Ultrafast relaxation dynamics of phosphine-protected, rod-shaped Au 20 clusters: interplay between solvation and surface trapping

• Published in: Physical chemistry chemical physics : PCCP 2014-09, Vol.16 (34), p.18288-18293
• Main Authors: Zhou, Meng, Long, Saran, Wan, Xiankai, Li, Yang, Niu, Yingli, Guo, Qianjin, Wang, Quan-Ming, Xia, Andong
• Format: Article
• Language: English
• ISSN: 1463-9076; 1463-9084
• DOI: 10.1039/C4CP02336F

The exact interaction between Au cores and surface ligands remains largely unknown because of the complexity of the structure and chemistry of ligand/Au-core interfaces in ligand-protected Au nanoclusters (AuNCs), which are commonly found in many organic–inorganic complexes. Here, femtosecond transient absorption measurement of the excited-state dynamics of a newly synthesized phosphine-protected cluster [Au 20 (PPhpy 2 ) 10 Cl 4 ]Cl 2 ( 1 ) is reported. Intramolecular charge transfer (ICT) from the Au core to the peripheral ligands was identified. Furthermore, we found that solvation strongly affected ICT at ligand/Au-core interfaces while by choosing several typical alcoholic solvents with different intrinsic solvation times, we successfully observed that excited-state relaxation dynamics together with displacive excited coherent oscillation of Au 20 clusters were significantly modulated through the competition between solvation and surface trapping. The results provide a fundamental understanding of the structure–property relationships of the solvation-dependent core–shell interaction of AuNCs for the potential applications in catalysis, sensing and nanoelectronics.