Liquid–Liquid Diffusion‐Assisted Crystallization: A Fast and Versatile Approach Toward High Quality Mixed Quantum Dot‐Salt Crystals

Here, a new, fast, and versatile method for the incorporation of colloidal quantum dots (QDs) into ionic matrices enabled by liquid–liquid diffusion is demonstrated. QDs bear a huge potential for numerous applications thanks to their unique chemical and physical properties. However, stability and processability are essential for their successful use in these applications. Incorporating QDs into a tight and chemically robust ionic matrix is one possible approach to increase both their stability and processability. With the proposed liquid–liquid diffusion‐assisted crystallization (LLDC), substantially accelerated ionic crystallization of the QDs is shown, reducing the crystallization time needed by one order of magnitude. This fast process allows to incorporate even the less stable colloids including initially oil‐based ligand‐exchanged QDs into salt matrices. Furthermore, in a modified two‐step approach, the seed‐mediated LLDC provides the ability to incorporate oil‐based QDs directly into ionic matrices without a prior phase transfer. Finally, making use of their processability, a proof‐of‐concept white light emitting diode with LLDC‐based mixed QD‐salt films as an excellent color‐conversion layer is demonstrated. These findings suggest that the LLDC offers a robust, adaptable, and rapid technique for obtaining high quality QD‐salts.     

Effect of Reciproc blue,XP‐endo shaper,and WaveOne gold instruments on dentinal microcrack formation: A micro‐computed tomographic evaluation

The purpose of this study was to evaluate and compare the effect of Reciproc Blue (RPCB), XP‐endo Shaper (XPS), and WaveOne Gold (WOG) single‐files on dentinal microcrack formation using micro‐computed tomography (micro‐CT). Twenty‐four mesial roots (24 mesio‐buccal and 24 mesio‐lingual canals) of mandibular molar teeth were prepared using RPCB, XPS, and WOG files (n = 8/each group). The samples were scanned with micro‐CT in the pre‐ and post‐preparation. Then, before preparation and after preparation cross‐sectional images of the teeth were evaluated to detect the presence of microcracks. For each group, the number of microcracks was calculated as a percentage rate. The data were statistically analyzed using McNemar at 5% significance level (p < .05). Dentinal microcracks were observed in 25.99% (2,103 of 7,813), 31.99% (2,482 of 7,758), and 36.66% (2,836 of 7,731) of cross‐sectional images of the XPS, WOG, and RPCB groups, respectively. In all the groups, all the dentinal microcracks seen in the post‐treatment cross‐sectional images were present in the corresponding pre‐treatment images. Within the limitations of this study, the XPS, WOG, and RPCB files did not cause new dentinal microcrack formation or propagation of existing dentinal microcracks.     

Covalent Immobilization of Tyrosinase on Electrospun Polyacrylonitrile/Polyurethane/Poly(m-anthranilic acid) Nanofibers: An Electrochemical Impedance Study

Polyacrylonitrile/polyurethane/poly(m-anthranilic acid) nanofibers were fabricated by electrospinning. Tyrosinase immobilization was performed by EDC/N-hydroxyl succinimide activation. Covalent binding of tyrosinase onto nanofibers was confirmed by Fourier transform infrared-attenuated total reflectance, and bicinchoninic acid assay revealed the amount of enzyme. Nanofiber morphology and composition were characterized by scanning electron microscopy/energy-dispersive X-ray spectroscopy (EDX). Nanofibers became smoother and thicker after tyrosinase immobilization. Effects of enzyme on nanofibers were investigated by electrochemical impedance spectroscopy and the data were fitted to equivalent electrical circuit model. EDX-mapping showed uniform distribution of enzyme. The solution resistance and charge transfer resistance of nanofibers decreased after enzyme immobilization.     

Determination of Membrane Protein Fouling by UV Spectroscopy and Electrochemical Impedance Spectroscopy

UV spectroscopy and electrochemical impedance spectroscopy were used to investigate the properties and performances of ultrafiltration membranes fabricated with different polymers. Membrane performances were studied by means of permeability and bovine serum albumin filtration. UV spectroscopy results showed that bovine serum albumin rejection was lowest in polyvinylidene fluoride membranes, whereas it was highest in polysulfone membranes. Electrochemical impedance spectroscopy data revealed that after bovine serum albumin filtration, resistance of the membranes was increased though double layer capacitances were decreased. Performance data of UV spectroscopy and electrochemical impedance spectroscopy were in correlation with each other. This study demonstrated that electrochemical impedance spectroscopy can be successfully used in filtration membrane studies.     

