共振光的大折射率

揭示了在多能级原子介质中的一种新现象:利用原子相干可使共振光获得明显大于1的折射率.     

混合溶液折射率对局域表面等离子体共振的影响

对水-二甲基亚砜二元混合溶液质量分数和温度与折射率的关系进行了理论和实验研究,对几种经典模型的拟合结果进行了比较,给出了适合水-二甲基亚砜混合溶液的经验公式。对水性金溶胶-二甲基亚砜混合溶液质量分数和温度对局域表面等离子体共振峰值波长的影响进行了理论和实验研究,结果表明:水性金溶胶-二甲基亚砜混合溶液质量分数对共振峰值波长的调节有较好的线性关系和较大的调节范围,当温度从20 ℃增大到60 ℃,混合溶液金溶胶的共振峰值波长增加了1367 pm,温度敏感度为34 pm/K,在0%~100%的质量分数范围内,混合溶液金溶胶的共振峰值波长平均产生8.5103 pm的增长。     

混合溶液折射率对局域表面等离子体共振的影响

对水-二甲基亚砜二元混合溶液质量分数和温度与折射率的关系进行了理论和实验研究,对几种经典模型的拟合结果进行了比较,给出了适合水-二甲基亚砜混合溶液的经验公式。对水性金溶胶-二甲基亚砜混合溶液质量分数和温度对局域表面等离子体共振峰值波长的影响进行了理论和实验研究,结果表明：水性金溶胶-二甲基亚砜混合溶液质量分数对共振峰值波长的调节有较好的线性关系和较大的调节范围,当温度从20 ℃增大到60 ℃,混合溶液金溶胶的共振峰值波长增加了1367 pm,温度敏感度为34 pm/K,在0%~100%的质量分数范围内,混合溶液金溶胶的共振峰值波长平均产生8.5103 pm的增长。     

螺旋形塑料光纤表面等离子体共振折射率传感器

研究了基于波长调制的螺旋形塑料光纤(plastic optical fiber, POF)表面等离子体共振(surface plasmon resonance, SPR)折射率传感器。采用机械热压和扭曲法将塑料光纤制备成螺旋形,在螺旋形POF上通过磁控溅射蒸镀一定厚度(约50 nm)的金属薄膜来激励SPR效应,从而形成螺旋形POF-SPR传感器。通过对螺旋形POF-SPR传感器的结构进行修饰,研究不同结构参数对折射率传感特性的影响。实验结果表明:由厚度为500μm扁平形POF扭制、螺纹数为4的螺旋形POF-SPR传感器具有较好的线性度和折射率传感特性,在折射率为1.335～1.400范围内测得的灵敏度为1 262 nm/RIU。该传感器具有成本较低、制备简单、结构稳定等优点。     

倾斜光纤光栅溶液折射率传感器的实验研究

根据倾斜光纤光栅(TFBG)和表面镀金的TFBG传感器测量折射率的基本原理,通过OptiGrating软件模拟了不同浓度溶液下TFBG的透射谱和芯层模与某阶包层模耦合引起的谐振峰,初步得出了TFBG各阶包层模随着外界折射率的增大而向右偏移、在一定的传感范围内中心波长与外界折射率呈线性关系的结论。用小型离子溅射仪对TFBG镀45 nm厚度左右的金膜,并用扫描电镜在微观上观察镀膜效果。通过不同浓度下的NaCl溶液、MgCl₂溶液、CaCl₂溶液实验,对比研究了裸TFBG和镀金TFBG传感器对溶液折射率的传感特性。从而验证了模拟仿真得出的结论并定量分析得知：镀金后具有表面等离子体共振的TFBG溶液折射率灵敏度大于500 nm·RIU-1,而裸TFBG为2 nm·RIU-1左右,大约提高了200～300倍,且在一定范围内中心波长与溶液折射率的线性拟合度都在0.99以上。     

兔红细胞的共振散射光谱研究

研究了液相兔血红细胞的共振散射光谱 (RSS)及非线性分频散射和倍频散射。兔红细胞浓度在0 0 15～ 31 1× 10 6个·(mL) -1范围与共振散射光强度成线性关系。对非线性散射机理进行了探讨。     

基于LabVIEW的表面等离激元共振测量液体折射率

利用LabVIEW编写硬件控制软件,搭建了基于表面等离激元共振原理的光强探测型液体折射率测量实验平台.实验测量纯水和纯酒精的表面等离激元共振的共振角分别与理论计算数据相吻合,证明该系统测量的共振角数值能正确地反映液体折射率的变化.利用该系统测量了不同浓度的酒精-水混合液的折射率.     

