금현성 교수

In2O3 thin-film transistors (TFTs) were fabricated on various dielectrics [SiO2, self-assembled nanodielectrics (SANDs)] by spin-coating In2O3 film precursor solutions consisting of ethanolamine (EAA) and InCl3 in methoxyethanol. Optimized film microstructures are characterized by the high-mobility In2O3 00 L orientation and are obtained only within a well-defined range of base: In3+ molar ratios. Electron mobilities as high as approximately 44 cm2 V(-1) s(-1) are measured for n+-Si/SAND/In2O3/A

Photocatalytic conversion of lignocellulose to valuable aromatics has significant potential for applications in biorefineries. The photocatalyst efficiency of lignocellulose conversion is typically limited by the buffering redox system in combination with oxidation and reduction of the photoexcited holes and electrons, respectively, which ensures high charge-recombination rates. Herein, Ag+-exchanged CdS is employed for easy photoexcited electron transfer to the oxidized intermediate, which resu

Silicalite-1 films (thickness = 400 nm) supported on both sides of glass plates (SL/G) were prepared, and hemicyanine dyes (HC-n) with different alkyl chain lengths (n, n = 3, 6, 9, 12, 15, 18, 22, and 24) were included into the silicalite-1 films by dipping SL/Gs into each methanol solution of HC-n (1 mM) for 1 d. The included numbers of HC-n per channel (N(C)) generally decreased with increasing n; that is, they were 6.4, 23.1, 15.4, 8.2, 5.7, 3.5, 0.9, and 1.2 molecules per channel, respectiv

We report a simple approach for preparing undoped and Pt-doped Fe(2)O(3) thin films with excellent photoactivity via facile hydrothermal growth. The photocurrent densities of undoped and Pt-doped Fe(2)O(3) thin films were recorded up to 1.2 and 1.38 mA cm(-2) at 0.23 V Ag/AgCl under 1 sun illumination, respectively.

Amorphous indium tin oxide (ITO)-based thin-film transistors (TFTs) were fabricated on various dielectrics [SiO(2) and self-assembled nanodielectrics (SANDs)] by spin-coating an ITO film precursor solution consisting of InCl(3) and SnCl(4) as the sources of In(3+) and Sn(4+), respectively, methoxyethanol (solvent), and ethanolamine (base). These films can be annealed at temperatures T(a) < or = 250 degrees C and afford devices with excellent electrical characteristics. The optimized [In(3+)]/[In

Zeolite-intercalated semiconductor quantum dots (QDs) have long been proposed to give very high third-order nonlinear optical (3NLO) responses. However, measurements of their 3NLO responses have not been possible due to the lack of methods to prepare optically transparent QD-incorporating zeolite films supported on optically transparent substrates and to confine QDs only within zeolite interiors. We found that the zeolite-Y films grown on indium-tin-oxide-coated glass plates (Ygs) remain firmly

The Co–P electrode synthesized in deep eutectic solution showed enhanced stability for electrocatalytic HMF oxidation into FDCA.

Unlike octadecyl-tethering hemicyanine (HC-18), nonyl-tethering hemicyanine (HC-9) entered the hydrophobic channels of silicalite-1 with a very small preference to the inclusion with the alkyl part first. Accordingly, while the degree of uniform orientation (DUO) of HC-18 in the channels was 0.67, that of HC-9 was only 0.08. This phenomenon was ascribed to the fact that HC-9 has a hydrophilic part at the center and two hydrophobic parts on both sides with almost equal hydrophobicities. Upon irra

The demand for nonlinear optical (NLO) materials with exceptional NLO properties is very large, and hence the search for such materials should be continued not only to enhance their functions in current applications but also to help expedite the materialization of photonics in which photons instead of electrons are used for signal processing, transmission, and storage. This article summarizes the preparation, characteristics, and the future perspectives of novel second order nonlinear optical (2

Zeolite Y films (0.35-2.5 μm), into which CdS and PbS quantum dots (QDs) were loaded, were grown on ITO glass. The CdS QD-loaded zeolite Y films showed a photovoltaic effect in the electrolyte solution consisting of Na(2)S (1 M) and NaOH (0.1 M) with Pt-coated F-doped tin oxide glass as the counter electrode. In contrast, the PbS QD-loaded zeolite Y films exhibited a negligible PV effect. This contrasting behavior was proposed to arise from the large difference in driving force for the electron

Sulfur mustard gas, also called HD, is one of the main chemical warfare agents and has claimed thousands of lives and left many more contaminated. The development of functional materials to promptly capture and detoxify sulfur mustard within a few minutes is extremely important to save the lives of the affected people. This has motivated us to explore excellent detoxification systems that can be deployed in the field to rapidly capture and hydrolyze mustard gas in a short time. To that end, we p