Vibrational spectroscopy of hydrated electron clusters (H2O)15-50- via infrared multiple photon dissociation

被引:72
作者
Asmis, Knut R.
Santambrogio, Gabriele
Zhou, Jia
Garand, Etienne
Headrick, Jeffrey
Goebbert, Daniel
Johnson, Mark A.
Neumark, Daniel M.
机构
[1] Max Planck Gesell, Fritz Haber Inst, D-14195 Berlin, Germany
[2] Free Univ Berlin, Inst Expt Phys, D-14195 Berlin, Germany
[3] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[4] Yale Univ, Sterling Chem Lab, New Haven, CT 06520 USA
[5] Lawrence Berkeley Natl Lab, Div Chem Sci, Berkeley, CA 94720 USA
基金
加拿大自然科学与工程研究理事会;
关键词
D O I
10.1063/1.2741508
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 ; 081704 ;
摘要
Infrared multiple photon dissociation spectra for size-selected water cluster anions (H2O)(n)(-), n=15-50, are presented covering the frequency range of 560-1820 cm(-1). The cluster ions are trapped and cooled by collisions with ambient He gas at 20 K, with the goal of defining the cluster temperature better than in previous investigations of these species. Signal is seen in two frequency regions centered around 700 and 1500-1650 cm(-1), corresponding to water librational and bending motions, respectively. The bending feature associated with a double-acceptor water molecule binding to the excess electron is clearly seen up to n=35, but above n=25; this feature begins to blueshift and broadens, suggesting a more delocalized electron binding motif for the larger clusters in which the excess electron interacts with multiple water molecules. (C) 2007 American Institute of Physics.
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页数:5
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