The effect of an anti-hydrogen bond on Fermi resonance:A Raman spectroscopic study of the Fermi doublet ν1-ν12 of liquid pyridine

The effects of an anti-hydrogen bond on the ν1-ν12 Fermi resonance(FR) of pyridine are experimentally investigated by using Raman scattering spectroscopy.Three systems,pyridine/water,pyridine/formamide,and pyridine/carbon tetrachloride,provide varying degrees of strength for the diluent-pyridine anti-hydrogen bond complex.Water forms a stronger anti-hydrogen bond with pyridine than with formamide,and in the case of adding non-polar solvent carbon tetrachloride,which is neither a hydrogen bond donor nor an acceptor and incapable of forming a hydrogen bond with pyridine,the intermolecular distance of pyridine will increase and the interaction of pyridine molecules will reduce.The dilution studies are performed on the three systems.Comparing with the values of the Fermi coupling coefficient W of the ring breathing mode ν1 and triangle mode ν12 of pyridine at different volume concentrations,which are calculated according to the Bertran equations,in three systems,we find that the solution with the strongest anti-hydrogen bond,water,shows the fastest change in the ν1-ν12 Fermi coupling coefficient W with the volume concentration varying,followed by the formamide and carbon tetrachloride solutions.These results suggest that the stronger anti-hydrogen bond-forming effect will cause a greater reduction in the strength of the ν1-ν12 FR of pyridine.According to the mechanism of the formation of an anti-hydrogen bond in the complexes and the FR theory,a qualitative explanation for the anti-hydrogen bond effect in reducing the strength of the ν1-ν12 FR of pyridine is given.     

混合溶液中CARS过程的非共振信号实验研究

相干反斯托克斯拉曼散射是一种非线性四波混频效应,但是通过探测共振信号不易进行物质成分的定量光谱分析。本文利用单频相干反斯托克斯拉曼散射光谱分析法,对不同体积比混合的乙醇溶液在远离双光子共振跃迁及其远离溶质与溶剂的特征拉曼共振态位置进行了光谱探测。通过对实验结果进行分析发现,在共振位置2 876 cm-1的信号强度随混合溶液中的乙醇的体积比增加而增加,呈二次方关系。而在远离共振态位置的非共振信号强度随混合溶液中乙醇的体积比增加而增加,且呈线性关系,进而说明了非共振信号强度随着分子数浓度N呈线性变化关系。因此,通过探测非共振信号强度与分子数浓度关系可以为混合物中特定成分的定量光谱分析提供一种研究途径。     

基于侧边抛磨光纤表面等离子体共振的折射率和温度传感研究

用轮式侧边抛磨法制作侧边抛磨光纤,通过磁控溅射法溅射金膜制成侧边抛磨光纤表面等离子体共振(SPR)传感器,并通过理论和实验对传感器的折射率灵敏度以及温度特性做了深入研究。结果表明表面等离子体共振波长随待测样品折射率的增大向长波长方向漂移,平均折射率灵敏度为4.1×103 nm/RIU(RIU为单位折射率),高于已报道的结果;共振波长随待测样品温度的升高向短波长方向漂移,平均温度灵敏度为0.36nm/℃,故该光纤SPR传感器具有更强抗温度漂移能力和更高的高折射率灵敏度,其在生物化学传感领域有重要的应用。     

分子间费米共振增强二元溶液体系的受激拉曼散射研究

研究了液芯光纤内不同体积比的甲苯和间二甲苯二元混合溶液的受激拉曼散射.实验结果表明:在不同的体积比之下二元溶液的环呼吸振动模式1002 cm^-1,甲基的CH伸缩振动模式2920 cm^-1 以及芳香环CH对称伸缩振动模式3058 cm^-1的拉曼带同时产生受激拉曼辐射,并且2920 cm^-1 和 3058 cm^-1 拉曼带的一阶受激拉曼散射阈值要低于1002 cm^-1拉曼带的二阶 关键词： 分子间费米共振 二元溶液 受激拉曼散射 拉曼散射截面     

Influence of pressure effect on Fermi resonance in binary solution

The Fermi resonance behaviours of the two groups of binary solutions --- pyridine and methanol, benzene and carbon tetrachloride, under different pressures are investigated according to their Raman spectra. The effect of pressure on Fermi resonance in binary solution differs significantly from that in pure liquid. In a binary solution, with the intermolecular distance shortening, the intermolecular interaction potential increases, the shift rates of the Raman spectral lines increase, the spectral line splitting occurs ahead of that in pure liquid, and the wavenumber separation Δ₀ between the unperturbed harmonic levels shifts more quickly, too. The Fermi resonance parameters, the coupling coefficient W and the intensity ratio R of the two Raman bands, decrease rapidly with pressure increasing, and the pressure at which Fermi resonance phenomenon disappears is much lower than that in pure liquid, especially in the solution whose molecules are of the same polarity. This article is valuable in the identification and the assignment of spectral lines under high pressure, as well as the study of high pressure effect, intermolecular interaction, and solvent effects in different cases, etc.     

