TY - JOUR
T1 - Long-lived charge-separated states in ligand-stabilized silver clusters
AU - Pelton, Matthew
AU - Tang, Yun
AU - Bakr, Osman
AU - Stellacci, Francesco
N1 - KAUST Repository Item: Exported on 2020-10-01
Acknowledgements: We thank A. Demortiere for assistance with freeze-pump-thaw preparation and D. Gosztola and G. Wiederrecht for helpful discussions. Work at the Center for Nanoscale Materials was supported by the U.S. Department of Energy, Office of Science, Office of Basic Energy Sciences, under Contract DE-AC02-06CH11357.
PY - 2012/7/16
Y1 - 2012/7/16
N2 - Recently developed synthesis methods allow for the production of atomically monodisperse clusters of silver atoms stabilized in solution by aromatic thiol ligands, which exhibit intense absorption peaks throughout the visible and near-IR spectral regions. Here we investigated the time-dependent optical properties of these clusters. We observed two kinetic processes following ultrafast laser excitation of any of the absorption peaks: a rapid decay, with a time constant of 1 ps or less, and a slow decay, with a time constant that can be longer than 300 ns. Both time constants decrease as the polarity of the solvent increases, indicating that the two processes correspond to the formation and recombination, respectively, of a charge-separated state. The long lifetime of this state and the broad optical absorption spectrum mean that the ligand-stabilized silver clusters are promising materials for solar energy harvesting. © 2012 American Chemical Society.
AB - Recently developed synthesis methods allow for the production of atomically monodisperse clusters of silver atoms stabilized in solution by aromatic thiol ligands, which exhibit intense absorption peaks throughout the visible and near-IR spectral regions. Here we investigated the time-dependent optical properties of these clusters. We observed two kinetic processes following ultrafast laser excitation of any of the absorption peaks: a rapid decay, with a time constant of 1 ps or less, and a slow decay, with a time constant that can be longer than 300 ns. Both time constants decrease as the polarity of the solvent increases, indicating that the two processes correspond to the formation and recombination, respectively, of a charge-separated state. The long lifetime of this state and the broad optical absorption spectrum mean that the ligand-stabilized silver clusters are promising materials for solar energy harvesting. © 2012 American Chemical Society.
UR - http://hdl.handle.net/10754/562247
UR - https://pubs.acs.org/doi/10.1021/ja303682m
UR - http://www.scopus.com/inward/record.url?scp=84864234485&partnerID=8YFLogxK
U2 - 10.1021/ja303682m
DO - 10.1021/ja303682m
M3 - Article
SN - 0002-7863
VL - 134
SP - 11856
EP - 11859
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 29
ER -