Changing Hydrogen-Bond Structure during an Aqueous Liquid-Liquid Transition Investigated with Time-Resolved and Two-Dimensional Vibrational Spectroscopy

被引:16
|
作者
Bruijn, Jeroen R. [1 ]
van der Loop, Tibert H. [1 ]
Woutersen, Sander [1 ]
机构
[1] Univ Amsterdam, Vant Hoff Inst Mol Sci HIMS, Sci Pk 904, NL-1098 XH Amsterdam, Netherlands
来源
关键词
SUPERCOOLED WATER; INFRARED-SPECTROSCOPY; PHASE-TRANSITION; DENSITY; CRYSTALLIZATION; SEPARATION; BEHAVIOR;
D O I
10.1021/acs.jpclett.5b02861
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 investigate the putative liquid-liquid phase transition in aqueous glycerol solution, using the OD-stretch mode in dilute OD/OH isotopic mixtures to probe the hydrogen-bond structure. The conversion exhibits Avrami kinetics with an exponent of n = 2.9 +/- 0.1 (as opposed to n = 1.7 observed upon inducing ice nucleation and growth in the same sample), which indicates a transition from one liquid phase to another. Two-dimensional infrared (2D-IR) spectroscopy shows that the initial and final phases have different hydrogen-bond structures: the former has a single Gaussian distribution of hydrogen-bond lengths, whereas the latter has a bimodal distribution consisting of a broad distribution and a narrower, ice-like distribution. The 2D-IR spectrum of the final phase is identical to that of ice/glycerol at the same temperature. Combined with the kinetic data this suggests that the liquid-liquid transformation is immediately followed by a rapid formation of small (probably nanometer-sized) ice crystals.
引用
收藏
页码:795 / 799
页数:5
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