Ultrafast Electron Dynamics in Thiolate-Protected Plasmonic Gold Clusters: Size and Ligand Effect
The influence of passivating ligand on electron-phonon relaxation dynamics of the smallest sized gold clusters was studied using ultrafast transient absorption spectroscopy and theoretical modeling. The electron dynamics in Au279, Au329, and Au329 passivated with TBBT, SC2Ph and SC6, respectively, were investigated. Ultrafast transient absorption measurements were also carried out on Au~1400 (SC6) and Au~2000 (SC6) to understand the influence of the size on electron-phonon relaxation with the same passivating ligand. The study has revealed interesting aspects on the role of ligand on electron-phonon relaxation dynamics wherein the aromatic passivating ligands, SC2Ph and TBBT, have shown smaller power dependence and higher plasmon bleach indicating dampened plasmon resonance while the cluster with aliphatic passivating ligand has behaved similarly to regular plasmonic gold nanoparticles. To model the effect of the ligand on the plasmonic properties of the investigated samples , free electron density correction factor of each one was calculated using three-layered Mie theory, and the results show that SC6 inter-acts least with core-gold while TBBT and SC2Ph have a greater effect on the surface electronic conductivity that is attributed to pi-interaction of the ligand with gold. The results also shed light on unusual electron-phonon relaxation and smaller slope observed for Au329 (SC2Ph) that is ascribed to surface gold-pi interaction creating a hybrid state. In contrast, extended pi-interaction is probably the reason for plasmonic nature observed in Au279 (TBBT) even though its size is smaller when compared to Au329. In addition, the results also have shown that the electron-phonon coupling has increased with an increase in the size of the cluster and theoretical modeling has shown higher electron conductivity for larger plasmonic gold clusters.