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ABSTRACTA new technique using impedance spectroscopy was developed to estimate the oxidation kinetics of the pyrolytic carbon interphase layer in SiCf/SiC ceramic matrix composites. The AC impedance Nyquist plot showed two semicircles that were curve-fitted using an equivalent circuit with two constant-phase element components. The analysis results revealed that the capacitance in the low-frequency region decreased with increasing oxidation time, whereas that in the high-frequency region remained relatively constant. This change in the capacitance in the low-frequency region was associated with the thickness of the oxidized SiO2 layer. This study might make a significant contribution to the literature, which has mostly focused on the characterization of ceramic matrix composites through measurements of mechanical properties. The limitations and potential applications of the developed method were also elucidated.

Redox mediators comprising I−, Co3+, and Ti3C2Tx MXene were applied to dye-sensitized solar cells (DSCs). In the as-prepared DSCs (I-DSCs), wherein hole conduction occurred via the redox reaction of I−/I3− ions, the power conversion efficiency (PCE) was not altered by the addition of Ti3C2Tx MXene. The I-DSCs were exposed to light to produce Co2+/Co3+-based cells (Co-DSCs), wherein the holes were transferred via the redox reaction of Co2+/Co3+ ions. A PCE of 9.01% was achieved in a Co-DSC with Ti3C2Tx MXene (Ti3C2Tx-Co-DSC), which indicated an improvement from the PCE of a bare Co-DSC without Ti3C2Tx MXene (7.27%). It was also found that the presence of Ti3C2Tx MXene in the redox mediator increased the hole collection, dye regeneration, and electron injection efficiencies of the Ti3C2Tx-Co-DSC, leading to an improvement in both the short-circuit current and the PCE when compared with those of the bare Co-DSC without MXene.

Metal–organic frameworks (MOFs) are porous materials assembled using metal and organic linkers, showing a high specific surface area and a tunable pore size. Large portions of metal open sites in MOFs can be exposed to electrolyte ions, meaning they have high potential to be used as electrode materials in energy storage devices such as supercapacitors. Also, they can be easily converted into porous metal oxides by heat treatment. In this study, we obtained high energy storage performance by preparing electrode materials through applying heat treatment to manganese MOFs (Mn-MOFs) under air. The chemical and structural properties of synthesized and thermally treated Mn-MOFs were measured by Fourier-transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). The surface area and porosity were investigated by nitrogen adsorption/desorption isotherms. The electrochemical properties were studied by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) using a three-electrode cell. It was found that Mn-MOF electrodes that underwent heat treatment at 400 °C under air consisted of Mn2O3 with high specific surface area and porosity. They also showed a superior specific capacitance of 214.0 F g−1 and an energy density value of 29.7 Wh kg−1 (at 0.1 A g−1) compared to non-treated Mn-MOFs.

MXenes consisting of thin layers of transition metal carbides or nitrides are good candidates for electrode materials due to their excellent electrical conductivity and fast ion transfer. Electrospun carbon nanofibers are highly porous and electrically conductive, making them attractive for electrode materials. In this study, free-standing electrodes were prepared by the dip-coating of carbon nanofibers (CNFs) in the MXene (Ti3C2) colloidal solution, which was synthesized via the wet-etching of MAX (Ti3AlC2) phase, and their chemical structures were investigated by X-ray diffraction and Fourier transform infrared spectroscopy. In addition, scanning and transmission electron microscopy were used to investigate the morphological and crystallographic features of MXene-coated CNFs. Surface area and pore volumes were investigated by nitrogen adsorption/desorption measurements. Supercapacitor performance was studied by assembling a 3-electrode system with 1M aqueous sodium sulfate solution as an electrolyte. MXene-coated CNFs exhibited a maximum specific capacitance of 514 F/g at 0.5 A/g, with energy and power densities of 71.4 Wh/kg at 0.5 A/g and 2.3 kW/kg at 5 A/g, respectively, which are relevantly higher compared to the pristine CNFs due to the pseudocapacitive behavior of MXenes. They also showed comparable cyclic stability during 5000 cycles with the CNFs. This result indicates that MXene-coated carbon nanofibers can be effective electrode materials for electrochemical energy storage.

