高质量三维光子晶体的实验制备及理论分析

对压强控制自组装法进行了改进,采用了密封硅胶颗粒的强吸水装置,为光子晶体样品的制备提供了一个稳定的温度、湿度和压强环境.将温度、压强分别控制在35 ℃、45 mmHg,利用直径为260 nm的聚苯乙烯胶体球进行了高质量三维光子晶体样品的制备.从理论计算和实验测量等方面对制备的光子晶体样品的结构、质量和性能进行了对比分析,结果表明,利用该实验装置进行光子晶体样品的制备时,可重复性高;制备的光子晶体样品具有较为完美有序的密堆结构,质量较好;在光子晶体样品的Г L方向有深且窄的光子带隙和陡峭的带隙边沿.光子带隙深度为83%,宽度为0.073,带隙边沿陡峭度为8%/nm,这为超快全光开关等先进的光学设备的研究奠定了基础.     

Raman spectroscopic studies on the conformational changes of calf thymus DNA induced by Cd~(2+) ions

We used Raman spectroscopy to study the conforniational changes of DNA induced by Cd2+ ions in different Cd2+ concentrations solution. The experimental results show that when the Cd2+/PO2- ratio R increased from 0 to 3.0, the band 835.0 cm-1 shifted about 8 cm-1, and the overlapping spectra of 1446.0 and 1461.0 cm-1 separated and moved to 1441.0 and 1458.0 cm-1, respectively. This indicates that the conformation of DNA has changed from a "normal" B-form to a "modified" B'-form. At the same time,     

高质量三维光子晶体的制备及其透射谱研究

设计了简易的压强可控自组装实验装置,制备了由直径为260 nm的聚苯乙烯(PS)胶体球组成的面心立方光子晶体.分析了压强的变化对光子禁带(PBG)深度及光子带隙边缘(PBE)坡度的影响,确定了合适的压强生长环境(P=5999.5 Pa).利用该实验装置,还进行了光子晶体的小批量制备,一次性制得了三块光子晶体,并从不同角度对每一块光子晶体的透射谱及不同光子晶体的透射谱进行了测量.同一光子晶体不同位置透射谱的重合、同一批次制备的不同光子晶体透射谱的一致性及光子禁带两侧的Fabry-Pérot振荡等均说明:该装置制备的光子晶体在大区域、大面积上是高度有序、均一和平整的;利用该实验装置进行光子晶体的小批量制备是可行的.     

金属纳米颗粒在Lu_2O_3薄膜中的应变场分析

利用有限元分析法对镶嵌在Lu2O3薄膜中的Au、Cu、Pt、Co金属纳米颗粒的应变场分布进行分析.分析表明:金属纳米颗粒在生长过程中受Lu2O3薄膜的压缩应力作用,从而在纳米颗粒内部和表面产生相应应变,应变分布与金属纳米颗粒的杨氏模量和泊松比有关.杨氏模量大的金属纳米颗粒表面应变和内部应变差异较大;而杨氏模量小的金属纳米颗粒内外应变差相对较小.随着金属纳米颗粒在基体材料内部不断生长,其受到的偏应变也逐渐增大.金属纳米颗粒生长过程中的这种偏应变的存在和变化将极大地影响其内部晶格结构和表面形貌,进而影响金属纳米颗粒的性能.     

Raman spectroscopic studies on the conformational changes of calf thymus DNA induced by Cd2+ ions

We used Raman spectroscopy to study the conformational changes of DNA induced by Cd2+ ions in different Cd2+ concentrations solution. The experimental results show that when the Cd2+/PO-2 ratio R increased from 0 to 3.0, the band 835.0 cm-1 shifted about 8 cm-1, and the overlapping spectra of 1446.0and 1461.0 cm-1 separated and moved to 1441.0 and 1458.0 cm-1, respectively. This indicates that the conformation of DNA has changed from a "normal" B-form to a "modified" B'-form. At the same time,changes of other bands demonstrate that parts of base stacking collapse and some hydrogen bonds between AT are disrupted, AT base pairs are damaged more larger than GC base pairs.