Absorptive reduction and width narrowing in Λ-type atoms confined between two dielectric walls

This paper investigates the absorptive reduction and the width narrowing of electromagnetically induced transparency （EIT） in a thin vapour film of A-type atoms confined between two dielectric walls whose thickness is comparable with the wavelength of the probe field. The absorptive lines of the weak probe field exhibit strong reductions and very narrow EIT dips, which mainly results from the velocity slow-down effects and transient behaviour of atoms in a confined system. It is also shown that the lines are modified by the strength of the coupling field and the ratio of L/λ, with L the film thickness and λthe wavelength of the probe field. A simple robust recipe for EIT in a thin medium is achievable in experiment.     

试论萍乡谚语的艺术特色

萍乡有着深厚的文化积淀。本文从萍乡谚语的创造手法、萍乡谚语的语法结构、萍乡谚语的用词、萍乡谚语的节奏四个方面讨论萍乡谚语的艺术特色。     

三新戊氧基溴硼亚酞菁薄膜材料的三阶非线性光学特性

通过单光束Z扫描技术 ,在波长为 1.0 6 4μm和 5 32nm、脉宽为 38ps条件下研究了一种新的酞菁相关化合物三新戊氧基溴硼亚酞菁薄膜材料的三阶非线性光学特性。观察到在 1.0 6 4μm(离强吸收带很远 )下的双光子吸收和在 5 32nm下的反饱和吸收现象 ,并计算出了相应的非线性吸收系数。在 1.0 6 4μm下的非共振三阶非线性极化率和在 5 32nm下的共振三阶非线性极化率 χ(3 ) 分别为 6 .1× 10 - 1 2 esu和 6 .7× 10 - 1 0 esu ,显著大于相关酞菁的值。这些结果表明三新戊氧基溴硼亚酞菁薄膜材料在非线性光学方面具有潜在的应用前景。     

High-field 19.6T 27Al solid-state MAS NMR of in vitro aluminated brain tissue

The combination of (27)Al high-field solid-state NMR (19.6T) with rapid spinning speeds (17.8 kHz) is used to acquire (27)Al NMR spectra of total RNA human brain temporal lobe tissues exposed to 0.10 mM Al(3+) (as AlCl(3)) and of human retinal pigment epithelial cells (ARPE-19), grown in 0.10 mM AlCl(3). The spectra of these model systems show multiple Al(3+) binding sites, good signal/noise ratios and apparent chemical shift dispersions. A single broad peak (-3 to 11 ppm) is seen for the aluminated ARPE-19 cells, consistent with reported solution-state NMR chemical shifts of Al-transferrin. The aluminated brain tissue has a considerably different (27)Al MAS NMR spectrum. In addition to the transferrin-type resonance, additional peaks are seen. Tentative assignments include: -9 to -3 ppm, octahedral AlO(6) (phosphate and water); 9 ppm, condensed AlO(6) units (Al-O-Al bridges); 24 ppm, tetrahedral AlO(3)N and/or octahedral Al-carbonate; and 35 ppm, more N-substituted aluminum and /or tetrahedral AlO(4). Thus, brain tissue is susceptible to a broad range of coordination by aluminum. Furthermore, the moderate (27)Al C(Q) values (all less than 10 MHz) suggest future NMR studies may be performed at 9.4T and a spin rate of 20 kHz.     

A new isomer in 136 Ba populated by deep inelastic collisions

Excited states in ¹³⁶Ba, populated in deep inelastic collisions by the interaction of 450 MeV ⁸²Se ions with a ¹³⁹La target, have been studied by means of in-beam -ray spectroscopy. A new isomer with has been identified at an excitation energy E_x = 3.357 MeV. The half-life was determined as ns. The extracted B(E2) value is much smaller than those in ¹³²Te and ¹³⁴Xe. This hindrance is investigated by a shell model calculation.Received: 22 September 2003, Revised: 11 November 2003, Published online: 6 April 2004PACS: 21.10.Tg Lifetimes - 23.20.Lv transitions and level energies - 27.60. + j      

