氢铵
分子
质子
星团(航天器)
化学物理
氢键
接受者
化学
水二聚体
光化学
物理
核物理学
计算机科学
凝聚态物理
有机化学
程序设计语言
作者
Conrad T. Wolke,Joseph A. Fournier,Laura C. Dzugan,Matias R. Fagiani,Tuguldur T. Odbadrakh,Harald Knorke,Kenneth D. Jordan,Anne B. McCoy,Knut R. Asmis,Mark A. Johnson
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2016-12-01
卷期号:354 (6316): 1131-1135
被引量:247
标识
DOI:10.1126/science.aaf8425
摘要
The Grotthuss mechanism explains the anomalously high proton mobility in water as a sequence of proton transfers along a hydrogen-bonded (H-bonded) network. However, the vibrational spectroscopic signatures of this process are masked by the diffuse nature of the key bands in bulk water. Here we report how the much simpler vibrational spectra of cold, composition-selected heavy water clusters, D+(D2O)n, can be exploited to capture clear markers that encode the collective reaction coordinate along the proton-transfer event. By complexing the solvated hydronium "Eigen" cluster [D3O+(D2O)3] with increasingly strong H-bond acceptor molecules (D2, N2, CO, and D2O), we are able to track the frequency of every O-D stretch vibration in the complex as the transferring hydron is incrementally pulled from the central hydronium to a neighboring water molecule.
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