一氯乙酸/FeCl_2·4H_2O催化合成聚苯乙烯遥爪预聚物

以一氯乙酸为引发剂 ,以FeCl2 ·4H2 O为新型催化剂 ,对苯乙烯进行了原子转移自由基聚合(ATRP) ,制得了含端羧基和端基氯的聚苯乙烯遥爪预聚物 ,并对聚苯乙烯与丙烯酸丁酯的嵌段共聚进行了研究 .结果表明 :利用ATRP技术可一步合成含端羧基和端基氯的聚苯乙烯遥爪预聚物 ,并可有效控制预聚物的相对分子质量及其相对分子质量分布 (1.3～ 1.6 ) ,预聚物的数均相对分子质量随单体转化率的提高而线性增加 ,ln([M ]0 / [M ])与时间呈线性关系 .表明该催化引发聚合反应具有活性可控聚合的特征 .

Uterine receptivity and the plasma membrane transformation

This review begins with a brief commentary on the diversity of placentation mechanisms, and then goes on to examine the extensive alterations which occur in the plasma membrane of uterine epithelial cells during early pregnancy across species. Ultrastructural, biochemical and more general morphological data reveal that strikingly common phenomena occur in this plasma membrane during early pregnancy despite the diversity of placental types-from epitheliochorial to hemochorial, which ultimately form in different species. To encapsulate the concept that common morphological and molecular alterations occur across species, that they are found basolaterally as well as apically, and that moreover they are an ongoing process during much of early pregnancy, not just an event at the time attachment, the term 'plasma membrane transformation' is suggested which also emphasises that alterations in this plasma membrane during early pregnancy are key to uterine receptivity.

Preparation of n-Atom GHZ State and Implementation of Quantum-State Transfer via Cavity Decay

We propose schemes to prepare n-atom Greenberger-Horn-Zeilinger （GHZ） state via two-sided cavities interacting with single-photon pulses, and achieve quantum state transfer （QST） from one atom to another atom. Entanglement particle pair and the control of coupling between qu bits are of no need in the QST process. Some practical quantum noises only decrease the success probabilities of the schemes but have no influence on the fidelity of prepared state. In addition, the success probabilities of our schemes are close to unity in the ideal case.

＂Pseudo-invariant Eigen-operator＂ Method for Deriving Energy-Gap of an Atom-Cavity Jaynes-Cummings Hamiltonian with Atomic Centre-of-Mass Motion

Using the ＂pseudo-invariant eigen-operator＂ method we find the energy-gap of the Jaynes-Cummings Hamiltonian model of an atom-cavity system. This model takes the atomic centre-of-mass motion into account. The supersymmetric structure is involved in the Hamiltonian of an atom-cavity system. By selecting suitable supersymmettic generators and using supersymmetrie transformation the Hamiltonian is diagonalized and energy eigenvectors are obtained.

Controlling Soliton Collisions of Condensates by Time-Dependence of Both Interactions and External Potential

Considering time-dependence of both interactions and external potential,we analytically study the collisional behaviors of two bright solitons in Bose-Einstein condensates by using Darboux transformation.It is found that for a closed external potential,the soliton-soliton distance is decreased with nonlinearly increased interactions,while the amplitude of each soliton increases and its width decreases.For linearly increased interactions but nonlinearly decreased external potential,especially,the atom transfer between two solitons is observed,different from previous theory of no atom transfer in solitons collision in a fixed external potential.In addition,it is shown that the collisional type,such as head-on,"chase",or collision period between two solitons,can be controlled by tuning both interactions and external potential.The predicted phenomena can be observed under the condition of the current experiments and open possibilities for future application in atoms transport.

Low band-gap benzodithiophene-thienothiophenecopolymers: the effect of dual two-dimensional substitutions on optoelectronic properties

Two new conjugated copolymers, PBDT-T6-TTF and PBDT-T12-TTF, were derived from a novel 4-fluorobenzoyl thienothi- ophene （TTF）. In addition, two types of benzodithiophene （BDT） units with 2,3-dihexylthienyl （T6） and 2,3-didodecylthienyl （T12） substituents, respectively, were successfully synthesized. The effect of the dual two-dimensional （2D） substitutions of the building blocks upon the optoelectronic properties of the polymers was investigated. Generally, the two polymers exhibited good solubility and broad absorption, showing similar optical band gaps of ~1.53 eV. However, PBDT-T6-TTF with its shorter alkyl chain length possessed a larger extinction coefficient in thin solid film. The highest occupied molecular orbital （HOMO） level of PBDT-T6-TTF was located at -5.38 eV while that of PBDT-T12-TTF was at -5.51 eV. In space charge-limited- current （SCLC） measurement, PBDT-T6-TTF and PBDT-T12-TTF displayed respective hole mobilities of 3.0~10-~ and 1.6x10 5 cm2 V-1 s-l. In polymer solar cells, PBDT-T6-TTF and PBDT-T12-TTF showed respective power conversion efficiencies （PCEs） of 2.86% and 1.67%. When 1,8-diiodooctane （DIO） was used as the solvent additive, the PCE of PBDT-T6-TTF was remarkably elevated to 4.85%, but the use of DIO for the PBDT-T12-TTF-blend film resulted in a lower PCE of 0.91%. Atomic force microscopy （AFM） indicated that the superior efficiency of PBDT-T6-TTF with 3% DIO （v/v） should be related to the better continuous phase separation of the blend film. Nevertheless, the morphology of the PBDT-T12-TTF deteriorated when the 3% DIO （v/v） was added. Our results suggest that the alkyl-chain length on the 2D BDT units play an important role in determining the optoelectronic properties of dual 2D BDT-TT-based polymers.

Al-doping effects on the photovoltaic performance of inverted polymer solar cells

The properties of Al-doped Zn O(AZO) play an important role in the photovoltaic performance of inverted polymer solar cells(PSCs), which is used as electron transport and hole blocking buffer layers. In this work, we study the effects of Al-doping level in AZO on device performance in detail. Results indicate that the device performance intensely depends on the Al-doping level. The AZO thin films with Al-doping atomic percentage of 1.0% possess the best conductivity. The resulting solar cells show the enhanced short current density and the fill factor(FF) simultaneously, and the power conversion efficiency(PCE) is improved by 74%, which are attributed to the reduced carrier recombination and the optimized charge transport and extraction between AZO and the active layer.