| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1332301 | Journal of Solid State Chemistry | 2008 | 6 Pages |
The phase transitions and proton dynamics of Cs5H3(SO4)4·0.5H2O single crystals were studied by measuring the NMR line shape, the spin-lattice relaxation time, T1, and the spin–spin relaxation time, T2, of the 1H and 133Cs nuclei. The “acid” protons and the “water” protons in Cs5H3(SO4)4·0.5H2O were distinguished. The loss of water protons was observed above TC1, whereas the content of water protons was found to recover above TC2. Therefore, the water protons play a special role in the stability of the superprotonic phase at high temperatures. The mechanism of fast proton conduction was found to consist of hydrogen-bond proton transfer involving the breakage of the weak part of the hydrogen bond and the formation of a new hydrogen bond. Thus, these structural phase transitions probably involve significant reorientation of the SO4 tetrahedra and dynamical disorder of the hydrogen bonds between them.
Graphical abstractThe phase transitions and proton dynamics of Cs5H3(SO4)4·0.5H2O were studied by the spin-lattice relaxation time and the spin–spin relaxation time of the 1H and 133Cs nuclei. The “acid” and the “water” protons were distinguished. Our NMR study has provided new information about the roles of acid protons, water protons, and cesium nuclei in Cs5H3(SO4)4·0.5H2O single crystals.Figure optionsDownload full-size imageDownload as PowerPoint slideFig. Temperature dependences of T1 and T2 for acid and water protons in a Cs5H3(SO4)4·H2O single crystal (●: T1 and ■: T2 for acid proton, ○: T1 and □: T2 for water proton).
