Monitoring Catalytic 2-Propanol Oxidation over Co3O4 Nanowires via In Situ Photoluminescence Spectroscopy

Spectroscopic methods enabling real-time monitoring of dynamic surface processes are a prerequisite for identifying how a catalyst triggers a chemical reaction. We present an in situ photoluminescence spectroscopy approach for probing the thermo-catalytic 2-propanol oxidation over mesostructured Co3O4 nanowires. Under oxidative conditions, a distinct blue emission at ~420 nm is detected that increases with temperature up to 280 °C, with an intermediate maximum at 150 °C. Catalytic data gained under comparable conditions show that this course of photoluminescence intensity precisely follows the conversion of 2-propanol and the production of acetone. The blue emission is assigned to the radiative recombination of unbound acetone molecules, the n - π* transition of which is selectively excited by a wavelength of 270 nm. These findings open a pathway for studying thermo-catalytic processes via in situ photoluminescence spectroscopy thereby gaining information about the performance of the catalyst and the formation of intermediate products.

Investigation of 4,4′- bis [(N carbazole) styryl] biphenyl (BSB4) for a pure blue fluorescent OLED with enhanced efficiency nearing the theoretical limit

4,4′-bis[(N-carbazole) styryl] biphenyl (BSB4 or BSBCz) is one of the widely studied organic fluorescent materials for blue organic electroluminescent devices in the recent times. In this work, BSB4 is used as a guest material to construct the host-guest matrix for the emissive layer (EML) of a pure blue fluorescent organic light-emitting diode (OLED). A pure blue emission suitable for display application with a Commission Internationale de l’Eclairage (CIE) coordinate of (0.147, 0.070) is achieved by the blue-shift of the emission spectrum of the host-guest matrix from that of the pristine guest (BSB4) molecules. The optimization of OLED structures is carried out by considering (i) charge balance in the emissive layer for high exciton density, and (ii) optical interference of generated light in the organic layers for increased light outcoupling. A thorough comparative study on the use of different combinations of widely used hole and electron transport layers to obtain charge balance in the EML of the OLED, thereby enhancing the external quantum efficiency (EQE) is shown. Optical interference effects in the fabricated OLEDs are analyzed by optical simulation of each device structure by transfer matrix method (TMM). With the optimized device structures, we are able to overcome the 2% EQE limit that has been reported so far for blue fluorescent OLEDs with BSB4 as light emitting material and achieve a maximum EQE of 4.08%, which is near to the theoretical limit of EQE for fluorescent OLEDs.

Synthesis and Characterization of Lightweight Beryllium Chloro Silicate Phosphor

In this chapter, low weight barium-based cholorsilicate Ba5Cl6Si2O6:Eu2+ is prepared through a solid-state reaction. To confirm the structure of the synthesized phosphors, powder photographs were obtained using an x-ray diffractometer. Photoluminescence spectra and FTIR spectra were recorded. Photoluminescence spectra are studied. The emission peak is observed at 407 nm at excitation 275 nm. The intense violet-blue emission is obtained. The broad excitation band and strong emission indicate that Ba5Cl6Si2O6:Eu2+could be a good phosphor candidate for blue LED and white LEDs. Decay curve indicates the phosphor has a long afterglow feature.

Surface modification strategy based on molecular engineering of organic cation toward spectrally stable deep-blue emission perovskites

All-inorganic perovskites (AIP) with three primary colors emission are all-important for AIP application in many field. However, poor spectral stability seriously hinders the development of blue-emission AIP. Here, we achieved...

Excitation induced asymmetric fluorescence emission in 2D-WS2 Quantum Dots

In this work, we synthesized 3-7 nm diameter tungsten disulfide quantum dots (WS2 QDs) by pulsed laser ablation in ethanol solvent, and observed strong, stable, excited independent blue emission. To...

Real-time photovoltaic parameters assessment of carbon quantum dots showing strong blue emission

Carbon QD showing bright blue fluorescence aid in improving the photovoltaic parameters in a co-sensitized solar cell. Time-dependent I–V analysis revealed the real-time functioning of the device.

Controlled Synthesis of Up-Conversion NaYF4:Yb,Tm Nanoparticles for Drug Release under Near IR-Light Therapy

Up-Conversion materials have received great attention in drug delivery applications in recent years. A specifically emerging field includes the development of strategies focusing on photon processes that promote the development of novel platforms for the efficient transport and the controlled release of drug molecules in the harsh microenvironment. Here, modified reaction time, thermal treatment, and pH conditions were controlled in the synthesis of NaYF4:Yb,Tm up-converted (UC) material to improve its photoluminescence properties. The best blue-emission performance was achieved for the UC3 sample prepared through 24 h-synthesis without thermal treatment at a pH of 5, which promotes the presence of the β-phase and smaller particle size. NaYF4:Yb,Tm has resulted in a highly efficient blue emitter material for light-driven drug release under near-IR wavelength. Thus, NaYF4:Yb,Tm up-converted material promotes the N-O bond cleavage of the oxime ester of Ciprofloxacin (prodrug) as a highly efficient photosensitized drug delivery process. HPLC chromatography and transient absorption spectroscopy measurements were performed to evaluate the drug release conversion rate. UC3 has resulted in a very stable and easily recovered material that can be used in several reaction cycles. This straightforward methodology can be extended to other drugs containing photoactive chromophores and is present as an alternative for drug release systems.