskite Nanoparticles by Ionic Metathesis: Bandgap Engineering Studies from Experiments and Theoretical Calculations.

Herein a newly discovered non-polar solvent based synthesis of MAPbX3 hybrid perovskite nanoparticles (NPs) is presented, where MA=Methylammonium and X=I, Br and Cl, as well as their mixed halide counterparts. The methodology proposed is simple and uses low-cost commercial precursors. The conventional method of hybrid perovskite preparation requires methylammonium halide precursors and highly polar solvents. Mandatory use of polar solvents and a particular perovskite precursor makes an intermediate compound which then requires a non-polar solvent to recover the NPs. In contrast here, a whole range of mixed halide perovskite NPs is fabricated without using a methylammonium halide precursor and a polar solvent. In this method, a non-polar solvent is used, which provides a better platform for the particle recovery. Organic cations on the nanoparticle surface prevent degradation from water, due to their hydrophobic nature, and hence offer a stable colloidal suspension in toluene for more than three months. Ab-initio calculations within density functional theory (DFT) predict lower formation energies compared to previously reported values, confirming better chemical stability for this synthesis pathway. Through the halide compositional tuning, these NPs exhibit a variety of emission and absorption starting from ultraviolet to near infrared (IR). The absorption spectra of various halide perovskite show a sharp band edge over the visible wavelength with high absorption coefficient. High oscillator strengths due to high excitonic binding energies combined with the simulated finite dipole transition probabilities point towards the observed high absorption. The emission spectra of mixed halide perovskites vary from 400 to 750 nm, which covers the whole range of visible spectra with sharp full-width at half maxima. Different halide perovskite exhibit average recombination lifetime from 5 to 227 ns. Ambient synthesis, chemical robustness and tunability of emission with varying halide compositions make MAPbX3 (X=I, Br and Cl) NPs appealing for the optoelectronic applications.

Effect of steam parboiling and hot soaking treatments on milling yield, physical, physicochemical, bioactive and digestibility properties of buckwheat (Fagopyrum esculentum L.).

Post-harvest hydrothermal processing of grains are targeted at improving milling performances and nutritional properties. In this study, the effects of two hydrothermal processes, namely steam parboiling and soaking in boiling water for different durations on properties of buckwheat (Fagopyrum esculentum L.) grown in the Indian Himalayan regions were assessed. Both treatments significantly improved milling yield. Changes in grain section morphology were evidenced under scanning electron microscope. Milder processing for 5 and 10 min mostly exerted annealing effect, represented by increased intensities of X-ray diffraction peaks. Starch gelatinization occurred upon prolonged processing for 15 and 20 min. This resulted in decreased crystallinity, increased sedimentation volume, paste thinning during rapid viscosity analysis and lower thermal transition in differential scanning calorimetry. Marginal changes in oil uptake suggested limited protein denaturation. Natural antioxidant compounds were variably denatured. Maillard browning was indicated by CIE L* a* b* colour and antioxidant levels. The starchy flour samples showed partial resistance to enzymatic amylolysis post retrogradation. Soaking in boiling water can be considered as a feasible alternative to conventional steam parboiling for better milling yield of buckwheat. Altered physicochemical and nutritional properties of buckwheat suggested that the hydrothermally modified flours can be used in ready to eat therapeutic food products.

Chemical Aspects of Halide Perovskite Nanocrystals.

Halide perovskite nanocrystals (HPNCs) are currently among the most intensely investigated group of materials. Structurally related to the bulk halide perovskites (HPs), HPNCs are nanostructures with distinct chemical, optical, and electronic properties and significant practical potential. One of the keys to the effective exploitation of the HPNCs in advanced technologies is the development of controllable, reproducible, and scalable methods for preparation of materials with desired compositions, phases, and shapes and low defect content. Another important condition is a quantitative understanding of factors affecting the chemical stability and the optical and electronic properties of HPNCs. Here we review important recent developments in these areas. Following a brief historical prospective, we provide an overview of known chemical methods for preparation of HPNCs and approaches used to control their composition, phase, size, and shape. We then review studies of the relationship between the chemical composition and optical properties of HPNCs, degradation mechanisms, and effects of charge injection. Finally, we provide a short summary and an outlook. The aim of this review is not to provide a comprehensive summary of all relevant literature but rather a selection of highlights, which, in the subjective view of the authors, provide the most significant recent observations and relevant analyses.

BiOBr Surface-Functionalized Halide Double-Perovskite Films for Slow Ion Migration and Improved Stability.

