Spectroscopic snapshots of the proton-transfer mechanism in water

被引:228
|
作者
Wolke, Conrad T. [1 ]
Fournier, Joseph A. [1 ,2 ,3 ]
Dzugan, Laura C. [4 ]
Fagiani, Matias R. [5 ,6 ]
Odbadrakh, Tuguldur T. [7 ]
Knorke, Harald [5 ]
Jordan, Kenneth D. [7 ]
McCoy, Anne B. [4 ,8 ]
Asmis, Knut R. [5 ]
Johnson, Mark A. [1 ]
机构
[1] Yale Univ, Dept Chem, 225 Prospect St, New Haven, CT 06520 USA
[2] Univ Chicago, James Franck Inst, 5640 S Ellis Ave, Chicago, IL 60637 USA
[3] Univ Chicago, Dept Chem, 5735 S Ellis Ave, Chicago, IL 60637 USA
[4] Ohio State Univ, Dept Chem & Biochem, Columbus, OH 43210 USA
[5] Univ Leipzig, Wilhelm Ostwald Inst Phys & Theoret Chem, D-04103 Leipzig, Germany
[6] Fritz Haber Inst Max Planck Gesell, D-14195 Berlin, Germany
[7] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15620 USA
[8] Univ Washington, Dept Chem, Seattle, WA 98195 USA
基金
美国国家科学基金会;
关键词
HYDRATED EXCESS PROTON; HYDROGEN-BONDS; LIQUID WATER; SPECTRAL SIGNATURES; INFRARED-SPECTRA; IR SPECTROSCOPY; CLUSTERS; TRANSPORT; ENERGY; VIBRATIONS;
D O I
10.1126/science.aaf8425
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
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 (D-2, N-2, 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.
引用
收藏
页码:1131 / 1135
页数:5
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