Observation of cavity polaritons in a metal-mirror Fabry-Pérot microcavity containing liquid-crystalline semiconductor based on perylene bisimide units.

We investigate the optical properties of a metal-mirror microcavity containing a liquid-crystalline (LC) perylene tetracarboxylic bisimide (PTCBI) derivative. Measurements of the transmission's incidence angle dependence show that the peaks are split in a complex way and shift as the angle changes. Further, measurements of the photoluminescence spectrum's emission angle dependence show that the peak also shifts with the angle, as in the transmission experiment.

Antiferroelectric Nature of CH3NH3PbI3-xClx Perovskite and Its Implication for Charge Separation in Perovskite Solar Cells.

Perovskite solar cells (PSCs) have been attracted scientific interest due to high performance. Some researchers have suggested anomalous behavior of PSCs to the polarizations due to the ion migration or ferroelectric behavior. Experimental results and theoretical calculations have suggested the possibility of ferroelectricity in organic-inorganic perovskite.

Nanoparticles speckled by ready-to-conjugate lanthanide complexes for multimodal imaging.

Multimodal and multifunctional contrast agents receive enormous attention in the biomedical imaging field. Such contrast agents are routinely prepared by the incorporation of organic molecules and inorganic nanoparticles (NPs) into host materials such as gold NPs, silica NPs, polymer NPs, and liposomes. Despite their non-cytotoxic nature, the large size of these NPs limits the in vivo distribution and clearance and inflames complex pharmacokinetics, which hinder the regulatory approval for clinical applications.

Synthesis of [111]- and {010}-faceted anatase TiO2 nanocrystals from tri-titanate nanosheets and their photocatalytic and DSSC performances.

[111]- and {010}-faceted anatase nanocrystals with controllable crystal size and morphology were synthesized from tri-titanate H2Ti3O7 nanosheets by hydrothermal reaction. The nanostructures and the formation reaction mechanism of the obtained TiO2 nanocrystals were investigated using XRD, FE-SEM, and TEM. Furthermore, the photocatalytic and dye-sensitized solar cell (DSSC) performances of the synthesized anatase nanocrystals were also characterized.

Auger ionization beats photo-oxidation of semiconductor quantum dots: extended stability of single-molecule photoluminescence.

Despite the bright and tuneable photoluminescence (PL) of semiconductor quantum dots (QDs), the PL instability induced by Auger recombination and oxidation poses a major challenge in single-molecule applications of QDs. The incomplete information about Auger recombination and oxidation is an obstacle in the resolution of this challenge. Here, we report for the first time that Auger-ionized QDs beat self-sensitized oxidation and the non-digitized PL intensity loss.

Modification of TiO₂ electrode with organic silane interposed layer for high-performance of dye-sensitized solar cells.

Back electron transfer from the TiO2 electrode surface to the electrolyte is the main reason behind the low-open circuit potential (Voc) and the low-fill factor (FF) of the dye-sensitized solar cells (DSSCs). Modifications to the TiO2 electrode, fabricated using {010}-faceted TiO2 nanoparticles with six different kinds of silane, are reported to decrease the back electron transfer on the TiO2 surface. The effect of alkyl chain length of hydrocarbon silanes and fluorocarbon silanes on adsorption parameters of surface coverage and adsorption constant, interfacial resistance, and photovoltaic performances were investigated.

Single-molecule photochemical reactions of Auger-ionized quantum dots.

Photoinduced electron transfer in donor-acceptor systems composed of quantum dots (QDs) and electron donors or acceptors is a subject of considerable recent research interest due to the potential applications of such systems in both solar energy harvesting and degradation of organic pollutants. Herein, we employed single-molecule imaging and spectroscopy techniques for the detection of photochemical reactions between 1,4-diaminobutane (DAB) and CdSe/ZnS single QDs. We investigated the reactions by analyzing photoluminescence (PL) intensity and lifetime of QDs at ensemble and single-molecule levels.

Blinking suppression in CdSe/ZnS single quantum dots by TiO2 nanoparticles.

The photoluminescence of semiconductor quantum dots and fluorescence of single molecules intermittently turn ON and OFF, a phenomenon referred to as blinking. In quantum dots, blinking occurs as a result of intermittent Auger ionization, which results in the formation of positively charged quantum dots. Due to strong Coulombic interactions, successive photoactivation of a charged quantum dot results in nonradiative carrier recombination, inducing long-lived OFF states in the intensity trajectories.

Enhancement and suppression of terahertz emission by a Fabry-Perot cavity structure with a nonlinear optical crystal.

We have fabricated Fabry-Perot (FP) cavities in the THz region with a ZnTe crystal as a cavity layer by a simple stacking method. We observed more than a three times enhancement of the THz emission intensity in the FP cavities compared with the bare ZnTe crystal at the frequencies of the resonant modes and stopband edges. On the other hand, suppression of the THz emission occurs at frequencies in the stopband.

Two-photon spectroscopy of core excitons in barium fluoride using synchrotron radiation and laser light.

We have conducted two-photon spectroscopy of core excitons in BaF(2). Synchrotron radiation and laser light were used for 5p core-electron excitation and Auger-free luminescence was detected as the signal. Two-photon excitation enables access to f and p orbitals that cannot be reached by one-photon excitation of electrons in p orbitals.