Electron-interface scattering during electron-phonon nonequilibrium in thin films creates another pathway for electron system energy loss as characteristic lengths of thin films continue to decrease. As power densities in nanodevices increase, excitations of electrons from sub-conduction-band energy levels will become more probable. These sub-conduction-band electronic excitations significantly affect the material’s thermophysical properties. In this work, the role of -band electronic excitations is considered in electron energy transfer processes in thin Au films. The electronic structure and density of states for gold are calculated using a plane wave pseudopotential density function approach. In thin films with thicknesses less than the electron mean free path, ballistic electron transport leads to electron-interface scattering. The ballistic component of electron transport is studied by a ballistic-diffusive approximation of the Boltzmann transport equation with input from ab initio calculations. The effects of -band excitations on electron-interface energy transfer are analyzed during electron-phonon nonequilibrium after short pulsed laser heating in thin films.
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1 September 2009
Research Article|
September 08 2009
Contribution of -band electrons to ballistic transport and scattering during electron-phonon nonequilibrium in nanoscale Au films using an ab initio density of states
Patrick E. Hopkins;
Patrick E. Hopkins
a)
Engineering Sciences Center,
Sandia National Laboratories
, Albuquerque, New Mexico 87185-0346, USA
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Derek A. Stewart
Derek A. Stewart
Cornell Nanoscale Science and Technology Facility,
Cornell University
, Ithaca, New York 14853-2700, USA
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a)
Author to whom correspondence should be addressed. Electronic mail: pehopki@sandia.gov.
J. Appl. Phys. 106, 053512 (2009)
Article history
Received:
April 20 2009
Accepted:
July 23 2009
Citation
Patrick E. Hopkins, Derek A. Stewart; Contribution of -band electrons to ballistic transport and scattering during electron-phonon nonequilibrium in nanoscale Au films using an ab initio density of states. J. Appl. Phys. 1 September 2009; 106 (5): 053512. https://doi.org/10.1063/1.3211310
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