Rapid Amorphization in MOF/Metal Selenite Nanocomposites for Enhanced Capacity in Supercapacitors.

MOF/inorganic nanocomposites combine the advantages of each component. Herein, two MOF/metal selenite nanocomposites, Co-NH2-BDC/CoSeO3·H2O and Co-BDC/CoSeO3·H2O, are prepared on nickel foam through a facile two-step hydrothermal method, which inherit the 2D morphology and porosity properties of their MOF precursors. Furthermore, during the electrochemical activation process, the crystallized nanocomposites can easily transform into amorphous structures in a short time of 20 min in the presence of an electric field, similar to CoSeO3·H2O. Due to amorphization, the electrochemical performance of the two nanocomposites is much enhanced relative to that of their MOF precursors. Specifically, the areal capacitances of Co-NH2-BDC/CoSeO3·H2O and Co-BDC/CoSeO3·H2O are 5.35 and 10.65 F·cm-2 at 2 mA·cm-2, respectively. The assembled asymmetric supercapacitor (ASC) using Co-NH2-BDC/CoSeO3·H2O as positive electrodes delivers an energy density of 0.207 mWh·cm-2 at a power density of 0.799 mW·cm-2 with outstanding cycling stability (93% capacity retention after 5000 cycles). Using Co-BDC/CoSeO3·H2O as positive electrodes, the ASC can reach a high energy density of 0.483 mWh·cm-2 at a power density of 0.741 mW·cm-2 and 84% capacity retention after 5000 cycles. This work provides an efficient strategy for constructing MOF/metal selenite nanocomposites for energy storage and conversion.

Synthesis, characterization, and aging resistance of the polyurethane dimethacrylate layer for dental restorations.

In this study, polyurethane dimethacrylate (PUDMA) was synthetized from different components and incorporated into a direct resin composite restoration system with the aim to buffer tooth-resin interfacial stresses and maintain the marginal adaptation. The tensile strength, elongation at fracture (ε), and thermal stability of the PUDMA layer were characterized, showing a tensile strength of 22 MPa, an ε of 112%, and a thermal decomposition temperature of about 282°C. In addition, the degree of conversion, water sorption/solubility, hydrophobicity, microtensile bond strength (µTBS), marginal leakage, and cytotoxicity in vitro were evaluated for the PUDMA layer. The data were analyzed using one-way ANOVA, except for leakage depths (which were analyzed using the Wilcoxon paired-rank test). The level of significance was set at 0.05. Compared with dental adhesives, PUDMA displayed a higher degree of conversion, lower water sorption/solubility, and improved hydrophobicity and biocompatibility in vitro. After thermocycling, the µTBS of the restoration system containing PUDMA had increased compared with the µTBS at 24 h. Restorations containing PUDMA showed lower leakage depths than those which did not contain PUDMA. In conclusion, because of its hydrophobic and elastic nature, the PUDMA layer, when used as an intermediate between tooth and resin restoratives, may buffer interfacial stresses, improve the stability and durability of the bonding interface, and reduce microleakage.

A red light-responsive photoswitch for deep tissue optogenetics.

Red light penetrates deep into mammalian tissues and has low phototoxicity, but few optogenetic tools that use red light have been developed. Here we present MagRed, a red light-activatable photoswitch that consists of a red light-absorbing bacterial phytochrome incorporating a mammalian endogenous chromophore, biliverdin and a photo-state-specific binder that we developed using Affibody library selection. Red light illumination triggers the binding of the two components of MagRed and the assembly of split-proteins fused to them. Using MagRed, we developed a red light-activatable Cre recombinase, which enables light-activatable DNA recombination deep in mammalian tissues. We also created red light-inducible transcriptional regulators based on CRISPR-Cas9 that enable an up to 378-fold activation (average, 135-fold induction) of multiple endogenous target genes. MagRed will facilitate optogenetic applications deep in mammalian organisms in a variety of biological research areas.

Polymerization shrinkage kinetics and degree of conversion of resin composites.

This study compared shrinkage strain, polymerization shrinkage kinetics, and degree of conversion (DC) of a set of resin composites and investigated their influencing factors. Ten commercial resin composites were assessed, and 5 specimens (n = 5) were developed for material and subjected to light curing using light emitting diode light at 650 mW/cm2 for 40 s. The laser triangulation method was adopted to assess the shrinkage strain, and Fourier transform infrared spectroscopy was used to measure DC. The shrinkage strain was monitored for 5 min in real time and its data were subjected to differential calculations to get the shrinkage strain rate curve with respect to time, obtaining the maximum shrinkage strain rate (Rmax) and gel time. The values of shrinkage strain varied from 1.28% to 2.10%. The Rmax values were between 5.17 µm/s and 21.83 µm/s. Gel time values varied from 3.08 s to 4.32 s. The DC yielded values ranging from 53.62% to 87.01%. The values of polymerization shrinkage and DC were dependent on the composition of materials, including the monomer matrix and filler system. Compared to the micro-filler materials, the nano-filler resin composites had higher values of DC. Some resin composites are suitable for clinical applications because of their superior polymerization shrinkage properties and DC.

The functions of hydrophobic elastic polyurethane combined with an antibacterial triclosan derivative in the dentin restoration interface.

Dentin restoration produces weak interfaces because of the effects of bacterial microflora, biofilms, and mechanical, thermal, and shrinkage stresses. This results in secondary caries. Therefore, hydrophobic elastic polyurethane (PU) containing different concentrations of triclosan derivatives was synthesized and applied to solve this problem. The antibacterial PU was characterized according to its tensile strength (TS) and elasticity (ε) via a universal testing machine, and water sorption (Wsp) and solubility testing (Wsl) was performed according to ISO 4049: 2009. Additionally, this study evaluated the antibacterial properties of PU against Streptococcus mutans (ATCC35668) and Escherichia coli (ATCC25922). A marginal leakage test was performed to evaluate the leakage prevention property. As a result, the antibacterial PU showed high TS (>17 MPa), high elasticity (ε > 65%), and low Wsp (>81.06 µg/mm3) and Wsl (>11.22 µg/mm3). The PU exhibited antibacterial effects against both Streptococcus mutans and Escherichia coli. The antibacterial rates were over 90% and >99% for the 3% and 5% groups, respectively. Moreover, the marginal level of leakage was 0. Based on the mechanical properties, Wsp and Wsl values and the antibacterial properties, the 3% group exhibited satisfactory performance and has been deemed a possible solution to reduce the occurrence of secondary caries.

Optical manipulation of the alpha subunits of heterotrimeric G proteins using photoswitchable dimerization systems.

Alpha subunits of heterotrimeric G proteins (Gα) are involved in a variety of cellular functions. Here we report an optogenetic strategy to spatially and temporally manipulate Gα in living cells. More specifically, we applied the blue light-induced dimerization system, known as the Magnet system, and an alternative red light-induced dimerization system consisting of Arabidopsis thaliana phytochrome B (PhyB) and phytochrome-interacting factor 6 (PIF6) to optically control the activation of two different classes of Gα (Gαq and Gαs). By utilizing this strategy, we demonstrate successful regulation of Ca2+ and cAMP using light in mammalian cells. The present strategy is generally applicable to different kinds of Gα and could contribute to expanding possibilities of spatiotemporal regulation of Gα in mammalian cells.