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Superatom State-Resolved Dynamics of the Au<sub>25</sub>(SC<sub>8</sub>H<sub>9</sub>)<sub>18</sub><sup>–</sup> Cluster from Two-Dimensional Electronic Spectroscopy
78
Citations
24
References
2016
Year
EngineeringChemistryElectronic Excited StateElectronic StructureMolecular DynamicsTwo-dimensional Electronic SpectroscopyQuantum MaterialsMolecular SpectroscopyCluster ScienceQuantum SciencePhysicsAtomic PhysicsPhysical ChemistryQuantum ChemistrySuperatom State-resolved DynamicsSolid-state PhysicSuperatom D ManifoldNanophysicsExcited State PropertyNatural SciencesCondensed Matter PhysicsApplied PhysicsCluster ChemistrySuperatom P States
Superatom state-resolved dynamics of the Au25(SC8H9)18(-) monolayer-protected cluster (MPC) were examined using femtosecond two-dimensional electronic spectroscopy (2DES). The electronic ground state of the Au25(SC8H9)18(-) MPC is described by an eight-electron P-like superatom orbital. Hot electron relaxation (200 ± 15 fs) within the superatom D manifold of lowest-unoccupied molecular orbitals was resolved from hot hole relaxation (290 ± 20 fs) in the superatom P states by using 2DES in a partially collinear pump-probe geometry. Electronic relaxation dynamics mediated by specific superatom states were distinguished by examining the time-dependent cross-peak amplitudes for specific excitation and detection photon energy combinations. Quantification of the time-dependent amplitudes and energy positions of cross peaks in the 2.21/1.85 eV (excitation/detection) region confirmed that an apparent energetic blue shift observed for transient bleach signals results from rapid hot electron relaxation in the superatom D states. The combination of structurally precise MPCs and state-resolved 2DES can be used to examine directly the influence of nanoscale structural modifications on electronic carrier dynamics, which are critical for developing nanocluster-based photonic devices.
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