Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA.
ACS Nano. 2010 Jun 22;4(6):3406-12. doi: 10.1021/nn1003524.
We report a systematic investigation of the optically excited vibrations in monolayer-protected gold clusters capped with hexane thiolate as a function of the particle size in the range of 1.1-4 nm. The vibrations were excited and monitored in transient absorption experiments involving 50 fs light pulses. For small quantum-sized clusters (< or =2.2 nm), the frequency of these vibrations has been found to be independent of cluster size, while for larger clusters (3 and 4 nm), we did not observe detectable optically excited vibrations in this regime. Possible mechanisms of excitation and detection of the vibrations in nanoclusters in the course of the transient absorption are discussed. The results of the current investigation support a displacive excitation mechanism associated with the presence of finite optical energy gap in the quantum-sized nanoclusters. Observed vibrations provide a new valuable diagnostic tool for the investigations of quantum size effects and structural studies in metal nanoclusters.
我们系统地研究了单层保护的金纳米簇在正己硫醇配体保护下的受激振动,这些纳米簇的粒径范围在 1.1-4nm 之间。通过涉及 50fs 光脉冲的瞬态吸收实验来激发和监测这些振动。对于小尺寸的量子点簇(≤2.2nm),我们发现这些振动的频率与簇的尺寸无关,而对于较大的簇(3nm 和 4nm),我们在这个范围内没有观察到可检测的受激振动。我们讨论了在瞬态吸收过程中纳米簇中振动的激发和检测的可能机制。当前研究的结果支持与量子点纳米簇中存在有限的光学能隙相关的位移激发机制。观察到的振动为研究量子尺寸效应和金属纳米簇的结构提供了一种新的有价值的诊断工具。