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排序方式: 共有1368条查询结果,搜索用时 15 毫秒
1.
Galia Pozina Elizaveta I. Girshova Konstantin M. Morozov Konstantin A. Ivanov Anton Yu. Egorov Mikhail A. Kaliteevski 《Annalen der Physik》2019,531(6)
Enhancement of spontaneous emission in a resonant Bragg quantum well (QW) structure with 60 periods of triple InAs monolayers embedded in a GaAs matrix is studied experimentally and theoretically. From measurements of the time‐resolved photoluminescence, besides the QW exciton at 1.47 eV, a specific super‐radiant (SR) emission demonstrating nonlinear properties is found. The SR mode shows a near‐quadratic dependence of intensity on excitation power, while its energy position follows the Bragg condition. It is revealed that the SR mode shows a peculiar non‐monotonic dependence of intensity on direction, with a maximum observed at approximately 40°. The enhancement in the SR emission at a specific direction is correlated well with suggested theoretical consideration of the modal Purcell factor for periodic quantum well structures. 相似文献
2.
During the course of our investigation of the electron transfer properties of some redox species through highly hydrophobic
long chain alkanethiol molecules on gold in aqueous and non-aqueous solvents, we obtained some intriguing results such as
unusually low interfacial capacitance, very high values of impedance and film resistance, all of which pointed to the possible
existence of a nanometer size interfacial gap between the hydrophobic monolayer and aqueous electrolyte. We explain this phenomenon
by a model for the alkanethiol monolayer—aqueous electrolyte interface, in which the extremely hydrophobic alkanethiol film
repels water molecules adjacent to it and in the process creates a shield between the monolayer film and water. This effectively
increases the overall thickness of the dielectric layer that is manifested as an abnormally low value of interfacial capacitance.
This behaviour is very much akin to the ‘drying transition’ proposed by Lum, Chandler and Weeks in their theory of length
scale dependent hydrophobicity. For small hydrophobic units consisting of apolar solutes, the water molecules can reorganize
around them without sacrificing their hydrogen bonds. Since for an extended hydrophobic unit, the existence of hydrogen bonded
water structure close to it is geometrically unfavourable, there is a net depletion of water molecules in the vicinity leading
to the possible creation of a hydrophobic interfacial gap. 相似文献
3.
We present all-atom molecular dynamics simulations ofn-hexane on the basal plane of graphite at monolayer and multilayer coverages. In keeping with experimental data, we find the
presence of ordered adsorbed layers both at single monolayer coverage and when the adsorbed layer coexists with excess liquid
adsorbate. Using a simulation method that does not impose any particular periodicity on the adsorbed layer, we quantitatively
compare our results to the results of neutron diffraction experiments and find a structural transition from a uniaxially incommensurate
lattice to a fully commensurate structure on increasing the coverage from a monolayer to a multilayer. The zig-zag backbone
planes of all the alkane molecules lie parallel to the graphite surface at the multilayer coverage, while a few molecules
are observed to attain the perpendicular orientation at monolayer coverage.
Dedicated to Professor C N R Rao on his 70th birthday 相似文献
4.
K. Dayananda R. Dhamodharan K. Vijayakumaran T. Rajamannar 《Journal of polymer science. Part A, Polymer chemistry》2004,42(21):5413-5423
A monolayer of covalently anchored, novel, binaphthyl ketone is used as a surface‐confined photochemical radical generator (PRG) for anchoring a variety of polymers to silicon surfaces. The precursor PRG is synthesized by the application of a facile and novel method for the oxidation of sterically hindered benzylic hydrocarbons to carbonyl compounds. Oxidation was carried out with a stoichiometric amount of potassium peroxydisulfate, in the presence of a catalytic amount of copper sulfate in an acetonitrile/water mixture. The PRG synthesized is characterized by 1H NMR, UV, and Fourier transform infrared (FTIR). The covalently attached monolayers are characterized by X‐ray photoelectron spectroscopy, ellipsometry, and water contact angle measurements. The method developed is applicable to the preparation of a monolayer of a variety of polymers on a wide range of substrates carrying surface hydroxyl groups. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 5413–5423, 2004 相似文献
5.
