偶氮聚合物光存储研究进展

着重阐明了偶氮聚合物光存储纪录的原理,分析了其双折射特性的微观机制,介绍了该课题近年来实验和理论上的最新进展,对这一充满希望和挑战的多学科交叉研究专题作了展望。     

Optical data storage by novel photoelectrochromic polymer

A novel elastic polymer containing 4,4′-bipyridinium salts with tetrakis[3,5-bis(trifluoromethyl)phenyl]borate as part of the main chain was synthesized. The cast film showed persistent and reversible colour changes due to photoinduced electron transfer upon excitation of an ion-pair charge-transfer band (_ex >365 nm) in vacuo. The lifetime of the coloured state markedly depended on temperature. The optically written data were stored without decay below 0°C and were erased thermally at elevated temperatures. The colour changes were reversibly repeatable for many times.     

共轭聚合物／C60复合体系及其在光伏打电池中的应用

共轭聚合物／C60复合体系在有机太阳能电池中的应用引起了化学工作者的广泛兴趣。本文介绍了共轭聚合物／C60复合体系的光诱导电子转移，以及近年来该体系在光伏打电池中的研究进展。     

2－芳基苯并噁唑的荧光猝灭和光诱导电子转移研究

本工作对两种不同的２－芳基苯并　唑化合物溶液荧光被四氯化碳所猝灭的机理进行了详细研究，通过多种途径研究表明该猝灭过程具有光诱导电子转移性质，工作还利用此电子转移所形成的活泼自由基来引发烯类单体的聚合，得到了有一定聚合度的聚甲基丙烯酸甲酯。     

带取代基硝酮化合物光环化反应的研究

本工作合成了一系列取代的硝酮类化合物。其中部分化合物仅一侧的苯环上带有取代基,而另部分化合物则两个苯环上均带有取代基。研究工作表明:取代基处于一侧的硝酮类化合物,不论取代基是给出电子或接受电子的,均有利于化合物光环化反应的进行。而当两个苯环分别带有给电子及接受电子的取代基形成推拉结构时,则大大减弱了化合物光环化反应的发生。文章对上述结果进行了初步讨论。     

竹红菌甲素衍生物13－SO_3Na－DDHA电化学及光诱导还原的研究

本工作研究了化合物１３－ＳＯ＿３Ｎａ－ＤＤＨＡ在不同ｐＨ的缓冲溶液中的电化学氧化还原行为．实验证明：化合物中羰基的还原电位与ｐＨ之间存在线性关系，其直线的斜率为６０ｍＶ／ｐＨ．并证明了此过程为一步两电子、两质子还原过程：Ｑ＋２Ｈ￣＋＋２ｅ＝ＱＨ＿２．ＤＭＦ作为非质子溶剂，具有很好的稳定自由基的作用．向缓冲溶液中加入ＤＭＦ后，化合物１３－ＳＯ＿３Ｎａ－ＤＤＨＡ为两步单电子还原过程，相应溶液中的光诱导电子转移吸收光谱证实了以上电化学的结果．     

含偶氮苯基团甲基丙烯酸酯单体的合成与表征

分别以对甲氧基苯胺和对硝基苯胺为原料,经重氮偶合、取代反应以及酯化反应,合成2种含偶氮苯基团甲基丙烯酸酯单体——4-[4-（4-甲氧基苯基偶氮）苯氧基]丁基甲基丙烯酸酯和4-[4-（4-硝基苯基偶氮）苯氧基]丁基甲基丙烯酸酯.利用红外光谱（FT-IR）和核磁共振氢谱（^1H-NMR）,对所合成的单体及反应中间体进行结构表征,并探讨合成反应条件.通过UV-Vis吸收光谱研究其紫外特征,其结果表明,由于引入柔性的丁基,含偶氮苯基团甲基丙烯酸酯单体的紫外吸收峰均没有发生明显位移.     

Optical,Electrical, and Magnetic Studies of Organic Solar Cells Based on Low Bandgap Copolymer with Spin ½ Radical Additives

The charge photogeneration and recombination processes in organic photovoltaic solar cells based on blend of the low bandgap copolymer, PTB7 (fluorinated poly‐thienothiophene‐benzodithiophene) with C60‐PCBM using optical, electrical, and magnetic measurements in thin films and devices is studied. A variety of steady state optical and magneto‐optical techniques were employed, such as photoinduced absorption (PA), magneto‐PA, doping‐induced absorption, and PA‐detected magnetic resonance (PADMR); as well as picosecond time‐resolved PA. The charge polarons and triplet exciton dynamics in films of pristine PTB7, PTB7/fullerene donor–acceptor (D–A) blend is followed. It is found that a major loss mechanism that limits the power conversion efficiency (PCE) of PTB7‐based solar cell devices is the “back reaction” that leads to triplet exciton formation in the polymer donor from the photogenerated charge‐transfer excitons at the D–A interfaces. A method of suppressing this “back reaction” by adding spin½ radicals Galvinoxyl to the D–A blend is presented; this enhances the cell PCE by ≈30%. The same method is not effective for cells based on PTB7/C70‐PCBM blend, where high PCE is reached even without Galvinoxyl radical additives.