Surface-tailored lead-free halide double-perovskite (Cs2AgBiX6) thin films are utilized for ion migration studies. A thin surface layer of BiOBr/Cl is grown via intentional annealing of the halide films in ambient conditions. Herein, we physically stacked the two films, viz., Cs2AgBiBr6 and Cs2AgBiCl6, to thermally activate the halide ion migration at different temperatures (room temperature (RT)-150 °C). While annealing, the films' color changes from orange to pale yellow and transparent brown to yellow as a result of the migration of Br- ions from Cs2AgBiBr6 to Cs2AgBiCl6 and Cl- ions from Cs2AgBiCl6 to Cs2AgBiBr6, respectively. Annealing helps in homogenizing the halide ions throughout the films, consequently leading to a mixed phase, i.e., Cs2AgBiClxBr6-x/Cs2AgBiBrxCl6-x (x = 0 to 6) formation. The movement of ions is understood by absorption studies performed at regular time intervals. These investigations reveal a redshift (from 366 to 386 nm) and a blueshift (from 435 to 386 nm) in absorption spectra, indicating the migration of Br- and Cl- toward Cs2AgBiCl6 and Cs2AgBiBr6, respectively. The films characterized using X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) reveal the presence of a peak at 2θ = 10.90° and binding energy of 158.1 eV, respectively, corresponding to the formation of Bi-O bonds at the film surface. Also, XRD studies show a lower 2θ shift of the diffraction peak in the case of Cs2AgBiCl6 films and a higher 2θ shift in the case of Cs2AgBiB6 films, which further confirms the migration of Cl- and Br- from one film to the other. XPS investigations confirm the compositional change with a gradual increment in the concentration of Br-/Cl- with an increase in heating time for Cs2AgBiCl6/Cs2AgBiBr6 films. All these studies confirm thermal diffusion of halide ions in double-perovskite films. Further, from the exponential decay of the absorption spectra, the rate constant for halide (Br) ion diffusion is calculated, which shows an increment from 1.7 × 10-6 s-1 at RT to 12.1 × 10-3 s-1 at 150 °C. The temperature-dependent rate constant follows Arrhenius behavior and renders an activation energy of 0.42 eV (0.35 eV) for bromide (chloride) ion mobility. A larger estimated value as compared to the reported values for Cs2AgBiBr6 wafers (∼0.20 eV) reveals a slow mobility of halide ions in thin films of Cs2AgBiBr6/Cl6. The formation of a BiOBr passivation layer at the surface of Cs2AgBiBr6 thin film might be one of the plausible causes of the slow anion diffusion in the present work. Slow ion migration is an indication that the films are stable and of high-quality.

Growth of Hybrid Perovskite Films via Single-Source Perovskite Nanoparticle Evaporation.

Herein, we demonstrate a vacuum-based evaporation approach to fabricate organic-inorganic perovskite thin films by using phase-formed halide perovskite nanoparticles (NPs) as a precursor/source. We are able to consistently obtain MAPbX3 (MA=CH3 NH3 and X=Cl, Br or I) thin films at various substrates (e. g., glass, ITO, or plastic). The perovskite phase formation in thin film form is confirmed by x-ray diffraction (XRD) studies. Small micro-strain (tensile) values of 1.64×10-3 , 1.42×10-3 and 6.85×10-4 obtained for MAPbCl3 , MAPbBr3 and MAPbI3 films respectively from Williamson-Hall equation indicate low structural distortions in perovskite thin films. The absorption spectra of thin films show sharp band edge having direct band gap, which is followed by narrow full width at half maxima (FWHM ∼0.1 eV) of the emission peak. Thin films of MAPbCl3 , MAPbBr3 and MAPbI3 show direct band gap of 3.1 eV, 2.4 eV and 1.6 eV, respectively. Small Urbach energy values of 33 meV, 44 meV and 66 meV for MAPbCl3 , MAPbBr3 and MAPbI3 films respectively indicates low defect density in various perovskite films. Scanning electron microscopy (SEM) along with energy-dispersive X-ray spectroscopy (EDS) shows high surface coverage and uniform chemical composition of MAPbX3 (X=Cl, Br and I) thin films deposited by the present method. We have successfully controlled the film thickness from 250 nm to 1 µm by varying the nanoparticle precursor amount. The perovskite thin films deposited by the present method are highly stable against the degradation under ambient conditions. Systematic XRD studies along with absorption data demonstrate that the MAPbCl3 and MAPbBr3 films stored under ambient conditions remained stable for more than 30 days and MAPbI3 films for more than 7 days.

Spontaneous Ion Migration via Mechanochemical Ultrasonication in Mixed Halide Perovskite Phase Formation: Experimental and Theoretical Insights.

We present a simple yet powerful synthesis process to prepare compound-phase perovskite nanoparticles (MAPbX3-nYn; MA = CH3NH3+ and X/Y = I, Br, or Cl). This is achieved by mixing two pure-phase perovskites (MAPbX3 and MAPbY3) by using ultrasonic vibration as a mechanochemical excitation. Unlike conventional methods, this procedure does not require any effort in designing a reaction or choosing any particular precursor. X-ray diffraction and TEM studies confirm compound-phase formation in all possible stoichiometries. The origin behind ultrasonic mixing lies in the generation of mechanical stress and high temperature arising from acoustic cavitation during reaction. Long-term experimental stability of the compound-phase is comprehended theoretically by simulating the temperature-dependent Gibbs free energy. Negative mixing entropy plays a crucial role during the synthesis which leads to better stabilization of the compound-phase perovskite over the pure-phase. The ease of synthesis and remarkable phase stability make this process effective and less cumbersome for perovskite nanoparticle synthesis.

Spontaneous anion-exchange synthesis of optically active mixed-valence Cs2Au2I6 perovskites from layered CsAuCl4 perovskites.

Cs2Au2I6, a lead-free photovoltaic material, has been synthesized via controlled and systematic addition of hydroiodic acid (HI) to CsAuCl4. X-ray diffraction studies suggest the formation of Cs2Au2I6 when a threshold concentration of HI is added to CsAuCl4. The final compound shows good stability against light, oxygen and moisture and at temperatures up to 140 °C without any phase degradation. The stability of Cs2Au2I6 is also confirmed by its high negative formation energy and the convex hull diagram constructed using Density Functional Theory (DFT). Absorption studies suggest an abrupt band shift from 2.31 eV to 1.06 eV when HI concentration reaches the threshold limit (∼100 µl). A sharp absorption edge was found for Cs2Au2I6 with an Urbach energy of 59 meV, indicating lower structural disorder and higher crystallinity.