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131.
Ju-Hyun Ahn 《Applied Surface Science》2007,253(21):8588-8591
Electrochemical synthesis of photoactive cadmium-indium-selenide (CdIn2Se4) thin films at ambient temperature was reported. The nanocrystalline nature and 1:2:4 elemental chemical stoichiometric ratio for Cd, In and Se were obtained from the X-ray diffraction and energy dispersive X-ray analysis, respectively. Irregular shaped islands of about 400-500 nm in sizes composed of large number of small (∼30-40 nm) spherical grains were confirmed from the atomic force microscopy and the scanning electron microscopy images. The photoelectrochemical measurement of CdIn2Se4 film electrode in presence of 1 M polysulphide electrolyte revealed 0.42% photoelectrochemical device conversion efficiency, under the light illumination intensity of 80 mW/cm2. 相似文献
132.
We propose double pass fiber Raman amplifier schemes based on Raman fiber oscillator in order to amplify optical signal with wavelengths from 1610 to 1650 nm efficiently. We experimentally demonstrate that the proposed double pass amplifier scheme has enhanced gain characteristics compared to a conventional single pass scheme. We also demonstrate a scheme for the proposed double pass amplifier to have small gain variation over the wavelength range by using two fiber Bragg gratings with different center wavelengths. 相似文献
133.
In this paper, we proposed a novel infrared absorbing structure for uncooled infrared detectors. The infrared absorber makes use of a quarter-wavelength structure composed of a dielectric layer, a protecting layer, an active layer, a supporting layer and a reflecting layer. Sputtered amorphous silicon is used as a dielectric layer because of its high refractive index. We fabricated the uncooled microbolometer with the proposed infrared absorbing structure by surface micromachining method. Then we characterized various bolometric properties such as thermal conductance, thermal time constant, responsivity and infrared absorptance. The fabricated bolometer showed the thermal conductance of 6.72 × 10−7 W/K, the thermal mass of 4.43 × 10−9 J/K, the thermal time constant of 6.6 ms and the responsivity of 7.76 × 103 V/W at 10 Hz chopper frequency and 9.22 μA bias current. From the results, the estimated absorptance is about 80%. We expect that the proposed absorbing structure shows high infrared absorption and high performance of uncooled microbolometer. 相似文献
134.
The reaction of AgX (X− = NO3
−, ClO4
−, or CF3SO3
−) with 1,3-bis(3-pyridyl)tetramethyldisiloxane (L) at room temperature affords 20-membered metallacyclodimers, [Ag(L)]2(X)2. For the macrocyclodimer, fine competition among argentophilic, electrostatic, and π···π interaction exists. The macrocyclodimer
is a unique molecular chair that tunes a transannular argentophilic interaction via the bite size of the counteranions. In
order to reversibly control the argentophilic interaction, anion exchange has been accomplished. The anion exchangeability
depends on the water solubility rather than the electrostatic interaction between silver(I) and anions. 相似文献
135.
Wongi Park Minyong Yang Hyewon Park Dr. Joanna M. Wolska Dr. Hyungju Ahn Prof. Dr. Tae Joo Shin Prof. Dr. Damian Pociecha Prof. Dr. Ewa Gorecka Prof. Dr. Dong Ki Yoon 《Chemistry (Weinheim an der Bergstrasse, Germany)》2021,27(24):7108-7113
Herein, it is reported that the polymorphism in the helical nanofilament (HNF, B4) liquid-crystalline phase depends on the fabrication methods, that is, UV-driven formation and template-assisted self-assembly in the nanoconfined geometry. As a result, uniaxially oriented HNFs with different helical structures were obtained, in which generation of the twisted-ribbon and cylindrical-ribbon polymorphs showed that even the molecular lattice has a different orientation. The detailed structures were directly observed by SEM and grazing-incidence X-ray diffraction with synchrotron radiation. The resultant polymorphs could be used in chiro-optical applications due to the capability for fine control of the helical structures. 相似文献
136.