Hai Huyen Dam Hans-Jürgen Zepernick Sven Nordholm Jörgen Nordberg 《Annals of Operations Research》2005,133(1-4):249-264
The performance of a code division multiple access system depends on the correlation properties of the employed spreading
code. Low cross-correlation values between spreading sequences are desired to suppress multiple access interference and to
improve bit error performance. An auto-correlation function with a distinct peak enables proper synchronization and suppresses
intersymbol interference. However, these requirements contradict each other and a trade-off needs to be established. In this
paper, a global two dimensional optimization method is proposed to minimize the out-of-phase average mean-square aperiodic
auto-correlation with average mean-square aperiodic cross-correlation being allowed to lie within a fixed region. This approach
is applied to design sets of complex spreading sequences. A design example is presented to illustrate the relation between
various correlation characteristics. The correlations of the obtained sets are compared with correlations of other known sequences. 相似文献
6.
Kenji Hara Keiji Iwahashi Satoru Takakusagi Kohei Uosaki Masaya Sawamura 《Surface science》2007,601(22):5127-5132
Functionalization of self-assembled monolayer (SAM) of alkanethiolate with metal containing unit is one of the versatile methods to obtain functional surfaces such as heterogeneous catalysts. However, organic molecules that strongly bind to transition metals at SAM terminal are limited. Recently N-heterocyclic carbenes (NHCs) such as cyclic diaminocarbenes have emerged as strongly σ-donating ligands forming a robust bond with broad spectrum of transition metals. In the present study, for the purpose of establishment of a new robust basement for heterogeneous metal catalysts, a SAM of the alkanethiolate terminated with NHC-rhodium(I) complex moiety was prepared by utilizing a newly designed disulfide molecule bearing NHC-metal complex terminals. X-ray photoelectron spectroscopy (XPS) analysis and angle resolved XPS measurement revealed successful formation of the Rh-complex-terminated SAM on a gold substrate. Infrared reflection absorption spectroscopy (IRRAS) analysis suggested that the linker methylene chains connecting the rhodium complex moiety and the gold surface are in a loosely packed structure. This unique chemical species, NHC, would be a promising candidate as a basement for the construction of functional surface. 相似文献
7.
辣根过氧化物酶活性膜结构及生物电催化性能 总被引:3,自引:0,他引:3
通过分子沉积法研究了在聚对苯二甲酸乙二醇酯(PET)表面及金电极表面组装辣根过氧化物酶(HRP)/聚对苯乙烯磺酸钠(PSS)多层生物活性膜,用原子力显微镜(AFM)研究了组装膜的表面形貌,并研究了组装膜的形貌、粗糙度和活性关系.应用循环伏安法(CV)研究了组装HRP膜后电极对H2O2的电化学催化还原作用.实验发现,采用亚甲基蓝(MB)溶液为介质,在H2O2浓度为0.2~5.0 mmol•L-1时,其响应电流对H2O2浓度变化基本呈线性. 相似文献
8.
J. H. Knox 《Chromatographia》1988,26(1):329-337
Summary Four Capillary Electroseparation methods are distinguished. All have an ultimate efficiency limited only by axial diffusion and are in principle capable of achieving 106 plates in <1 hour.The main limitation to performance arises from Ohmic heating of the electrolyte. While forced convection at 10ms–1 is recommended to keep tubes cool, the parabolic temperature profile within the electrolyte limits the tube bore which can be used. A simple limiting expression is derived: (dc/m)3 (E/kV m–1)3 (c/mol dm–3) <3.3×109.Values of constants underlined 相似文献
9.
Gold electrodes were chemically modified with thioctic acid monolayer designed to mimic biological ion-channel membranes. The technique was then used in the determination of alkali, alkaline earth, thallium(I), and lanthanum metal cations as analytes. Cyclic voltammograms (CV) of [Fe(CN)6]3− an electroactive marker, were measured in the presence of the various types of analyte cations. In the absence of the analyte cation, electrostatic repulsion between the marker anions and the carboxylate groups of the receptor monolayer hindered the approach of the marker anion to the electrode surface and hence hindered its reduction. The modified electrodes responded well to the metal cations except the alkali metal cations. The sensors could detect the trivalent cation La3+ at concentrations as low as 10−8 M. The response of the sensor to the metal cations increase in the order alkali metal3+ can be discriminated in the ratio 1:100. This makes it possible to determine the trivalent ion in a sample matrix containing monovalent and divalent cations. Thallium(I) ion showed marked deviation in its response as compared to monovalent ions of the alkali metals. The ion-channel sensor based on self-assembled monolayer of thioctic acid therefore offers a potential alternative technique for the selective determination of metal ions. 相似文献
10.