Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations
Rovibrational Raman spectra of CO molecules isolated in solid Ar were measured for the 9–30 K temperature range and compared to past and present IR spectra. The fundamental band appears as a triplet-split structure, where the center peak shows completely different response to temperature in the Ra...
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| Дата: | 2012 |
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| Автори: | , , , |
| Формат: | Стаття |
| Мова: | English |
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Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України
2012
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| Назва видання: | Физика низких температур |
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| Назва журналу: | Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| Цитувати: | Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations / J. Lindgren, A. Olbert-Majkut, M. Pettersson, T. Kiljunen // Физика низких температур. — 2012. — Т. 38, № 8. — С. 894-904. — Бібліогр.: 46 назв. — англ. |
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Digital Library of Periodicals of National Academy of Sciences of Ukraine| id |
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irk-123456789-1174182017-05-24T03:04:24Z Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations Lindgren, J. Olbert-Majkut, A. Pettersson, M. Kiljunen, T. Low Temperature Spectroscopy and Radiation Effects Rovibrational Raman spectra of CO molecules isolated in solid Ar were measured for the 9–30 K temperature range and compared to past and present IR spectra. The fundamental band appears as a triplet-split structure, where the center peak shows completely different response to temperature in the Raman and IR spectroscopies. The peak is sharp and stable in Raman but reversibly broadens beyond recognition in IR upon annealing. The red-shifted, intense line of the triplet is found thermally inert similarly in both spectroscopies. The third line is the weakest, and as concentration dependent, it is assigned to a dimer as before. The CO–H₂O impurity complex is identified as a side band. We employ crystal field and quantum chemical modeling to interpret the disparity between the spectroscopies. The stable and broadening lines are given assignments to double- and singlesubstitution sites, respectively. Thermal excitations are not effective in the former case of angularly tightconfined, deep potential well. In the single-substitutional case, the librational level structure shows up in discriminating between the Raman and IR selection rules. An effectively ΔJ = 0 totally symmetric transition is found for Raman that is uncoupled from lattice phonons and corresponding broadening mechanisms. The low-temperature limit necessitates the use of a fixed lattice approach while the warmer end of the range is best described with an adiabatic, pseudorotating lattice approach. 2012 Article Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations / J. Lindgren, A. Olbert-Majkut, M. Pettersson, T. Kiljunen // Физика низких температур. — 2012. — Т. 38, № 8. — С. 894-904. — Бібліогр.: 46 назв. — англ. 0132-6414 PACS: 33.20.Ea, 33.20.Fb, 33.20.Vq, 34.20.Gj, 31.15.xv http://dspace.nbuv.gov.ua/handle/123456789/117418 en Физика низких температур Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України |
| institution |
Digital Library of Periodicals of National Academy of Sciences of Ukraine |
| collection |
DSpace DC |
| language |
English |
| topic |
Low Temperature Spectroscopy and Radiation Effects Low Temperature Spectroscopy and Radiation Effects |
| spellingShingle |
Low Temperature Spectroscopy and Radiation Effects Low Temperature Spectroscopy and Radiation Effects Lindgren, J. Olbert-Majkut, A. Pettersson, M. Kiljunen, T. Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations Физика низких температур |
| description |
Rovibrational Raman spectra of CO molecules isolated in solid Ar were measured for the 9–30 K temperature
range and compared to past and present IR spectra. The fundamental band appears as a triplet-split structure,
where the center peak shows completely different response to temperature in the Raman and IR spectroscopies.
The peak is sharp and stable in Raman but reversibly broadens beyond recognition in IR upon annealing. The
red-shifted, intense line of the triplet is found thermally inert similarly in both spectroscopies. The third line is
the weakest, and as concentration dependent, it is assigned to a dimer as before. The CO–H₂O impurity complex
is identified as a side band. We employ crystal field and quantum chemical modeling to interpret the disparity
between the spectroscopies. The stable and broadening lines are given assignments to double- and singlesubstitution
sites, respectively. Thermal excitations are not effective in the former case of angularly tightconfined,
deep potential well. In the single-substitutional case, the librational level structure shows up in discriminating
between the Raman and IR selection rules. An effectively ΔJ = 0 totally symmetric transition is found
for Raman that is uncoupled from lattice phonons and corresponding broadening mechanisms. The low-temperature
limit necessitates the use of a fixed lattice approach while the warmer end of the range is best described
with an adiabatic, pseudorotating lattice approach. |
| format |
Article |
| author |
Lindgren, J. Olbert-Majkut, A. Pettersson, M. Kiljunen, T. |
| author_facet |
Lindgren, J. Olbert-Majkut, A. Pettersson, M. Kiljunen, T. |
| author_sort |
Lindgren, J. |
| title |
Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations |
| title_short |
Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations |
| title_full |
Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations |
| title_fullStr |
Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations |
| title_full_unstemmed |
Librational motion of CO in solid Ar: Raman and IR spectra and quantum simulations |
| title_sort |
librational motion of co in solid ar: raman and ir spectra and quantum simulations |
| publisher |
Фізико-технічний інститут низьких температур ім. Б.І. Вєркіна НАН України |
| publishDate |
2012 |
| topic_facet |
Low Temperature Spectroscopy and Radiation Effects |
| url |
http://dspace.nbuv.gov.ua/handle/123456789/117418 |
| citation_txt |
Librational motion of CO in solid Ar:
Raman and IR spectra and quantum simulations / J. Lindgren, A. Olbert-Majkut, M. Pettersson, T. Kiljunen // Физика низких температур. — 2012. — Т. 38, № 8. — С. 894-904. — Бібліогр.: 46 назв. — англ. |
| series |
Физика низких температур |
| work_keys_str_mv |
AT lindgrenj librationalmotionofcoinsolidarramanandirspectraandquantumsimulations AT olbertmajkuta librationalmotionofcoinsolidarramanandirspectraandquantumsimulations AT petterssonm librationalmotionofcoinsolidarramanandirspectraandquantumsimulations AT kiljunent librationalmotionofcoinsolidarramanandirspectraandquantumsimulations |
| first_indexed |
2023-10-18T20:29:45Z |
| last_indexed |
2023-10-18T20:29:45Z |
| _version_ |
1796150350208565248 |