Soojin Park Wha‐Keun Ahn Sunyoung Lee Sang Yun Han Bum Ku Rhee Han Bin Oh 《Rapid communications in mass spectrometry : RCM》2009,23(23):3609-3620
Ultraviolet (UV) photodissociation (PD) experiments using 266 nm light were performed for a series of phosphopeptide cations in a Fourier transform mass spectrometer. The objective of the experiments was to determine whether 266 nm UV irradiation on the phosphopeptide cations would induce unique peptide backbone dissociation. In addition, the general behavior of the phosphate loss (?80 or ?98 Da) was monitored, particularly for those phosphopeptides with a phosphotyrosine residue that itself is a UV chromophore. For phosphopeptides with a UV chromophore, their photodissociation behavior was very similar to that of low‐energy sustained off‐resonance irradiation collisionally activated dissociation (SORI‐CAD), with a few exceptions. For example, b‐ and y‐type peptide backbone fragments were prevalent, and their dephosphorylation behavior was consistent with that of the SORI‐CAD results. For phosphoserine peptides, the loss of a phosphate group was always observed. On the other hand, for phosphotyrosine peptides, the phosphate loss was found to be dependent on the presence of a basic amino group in the sequence and the charge state of the precursor ions, in agreement with the CAD results in the literature. However, hydrogen atom loss or aromatic side chain loss, which is known to be the excited state specific fragmentation pathway, was rarely observed in our 266 nm UV PD experiments, in contrast to the previous UV PD literature (particularly at 220 nm). The mechanism for these observations is described in terms of dominant internal conversion followed by intramolecular vibrational energy redistribution (IVR). Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
137.
138.
A series of crosslinked polymer electrolyte membranes were prepared by blending cellulose and sulfosuccinic acid (SA) for
fuel cell applications. The crosslinking reaction of membranes occurred via the esterification between –OH of cellulose and
–COOH of SA, as confirmed by FT-IR spectroscopy. Both the ion exchange capacity and the proton conductivity increased in proportion
to the increase of SA concentrations due to the increasing portion of charged groups in the membrane. In contrast, the water
uptake linearly increased up to 25 wt.% of SA concentration, above which it decreased abruptly. The maximum behavior of water
uptake may be a result of competitive effect between the increasing number of ionic sites and the increasing degree of crosslinking
with the SA concentrations. Wide angle X-ray scattering also showed that the crystalline structures of cellulose disappeared
upon the introduction of SA. The mechanical properties of cellulose/SA membranes, i.e., tensile strength at break and Young’s
modulus, showed a maximum at 15 wt.% of SA, as revealed by universal testing machine. These membranes exhibited good thermal
stability up to 250 °C, as revealed by thermal gravimetric analysis. 相似文献
139.
Relationships between an assembler and a vendor in a supply chain are investigated in two-period models when the assembler wants to reduce response time by incentive systems. The assembler may offer myopic or farsighted incentive contracts to the vendor, under short-term or long-term relationships. Incentive schemes, effort levels, and expected payoffs under different perspectives and relationships are examined. We find that a farsighted assembler provides the vendor with a higher incentive than a myopic assembler in the first period. A long (short)-term relationship is preferred if the value of farsightedness under a long-term relationship is greater (less) than the switching option value under a short-term relationship. We propose several sufficient conditions regarding which perspectives and relationships are preferred. 相似文献
140.
Soon Kil Ahn Nam Song Choi Byeong Seon Jeong Kye Kwang Kim Duck Jin Journ Joon Kyum Kim Sang Joon Lee Jung Woo Kim Chung Hong Sang‐Sup Jew 《Journal of heterocyclic chemistry》2000,37(5):1141-1144
A practical semi‐synthetic method of (S)‐7‐(2‐isopropylamino)ethylcamptothecin hydrochloride has been developed. The Mannich reaction of (S)‐7‐methylcamptothecin with isopropylamine hydrochloride in dimethyl sulfoxide as a formaldehyde source gave the desired product in moderate yield. 相似文献