Song Youlin, Zhao Ke, Jia Yu, Hu Xing, Zhang Zhenyu
School of Physics and Engineering, Zhengzhou University, Zhengzhou, China.
J Chem Phys. 2008 Nov 28;129(20):204506. doi: 10.1063/1.3009293.
Finite size effects on the optical properties of one-dimensional (1D) and two-dimensional (2D) nanoshell dimer arrays are investigated using generalized Mie theory and coupled dipole approximation within the context of surface-enhanced Raman spectroscopy (SERS). It is shown that the huge enhancement in the electromagnetic (EM) field at the center of a given dimer oscillates with the length of the 1D array. For an array of fixed length, the EM enhancement also oscillates along the array, but with a different period. Both types of oscillations can be attributed to the interference of the dynamic dipole fields from different dimers in the array. When generalized to 2D arrays, EM enhancement higher than that of the 1D arrays can be gained with a constant magnitude, a salient feature advantageous to experimental realization of single-molecule SERS.
在表面增强拉曼光谱(SERS)的背景下,利用广义米氏理论和耦合偶极近似,研究了有限尺寸对一维(1D)和二维(2D)纳米壳二聚体阵列光学性质的影响。结果表明,给定二聚体中心处的电磁(EM)场的巨大增强随一维阵列的长度振荡。对于固定长度的阵列,EM增强也沿阵列振荡,但周期不同。这两种振荡都可归因于阵列中不同二聚体的动态偶极场的干涉。当推广到二维阵列时,可以获得比一维阵列更高且幅度恒定的EM增强,这是有利于单分子SERS实验实现的一个显著特征。