Asymmetric Colliding-Pulse Mode-Locking in InGaAsP Semiconductor Lasers

Asymmetric colliding-pulse mode-locking was successfully demonstrated in an InGaAsP laser. This laser had a single saturable absorber section located partway along the cavity length, and showed mode-locking operation at harmonics of the cavity roundtrip frequency. The method verified that optical pulse repetition up to subterahertz rates can be generated with nearly 1-mm-long mode-locked InGaAsP lasers.     

利用4400系统构造具有光学多道分析功能的信号处理系统

基于4400系统,通过引入光电二极管列阵作为传感器,构造了具有光学多道分析功能的信号处理系统。利用该系统对实际的激光空间分布进行了描绘,给出了高斯场分布的相应参数。通过进一步观测p偏振光在K9玻璃上下表面反射光强比(γ)的角度调制曲线,获得了玻璃表面层的光学参数。实验结果表明,该系统测量精度高,可应用在激光时间信号及空间场分布的表征与测量领域。     

磷光染料/宽禁带半导体聚合物高效率能量转移体系的电致发光

小分子磷光染料掺杂的聚合物发光器件具有发光效率高、制备工艺简单等优点，但是应该注意小分子染料的聚集与相分离问题，特别是在高掺杂浓度时更应注意防止相分离现象的发生。我们的思路是通过使用聚芴(Polyfluorene，PF)改性后的母体聚合物材料PC(poly[2，7-(9，9-dihexyl fluorene)-co-alt-2，10-(cyclohex—ane-1-spiro-6／-dibenzo[d，f][1，3]dioxepin)])，由于其发光峰位蓝移到紫外区，这就与作为掺杂分子的Ir(ppy)3配合物的吸收匹配得更好，进而达到提高能量转移效率的目的。在此条件下，可以实现较低掺杂浓度的发光，这对降低小分子染料的聚集以及相分离现象的发生是有帮助的。采用的器件结构为ITO／PEDOT：PSS/polymer:Ir(ppy)3／Ba／Al.当使用传统PF材料作为母体时，Ir(ppy)3需达到4％的掺杂比例才能实现能量的完全转移，而当采用改进后的PF作为母体时，Ir(ppy)3配合物只需达到0．5％的掺杂比例就能实现能量的完全转移，改进后的器件掺杂比例大幅度降低。     

寻找顶夸克的漫长过程

本文描述寻找顶夸克的漫长过程。从70年代末开始,美国的PEP,德国的PETRA,80年代日本的TRISTAN,欧洲核子中心CERN的SP PS质子反质子对撞机,90年代的CERN的LEP大型电子正电子对撞机,最后于1997年才由美国费米国家实验室的D0和CDF国际合作组找到了顶夸克存在的证据,并给出了顶夸克的质量为:174.3±3.2±4.0GeV。人们可以从这段历史获得有益的启示。     

Nearly light cycles in embedded graphs and crossing‐critical graphs

We find a lower bound for the proportion of face boundaries of an embedded graph that are nearly light (that is, they have bounded length and at most one vertex of large degree). As an application, we show that every sufficiently large k‐crossing‐critical graph has crossing number at most 2k + 23. © 2006 Wiley Periodicals, Inc. J Graph Theory 53: 151–156, 2006     

White electroluminescence from a single polyfluorene containing bis‐DCM units

A series of fluorene‐based copolymers composed of blue‐ and orange‐light‐emitting comonomers were synthesized through palladium‐catalyzed Suzuki coupling reactions. 9,9‐Dihexylfluorene and 2‐(2,6‐bis‐{2‐[1‐(9,9‐dihexyl‐9H‐fluoren‐2‐yl)‐1,2,3,4‐tetrahydroquinolin‐6‐yl]‐vinyl}‐pyran‐4‐ylidene)‐malononitrile (DCMF) were used as the blue‐ and orange‐light‐emitting chromophores, respectively. The resulting single polymers exhibited simultaneous blue (423/450 nm) and orange (580–600 nm) emissions from these two chromophores. By adjusting the fluorene and DCMF contents, white light emission could be obtained from a single polymer; a device with an ITO/PEDOT:PSS/polymer/Ca/Al configuration was found to exhibit pure white electroluminescence with Commission Internationale de L'Eclairage (CIE) coordinates of (0.33, 0.31), a maximum brightness of 1180 cd/m², and a current efficiency of 0.60 cd/A. Furthermore, the white light emission of this device was found to be very stable with respect to variation of the driving voltage. The CIE coordinates of the device were (0.32, 0.29), (0.32, 0.29), and (0.33, 0.31) for driving voltages of 7, 8, and 10 V, respectively. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 3380–3390, 2007     

