Glasslike Behavior in Aqueous Electrolyte Solutions
| dc.creator | Turton, David A. | |
| dc.creator | Hunger, Johannes | |
| dc.creator | Hefter, Glenn | |
| dc.creator | Buchner, Richard | |
| dc.creator | Wynne, Klaas | |
| dc.date | 2009-04-04 | |
| dc.date.accessioned | 2026-07-07T13:00:39Z | |
| dc.date.available | 2026-07-07T13:00:39Z | |
| dc.description | When salts are added to water, the viscosity generally increases suggesting the ions increase the strength of the water's hydrogen-bond network. However, infrared pump-probe measurements on electrolyte solutions have found that ions have no influence on the rotational dynamics of water molecules implying no enhance-ment or breakdown of the hydrogen-bond network. Here we report optical Kerr-effect and dielectric relaxa-tion spectroscopic measurements, which have enabled us to separate the effects of rotational and transitional motions of the water molecules. These data show that electrolyte solutions behave like a supercooled liquid approaching a glass transition in which rotational and translational molecular motions are decoupled. It is now possible to understand previously conflicting viscosity data, nuclear magnetic resonance relaxation, and ultrafast infrared spectroscopy in a single unified picture. | |
| dc.identifier | https://arxiv.org/abs/0904.0717 | |
| dc.identifier | http://arxiv.org/abs/0904.0717 | |
| dc.identifier | J. Chem. Phys. Communication, 128, 161102 (2008) | |
| dc.identifier | doi:10.1063/1.2906132 | |
| dc.identifier.uri | http://salesiana.dossiersoluciones.com/handle/123456789/225906 | |
| dc.subject | Chemical Physics | |
| dc.title | Glasslike Behavior in Aqueous Electrolyte Solutions | |
| dc.type | text |