Department of Applied Chemistry, National Chiayi University, Chiayi City, Taiwan.
Chemphyschem. 2010 Jun 7;11(8):1742-8. doi: 10.1002/cphc.200900842.
Herein, we find that the surface plasmon resonance (SPR) spectra of silver nanoprisms in the presence of halide ions change gradually with reaction time. The changes in the spectra correspond to the shape transformation of silver nanoprisms. There are threshold concentrations of halide ions that initiate the shape-transformation reaction. The threshold concentrations for Cl(-), Br(-), and I(-) are about 3x10(-4) M, 1x10(-6) M, and 1.5x10(-6) M, respectively. Any concentrations of the added halide ions above these thresholds can eventually etch the silver nanoprisms into nanodisks if the reaction time is long enough. The higher the concentration of the halide ions, the higher the etching rate will be. The kinetics of the shape transformation of the silver nanoprisms can be studied by recording their time-dependent surface plasmon resonance (SPR) spectra on a commercial UV/Vis-NIR spectrometer. The peak positions of in-plane dipole SPR bands of silver colloids in the presence of chloride and bromide ions can be fitted very well with the biexponential functions. We propose that the fast components of the biexponential behaviors should correlate to the truncating effect on the corners of silver nanoprisms, and the slow component should correlate to the redeposition of the truncated residues onto the basal plane of the nanoplates.
在此,我们发现银纳米棱柱体在卤离子存在下的表面等离子体共振(SPR)光谱随反应时间逐渐发生变化。光谱的变化对应于银纳米棱柱体的形状转变。卤离子存在引发形状转变反应的阈值浓度。Cl(-)、Br(-)和 I(-)的阈值浓度分别约为 3x10(-4) M、1x10(-6) M 和 1.5x10(-6) M。如果反应时间足够长,任何高于这些阈值的添加卤离子浓度最终都会将银纳米棱柱体蚀刻成纳米盘。卤离子的浓度越高,蚀刻速率就越高。通过在商业 UV/Vis-NIR 分光光度计上记录其随时间变化的表面等离子体共振(SPR)光谱,可以研究银纳米棱柱体的形状转变动力学。在氯化物和溴化物离子存在下,银胶体的面内偶极 SPR 带的峰值位置可以很好地用双指数函数拟合。我们提出,双指数行为的快分量应与银纳米棱柱体角的截断效应相关,而慢分量应与截断残余物重新沉积到纳米板的基面相关。