State Key Laboratory of Molecular Reaction Dynamics, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, 116023 Dalian, China.
University of Chinese Academy of Sciences, 100049 Beijing, China.
Proc Natl Acad Sci U S A. 2020 Jul 7;117(27):15423-15428. doi: 10.1073/pnas.2000601117. Epub 2020 Jun 15.
Infrared spectroscopic study of neutral water clusters is crucial to understanding of the hydrogen-bonding networks in liquid water and ice. Here we report infrared spectra of size-selected neutral water clusters, (HO) ( = 3-6), in the OH stretching vibration region, based on threshold photoionization using a tunable vacuum ultraviolet free-electron laser. Distinct OH stretch vibrational fundamentals observed in the 3,500-3,600-cm region of (HO) provide unique spectral signatures for the formation of a noncyclic pentamer, which coexists with the global-minimum cyclic structure previously identified in the gas phase. The main features of infrared spectra of the pentamer and hexamer, (HO) ( = 5 and 6), span the entire OH stretching band of liquid water, suggesting that they start to exhibit the richness and diversity of hydrogen-bonding networks in bulk water.
中性水分子团的红外光谱研究对于理解液态水和冰中的氢键网络至关重要。在这里,我们报告了基于可调谐真空紫外自由电子激光的阈上光电离,在 OH 伸缩振动区域中性水团簇(HO)(n=3-6)的红外光谱。在(HO)的 3500-3600cm-1 区域中观察到的独特 OH 伸缩振动基频为非环状五聚体的形成提供了独特的光谱特征,该五聚体与先前在气相中确定的全局最小环状结构共存。五聚体和六聚体(HO)(n=5 和 6)的红外光谱的主要特征跨越了液态水的整个 OH 伸缩带,表明它们开始表现出与体相水中丰富多样的氢键网络相似的特征。