显微镜产品质量光电检测的研究

显微镜产品质量光电检测的实施是光、机、光电、计算机技术的综合运用。本文是笔者多年来研究成果总结，包括了已研制出的ＸＪ－１型生物显微镜多功能光电质检仪及其改进；对显微镜离焦性能检测的探索，共可实现显微镜产品质量七个考核项目的检测与等级分拣。这些成果给显微镜行业提供了先进的检测工具；同时为发展我国显微镜产品检测技术、提高检测水平起积极的促进作用。     

氮原子在Ni平坦和缺陷表面上的吸附和振动

 构造了氮－镍相互作用的5－参数Morse势，研究了氮原子在Ni（\r\n100），Ni（110）和Ni（111）平坦表面的吸附和振动，获得了氮原子\r\n在三个低指数表面的吸附位、吸附构型、结合能和本征振动等数据，计\r\n算结果与实验结果非常吻合．同时，与Ni（100）表面对比，系统研究\r\n了氮原子在Ni（510）台阶面的吸附和扩散．计算结果表明，氮原子在\r\n台阶下部形成最稳定的吸附态，台阶对下台面上扩散的氮原子形成捕获\r\n势，对上台面上扩散的氮原子形成反射势．     

气相反应C_(60)+O_3=C_(6O)(C_(2v))+O_2热力学函数的计算

计算了气相反应C60＋O3＝C6O（C2v）＋O2的热力学函数．得到了该反应Gibbs自由能的具体数值，结果表明在所研究的温度范围内Gibbs自由能为负值，从热力学角度来说，该反应可以自发进行,在计算该气相反应热力学函数的基础上，给出了气相C6O（C2v）的标准热力学函数     

面向半导体照明的光学

以发光二极管(LED)为核心的半导体照明光源成为世界公认的第三代照明光源.通常基于蓝光LED抽运黄色荧光粉产生白光的方案,因荧光粉的斯托克斯位移和宽光谱,其具有产业化价值的发光效率上升范围受到极大限制.另外,传统封装LED因其朗伯型发光分布和超高亮度会造成严重的眩光以及光分布难以满足照明应用要求从而导致光污染、光浪费,...     

Tuning the Reactivity of Cyclopropenes from Living Ring‐Opening Metathesis Polymerization (ROMP) to Single‐Addition and Alternating ROMP

Ring‐opening metathesis polymerization (ROMP) has become one of the most important living polymerizations. Cyclopropenes (CPEs) remain underexplored for ROMP. Described here is that the simple swap of 1‐methyl to 1‐phenyl on 1‐(benzoyloxymethyl)CPEs elicited strikingly different modes of reactivity, switching from living polymerization to either selective single‐addition or living alternating ROMP. The distinct reactivity stems from differences in steric repulsions at the Ru alkylidene after CPE ring opening. Possible olefin or oxygen chelation from ring‐opened CPE substituents was also observed to significantly affect the rate of propagation. These results demonstrate the versatility of CPEs as a new class of monomers for ROMP, provide mechanistic insights for designing new monomers with rare single‐addition reactivity, and generate a new functionalizable alternating copolymer scaffold with controlled molecular weight and low dispersity.     

Experimental phase diagram of a model colloid-polymer mixture in the protein limit

Sterically stabilized silica nanoparticles were synthesized, and turbidity measurements confirmed that they behaved as hard spheres in cyclohexane. Poly(isoprene) was added to give mixtures in the protein limit with a polymer coil/colloid radius ratio of 4.8. Their phase behavior under good solvent conditions was studied experimentally. The critical colloid volume fraction was phi = 0.13, whereas recent simulations (Bolhuis, P. G.; Meijer, E. J.; Louis, A. A. Phys. Rev. Lett. 2003, 90, 068304) predicted phi = 0.24. This difference is ascribed to the fact that many systems showing good solvent scaling behavior of the polymer still have a Flory-Huggins parameter close to 0.5, for instance, chi = 0.45 in this work.     

显微摄影装置的优化设计

本文是作者根据图片资料对国外先进的显微摄影装置进行“反求”价值分析后，自主地设计出达到或优于国外同类产品的小结，其中包括了无限远像距光学系统的创新应用。可见在工程光学设计中运用价值工程这一先进的管理技术与思想方法也是大有可为的。     

氢原子在Pd(997)台阶面上的吸附和扩散

用对势方法研究了氢原子在Pd（997）台阶面上的吸附和扩散．计算结果表明，氢原子在台阶下形成最稳定的吸附态，并分析了其新的振动模式．理论分析表明，台阶对下台面上扩散的氢原子形成捕获势，对上台面扩散的氢原子形成反射势，很好地支持了实验结果．     

Dinaphthobenzo[1,2:4,5]dicyclobutadiene: Antiaromatic and Orthogonally Tunable Electronics and Packing

Polycyclic conjugated hydrocarbons containing antiaromatic four‐membered cyclobutadienoids (CDB) are of great fundamental and technical interest. However, their challenging synthesis has hampered the exploration and understanding of such systems. Reported herein is a modular and efficient synthesis of novel CBD‐containing acene analogues, dinaphthobenzo[1,2:4,5]dicyclobutadiene (DNBDCs), with orthogonally tunable electronic properties and molecular packing. The design also features strong antiaromaticity of the CBD units, as revealed by nucleus‐independent chemical shift and anisotropy of the induced current density calculations, as well as X‐ray crystallography. Tuning the size of silyl substituents resulted in the most favorable “brick‐layer” packing for triisobutylsilyl‐DNBDC and a charge mobility of up to 0.52 cm² V^?1 s^?1 in field‐effect transistors.     

Air-stable,long-length,solution-based graphene nanoribbons

Within the context of nanoelectronics, general strategies for the development of electronically tunable and air stable graphene nanoribbons are crucial. Previous studies towards the goal of processable nanoribbons have been complicated by ambient condition instability, insolubility arising from aggregation, or poor cyclization yield due to electron deficiency. Herein, we present a general strategy for the elongation of smaller graphene nanoribbon fragments into air-stable, easily processed, and electronically tunable nanoribbons. This strategy is facilitated by the incorporation of electron-rich donor units between electron-poor acceptor perylene diimide oligomeric units. The ribbons are processed in solution via a visible-light flow photocyclization using LEDs. The resulting long nanoribbons can be solution-cast and imaged, which are necessary characteristics for device fabrication. The ribbons become conductive after thermolysis of the pendent side-chains. The electron-accepting character of these nanoribbons in solution is reversible, and the conductivity of the thermolyzed species as a solid remains stable. This work highlights our general strategy for the mild and reliable fabrication of tunable and ambient-stable graphene nanoribbons, and charts a straightforward route for facile device incorporation.

A strategy is shown for the elongation of graphene nanoribbon (GNR) fragments into air-stable, solution processable and electronically tunable GNRs, aided by incorporating electron-rich donor units between electron-poor oligomeric acceptor units.