大粒子对高斯波束散射的数值模拟

基于广义米氏理论，精确的求解了球形粒子对高斯波束和平面波的散射，采用Matlab编程， 改进了计算方法，所能够计算的粒子的尺寸参数已突破80000. 给出了平面波与高斯波入射 时，均匀粒子以及镀层粒子的散射分布，比较了吸收粒子和非吸收粒子散射分布. 关键词： 广义米氏理论 高斯波束 光散射 波束因子     

Synthesis,photophysics, structure‐tunable photoluminescence,and electrochemical properties of soluble poly(p‐phenylenevinylene)‐based polymers with adjacent 1,3,4‐oxadiazoles in the backbone

Three new poly(p‐phenylenevinylene)‐based polymers containing two 1,3,4‐oxadiazole moieties in the main chain per repeat unit were synthesized by Heck coupling. A single, double, or triple bond was introduced between the oxadiazoles to provide a means for modifying the polymer properties. The polymers were readily soluble in common organic solvents and showed T_g values lower than 50 °C. The color of the emissive light in both the solid state and the solution could be tuned by a change in the nature of the bond between the oxadiazole rings. The polymers emitted ultraviolet‐green light in solution with a photoluminescence (PL) emission maximum at 345–483 nm and blue‐green light at 458–542 nm in thin films. The PL quantum yields in solution were 0.36–0.43. The electrochemical properties are affected by the nature of the bond between the oxadiazoles as well. In polymers with a single bond between the oxadiazoles, a lower ionization potential was observed than in polymers with a double or triple bond. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 3079–3090, 2005     

Synthesis and self‐assembly of highly incompatible polybutadiene–poly(hexafluoropropylene oxide) diblock copolymers

A versatile coupling reaction for the preparation of polybutadiene–poly‐(hexafluoropropylene oxide) (BF) diblock copolymers is described. Six diblock copolymers with different block lengths were characterized by nuclear magnetic resonance spectroscopy and size exclusion chromatography; all six had total molecular weights below 15,000. Microphase separation of the block copolymers in the bulk state was established by small‐angle X‐ray scattering (SAXS) and differential scanning calorimetry. SAXS data suggest that the diblocks are characterized by an unusually large Flory‐Huggins interaction parameter, χ, on the order of 10. However, extraction of χ from the order–disorder transition gave large (order 1) but significantly different values, thereby suggesting that these copolymers are too small and too strongly interacting to be described by block copolymer mean‐field theory. Dynamic light scattering was used to analyze dilute solutions of the title block copolymers in four selective organic solvents; the sizes of the micelles formed were solvent dependent. The micellar aggregates were large and nonspherical, and this is also attributed to the high degree of incompatibility between the two immiscible blocks. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 43: 3685–3694, 2005     

Investigation of the Effective Space–Time of the Vacuum Nonlinear Electrodynamics in a Magnetic Dipole Field

The metric tensor of the effective pseudo-Riemannian space–time for an electromagnetic wave propagating in the magnetic dipole field and the gravitational field of a neutron star is obtained within a parameterized post-Maxwellian vacuum electrodynamics. The angles of the nonlinear electrodynamic and gravitational ray bending for electromagnetic waves propagating in the magnetic equatorial plane of the star are calculated based on an analysis of isotropic geodesics of this space. We show that for all nonlinear theories whose post-Maxwellian parameters do not coincide, the velocity of the electromagnetic signal propagation in external fields and the rays along which these signals propagate depend on the polarization of the electromagnetic waves. The difference of the source-to-detector propagation time of these signals for two principal polarization states is calculated.