采用选择激发研究光系统Ⅱ反应中心β-Car的物理特性

光系统Ⅱ反应中心包含有2个去镁叶绿素分子(Pheo),2个β胡萝卜素分子(β-Car)和6个叶绿素a分子(Chla).对反应中心的时间分辨荧光光谱表明,两个β-Car具有不同的吸收光谱,吸收峰分别为489 nm(Car489)和507 nm(Car507),Car489靠近吸收峰为667 nm和675 nm的叶绿素a(Chl a),它的主要功能是保护反应中心免受单态氧的破坏,而不能将激发能传递给光化学反应活性的色素分子P680;Car507靠近吸收峰为669 nm的Chl a分子;能够将激发能传递给P680,进行电荷分离.采用全局优化拟合的方法对荧光光谱进行处理,Car489在61 ps时间内将能量传递给Chl a672, 随后传给Chl a677,处于激发态的Chl a677在3 ns衰减到基态;Car507在274 ps时间内将能量传递给P680,P680＋Pheo-的电荷重组发生在3.8 ns和16 ns.     

Molecular Dynamics Simulations of Helium Behaviour in Titanium Crystals

Molecular dynamics simulations are performed to investigate the behaviour of helium atoms in titanium at a temperature of 30OK. The nucleation and growth of helium bubble has been simulated up to 50 helium atoms. The approach to simulate the bubble growth is to add helium atoms one by one to the bubble and let the system evolve. The titanium cohesion is based on the tight binding scheme derived from the embedded atom method, and the helium-titanium interaction is characterized by fitted potential in the form of a Lennard-Jones function. The pressure in small helium bubbles is approximately calculated. The simulation results show that the pressure will decrease with the increasing bubble size, while increase with the increasing helium atoms. An analytic function about the quantitative relationship of the pressure with the bubble size and number of helium atoms is also fitted.     

Fibre Optical Parametric Amplification in Defect Bragg Fibres with Zero Dispersion Slow Light Effect

Nonlinearity enhancement by slow light effect and strong light confinement in defect Bragg fibres is demonstrated and anMysed in applications of fibre optical parametric amplifiers. Broadband low group velocity and zero dispersion as well as the strong light confinement by band gap enhances the nonlinear coefficient up to more than one order than the conventional high nonlinear fibres. Moreover, the zero dispersion wavelength of coupled core mode can be designed arbitrarily, under which the phase-matching bandwidth of the nonlinear process can be extended.     

Observation of Nano-Dots on HOPG Surface Induced by Highly Charged Arq+ Impact

Highly charged ions （HCIs） have huge potential energy due to their high charge state. When a HCI reaches a solid surface, its potential energy is released immediately on the surface to cause a nano-scale defect. Thus, HCIs are expected to be useful for solid-surface modifications on the nano-scale. We investigate the defects on a highly oriented pyrolytic graphite （HOPG） surface induced by slow highly charged Ar^q＋ ions with impact energy of 20-2000qeV with scanning probe microscopy （SPM）. In order to clarify the role of kinetic and potential energies in surface modification, the nano-defects are characterized in lateral size and height corresponding to the kinetic energy and charge state of the HCIs. Both the potential energy and kinetic energy of the ions may influence the size of nano-defect. Since potential energy increases dramatically with increasing charge state, the potential energy effect is expected to be much larger than the kinetic energy effect in the case of extremely high charge states. This implies that pure surface modification on the nano-scale could be carried out by slow highly charged ions. The mean size of nano-defect region could also be controlled by selecting the charge state and kinetic energy of HCI.     

Third-Order Optical Nonlinearity in Novel Porphyrin Dimers

We investigate the third-order optical nonlinearities in four novel porphyrin dimers （dimers A to D） and a monomeric porphyrin H2 CPTPP measured by using the single-beam z-scan technique with a pulsed Q-switched Nd：YAG nanosecond laser at 532nm. All the samples show strong excited state absorption （ESA） and high value of Х^（3） in the ns domain at this wavelength. We perform a comparison between dimer A and its monomer H2 CPTPP in their third-order optical nonlinearity, and discuss the relationships between the values of Х^（3） and the different bridging groups for all the dimers.     

热对流作用下筒壁涂层的边裂行为

边裂(边缘开裂)是涂层热致损伤的主要模式之一. 边缘裂纹穿透涂层后,常导致界面脱粘从而驱使涂层与基体剥离,最终丧失对基体的保护作用. 本文以热应力强度因子表征边缘裂纹的扩展驱动力,研究筒壁涂层在热对流作用下的边裂行为. 首先,利用拉普拉斯变换法,得到了瞬态温度场及热应力场的封闭解. 其次,运用Fett等的三参数法确定了筒壁涂层边缘裂纹的权函数. 最后,基于叠加原理和权函数方法计算了边缘裂纹的热应力强度因子. 探讨了无量纲时间、边缘裂纹深度、基体/涂层厚度比、热对流强度等参数对热应力强度因子的影响规律. 结果表明:热应力强度因子的峰值既非发生在热载荷初始时刻,也非发生在热稳态时刻,而出现在时间历程的中间时刻;增大热对流强度不仅可提高热应力强度因子的峰值,而且使峰值提前出现;其他条件相同时,热应力强度因子随着边缘裂纹长度的增大而降低;增大涂层厚度或减小基体厚度可增强涂层抵抗瞬态热载荷的能力.      

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正关键词:Arrhenius公式的物理内涵·反应动力学W.Schmickler,Y.X.Chen,E.Santos,Z.He.The Pre-Exponential Factor in Electrochemistry,Angew.Chem.Int.Ed.,2018.DOI:10.1002/anie.201800130.中国科学技术大学合肥微尺度物质科学国家实验室和化学物理系陈艳霞教授课题组与德国Ulm大学的Schmickler教授课题组,在系统分析了文献中探究电催化反应的活化能与指前因子的理论和实验研究成果的基础上,基于Kramer理论给出了     

数字激光散斑照相技术测金属的热胀系数

利用数字激光散斑照相技术对金属热胀系数进行了测量。产生激光散斑的散射体(毛玻璃片)随被测金属棒受热膨胀而相应移动,数字照相机(CCD)将一系列随温度上升而平移的激光散斑场记录下来。通过计算机程序对采集到的图像进行频谱分析,获得两幅数字激光散斑场相对应的干涉条纹图像,计算条纹间距从而得到温度变化导致的金属棒伸长量,并计算出金属材料的膨胀系数。     

匀强及非匀强磁场中Heisenberg XXX链的纠缠研究

研究了匀强及非匀强磁场中反铁磁体Heisenberg XXX链的近邻和次近邻纠缠.结果表明对基态情形,纠缠随磁场B变化呈现阶梯型结构,这可用来构建量子纠缠"放大器"或量子纠缠"开关".对有限温度情形,引进一非匀强磁场Bi=(-1)iB可以使近邻格点间纠缠在某些区域明显增大,而次近邻格点间纠缠则完全消失;同时引进非匀强磁场Bi=(-1)iB还可以使近邻格点纠缠的临界温度Tcn增大,且Tcn随B的增大而升高,这意味着我们可以通过调节B的大小而在任意温度下得到纠缠.