ABSTRACT
Atomic-force microscopic images, x-ray diffraction patterns, Urbach energies and photoluminescence quenching experiments show that the interfacial contact quality between the hydrophobic [6,6]-phenyl-C61-buttric acid methyl ester (PCBM) thin film and hydrophilic CH3NH3PbI3(MAPbI3) thin film can be effectively improved by using a binary antisolvent mixture (toluene:dichloromethane or chlorobenzene:dichloromethane) in the anti-solvent mixture-mediated nucleation process, which increases the averaged power conversion efficiency of the resultant PEDOT:PSS (P3CT-Na) thin film based MAPbI3solar cells from 13.18% (18.52%) to 13.80% (19.55%). Beside, the use of 10% dichloromethane (DCM) in the binary antisolvent mixture results in a nano-textured MAPbI3thin film with multicrystalline micrometer-sized grains and thereby increasing the short-circuit current density and fill factor (FF) of the resultant solar cells. It is noted that a remarkable FF of 80.33% is achieved, which can be used to explain the stable photovoltaic performance without additional encapsulations.
ABSTRACT
The methods to enhance contrast ratios (CRs) in scattering-type transflective liquid crystal displays (ST-TRLCDs) based on polymer-network liquid crystal (PNLC) cells are investigated. Two configurations of ST-TRLCDs are studied and are compared with the common ST-TRLCDs. According to the comparisons, CRs are effectively enhanced by assembling a linear polarizer at the suitable position to achieve better dark states in the transmissive and reflective modes of the reported ST-TRLCDs with the optimized configuration, and its main trade-off is the loss of brightness in the reflective modes. The PNLC cell, which works as an electrically switchable polarizer herein, can be a PN-90° twisted nematic LC (PN-90° TNLC) cell or a homogeneous PNLC (H-PNLC) cell. The optoelectric properties of PN-90° TNLC and those of H-PNLC cells are compared in detail, and the results determine that the ST-TRLCD with the optimized configuration using an H-PNLC cell can achieve the highest CR. Moreover, no quarter-wave plate is used in the ST-TRLCD with the optimized configuration, so a parallax problem caused by QWPs can be solved. Other methods for enhancing the CRs of the ST-TRLCDs are also discussed.
ABSTRACT
In cultured rat cerebellar granule cells, glutamate or N-methyl-d-aspartate (NMDA) activation of the NMDA receptor caused a sustained increase in cytosolic Ca(2+) levels ([Ca(2+)](i)), reactive oxygen species (ROS) generation, and cell death (respective EC(50) values for glutamate were 12, 30, and 38 microM) but no increase in caspase-3 activity. Removal of extracellular Ca(2+) blocked all three glutamate-induced effects, whereas pretreatment with an ROS scavenger inhibited glutamate-induced cell death but had no effect on the [Ca(2+)](i) increase. This indicates that glutamate-induced cell death is attributable to [Ca(2+)](i) increase and ROS generation, and the [Ca(2+)](i) increase precedes ROS generation. Apoptotic cell death was not seen until 24 h after exposure of cells to glutamate. S-nitrosoglutathione abolished glutamate-induced ROS generation and cell death, and only a transient [Ca(2+)](i) increase was seen; similar results were observed with another nitric oxide (NO) donor, S-nitroso-N-acetylpenicillamine, but not with glutathione, which suggests that the effects were caused by NO. The transient [Ca(2+)](i) increase and the abolishment of ROS generation induced by glutamate and S-nitrosoglutathione were still seen in the presence of an ROS scavenger. Glial cells, which were present in the cultures used, showed no [Ca(2+)](i) increase in the presence of glutamate, and glutamate-induced granule cell death was independent of the percentage of glial cells. In conclusion, NO donors protect cultured cerebellar granule cells from glutamate-induced cell death, which is mediated by ROS generated by a sustained [Ca(2+)](i) increase, and glial cells provide negligible protection against glutamate-induced excitotoxicity.
