TY - JOUR
T1 - Ultrafast temperature jump in polymers
T2 - Phonons and vibrations heat up at different rates
AU - Wen, Xiaoning
AU - Tolbert, William A.
AU - Dlott, Dana D.
PY - 1993
Y1 - 1993
N2 - Optical calorimetry is used to study the dynamics of a polymer, poly-(methyl methylacrylate), (PMMA), subjected to a temperature jump which is faster than the time required for Boltzmann equilibrium. The temperature jump is produced by exciting a near-infrared dye embedded in the polymer with a 23 ps duration optical pulse. The magnitude of the temperature jump ΔT was as large as 125 degrees. To attain such a large temperature jump with good spatial uniformity requires optical heating pulses which strongly saturate the heater dye absorption. A formalism is developed to quantitatively treat optical heating with saturation. The heat capacity of the polymer, Cpol, can be determined to an accuracy of 8% using this method. The temperature jump data could not be fit by assuming the polymer heats up in a single stage. A quasitemperature model with two-stage heating, where the dye first excites polymer phonons and then the phonons excite polymer vibrations by multiphonon up pumping, gave quantitative agreement. The data at several values of ΔT were simultaneously fit using three adjustable parameters: κvc, the molecular thermal conductivity for vibrational cooling of the heater dye; κup, the molecular thermal conductivity for multiphonon up pumping; and Cpol. The value of κvc was the same magnitude as kth, the thermal conductivity of the polymer, despite the fact that the vibrational cooling process occurs on the 1 nm length scale. The value of κup was 2 orders of magnitude smaller than κth.
AB - Optical calorimetry is used to study the dynamics of a polymer, poly-(methyl methylacrylate), (PMMA), subjected to a temperature jump which is faster than the time required for Boltzmann equilibrium. The temperature jump is produced by exciting a near-infrared dye embedded in the polymer with a 23 ps duration optical pulse. The magnitude of the temperature jump ΔT was as large as 125 degrees. To attain such a large temperature jump with good spatial uniformity requires optical heating pulses which strongly saturate the heater dye absorption. A formalism is developed to quantitatively treat optical heating with saturation. The heat capacity of the polymer, Cpol, can be determined to an accuracy of 8% using this method. The temperature jump data could not be fit by assuming the polymer heats up in a single stage. A quasitemperature model with two-stage heating, where the dye first excites polymer phonons and then the phonons excite polymer vibrations by multiphonon up pumping, gave quantitative agreement. The data at several values of ΔT were simultaneously fit using three adjustable parameters: κvc, the molecular thermal conductivity for vibrational cooling of the heater dye; κup, the molecular thermal conductivity for multiphonon up pumping; and Cpol. The value of κvc was the same magnitude as kth, the thermal conductivity of the polymer, despite the fact that the vibrational cooling process occurs on the 1 nm length scale. The value of κup was 2 orders of magnitude smaller than κth.
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U2 - 10.1063/1.466110
DO - 10.1063/1.466110
M3 - Article
AN - SCOPUS:25944444845
SN - 0021-9606
VL - 99
SP - 4140
EP - 4151
JO - Journal of Chemical Physics
JF - Journal of Chemical Physics
IS - 5
ER -