Study of asymmetric wavenumber shift of the Fermi doublet ν1 − 2ν2 in the Raman spectrum of liquid carbon disulfide

The Raman spectra of liquid carbon disulfide (CS₂) diluted with benzene (C₆H₆) have been measured. By changing the CS₂, the concentration, we found an asymmetric wavenumber shift phenomenon. With decreasing concentration of CS₂, the position of the ν₁ (655 cm⁻¹) band remains practically unchanged, and the 2ν₂ (796 cm⁻¹) band shifts toward higher wavenumbers. To interpret this asymmetric wavenumber shift phenomenon of the Fermi doublet ν₁ − 2ν₂ in the Raman spectra satisfactorily, we propose a modified Bertran model. The values of the Fermi resonance (FR) parameters of CS₂ at different concentrations were calculated using the Bertran equations. In addition, we found the fundamental ν₂, which should be independent of the FR interaction, shifted to higher wavenumbers as the concentration decreased. This shift was probably driven by the tuning of the FR. Copyright © 2009 John Wiley & Sons, Ltd.     

高压拉曼光谱方法研究联苯分子费米共振

测量了0—15 GPa压强下联苯分子的拉曼光谱. 结果表明,随压强增加,分子内和分子间π-π共轭和离域效应增强,谱线的绝对强度变大、蓝移. 联苯分子的两费米共振谱线强度比R_f/a减少,频率差Δ增加,当压强为8 GPa时,费米共振现象消失,利用Betran理论得出了固有频率差Δ₀和耦合系数ω随压强的变化关系,通过高压下相变进行了解释,并探讨了高压下费米共振耦合变弱的机理. 关键词： 联苯 费米共振 高压 拉曼光谱     

Pressure dependence of the refractive index and of the sound velocity of methanol-ethanol solution: A Brillouin scattering study

Abstract

The pressure dependence of the refractive index n(P) and of the longitudinal acoustic velocities of 4.1 methanol-ethanol solution have been measured in a diamond anvil cell up to 8.1 GPa. We utilize Brillouin scattering methods for this determination and detect, in the same back scattering configuration, acoustic wave propagation parallel to the faces of the diamond anvils as well as along the incident laser radiation direction. We also deduce that the polarizability of the fluid is reduced by about 15% over the pressure range studied.     

四氯化碳费米共振的拉曼光谱研究

费米共振现象是一种广泛存在于分子振动光谱中的现象,特别是结构比较复杂的多原子分子.在多原子分子中当振动倍频或组合频位于某一基频附近,由于发生振动耦合,会出现两个新峰,峰的位置向两侧发生移动,二者谱线强度发生变化,把这种现象称为费米共振.费米共振现象不仅存在于红外光谱中,也存在于拉曼光谱中.文章中测量了CCl4的拉曼光谱,利用所得到的谱线峰位和用Originpro7.5软件程序获得积分强度,用费米共振的相关理论计算了C-Cl的a1对称伸缩振动频率v1与C-Cl2的f对称弯曲振动频率v4的组合频(v1 v4)与(某一未知基频)C-Cl的f对称伸缩振动频率v03的费米共振特征参数,进而计算出了耦合系数W和这一未知基频v03.该文对理解费米共振,了解分子振动频率,研究分子结构有很重要的参考价值.     

改进的油浸法测量聚硅氧烷微球的折射率

在传统的油浸法基础上,引入透光率指标来判断粉体与浸液折射率的差异,测量了聚硅氧烷微球粉体的折射率.该方法将传统油浸法的适用范围扩展至超细粉体甚至纳米粉体的折射率测量.     

The effect of anti-hydrogen bond on Fermi resonance: A Raman spectroscopic study of the Fermi doublet ν1—ν12 of liquid pyridine

The effects of anti-hydrogen bond on the ν₁—ν₁₂ Fermi resonance (FR) of pyridine are experimentally investigated by using Raman scattering spectroscopy. Three systems, pyridine/water, pyridine/formamide, pyridine/carbon tetrachloride, provide varying degrees of strength for the diluent-pyridine anti-hydrogen bond complex. Water forms a stronger anti-hydrogen bond with pyridine than with formamide, and in the case of adding non-polar solvent carbon tetrachloride, which is neither a hydrogen bond donor nor an acceptor and incapable of forming hydrogen bond with pyridine, the intermolecular distance of pyridine will increase and the interaction of pyridine molecules will reduce. The dilution studies are performed on the three systems. Comparing with the values of Fermi coupling coefficient W of the ring breathing mode ν ₁ and triangle mode ν ₁₂ of pyridine at different volume concentrations, which are calculated according to the Bertran equations, in three systems, we find that the solution with the strongest anti-hydrogen bond, water, shows the fastest change in the ν₁—ν₁₂ Fermi coupling coefficient W with the volume concentration varying, followed by the formamide and carbon tetrachloride solutions. These results suggest that the stronger anti-hydrogen bond-forming effect will cause a greater reduction in the strength of the ν₁—ν₁₂ FR of pyridine. According to the mechanism of the formation of anti-hydrogen bond in the complexes and the FR theory, a qualitative explanation for the anti-hydrogen bond effect in reducing the strength of the ν₁—ν₁₂ FR of pyridine is given.