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1.
Criteria for the near and far electromagnetic fields of ultrawideband radiation are considered based on a numerical simulation.
To estimate the field boundaries for ultrawideband radiation, it is proposed to use the condition of the maximum (near field)
and minimum (far field) differences between the time dependences of the electromagnetic field components. The approach proposed
has been approved for an axially symmetric radiator excited by voltage pulses of varied waveform and duration.
Translated from Izvestiya Vysshikh Uchebnykh Zavedenii, Fizika, No. 9, pp. 46–50, September, 2008. 相似文献
2.
The surface characteristics of titanium oxide films evaluated by gray level co-occurrence matrices (GLCMs) and entropy are demonstrated experimentally. A PC-based measurement system was set up to detect the interference fringe of optical coating surface as captured by a Fizeau interferometer. Titanium oxide films were prepared by an electron-beam gun evaporation method. The proposed measuring system was used to evaluate the surface flatness of titanium oxide films coated on glass substrates. The variation of entropy in titanium oxide films before and after film deposition was found to be related to the root-mean-square (rms) surface roughness. Surface characteristics of thin films were fast measured by our proposed method and the test results were verified by atomic force microscopy (AFM) and scanning electrical microscopy (SEM). 相似文献
3.
Separations of small ions were carried out under nonequilibrated conditions using capillaries treated with NaOH, HCl, or tris(hydroxymethyl)aminomethane (Tris) prior to analysis. For separations of benzoic acid isomers or acids and amines under weakly acidic conditions, capillaries flushed with 0.1 M NaOH and subsequently with running buffers prior to analysis were used. Separations of six benzoic acid isomers were accomplished in 4 min in 1 mM phosphate buffers, pH 4.01, containing 2.5 mM hydroxypropyl-beta-cyclodextrin. Without additives, the separation of biological amines and acids were also achieved in 10 min at pH 4.01. Capillaries treated with 0.1 M HCl prior to analysis were tested in separations of six phenols in 5 mM Tris solutions at pH 7.0. As a result of small electrophoretic mobilities of phenols against a small electroosmotic flow, resolution was optimized. We also found that reproducibility was improved using capillaries treated with HCl. The relative standard deviations of migration mobility of phenols were less than 1%, which were smaller than those obtained using capillaries treated with 0.1 M NaOH or Tris. 相似文献
4.
Zheng-Ming Wang Noriko Yoshizawa Katsunori Kosuge Wendong Wang Geoffrey A. Ozin 《Adsorption》2014,20(2-3):267-274
Quiescent hydrothermal conditions were applied to synthesis of the sandwich nanocomposites of reduced graphite oxide (rGO) and periodic mesoporous silica (PMS) with vertically aligned mesochannels. It was found that the formation of the PMS–rGO–PMS sandwich structure is very sensitive to the surface and synthesis conditions. Although a higher temperature hydrothermal condition promotes reduction of GO and formation of bulky mesoporous nanoparticles, quiescent hydrothermal condition can serve as an alternative approach to obtain the unusual nanocomposites and slightly promote the structural stability of PMS on the surface of rGO. 相似文献
5.
Weiyi Li Geng Leng Caiqin Li Yajing Lyu 《International journal of quantum chemistry》2020,120(8):e26150
The mechanisms of CO2 coupling with the propargylic alcohol using alkali carbonates M2CO3 (M = Li, Na, K, Cs) have been investigated by means of density functional theory calculations. The calculations reveal that the target product tetronic acid (TA) is yielded through two stages: (a) the formation of the α-alkylidene cyclic carbonate (αACC) intermediate via Cs2CO3-mediated carboxylative cyclization of the propargylic alcohol with CO2, and (b) the conversion of the αACC intermediate with Cs2CO3 to produce the cesium salt of the TA. Since the overall kinetic barriers for the two stages are comparable and affordable, the excellent chemoselectivity to the TA should be primarily originated from the high thermodynamic stability of the cesium salt of the TA. Moreover, relative to the TA, the possibility to yield the by-product acyclic carbonate can be excluded due to the both kinetics and thermodynamic inferiority. This result is different from the organic base-mediated reaction. Alternatively, our calculations predict that CsHCO3 together generated with the cesium salt of the TA might also be an available mediating reagent for the incorporation of CO2 with the propargylic alcohol. Compared to other alkali carbonates M2CO3 (M = Li, Na, K), the stronger basicity of Cs2CO3 and the lower ionic potential of cesium ion can raise the effective concentration of the αACC intermediate, and thus the conversion of the αACC intermediate into the cesium salt of the TA can be achieved with high yield. 相似文献
6.
Prof. Pedro Laborda Yong-Mei Lyu Dr. Fabio Parmeggiani Dr. Ai-Min Lu Wen-Jiao Wang Ying-Ying Huang Dr. Kun Huang Juan Guo Prof. Li Liu Prof. Sabine L. Flitsch Prof. Josef Voglmeir 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(13):5346-5349
Chitin is one of the most abundant and cheaply available biopolymers in Nature. Chitin has become a valuable starting material for many biotechnological products through manipulation of its N-acetyl functionality, which can be cleaved under mild conditions using the enzyme family of de-N-acetylases. However, the chemoselective enzymatic re-acylation of glucosamine derivatives, which can introduce new stable functionalities into chitin derivatives, is much less explored. Herein we describe an acylase (CmCDA from Cyclobacterium marinum) that catalyzes the N-acylation of glycosamine with a range of carboxylic acids under physiological reaction conditions. This biocatalyst closes an important gap in allowing the conversion of chitin into complex glycosides, such as C5-modified sialosides, through the use of highly selective enzyme cascades. 相似文献
7.
