Salivary α-amylase as a stress biomarker in mentally and physically disabled individuals during COVID-19 times.

Background: Stress is faced by every individual in their day-to-day life activities. During pandemic, most people have experienced multiple episodes of depression, anxiety, and insomnia. Several medical and dental problems are reported with stress and the fastest and easiest way to study and investigate is through body fluids, mainly saliva. Hence, we aim to study salivary α amylase in disabled individuals and hypothesize that salivary α amylase could be a reliable stress biomarker in disabled individuals. Materials and Methods: Cross-sectional study was conducted including 200 individuals grouped into controls (100) and disabled individuals (100). Disabled individuals were further grouped into physically (50) and mentally (50) disabled. Stimulated and unstimulated saliva was collected from all the participants and were investigated for salivary α-amylase by direct substrate method. The enzyme activity was analyzed using a spectrophotometer and the obtained were analyzed statistically. Result: Salivary α-amylase showed significant difference between controls and disabled group (p = 0.000). Salivary α-amylase was least in the mentally disabled group compared to physically disabled group. Age related comparison of salivary α-amylase was higher in physically disabled whereas gender related comparison showed females in physically disabled group to be more affected than controls. Conclusion: Saliva, the easy and most researched fluid, is rich in salivary α-amylase. Salivary α-amylase is a potential biomarker to assess stress. Further diagnostic studies are required to know the salivary changes and their influence on individual general health status.

Polyvinyl Butyral Polymeric Host Material-Based Fluorescent Thin Films to Achieve Highly Efficient Red and Green Colour Conversion for Advanced Next-Generation Displays.

Rare-earth element-free fluorescent materials are eco-friendlier than other traditional fluorescent precursors, such as quantum dots and phosphors. In this study, we explore a simple and facile solution-based technique to prepare fluorescent films, which are highly stable under ordinary room conditions and show hydrophobic behaviour. The proposed hybrid material was designed with hybrid composites that use polyvinyl butyral (PVB) as a host doped with organic dyes. The red and green fluorescent films exhibited quantum yields of 89% and 80%, respectively, and both are very uniform in thickness and water resistant. Additionally, PVB was further compared with another polymeric host, such as polyvinylpyrrolidone (PVP), to evaluate their binding ability and encapsulation behaviour. Next, the effect of PVB on the optical and chemical properties of the fluorescent materials was studied using UV spectroscopy and Fourier transform infrared spectroscopy. The analysis revealed that no new bond was formed between the host material and fluorescent precursor during the process, with intermolecular forces being present between different molecules. Moreover, the thickness of the fluorescent film and quantum yield relation were evaluated. Finally, the hydrophobic nature, strong binding ability, and optical enhancement by PVB provide a powerful tool for fabricating a highly efficient fluorescent film with enhanced stability in an external environment based on its promising encapsulation properties. These efficient fluorescent films have a bright potential in colour conversion for next-generation display applications.

Review on Fluorescent Carbon/Graphene Quantum Dots: Promising Material for Energy Storage and Next-Generation Light-Emitting Diodes.

Carbon/graphene quantum dots are 0D fluorescent carbon materials with sizes ranging from 2 nm to around 50 nm, with some attractive properties and diverse applications. Different synthesis routes, bandgap variation, higher stability, low toxicity with tunable emission, and the variation of physical and chemical properties with change in size have drawn immense attention to its potential application in different optoelectronics-based materials, especially advanced light-emitting diodes and energy storage devices. WLEDs are a strong candidate for the future of solid-state lighting due to their higher luminance and luminous efficiency. High-performance batteries play an important part in terms of energy saving and storage. In this review article, the authors provide a comparative analysis of recent and ongoing advances in synthesis (top-down and bottom-up), properties, and wide applications in different kinds of next-generation light-emitting diodes such as WLEDs, and energy storage devices such as batteries (Li-B, Na-B) and supercapacitors. Furthermore, they discuss the potential applications and progress of carbon dots in battery applications such as electrode materials. The authors also summarise the developmental stages and challenges in the existing field, the state-of-the-art of carbon/graphene quantum dots, and the potential and possible solutions for the same.

Enhanced Efficiency of Semitransparent Perovskite Solar Cells via Double-Sided Sandwich Evaporation Technique for Four Terminal Perovskite-Silicon Tandem Application.

Halide perovskite based solar cells (PSC's) have shown tremendous potential based on its facile fabrication technique, and the low cost of perovskite thin film formation with efficiency passing through an unmatched growth in recent years. High quality film along with morphology and crystallinity of the perovskite layer influences the efficiency and other properties of the perovskite solar cell (PSC). Furthermore, semitransparent perovskite solar cells (ST-PSC) are an area of attraction due to its application in tandem solar cells, although various factors like suitable transparent rear electrodes and optimized technique limit the power conversion efficiency (PCE). In this article, we fabricated perovskite film using a technique termed Double-sided sandwich evaporation technique (DS-SET) resulting in high quality perovskite film (MAPbI3 and MAPbIxCl3-x). Using this fabrication approach as compared to the traditional spin-coating method, we reported an enhanced photovoltaic performance of the PSC with a better surface morphology and homogeneity. The best parameter via DS-SET was found to be SET 30 min, which demonstrated a PCE (%) up to 14.8% for MAPbI3 and 16.25% for MAPbIxCl3-x, respectively. Addressing the tandem solar cell, incorporating thin Ag as a transparent electrode with a thickness of 20 nm onto the PSC's as the top cell and further combining with the Si solar cell results in the four terminal (4T) tandem solar cell exhibiting a PCE (%) of 24.43%.

Acid anion electrolyte effects on platinum for oxygen and hydrogen electrocatalysis.

Platinum is an important material with applications in oxygen and hydrogen electrocatalysis. To better understand how its activity can be modulated through electrolyte effects in the double layer microenvironment, herein we investigate the effects of different acid anions on platinum for the oxygen reduction/evolution reaction (ORR/OER) and hydrogen evolution/oxidation reaction (HER/HOR) in pH 1 electrolytes. Experimentally, we see the ORR activity trend of HClO4 > HNO3 > H2SO4, and the OER activity trend of HClO4 [Formula: see text] HNO3 ∼ H2SO4. HER/HOR performance is similar across all three electrolytes. Notably, we demonstrate that ORR performance can be improved 4-fold in nitric acid compared to in sulfuric acid. Assessing the potential-dependent role of relative anion competitive adsorption with density functional theory, we calculate unfavorable adsorption on Pt(111) for all the anions at HER/HOR conditions while under ORR/OER conditions [Formula: see text] binds the weakest followed by [Formula: see text] and [Formula: see text]. Our combined experimental-theoretical work highlights the importance of understanding the role of anions across a large potential range and reveals nitrate-like electrolyte microenvironments as interesting possible sulfonate alternatives to mitigate the catalyst poisoning effects of polymer membranes/ionomers in electrochemical systems. These findings help inform rational design approaches to further enhance catalyst activity via microenvironment engineering.