Vibrational Spectroscopy of the Water Dimer at Jet-Cooled and Atmospheric Temperatures
Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt
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Vibrational Spectroscopy of the Water Dimer at Jet-Cooled and Atmospheric Temperatures. / Vogt, Emil; Kjaergaard, Henrik G.
I: Annual Review of Physical Chemistry, Bind 73, 2022, s. 209-231.Publikation: Bidrag til tidsskrift › Review › Forskning › fagfællebedømt
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TY - JOUR
T1 - Vibrational Spectroscopy of the Water Dimer at Jet-Cooled and Atmospheric Temperatures
AU - Vogt, Emil
AU - Kjaergaard, Henrik G.
PY - 2022
Y1 - 2022
N2 - The vibrational spectroscopy of the water dimer provides an understanding of basic hydrogen bonding in water clusters, and with about one water dimer for every 1,000 water molecules, it plays a critical role in atmospheric science. Here, we review how the experimental and theoretical progress of the past decades has improved our understanding of water dimer vibrational spectroscopy under both cold and warm conditions. We focus on the intramolecular OH-stretching transitions of the donor unit, because these are the ones mostly affected by dimer formation and because their assignment has proven a challenge. We review cold experimental results from early matrix isolation to recent mass-selected jet expansion techniques and, in parallel, the improvements in the theoretical anharmonic models. We discuss and illustrate changes in the vibrational spectra of complexes upon increasing temperature, and the difficulties in recording and calculating these spectra. In the atmosphere, water dimer spectra at ambient temperature are crucial.
AB - The vibrational spectroscopy of the water dimer provides an understanding of basic hydrogen bonding in water clusters, and with about one water dimer for every 1,000 water molecules, it plays a critical role in atmospheric science. Here, we review how the experimental and theoretical progress of the past decades has improved our understanding of water dimer vibrational spectroscopy under both cold and warm conditions. We focus on the intramolecular OH-stretching transitions of the donor unit, because these are the ones mostly affected by dimer formation and because their assignment has proven a challenge. We review cold experimental results from early matrix isolation to recent mass-selected jet expansion techniques and, in parallel, the improvements in the theoretical anharmonic models. We discuss and illustrate changes in the vibrational spectra of complexes upon increasing temperature, and the difficulties in recording and calculating these spectra. In the atmosphere, water dimer spectra at ambient temperature are crucial.
KW - infrared
KW - intensities
KW - intermolecular modes
KW - OH-stretching transitions
KW - radiative transfer
U2 - 10.1146/annurev-physchem-082720-104659
DO - 10.1146/annurev-physchem-082720-104659
M3 - Review
C2 - 35044791
AN - SCOPUS:85128801960
VL - 73
SP - 209
EP - 231
JO - Annual Review of Physical Chemistry
JF - Annual Review of Physical Chemistry
SN - 0066-426X
ER -
ID: 307334285