一种新型有机电致微腔结构的双模发射

采用结构Glass／DBR／ITO／NPB／NPB：Alq／Alq／Al制作了有机微腔电致发光器件。将空穴传输材料与发光材料以一定比例混合作为发光层，为了便于对比，在不改变有机层的膜厚的情况下同时制作了传统的异质结微腔器件，发现两种器件的发光光谱有很大不同，器件的复合效率与传统的异质结器件相比也得到了很大提高，这是因为将两种有机材料混合能消除界面势垒，提高器件的复合效率，从而提高了器件的发光性能，实现了微腔双模发射，且两个模式的半峰全宽分别为8nm和12nm。通过进一步优化器件结构可以实现微腔白光发射。     

A high-gain porous silicon metal–semiconductor–metal photodetector through rapid thermal oxidation and rapid thermal annealing

2 tungsten lamp at 1.83 mA excited by a 0.85-mW 675-nm laser diode. We also demonstrate that the dark current could be greatly reduced through rapid thermal oxidation and rapid thermal annealing. Received: 4 August 1997/Accepted: 28 May 1998     

Comparative analysis of (p,d), (d,t) and (3He, α) reactions on13C nucleus

The angular distributions of the (p, d), (d, t) and(³He, ) reactions on¹³C have been analysed within the framework of DWBA in which additional information on nuclear vertex constants was introduced. Although all these reactions seem to be similar single nucleon transfer, their mechanism is shown to be quite different and so is the information extracted thereof. While from the (p, d) reactions spectroscopic factors may be extracted unambiguously, from the (d, t) reactions it is possible to obtain directly the values of vertex constants only, which in turn are consistent with those determined by extrapolation of the experimental cross sections of the (p, d) reactions to the pole.In the case of (³He, ) reactions, however, the analysis indicates inadequacy of the DWBA concerning the calculations of central partial amplitudes. For a more reliable extraction of structural information, besides the correct normalization of peripheral amplitudes, a contribution of more complex mechanisms must be taken into account.     

激发态卟啉衍生物研究(Ⅶ)——取代基对卟啉—硝基苯化合物发光特性的影响

本文报导共价链相连的X-P-Y“三合板”型化合物在二甲基甲酰胺(DMF)和苯溶液中的发光特性.结果发现:引入取代基X=Cl—,CH3O—和Y=苯、硝基苯对中心卟啉的吸收和荧光光谱均无明显影响,仅其峰值频率将因溶剂不同而有所偏移.此外,由Cl—取代的卟啉—苯的荧光强度总比CH3O—取代时高;若将Y取代基由苯改换为硝基苯时,将使CH3O—P—Y化合物的荧光增强,但在Cl—P—Y化合物中则出现相反的趋势.不论在何种化合物中,在Y取代基中的苯环上引入NO2—基后,均可使其消光系数减小,而且当硝基在邻位取代时,这一效应更为显著.所有这些变化规律均不因溶剂不同而异.如果我们认为X—P—Y化合物的发光强度变化和其中心的卟啉大环上的π电子云密度偏移有规律性的关联,那么上述的一些取代基效应是可以理解的.进而,我们认为:本文所报导的事实将有助于充实巧妙设计高效利用太阳能的分子体系的科学依据.     

Extension to R + n+1 of singular integrals and fractional integrals

In this paper, a natural R ₊ ⁿ⁺¹ extension of singular integrals, i.e.,T _κ:f→K*φ _t *t with K a standard C-Z kernel and ϕ usual one, is investigated. One of the main results is: Let (dμ, udx) ∈C₁ and u-Mw, w∈A_∞, then T_k is of type (L^p(udx), L^p(dμ)). As a related topic, a maximal operator is proved to be of type , where , provided (dμ, udx) ∈C₁ and u∈ A_∞. Supported by National Science Foundation of China     

Spectroscopic factors of9Be,10B and13C from (d,t) reactions

The differential cross sections of tritons from the (d, t) reaction on⁹Be,¹⁰B and¹³C targets have been measured in the angular range of 5° _LAB110° with relatively small errors, 5%. The experimental data were analysed in terms of the standard DWBA using both zero-range and exact finite-range approaches.