Au/PANA/PVAc and Au/P(ANA-co-CNTA)/PVAc electrospun nanofibers as tyrosinase immobilization supports

Au/poly anthranilic acid/poly vinyl acetate and Au/poly(anthranilic acid-co-3-carboxy-N-(2-thenylidene)aniline)/poly vinyl acetate nanofibers through electrospinning and their modification with covalent tyrosinase (Ty) immobilization was performed. It was realized by surface activation using N-(3-dimetylaminopropyl)-N-ethylcarbodimide hydrochloride/N-hydroxysuccinimide chemistry. Electrochemical impedance spectroscopy (EIS), FTIR–ATR, Raman spectroscopy, and bicinchoninic acid assay analyses demonstrated that Ty was stably and covalently bonded onto the nanofibers. Increase in surface roughness [atomic force microscopy (AFM)] and the presence of Cu atoms in the nanofiber composition after enzyme immobilization confirmed the Ty immobilization. The charge transfer resistances of the nanofibers decreased due to changes in the nanofiber surfaces after attachment of enzyme.     

The effect of deposition on electrochemical impedance properties of TiO<Subscript>2</Subscript>/FTO photoanodes

The integration of TiO₂ layers onto a substrate is challenging and limits the application potential of TiO₂. Even though, several studies have been reported to solve this problem by applying various deposition methods, there is still lack of information about how these methods affect the electrochemical and photo-electrochemical properties of resulting electrodes. The TiO₂ layers possessing different morphologies, deposited on the conductive FTO glass by means of various different deposition techniques (dip-coating, electrospinning and electrospraying), were used as photoanode (and working electrode) in the three-compartment electrochemical cell. The TiO₂ electrodes were calcinated at 450 °C and after that all samples revealed the crystallographic form of anatase. Using these three deposition techniques, three different morphologies were obtained. They consisted of a thin TiO₂ nanoparticle layer, TiO₂ nanoparticle/nanofiber layer and TiO₂ nanorod layer, respectively. The crystallinity and surface properties of the calcinated layers were determined by XRD, Raman spectroscopy, FTIR-ATR and SEM analyses. The electrochemical impedance (EIS) and photo-induced properties of photoanodes were studied by electrochemical measurements. The effects of surface morphology and crystal size of nanostructured layers on electrochemical impedance and photo-electrochemical properties were investigated. The electrodes prepared by dip-coating technique showed the best electrochemical impedance and photo-electrochemical results compared to other two types of electrodes. Dip-coating TiO₂ layer possesses the biggest crystal size and lowest charge transfer resistance which result the highest photocurrent density.     

Evaluation of antibacterial effects of contemporary orthodontic bonding materials

Aim: The aim of this study was to evaluate the antibacterial effects of five orthodontic bonding materials commonly used in orthodontics. Materials and Methods: The antibacterial effects of five orthodontic bonding materials were evaluated against Streptococcus mutans and Streptococcus salivarius by direct contact test (DCT). Using the DCT technique, quintet specimens of Transbond XT, Blugloo, Grengloo, Light Bond, and Opal Bond were applied to the bottom and the walls of the five wells of a 96-microtiter plate with a height of 2 mm. Samples were prepared in two sets: 1-day samples and 7-day samples. Ten microliters of bacterial suspension were added to each well for direct contact with each material for 1h at 37 °C. Bacterial growth was then measured in a microplate spectrophotometer hourly at 600 nm for 24 h. Five uncoated wells with identical inoculum sizes served as positive controls. The data obtained at the end of 24 h was statistically analyzed with one-way ANOVA, and post hoc comparisons were done using Tamhane’s T2 test. Results: Blugloo generally showed better antibacterial activity than the other materials. Transbond XT did not show any antibacterial activity. There was a statistically significant difference between Transbond XT and Light Bond in the 1-day sample against S. mutans (p < 0.05). No statistically significant differences were found among the other groups (p > 0.05). Conclusion: Blugloo had the most potent antibacterial activity against S. salivarious.