The TiO2 films were modified with a dianion compound, 1,2-ethanedisulfonic acid disodium salt (ESD), to give a negative charge (ethane sulfonate anion) on the TiO2 surface, i.e., TiO2-O-SO2-CH2-CH2-SO3−), and effects of repulsion between the negative charge and ions (I3−) of the electrolyte on the performance of dye-sensitized solar cells (DSSCs) were investigated. The reference device without any modification showed a power conversion efficiency (PCE) of 9.89%, whereas for the device with ESD(20)-TiO2/FTO, which was prepared by soaking bare TiO2/FTO in an ESD solution for 20 min, the PCE was increased to 10.97%, due to an increase in both short-circuit current (Jsc) and open-circuit voltage(Voc). It was verified from the measurements of electrochemical impedance, open-circuit voltage decay and dark current that the enhancement in the Jsc and Voc values was attributed to the reduced back reaction between photoinjected electrons and I3− ions, resulting from the presence of the ethane sulfonate anions on the TiO2 surface. Keywords: Dianion compound, 1,2-Ethanedisulfonic acid disodium salt, Dye-sensitized solar cell, Back reaction

An ionic liquid, 1-methyl-3-propylimidazolium iodide (MPII), was solidified with an organic hole-transporting material, 4,4′,4″-tris[(3-methylphenyl)phenylamino]triphenylamine (m-MTDATA), and the resulting solid-state redox mediator (RM) (m-MTDATA-solidified MPII) was employed in solar devices to realize solid-state dye-sensitized solar cells (sDSSCs). Solar devices with only MPII or m-MTDATA as an RM showed almost 0 mA/cm2 of short-circuit current (Jsc) and thus 0% power conversion efficiency (PCE). However, an sDSSC with the m-MTDATA-solidified MPII exhibited 4.61 mA/cm2 of Jsc and 1.80% PCE. It was found that the increased Jsc and PCE were due to the formation of I3−, which resulted from a reaction between the iodie (I−) of MPII and m-MTDATA cation. Further enhancement in both Jsc (9.43 mA/cm2) and PCE (4.20%) was observed in an sDSSC with 4-tert butylpyridine (TBP) as well as with m-MTDATA-solidified MPII. We attributed the significant increase (about 230%) in PCE to the lowered diffusion resistance of I−/I3− ions in the solid-state RM composed of the m-MTDATA-solidified MPII and TBP, arising from TBP’s role as a plasticizer.

ZnO nanorods were formed by chemical bath deposition on fluorine–doped tin oxide (FTO) glass and the photovoltaic performance of ZnO-based dye-sensitized solar cells (DSCs) was investigated. A DSC with 8 h-grown ZnO nanorods showed a higher power conversion efficiency (PCE) than devices with 4, 6, and 10 h-grown ones. Further improvement in PCE was achieved in a cell with a silver-ion-deposited ZnO/FTO electrode. By deposition of Ag+ on the surface of the 8 h-grown ZnO nanorods, the dye-loading amount increased by approximately 210%, compared to that of pristine ZnO nanorods, resulting in a 1.8-times higher PCE. A DSC with the pristine ZnO/FTO electrode showed a PCE of 0.629%, while in a device with the silver-ion-deposited ZnO/FTO, the PCE increased to 1.138%. In addition, interfacial resistance at the ZnO/dye/electrolyte was reduced to approximately 170 Ω from 460 Ω for the control cell with the pristine ZnO/FTO. We attributed the higher dye-loading amount in the silver-ion-deposited ZnO/FTO to the electrostatic attraction between the positively charged ZnO and carboxylate anions (–COO−) of the N719 dyes.

