Search Results (5)

In this study, we investigated the influence of an epoxy end-capped polypropylene oxide crosslinker (epoxy-PPO) on the formation of the crosslinked network structure, the stress–strain response, and the electro-mechanical actuation performance of a maleic anhydride functionalized liquid isoprene rubber (LIR). The crosslinker amount varied from 10 (C-LIR-10) to 50 (C-LIR-50) weight parts per hundred parts (phr) of LIR. The swelling test of the cured rubbers revealed that C-LIR-20 formed the densest crosslinked network with the lowest chloroform uptake value within this series. The crosslinked rubber became stiffer in tensile response upon increasing the epoxy-PPO amount from C-LIR-10 to C-LIR-20 and then softened at higher amounts. The SEM measurements were used to relate this composition-induced softening of the rubbers to the phase morphology evolution from nanoscale homogeneity in C-LIR-10 to microscale segregations of excess crosslinkers in C-LIR-50. The use of epoxy-PPO improved the dielectric constant value of LIR; however, the leakage current through the films also increased from 25 µA DC to 320 µA DC for LIR-30 and LIR-50, respectively, during DEA operation. The electro-mechanical actuation tests with circular actuators showed that the C-LIR-10 elastomer film demonstrated a radial strain of 1.7% on activation at an electric field strength of 17.5 V/µm. At higher crosslinker amounts, the close proximity of excess epoxy-PPO molecules caused leakage current across elastomer films thus diminishing the actuation strain of otherwise relatively softer elastomers with higher dielectric constant values. Full article

Tumor Treating Fields (TTFields) are electric fields that exert physical forces to disrupt cellular processes critical for cancer cell viability and tumor progression. TTFields induce anti-mitotic effects through the disruption of the mitotic spindle and abnormal chromosome segregation, which trigger several forms of cell death, including immunogenic cell death (ICD). The efficacy of TTFields concomitant with anti-programmed death-1 (anti-PD-1) treatment was previously shown in vivo and is currently under clinical investigation. Here, the potential of TTFields concomitant with anti- PD-1/anti-cytotoxic T-lymphocyte-associated protein 4 (anti-CTLA-4) or anti-programmed death-ligand 1 (anti-PD-L1) immune checkpoint inhibitors (ICI) to improve therapeutic efficacy was examined in lung tumor-bearing mice. Increased circulating levels of high mobility group box 1 protein (HMGB1) and elevated intratumoral levels of phosphorylated eukaryotic translation initiation factor 2α (p-eIF2α) were found in the TTFields-treated mice, indicative of ICD induction. The concomitant application of TTFields and ICI led to a significant decrease in tumor volume as compared to all other groups. In addition, significant increases in the number of tumor-infiltrating immune cells, specifically cytotoxic T-cells, were observed in the TTFields plus anti-PD-1/anti-CTLA-4 or anti-PD-L1 groups. Correspondingly, cytotoxic T-cells isolated from these tumors showed higher levels of IFN-γ production. Collectively, these results suggest that TTFields have an immunoactivating role that may be leveraged for concomitant treatment with ICI to achieve better tumor control by enhancing antitumor immunity. Full article

In our previous work, epitaxial Ba(Zr_0.2Ti_0.8)O₃ thick films (~1–2 μm) showed an excellent energy storage performance with a large recyclable energy density (~58 J/cc) and a high energy efficiency (~92%), which was attributed to a nanoscale entangled heterophase polydomain structure. Here, we propose a detailed analysis of the structure–property relationship in these film materials, using an annealing process to illustrate the effect of nanodomain entanglement on the energy storage performance. It is revealed that an annealing-induced stress relaxation led to the segregation of the nanodomains (via detailed XRD analyses), and a degraded energy storage performance (via polarization-electric field analysis). These results confirm that a nanophase entanglement is an origin of the high-energy storage performance in the Ba(Zr_0.2Ti_0.8)O₃ thick films. Full article

Inexpensive perovskite light-emitting devices fabricated by a simple wet chemical approach have recently demonstrated very prospective characteristics such as narrowband emission, low turn-on bias, high brightness, and high external quantum efficiency of electroluminescence, and have presented a good alternative to well-established technology of epitaxially grown III-V semiconducting alloys. Engineering of highly efficient perovskite light-emitting devices emitting green, red, and near-infrared light has been demonstrated in numerous reports and has faced no major fundamental limitations. On the contrary, the devices emitting blue light, in particular, based on 3D mixed-halide perovskites, suffer from electric field-induced phase separation (segregation). This crystal lattice defect-mediated phenomenon results in an undesirable color change of electroluminescence. Here we report a novel approach towards the suppression of the segregation in single-layer perovskite light-emitting electrochemical cells. Co-crystallization of direct band gap CsPb(Cl,Br)${}_3$ and indirect band gap Cs${}_4$Pb(Cl,Br)${}_6$ phases in the presence of poly(ethylene oxide) during a thin film deposition affords passivation of surface defect states and an increase in the density of photoexcited charge carriers in CsPb(Cl,Br)${}_3$ grains. Furthermore, the hexahalide phase prevents the dissociation of the emissive grains in the strong electric field during the device operation. Entirely resistant to 5.7 × 10${}^6$ V·m${}^{-1}$ electric field-driven segregation light-emitting electrochemical cell exhibits stable emission at wavelength 479 nm with maximum external quantum efficiency 0.7%, maximum brightness 47 cd·m${}^{-2}$, and turn-on bias of 2.5 V. Full article

Manipulation of particles at the surface of a droplet can lead to the formation of structures with heterogeneous surfaces, including patchy colloidal capsules or patchy particles. Here, we study the assembly and rearrangement of microparticles confined at the surface of oil droplets. These processes are driven by electric-field-induced hydrodynamic flows and by ‘electro-shaking’ the colloidal particles. We also investigate the motion of an intruder particle in the particle film and present the possibility of segregating the surface particles. The results are expected to be relevant for understanding the mechanism for particle segregation and, eventually, lead to the formation of new patchy structures. Full article