Dr. Yui Sasaki Satoshi Ito Zhoujie Zhang Xiaojun Lyu Dr. Shin-ya Takizawa Dr. Riku Kubota Prof. Dr. Tsuyoshi Minami 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(69):16236-16240
An artificial tongue that detects astringent components for a comprehensive evaluation of taste has not been established to date. Herein, we first propose fluorescent polythiophene (PT) derivatives ( S1 – S3 ) modified with 3-pyridinium boronic acid as supramolecular chemosensors for wine components including astringent procyanidin C1. After numerous attempts for the synthetic conditions, more than 95 mol % of the PT unit was modified with the pyridinium boronic acid moiety. To evaluate the PT derivatives as chemosensors of the artificial tongue, qualitative and quantitative analyses were performed with four types of wine components (i.e., sweet, sour, bitter, and astringent tastes) in combination with pattern recognition models. Notably, procyanidin C1 in the actual wine sample was successfully detected in a quantitative manner. In other words, we have established an authentic artificial tongue using PT based supramolecular chemosensors. 相似文献
8.
Wenyuan Lyu Dr. Yang Liu Jingyi Zhou Datong Chen Dr. Xin Zhao Dr. Ruiqi Fang Dr. Fengliang Wang Prof. Yingwei Li 《Angewandte Chemie (International ed. in English)》2023,62(42):e202310733
Photocatalytic conversion of low-concentration CO2 is considered as a promising way to simultaneously mitigate the environmental and energy issues. However, the weak CO2 adsorption and tough CO2 activation process seriously compromise the CO production, due to the chemical inertness of CO2 molecule and the formed fragile metal-C/O bond. Herein, we designed and fabricated oxygen vacancy contained Co3O4 hollow nanoparticles on ordered macroporous N-doped carbon framework (Vo−HCo3O4/OMNC) towards photoreduction of low-concentration CO2. In situ spectra and ab initio molecular dynamics simulations reveal that the constructed oxygen vacancy is able to break the local structural symmetry of Co−O−Co sites. The formation of asymmetric active site switches the CO2 configuration from a single-site linear model to a multiple-sites bending one with a highly stable configuration, enhancing the binding and structural polarization of CO2 molecules. As a result, Vo−HCo3O4/OMNC shows unprecedent activity in the photocatalytic conversion of low-concentration CO2 (10 % CO2/Ar) under laboratory light source or even natural sunlight, affording a syngas yield of 337.8 or 95.2 mmol g−1 h−1, respectively, with an apparent quantum yield up to 4.2 %. 相似文献
9.
B. Hari Babu Chengkun Lyu Hongwei Zhang Zhihao Chen Fenghong Li Lin Feng Xiao‐Tao Hao 《中国化学》2020,38(8):817-822
Interfacial engineering is expected to be a feasible strategy to improve the charge transport properties of the hole transport layer (HTL), which is of crucial importance to boost the device performance of organic solar cells (OSCs). In this study, two types of alcohol soluble materials, 2,3,5,6‐tetrafluoro‐7,7,8,8‐tetracyanoquinodimethane (F4‐TCNQ) and di‐tetrabutylammoniumcis–bis(isothiocyanato)bis (2,2’‐bipyridyl‐4,4’‐dicarboxylato) ruthenium(II) (N719) dye were selected as the dopant for HTL. The doping of F4‐TCNQ and N719 dye in poly (ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) with and without integrating a graphene quantum‐dots (G‐QDs) layer has been explored in poly[[2,6′‐4‐8‐di(5‐ethylhexylthienyl)benzo[1,2‐b:3,3‐b]dithiophene][3‐fluoro‐2[(2‐ethylhexyl)carbonyl]thieno[3,4‐b]thio‐phenediyl:(2,2′‐((2Z,2′Z)‐(((4,4,9, 9‐tetrakis(4‐hexylphenyl)‐4,9‐dihydro‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene‐2,7‐diyl)bis(4‐((2‐ethylhexyl)oxy)thiophene‐5,2‐diyl))bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (PTB7‐Th:IEICO‐4F) OSCs. The power conversion efficiency of the non‐fullerene OSCs has been increased to 10.12% from 8.84%. The influence of HTL modification on the nano‐morphological structures and photophysical properties is analyzed based on the comparative studies performed on the control and modified devices. The use of chemical doping and bilayer strategy optimizes the energy level alignment, nanomorphology, hole mobility, and work‐function of HTL, leading to considerable reduction of the leakage current and recombination losses. Our work demonstrates that the doping of HTL and the incorporation of G‐QDs layer to constitute a bilayer HTL is an promising strategy to fabricate high performance non‐fullerene polymer solar cells 相似文献
10.
Chen Li Wendong Wang Congying Xu Yuanxu Liu Bo He Chusheng Chen .CAS Key Laboratory of Materials for Energy Conversion University of Science Technology of China Hefei Anhui China 《天然气化学杂志》2011,(4):345-349
The double perovskite oxides Sr2Mg1-xF exMoO6-δ were investigated as catalysts for the methane oxidation.The structural properties of catalysts were characterized in detail by X-ray diffraction,X-ray photoelectron spectroscopy and X-ray absorption spectroscopy.The catalytic property was strongly influenced by the Fe substitution.The relation between catalytic performance and the degree of Fe substitution was examined with regard to the structure and surface characteristics of the mixed oxides.The Fe-containing catalysts exhibited higher activity attributable to the possible(Fe2+,Mo6+) and (Fe3+,Mo5+)valency pairs,and the highest activity was observed for Sr2Mg0.2Fe0.8MoO6-δ.The enhancement of the catalytic activity may be correlated with the Fe-relating surface lattice oxygen species and was discussed in view of the presence of oxygen vacancies. 相似文献