Highly luminescent, fast switching electro-optical device based on core-shell bimetallic nanoparticles/ ferroelectric liquid crystal composites.

Owing to the passive nature of liquid crystal (LC) materials, achieving luminous displays using pure LC materials is challenging. In addition, it is difficult to achieve a fast switching time using pristine ferroelectric LC devices without compromising their cell thickness. Herein, we have developed a fast switching and highly luminescent electro-optical device by dispersing a minute concentration of bimetallic nanoparticles (Au@Ag NPs) having a spherical gold core and a silver shell within a ferroelectric liquid crystal (FLC) host matrix, ZLI3654. Au@Ag core-shell NPs having synergic attributes of both counterparts were successfully synthesized by a facile seed-mediated route. The Au core helps to tune the shape of the Ag shell and provides enhanced electron density as well as improved stability against oxidation. Introducing nanoparticles induces little structural modifications to the host FLC, resulting in an improvement in the mesogenic alignment. Interestingly, ∼29-fold enhancement in the photoluminescence (PL) intensity is observed on dispersing 0.25 wt% of Au@Ag NPs into the FLC host matrix. The enhanced electromagnetic field in the FLC-nanocomposite is attributed to the Localized Surface Plasmon Resonance of Au@Ag NPs, which strengthens the photon absorption rates by the FLC molecules, culminating in the massive enrichment of the PL intensity. In addition, the improved localized electric field inside the FLC device led to a noticeable enhancement in the spontaneous polarization, dielectric permittivity, and, most interestingly, ∼53% fastening in the switching time at an optimum concentration (0.25 wt%) of Au@Ag NPs. The improved electro-optical parameters of the Au@Ag NPs/FLC composite have been compared with the performance of both pristine Au NPs/FLC and Ag NPs/FLC composites, respectively, for the comprehensiveness of the study. The present study paves a systematic way to develop FLC-based advanced electro-optical devices with faster switching and higher luminescence properties.

Nanocellulose-based cobalt(II) coordinated malonic acid hybrid aerogels exhibiting reversible thermochromism and moisture sensor properties.

The emergence of sustainable polymers and technologies has led to the development of innovative materials with minimal carbon emissions which find extensive applications in wearable electronics, biomedical sensors, and Internet of Things (IoT)-based monitoring systems. Nanocellulose which can be generated from abundant biomass materials has been widely recognized as a sustainable alternative for a diverse range of applications due to its remarkable properties and eco-friendly nature. By making use of the unique and easily accessible coordination transformation property of Co(II) ions and associated visible light absorption changes, we report a novel Co(II) cation-incorporated nanocellulose/malonic acid hybrid aerogel material that exhibits reversible thermochromism induced by thermal stimulus in the presence of atmospheric moisture. This effect is accentuated by the highly porous nature of the nanocellulose aerogel material we have developed. Besides the reversible thermochromic property which Co(II) ions exhibit, the metal ions act as very efficient reinforcing units contributing significantly to the structural stability and rigidity of the hierarchical aerogels by coordinative cross-linking through carboxylate moieties present in the TEMPO-oxidized cellulose nanofibers (TCNF) and additionally adding malonic acid to provide sufficient COO- for cross-linking. Thorough characterization and detailed investigation of as-prepared hybrid aerogels was conducted to evaluate their overall properties including reversible thermochromism and moisture sensor behaviour. Further, an Android mobile-based application was developed to demonstrate the real-world application of the aerogels for atmospheric humidity sensing.

Remediation Approaches to Reduce Hydrocarbon Contamination in Petroleum-Polluted Soil.

Heavy metals pollution associated with oil spills has become a major concern worldwide. It is essential to break down these contaminants in the environment. In the environment, microbes have been used to detoxify and transform hazardous components. The process can function naturally or can be enhanced by adding nutrients, electron acceptors, or other factors. This study investigates some factors affecting hydrocarbon remediation technologies/approaches. Combinations of biological, chemical, and eco-toxicological techniques are used for this process while monitoring the efficacy of bacterial products and nutrient amendments to stimulate the biotransformation of contaminated soil. Different hydrocarbon removal levels were observed with bacterial augmentation (Beta proteobacterium and Rhodococcus ruber), exhibiting a total petroleum hydrocarbon (TPH) reduction of 61%, which was further improved to a 73% reduction using bacterial augmentation combined with nutrient amendment (nitrogen, potassium, and phosphorus). A heavy metal analysis of the polluted soils showed that the combination of nutrient and bacterial augmentation resulted in a significant reduction (p-value < 0.05) in lead, zinc, and barium. Toxicity testing also showed that a reduction of up to 50% was achieved using these remediation approaches.

