Infrared study of high-pressure molecular phases of carbon dioxide

The infrared absorption spectra of the high-pressure crystalline phases II, III and IV of solid CO₂ were studied by using a resistive heated diamond anvil cell up to 30 GPa. The employment of crystal slabs having thickness of ~ 2 m allowed the study of the strongly absorbing fundamental bending a...

Повний опис

Збережено в:
Бібліографічні деталі
Опубліковано в: :Физика низких температур
Дата:2006
Автори: Giordano, V.M., Gorelli, F.A., Bini, R.
Формат: Стаття
Мова:Англійська
Опубліковано: Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України 2006
Теми:
Онлайн доступ:https://nasplib.isofts.kiev.ua/handle/123456789/120879
Теги: Додати тег
Немає тегів, Будьте першим, хто поставить тег для цього запису!
Назва журналу:Digital Library of Periodicals of National Academy of Sciences of Ukraine
Цитувати:Infrared study of high-pressure molecular phases of carbon dioxide / V.M. Giordano, F.A. Gorelli, R. Bini // Физика низких температур. — 2006. — Т. 32, № 11. — С. 1402–1408. — Бібліогр.: 24 назв. — англ.

Репозитарії

Digital Library of Periodicals of National Academy of Sciences of Ukraine
Опис
Резюме:The infrared absorption spectra of the high-pressure crystalline phases II, III and IV of solid CO₂ were studied by using a resistive heated diamond anvil cell up to 30 GPa. The employment of crystal slabs having thickness of ~ 2 m allowed the study of the strongly absorbing fundamental bending and antisymmetric stretching modes without saturation. These are the first data for phases II and IV in the fundamental modes spectral region, furthermore the high samples quality allowed to improve, with respect to previous studies, the characterization of the infrared spectra of phases I and III. The comparison of the spectral structure and of the frequency evolution with pressure of the crystal modes between phase I and the higher pressure phases clearly indicates the close resemblance among all these phases. In particular, the dramatic change of the intermolecular interaction claimed for phases II (dimeric association) and IV (large molecular bending) can be ruled out and, as a consequence, the hypothesis of a transition from the molecular phase I to the silica-like phase V through intermediate nonmolecular phases discarded.
ISSN:0132-6414