Time-resolved intraband electronic relaxation dynamics of Hgn- clusters (n=7-13,15,18) excited at 1.0 eV -: art. no. 054314

被引:25
作者
Bragg, AE
Verlet, JRR
Kammrath, A
Cheshnovsky, O
Neumark, DM [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[2] Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
[3] Tel Aviv Univ, Sackler Fac Exact Sci, Sch Chem, IL-69978 Tel Aviv, Israel
关键词
D O I
10.1063/1.1828042
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
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. (C) 2005 American Institute of Physics.
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页数:11
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