Tailored synthesis of ultra-stable Au@Pd nanoflowers with enhanced catalytic properties using cellulose nanocrystals.

A green strategy for the synthesis of bimetallic core-shell Au@Pd nanoflowers (NFs) employing banana pseudo-stem-derived TEMPO-oxidized cellulose nanocrystals (TCNC) as both capping and shape-directing agent via seed-mediated method is presented. Flower-like nanostructures of Au@Pd bound to TEMPO-oxidized cellulose nanocrystals (TCNC-Au@Pd) were decorated on amino-functionalized graphene (NH2-RGO) without losing their unique structure, allowing them to be deployed as an efficient, reusable and a green alternative heterogeneous catalyst. The decisive role of TCNC in the structural metamorphosis of nanoparticle morphology were inferred from the structural and morphology analyses. According to our study, the presence of -OH rich TCNC appears to play a pivotal role in the structured evolution of intricate nanostructure morphology. The feasibility of the bio-supported catalyst has been investigated in two concurrently prevalent model catalytic reactions, namely the oxygen reduction reaction (ORR) and the reduction of 4-nitrophenol, the best model reactions in fuel cell and industrial catalytic applications, respectively.

ZnO-ZnS Heterojunctions: A Potential Candidate for Optoelectronics Applications and Mineralization of Endocrine Disruptors in Direct Sunlight.

Simple solution combustion synthesis was adopted to synthesize ZnO-ZnS (ZSx) nanocomposites using zinc nitrate as an oxidant and a mixture of urea and thiourea as a fuel. A large thiourea/urea ratio leads to more ZnS in ZSx with heterojunctions between ZnS and ZnO and throughout the bulk; tunable ZnS crystallite size and textural properties are an added advantage. The amount of ZnS in ZSx can be varied by simply changing the thiourea content. Although ZnO and ZnS are wide band gap semiconductors, ZSx exhibits visible light absorption, at least up to 525 nm. This demonstrates an effective reduction of the optical band gap and substantial changes in its electronic structure. Raman spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and secondary-ion mass spectrometry results show features due to ZnO and ZnS and confirm the composite nature with heterojunctions. The above mentioned observations demonstrate the multifunctional nature of ZSx. Bare ZSx exhibits a promising sunlight-driven photocatalytic activity for complete mineralization of endocrine disruptors such as 2,4-dichlorophenol and endosulphan. ZSx also exhibits photocurrent generation at no applied bias. Dye-sensitized solar cell performance evaluation with ZSx shows up to 4% efficiency and 48% incident photon conversion efficiency. Heterojunctions observed between ZnO and ZnS nanocrystallites in high-resolution transmission electron microscopy suggest the reason for effective separation of electron-hole pairs and their utilization.

[Study regarding coronal fracture probability in posterior amalgam restorations]. / Studiul privind evaluarea probabilitatii de fractura coronara la restaurarile din amalgam pe dintii laterali.

Despite minimal invasive orientation in restorative dentistry, in Romania the necessary for extensive restorative treatment in posterior teeth is still high. The silver amalgam still remains a social treatment option for such situation. The purpose of this study was to analyze the efficiency of a new method for analytical determination of the volume of restoration in posterior teeth, knowing that the risk for coronal fracture depends on the size of restoration. The study correlated the results obtained through this method with the real values (mathematically determined) of restorations and the anatomical crowns volumes in order to assess the risk fracture. Amalgam restorations of different types and sizes were placed in 24 extracted premolars and molars. A good global correlation was observed between the true and calculated value (98.321%). The best correlation was observed for MOD restorations (93.042%) while the worst coefficient was obtained for MO restorations (83.378%). The medium restorations presented o correlation of 99.288% and the extensive restorations had an index around 96.957%. This method is based on physics principles and objective measurement resulting in a good correlation with the real dimensions of cavities. Therefore it could be used to assess the risk of crown fracture in teeth with amalgam restorations.