Hydrogen bond reorganization and vibrational relaxation in water studied with ultrafast infrared spectroscopy

Water consists of an extended hydrogen bond network that is constantly evolving. More than just a description of the time averaged structure is necessary to understand any process that occurs in water. In this thesis we study the dynamic regime, which involves fluctuations and rearrangements that occur on the tens of femtoseconds to picosecond time scale. The dynamic regime involves hydrogen bond breaking and forming which interlaces with translations and reorientation and ultimately largescale reorganization. Our experimental technique is ultrafast infrared spectroscopy of the OX stretch (where X = H, D, or T) of isotopically dilute water. The OX stretch frequency is sensitive to its environment, and loss of frequency correlation provides a picture of local and collective hydrogen bond dynamics. With pump-probe experiments we are also able to measure vibrational relaxation and reorientational dynamics of water. We present the first infrared linear absorption spectrum of the OT stretch of isotopically dilute tritiated water and compare line shape parameters to the other water isotopologues to provide further evidence that electric field fluctuations properly describe line broadening of the infrared spectrum of water. Measurement of the infrared spectrum of tritiated water is the first step towards an experiment that may be capable of directly monitoring the relative geometry between two water molecules during a hydrogen bond switch. We calculate the change in electric field and transition dipole coupling during an idealized hydrogen switch to determine the correlated frequency shifts one might observe in such an experiment. To test the proposed vibrational relaxation pathway in isotopically dilute water, we present the first pump-probe of tritiated water and the temperature-dependent lifetime of deuterated water (or HOD in H20). For the OT and OH stretch, our experimental findings agree with the proposed mechanism in which the vibrational energy first relaxes to the intramolecular bend. However, evidence from the temperature-dependent measurements of the OD stretch show multiple pathways may be in competition that have different dependencies on temperature. Our results call for further experimental and theoretical studies. We acquire temperature-dependent 2D IR and pump-probe anisotropy measurements of the OD stretch of HOD in H20 in order to test if spectral diffusion, which reports on hydrogen bond rearrangements, and reorientation are correlated in water. We compare the temperature dependence of the picosecond decay to a number of measures of structural relaxation and find similar activation barrier heights and slightly non-Arrhenius behavior, which suggests that the reaction coordinate for hydrogen bond reorganization in water is collective.

Department dc:contributor.department

Massachusetts Institute of Technology. Dept. of Chemistry.

Grantor dc:publisher

Massachusetts Institute of Technology

Year dc:date.issued

2011

Author dc:creator

• Nicodemus, Rebecca Anne

Advisor dc:contributor.advisor

• Andrei Tokmakoff.

• Chemistry.

Statement dc:rights

• M.I.T. theses are protected by copyright. They may be viewed from this source for any purpose, but reproduction or distribution in any format is prohibited without written permission. See provided URL for inquiries about permission.

Licence dc:rights.uri

• http://dspace.mit.edu/handle/1721.1/7582

Language dc:language.iso

eng

Handle dc:identifier.uri

http://hdl.handle.net/1721.1/62727

OAI identifier oai:identifier

oai:dspace.mit.edu:1721.1/62727