The local structure of protonated water from x-ray absorption and density functional theory

被引:47
作者
Cavalleri, Matteo [1 ]
Naslund, Lars-Ake
Edwards, David C.
Wernet, Philippe
Ogasawara, Hirohito
Myneni, Satish
Ojamae, Lars
Odelius, Michael
Nilsson, Anders
Pettersson, Lars G. M.
机构
[1] Stockholm Univ, AlbaNova Univ Ctr, Fysikum, SE-10691 Stockholm, Sweden
[2] Stanford Synchrotron Radiat Lab, Stanford, CA 94309 USA
[3] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
[4] Stanford Synchrotron Radiat Lab, Stanford, CA 94309 USA
[5] BESSY, D-12489 Berlin, Germany
[6] Princeton Univ, Dept Geosci, Princeton, NJ 08544 USA
[7] Linkoping Univ, IFM, Dept Chem, SE-58183 Linkoping, Sweden
基金
美国国家科学基金会;
关键词
D O I
10.1063/1.2199828
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
We present a combined x-ray absorption spectroscopy/computational study of water in hydrochloric acid (HCl) solutions of varying concentration to address the structure and bonding of excess protons and their effect on the hydrogen bonding network in liquid water. Intensity variations and energy shifts indicate changes in the hydrogen bonding structure in water as well as the local structure of the protonated complex as a function of the concentration of protons. In particular, in highly acidic solutions we find a dominance of the Eigen form, H3O+, while the proton is less localized to a specific water under less acidic conditions. (c) 2006 American Institute of Physics.
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页数:8
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