The leakage and volatilization of liquid electrolytes limit the commercialization of dye-sensitized solar cells (DSCs). As solid-state (ss) hole-transporting materials, free from leakage and volatilization, biscarbazole-based polymers with different molecular weights (PBCzA-H (21,200 g/mol) and PBCzA-L (2450 g/mol)) were applied in combination with additives to produce ssDSCs. An ssDSC with PBCzA-H showed a better short-circuit current (Jsc), open-circuit voltage (Voc), and fill factor (FF) than a device with PBCzA-L, resulting in 38% higher conversion efficiency. Compared to the PBCzA-L, the PBCzA-H with a higher molecular weight showed faster hole mobility and larger conductivity, leading to elevations in Jsc via rapid hole transport, Voc via rapid hole extraction, and FF via lowered series and elevated shunt resistances. Thus, it is believed that PBCzA-H is a useful candidate for replacing liquid electrolytes.

By simple soaking titanium dioxide (TiO2) films in an aqueous Na2S solution, we could prepare surface-modified photoanodes for application to dye-sensitized solar cells (DSSCs). An improvement in both the open-circuit voltage (Voc) and the fill factor (FF) was observed in the DSSC with the 5 min-soaked photoanode, compared with those of the control cell without any modification. The UV−visible absorbance spectra, UPS valence band spectra, and dark current measurements revealed that the Na2S modification led to the formation of anions on the TiO2 surface, and thereby shifted the conduction band edge of TiO2 in the negative (upward) direction, inducing an increase of 29 mV in the Voc. It was also found that the increased FF value in the surface-treated device was attributed to an elevation in the shunt resistance.

At an elevated temperature of 90 °C, a chemical bath deposition using an aqueous solution of Zn(NO3)2·6H2O and (CH2)6N4 resulted in the formation of both nanoflowers and microrods of ZnO on F-doped SnO2 glass with a seed layer. The nanoflowers and microrods were sensitized with dyes for application to the photoelectrodes of dye-sensitized solar cells (DSSCs). By extending the growth time of ZnO, the formation of nanoflowers was reduced and the formation of microrods favored. As the growth time was increased from 4 to 6 and then to 8 h, the open circuit voltage (Voc) values of the DSSCs were increased, whilst the short circuit current (Jsc) values varied only slightly. Changes in the dye-loading amount, dark current, and electrochemical impedance were monitored and they revealed that the increase in Voc was found to be due to a retardation of the charge recombination between photoinjected electrons and I3− ions and resulted from a reduction in the surface area of ZnO microrods. A reduced surface area decreased the dye contents adsorbed on the ZnO microrods, and thereby decreased the light harvesting efficiency (LHE). An increase in the electron collection efficiency attributed to the suppressed charge recombination counteracted the decreased LHE, resulting in comparable Jsc values regardless of the growth time.

Here we report the influences of the sheet resistance (Rsheet) of a hole-collecting electrode (indium tin oxide, ITO) and the conductivity of a hole-collecting buffer layer (poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate), PEDOT:PSS) on the device performance of flexible plastic organic photovoltaic (OPV) devices. The series resistance (RS) of OPV devices steeply increases with increasing Rsheet of the ITO electrode, which leads to a significant decrease of short-circuit current density (JSC) and fill factor (FF) and power conversion efficiency, while the open-circuit voltage (VOC) was almost constant. By applying high-conductivity PEDOT:PSS, the efficiency of OPV devices with high Rsheet values of 160 Ω/□ and 510 Ω/□ is greatly improved, by a factor of 3.5 and 6.5, respectively. These results indicate that the conductivities of ITO and PEDOT:PSS will become more important to consider for manufacturing large-area flexible plastic OPV modules.

We developed a single-panel LCD microdisplay system using a field-sequential color (FSC) driving method and an organic light-emitting diode (OLED) as a backlight unit (BLU). The 0.76′′ OLED BLU with red, green, and blue (RGB) colors was fabricated by a conventional UV photolithography patterning process and by vacuum deposition of small molecule organic layers. The field-sequential driving frequency was set to 255 Hz to allow each of the RGB colors to be generated without color mixing at the given display frame rate. A prototype FSC LCD microdisplay system consisting of a 0.7′′ LCD microdisplay panel and the 0.76′′ OLED BLU successfully exhibited color display and moving picture images using the FSC driving method.