叶绿素a分子在乙醇溶剂中的瞬态吸收研究

The excited state of Chlorophyll a is investigated by femtosecond transient absorption. The transient absorption spectra of Q band and By band of Chlorophyll a in ethanol have been observed. The fast kinetics of Chlorophyll a which exhibit two ultrafast components were also measured. The one is assigned to transient absorption of the inhomogeneously broadened ground state absorption spectrum, while the other is the response of the solvent to the change of the electron configuration in the excited state due to salvation dynamics of the polar solvent molecules. To understand the anisotropy of Chlorophyll a in ethanol, the anisotropy profile was also performed by 405 nm excitation and found that the anisotropy profile is 0.143. The possible combination of θda, θdb and η at excitation of By band has been simulated.     

An approach to analysis of single pier based on the variational principle in multi-layered soil

In this study, a variational approach to the settlement analysis of an axially loaded pier embedded in a multi-layered soil profile is presented. In this method, the soil profile and the embedded pier are divided into a number of sub-layers according to the actual number of soil layers observed in the field. The displacement shape function of each soil layer is given as a product of an exponential equation along the pier depth and the Bessel's solution in the radial direction. The displacement relationship among the layers can be derived through the transformation matrices. One of the major features of this method is that the total number of pier elements is the same as that of soil sub-layers. All the field components, such as the displacement, stress, and strain in the soil, can be calculated by closed-form solutions except that the only unknown variable is the value β which can be determined by iteration techniques. Comparisons were made with the results of finite element analysis and the field observation in pile-loaded tests.     

Optimal dividends in the dual model

The optimal dividend problem proposed by de Finetti [de Finetti, B., 1957. Su un’impostazione alternativa della teoria collettiva del rischio. In: Transactions of the XVth International Congress of Actuaries, vol. 2. pp. 433-443] is to find the dividend-payment strategy that maximizes the expected discounted value of dividends which are paid to the shareholders until the company is ruined or bankrupt. In this paper, it is assumed that the surplus or shareholders’ equity is a Lévy process which is skip-free downwards; such a model might be appropriate for a company that specializes in inventions and discoveries. In this model, the optimal strategy is a barrier strategy. Hence the problem is to determine b^∗, the optimal level of the dividend barrier. A key tool is the method of Laplace transforms. A variety of numerical examples are provided. It is also shown that if the initial surplus is b^∗, the expectation of the discounted dividends until ruin is the present value of a perpetuity with the payment rate being the drift of the surplus process.     

Imaging the reaction dynamics of OH + CD4. 2. Translational energy dependencies

The reaction of OH + CD4 is investigated in a crossed-beam experiment over the collisional energies ranging from reaction threshold of about 5 to 16 kcal/mol. Exploiting a time-sliced ion velocity imaging detection scheme, the coincident information on the two polyatomic product pairs, HOD and CD3, is revealed in a state-correlated manner. The recently discovered vibrational mode-correlation between the two products is found to persist over the full range of collision energies of this study. In addition, the energy dependencies of the correlated cross section, state distribution, and angular distribution are elucidated, providing an unprecedented insight into this important reaction.     

Rotationally selected product pair correlation in F+CD(4)-->DF(nu('))+CD(3)(nu=0,N)

The title reaction was studied in a crossed-beam experiment by imaging of state-selected products. The rotational state selection of the CD(3) products was achieved using (2+1) resonance-enhanced multiphoton ionization. The coincident information on the DF coproducts was revealed in a state-resolved manner from time-sliced velocity map images. Significant dependences of both the correlated differential cross sections and the DF vibrational branching ratios on the "tagged" CD(3) rotation states were found. The dynamical implications of one of the major findings are discussed.     

以(真空紫外光+紫外光)-共振加强式多光子游离法侦测交叉分子束之甲基生成物

用(真空紫外光+紫外光)-共振加强式多光子游离法侦测甲基自由基.为证明此法之灵敏度,实验用交叉分子束反应F+CH4(CD4)→HF(DF)+CH3(CD3),其绝对灵敏度可达107/cm3.由所得之光谱,更精确地得到两个里德堡态3d2E″及3d 2A1′之光谱系数.     

Alkaline‐Earth Metal Cations as Structure Building Blocks for Molecular Cages with Entrapment and Controlled Release of Quintuple Ionic Aggregates

Currently, main‐group metal cations are totally neglected as the structure‐building blocks for the self‐assembly of supramolecular coordination metallocages due to the lack of directional bonding. However, here we show that a common Arrhenius acid–base neutralization allows the alkaline‐earth metal cations to act as charged binders, easily connecting two or more highly directional anionic transition‐metal‐based metalloligands to coordination polymers. With a metal salt such as K⁺PF₆^? added during the neutralization, the main‐group metal‐connected skeleton can be templated by the largest yet reported ionic‐aggregate anion, K₂(PF₆)₃^?, formed from KPF₆ in solution, into molecular metallocages, encapsulating the ion. Crystal‐structure details, DFT‐calculation results, and controlled‐release behavior support the presence of K₂(PF₆)₃^? as a guest in the cage. Upon removal of PF₆^? ions, the cage stays intact. Other ions like BF₄^? can be put back in.     

Plasmonic Zener tunneling in metal-dielectric waveguide arrays

We elucidate in this Letter plasmonic Zener tunneling (PZT) in metal-dielectric waveguide arrays (MDWAs) by using numerical simulations and theoretical analyses. PZT in MDWAs occurs at the waveguide entrance and wherever the beam completes Bloch oscillations, because the bandgap between the first and second bands is minimal at the center of the first Brillouin zone. This feature significantly differs from that of optical Zener tunneling in dielectric waveguide arrays. The dependence of the simulated tunneling rate on the gradient of the relative permittivity of the dielectric layers correlates with the tunneling theory, thus confirming the occurrence of PZT in MDWAs.     

Sound absorption and compressive property of PU foam‐filled composite sandwiches: Effects of needle‐punched fabric structure,porous structure,and fabric‐foam interface

The flexible polyurethane (PU) foam‐filled composite sandwiches are constructed using three types of needle‐punched fabrics (upper layer), PU foam (core layer), and nylon (bottom layer). Different contents of deionized water were used to adjust the pore size and bulk density of PU foam by free‐foaming. Effects of needle‐punched fabric components, cell structure, and fabric‐foam interface on sound absorption and compressive property of the composite sandwiches were investigated. Fabric‐foam interface contributes to improve high‐frequency sound absorption efficiency. When containing 0.5 wt% water in the core and nylon‐glass grid needle‐punched composite fabric (NPUN‐G) in the upper face, the composite sandwiches exhibited optimal sound absorption of 0.78 at low frequency of 450 Hz, and optimal compressive strength of 14.4 kPa. Combination of needle‐punched composite fabric improved the sound absorption coefficient and compressive strength, as high as 223% and 121%, respectively, compared with pure PU foam. This study provided an important basis for the preparation of high‐strength composite sandwiches with low‐frequency sound absorption.