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掺杂磺基罗丹明的脱氧核糖核酸(DNA)薄膜的光致发光和激光发射。

Photoluminescence and lasing from deoxyribonucleic acid (DNA) thin films doped with sulforhodamine.

作者信息

Yu Z, Li W, Hagen J A, Zhou Y, Klotzkin D, Grote J G, Steckl A J

机构信息

Nanoelectronics Laboratory, University of Cincinnati, Cincinnati, Ohio 45221-0030, USA.

出版信息

Appl Opt. 2007 Mar 20;46(9):1507-13. doi: 10.1364/ao.46.001507.

Abstract

Thin solid films of salmon deoxyribonucleic acid (DNA) have been fabricated by treatment with a surfactant and used as host for the laser dye sulforhodamine (SRh). The DNA films have an absorption peak at approximately 260 nm owing to absorption by the nitrogenous aromatic bases. The SRh molecules in the DNA films have absorption and emission peaks at 578 and 602 nm, respectively. The maximum emission was obtained at approximately 1 wt. % SRh in DNA, equivalent to approximately 100 DNA base pairs per SRh molecule. A distributed feedback grating structure was fabricated on a SiO(2)-Si substrate using interference lithography. The grating period of 437 nm was selected, corresponding to second-order emission at the amplified spontaneous emission wavelength of 650 nm. Lasing was obtained by pumping with a doubled Nd:YAG laser at 532 nm. The lasing threshold was 3 microJ, corresponding to approximately 30 microJ/cm(2) or 4 kW/cm(2). The emission linewidth decreased from approximately 30 nm in the amplified spontaneous emission mode to <0.4 nm (instrument limited) in the lasing mode. The slope efficiency of the lasing was approximately 1.2%.

摘要

通过用表面活性剂处理制备了鲑鱼脱氧核糖核酸(DNA)的固体薄膜,并将其用作激光染料磺基罗丹明(SRh)的主体。由于含氮芳香碱基的吸收,DNA薄膜在约260nm处有一个吸收峰。DNA薄膜中的SRh分子分别在578和602nm处有吸收峰和发射峰。在DNA中约1wt.%的SRh时获得最大发射,相当于每个SRh分子约100个DNA碱基对。使用干涉光刻在SiO(2)-Si衬底上制备了分布反馈光栅结构。选择437nm的光栅周期,对应于650nm放大自发发射波长处的二阶发射。通过用532nm的倍频Nd:YAG激光泵浦获得激光。激光阈值为3微焦,对应于约30微焦/平方厘米或4千瓦/平方厘米。发射线宽从放大自发发射模式下的约30nm减小到激光模式下的<0.4nm(仪器限制)。激光的斜率效率约为1.2%。

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