Thickness measurement of GaN epilayer using high resolution X-ray diffraction technique

In this paper we propose a new method for measuring the thickness of the GaN epilayer, by using the ratio of the integrated intensity of the GaN epilayer X-ray diffraction peaks to that of the sapphire substrate ones. This ratio shows a linear dependence on the GaN epilayer thickness up to 2 μm. The new method is more accurate and convenient than those of using the relationship between the integrated intensity of GaN epilayer diffraction peaks and the GaN thickness. Besides, it can eliminate the absorption effect of the GaN epilayer.     

A low-molecular-mass gelator with an electroactive tetrathiafulvalene group: tuning the gel formation by charge-transfer interaction and oxidation

A new low-molecular-mass gelator with one TTF and one urea group is described. It was found that the gel formation can be tuned by formation of CT complexes and oxidation.     

NMR heteronuclear correlation between quadrupolar nuclei in solids

We show for the first time that it is possible to acquire high-resolution heteronuclear NMR correlation experiments in solid state between second-order-broadened half integer quadrupolar nuclei (i.e., 27Al and 17O) using the scalar J-coupling. The sensitivity of the experiment is dramatically improved at high fields (gain proportional to the fourth power of the principal field) with a combination of signal enhancement techniques. This turns a challenging experiment into a real tool. We apply this experiment to characterize a calcium aluminate glass in which we prove the presence of tricluster mu3 oxygen sites and describe the signature of their directly bonded aluminum sites. Applications involve a large range of possible pairs of quadrupolar nuclei in different materials, such as glasses, porous or mesoporous framework materials, zeolites, hybrid organic-inorganic, and bioinvolved materials.     

Superexchange and sequential mechanisms in charge transfer with a mediating state between the donor and acceptor

The rate of intramolecular charge transfer from biphenyl to naphthalene was determined for the radical anions and radical cations of molecules with the general structure: (2-naphthyl)-(steroid spacer)-(4-biphenylyl). Varied degrees of unsaturation (one double bond, NSenB; two double bonds, NSen(2)B; and the b-ring completely aromatized, NSarB) were incorporated into the steroid spacer to examine the effect it would have on the charge transfer rate. The charge transfer rate, as inferred from the decay of the biphenyl radical ion absorption, increased in all cases relative to the completely saturated 3-(2-naphthyl)-16-(4-biphenylyl)-5alpha-androstane (NSB) reference molecule. For the anion charge transfer, the decay rates increased by factors of 1.4, 4.2, and 5.1, respectively, and for the cation, the decay rates increased by factors of 5, 276, and 470. To explain the results, the charge-transfer process was viewed as a combination of two independent mechanisms: a single-step, superexchange mechanism, and a two-step, sequential charge transfer. Using a low level of theory, simple models of the superexchange and two-step mechanisms were developed to elucidate the nature and differences between the two mechanisms. The critical variable for this analysis is the free energy of formation (DeltaG(I) degrees ) of the intermediate state: (2-naphthyl)-[spacer](1)+/--(4-biphenylyl). The conclusion from this treatment is that superexchange is the dominant mechanism when DeltaG(I) degrees is large, but at small DeltaG(I) degrees , the sequential mechanism will dominate. This is because the superexchange rate is shown to have a weak dependence on DeltaG(I) degrees , changing 10-fold for a change in DeltaG(I) degrees of 2 eV, compared to the sequential mechanism in which the rate can change over 10(3) for 0.5 V.     

A novel multisignaling optical-electrochemical chemosensor for anions based on tetrathiafulvalene

[structure: see text] A multisignaling optical-electrochemical receptor for anions based on a triad with anthracene and TTF units was prepared. It showed a unique selectivity for fluoride ion over various anions with dramatic fluorescence enhancement in neutral condition and displayed a special recognition of H2PO4(-) in electrochemical studies with remarkable cathodic displacement of the first oxidation potential E(ox)1 of the TTF unit.