TY - JOUR
T1 - Time-resolved intraband electronic relaxation dynamics of Hg n - clusters (n=7-13,15,18) excited at 1.0eV
AU - Bragg, Arthur E.
AU - Verlet, Jan R.R.
AU - Kammrath, Aster
AU - Cheshnovsky, Ori
AU - Neumark, Daniel M.
PY - 2005
Y1 - 2005
N2 - Time-resolved photoelectron imaging has been used to study the relaxation dynamics of small Hg n - clusters (n=7-13,15,18) following intraband electronic excitation at 1250 nm (1.0 eV). This study furthers our previous investigation of single electron, intraband relaxation dynamics in Hg n - clusters at 790 nm by exploring the dynamics of smaller clusters (n=7-10), as well as those of larger clusters (n=11-13,15,18) at a lower excitation energy. We measure relaxation time scales of 2-9 ps, two to three times faster than seen previously after 790 nm excitation of Hg n -, n=11-18. These results, along with size-dependent trends in the absorption cross-section and photoelectron angular distribution anisotropy, suggest significant evolution of the cluster anion electronic structure in the size range studied here. Furthermore, the smallest clusters studied here exhibit 35-45 cm -1 oscillations in pump-probe signal at earliest temporal delays that are interpreted as early coherent nuclear motion on the excited potential energy surfaces of these clusters. Evidence for evaporation of one or two Hg atoms is seen on a time scale of tens of picoseconds.
AB - Time-resolved photoelectron imaging has been used to study the relaxation dynamics of small Hg n - clusters (n=7-13,15,18) following intraband electronic excitation at 1250 nm (1.0 eV). This study furthers our previous investigation of single electron, intraband relaxation dynamics in Hg n - clusters at 790 nm by exploring the dynamics of smaller clusters (n=7-10), as well as those of larger clusters (n=11-13,15,18) at a lower excitation energy. We measure relaxation time scales of 2-9 ps, two to three times faster than seen previously after 790 nm excitation of Hg n -, n=11-18. These results, along with size-dependent trends in the absorption cross-section and photoelectron angular distribution anisotropy, suggest significant evolution of the cluster anion electronic structure in the size range studied here. Furthermore, the smallest clusters studied here exhibit 35-45 cm -1 oscillations in pump-probe signal at earliest temporal delays that are interpreted as early coherent nuclear motion on the excited potential energy surfaces of these clusters. Evidence for evaporation of one or two Hg atoms is seen on a time scale of tens of picoseconds.
UR - http://www.scopus.com/inward/record.url?scp=22944466880&partnerID=8YFLogxK
U2 - 10.1063/1.1828042
DO - 10.1063/1.1828042
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AN - SCOPUS:22944466880
SN - 0021-9606
VL - 122
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 5
M1 - 054314
ER -