硅基发光材料研究进展

微电子技术是高技术中的关键技术，硅是微电子技术的基础材料，但是硅是一种非发光材料，为了发展光电集成技术，必须大力发展硅基发光材料，多孔硅是一种有希望的硅基发光材料，它表明纳米晶粒中的量子限制效应对光发射是极有效的，随之涌现出一系列量子限制硅基发光材料，为发展光电子集成提供了新的途径。     

Synthesis and characterization of new sulfone‐derivatized phenylenevinylene‐based conjugated copolymers with evolving energy levels and gaps

A new series of stable, processable, and chain end functionalizable sulfone‐derivatized phenylenevinylene‐based conjugated polymers (SFPVs) containing different donor type comonomers have been synthesized and characterized. The polymer main chains are consisted of a sulfone‐phenylene electron accepting unit coupled with an electron donating unit which is derived from one of the dialdehyde comonomers based on benzene, thiophene, and pyrrole (with or without alkoxy side chains). The optical energy gaps (E_g) of the new polymers (in solvent) are in a range of 1.9–2.3 eV, with the lowest energy gap obtained from the polymer containing pyrrole as the donor unit. By using a combination of strong donor unit (such as pyrrole) and a relatively weak but stable acceptor unit (sulfone‐substituted benzene), E_g of the conjugated polymers can be tailored to below 2 eV, while the vinylene bonds on the polymer main chain are still chemically stable to survive strong basic conditions as compared with the S,S‐dioxo‐thiophene‐based PTV polymers developed earlier for potential supra‐molecular block copolymer systems. The lowest energy gap P(Pyrrole‐SFPV) exhibited 10 times better photoelectric power conversion efficiency than P(TV‐SFPV). © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Donor-Acceptor Type Covalent Organic Frameworks

Intermolecular charge transfer (ICT) effect has been widely studied in both small molecules and linear polymers. Covalently-bonded donor-acceptor pairs with tunable bandgaps and photoelectric properties endow these materials with potential applications in optoelectronics, fluorescent bioimaging, and sensors, etc. However, owing to the lack of charge transfer pathway or effective separation of charge carriers, unfavorable charge recombination gives rise to inevitable energy loss. Covalent organic frameworks (COFs) can be mediated with various geometry- and property-tailored building blocks, where donor (D) and acceptor (A) segments are connected by covalent bonds and can be finely arranged to form highly ordered networks (namely D−A COFs). The unique structural features of D−A COFs render the formation of segregated D−A stacks, thus provides pathways and channels for effective charge carriers transport. This review highlights the significant progress on D−A COFs over the past decade with emphasis on design principles, growing structural diversities, and promising application potentials.     

A Conjugated Thiophene‐Based Rotaxane: Synthesis,Spectroscopy, and Modeling

A dithiophene rotaxane 1 ?β‐CD and its shape‐persistent corresponding dumbbell 1 were synthesized and fully characterized. 2D NOESY experiments, supported by molecular dynamics calculations, revealed a very mobile macrocycle (β‐CD). Steady‐state and time‐resolved photoluminescence experiments in solution were employed to elucidate the excited‐state dynamics for both systems and to explore the effect of cyclodextrin encapsulation. The photoluminescence (PL) spectrum of 1 ?β‐CD was found to be blueshifted with respect to the dumbbell 1 (2.81 and 2.78 eV, respectively). Additionally, in contrast to previous observations, neither PL spectra nor the decay kinetics of both threaded and unthreaded systems showed changes upon increasing the concentration or changing the polarity of the solutions, thereby providing evidence for a lack of tendency toward aggregation of the unthreaded backbone.     

DNA‐Based Polymers as Chiral Templates for Second‐Order Nonlinear Optical Materials

The unique symmetry properties of chiral systems allow the emergence of coherent second harmonic generation in polymeric materials lacking polar order. Deoxyribonucleic acid (DNA) treated with the surfactant cetyltrimethylammonium (CTMA) was drop‐cast to spontaneously form films that are active for coherent second harmonic generation (SHG). SHG images acquired as a function of incident and exigent polarization are in good agreement with theoretical predictions assuming nonpolar D_∞ symmetry for the double‐stranded DNA chains. Doping the DNA films with crystal violet substantially increases the efficiency of SHG, but does not significantly alter the polarization‐dependence, suggesting that the SHG generated upon doping arises from the same chiral‐specific origin, presumably templated by the DNA. These results raise the possibility of new design strategies for organic nonlinear optical materials based on soft chiral polymers that do not require polar order.     

光学课程和高、新科技结合探索

对光学课程教学现代化问题进行了探索和实践,一是光学基本原理与科技前沿典型实例结合,二是从激光新技术讲授光学基本概念,三是从光电技术发展探讨光学课程中的新仪器,新器件。     

Synthesis and self‐assembly in water of coil‐rod‐coil amphiphilic block copolymers with central π‐conjugated sequence

The purpose of this study is to correlate the nano‐organization in water of coil‐rod‐coil amphiphilic block copolymers constituted of a conjugated segment to their optoelectronic properties. The ABA block copolymer structures, easily achieved via coupling reactions, are based on conjugated rod of dihexylfluorene and 3,4‐ethylenedioxythiophene units linked to two flexible poly(ethylene oxide) or poly[(ethylene oxide)‐ran‐(propylene oxide)] chains. These well‐defined copolymers exhibited a range of specific morphologies in water, a good solvent of coil blocks and a bad solvent of the conjugated rod. Particularly, vesicles and micelles with spherical, cylindrical, or elongated shape were noticed. Correlations were attempted to be established between the weight percent of the conjugated sequence contained in the copolymers, the morphology of the nanostructures obtained by self‐assembly in solution and the resulting optical properties. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 4602–4616, 2008     

Fabrication of ZnO nanorods for optoelectronic device applications

Hydroxyl free zinc oxide nanorods have been synthesized by a catalyst free surfactant based one-step solid state reaction process. The powder X-ray diffraction studies reveal well defined wurtzite peaks due to crystalline ZnO, while optical absorption spectra represent prominent exciton absorption and remarkable blueshift in the onset of absorption. As predicted by transmission electron microscopy, the ZnO nanorods are ∼100 nm long and of ∼20 nm dia. Further, luminescence aspects of such nanorods are studied for possible deployment in optoelectronics devices.      

减小外差干涉一次谐波非线性误差的方法

为了补偿激光外差干涉纳米测量中的非线性误差,提出了一种减小非线性误差的一次谐波方法。基于全反射理论分析了镀膜实体角锥棱镜反射光偏振特性,并由此推导出角锥棱镜反射光偏振特性及测量角锥棱镜以其运动方向为轴线的轴向旋转对激光外差干涉非线性误差一次谐波的影响模型。理论分析表明,测量角锥棱镜以其运动方向为轴线的轴向旋转会减小非线性误差一次谐波,当测量角锥棱镜轴向旋转97°时,可使非线性误差一次谐波达到最小,约为原有非线性误差一次谐波分量的1/20倍。当激光器出射的两束线偏振光存在6°非正交误差时,镀膜实体测量角锥棱镜轴向旋转角度从0°增加到97°,非线性误差一次谐波由5.30 nm减小到0.30 nm。