Kinetic Studies of the Photogeneration of Silver Nanoparticles

被引:11
作者
Baker, Thomas A.
Monti, Oliver L. A.
Nesbitt, David J. [1 ]
机构
[1] Univ Colorado, JILA, Boulder, CO 80309 USA
基金
美国国家科学基金会;
关键词
ENHANCED RAMAN-SCATTERING; SURFACE-PLASMON RESONANCE; LINKED PVA/PAA FILMS; METAL NANOPARTICLES; COLLOIDAL NANOPARTICLES; NANOSPHERE LITHOGRAPHY; OPTICAL-PROPERTIES; PHASE-CHANGE; SERS; SHAPE;
D O I
10.1021/jp200161j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Stable, intensely Raman active silver nanopartides are photogenerated by visible light from silver ions in a thin polymer film within a diffraction-limited focal area. The emission is resolved both spectrally and temporally to demonstrate that the source of the signal is surface-enhanced Raman scattering (SERS) from multiple silver nanoparticles generated in the diffraction-limited spot. The time evolution of the SERS signal is sigmoidal in shape and well described by Avrami phase transformation kinetics. The rate constant for the Avrami transformation depends linearly on illumination intensity, consistent with single photon photoreduction of the silver percholorate starting material as the limiting step to form silver nanoparticles. The asymptotic kinetic growth SERS signal exhibits a linear dependence on illumination intensity. Avrami analysis of the kinetics indicates that transformation is constrained to two dimensions, consistent with the similar to 10 nm thin film nature of the sample. The technique presented provides a novel route to large-scale periodic molecular sensor arrays with long-term stability, diffraction-limited resolution (<1 mu m), and laser-based spatial/temporal control of the formation kinetics.
引用
收藏
页码:9861 / 9870
页数:10
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