Abstract
The role of thermoelectric power and/or charge separation-generated electric fields upon Cr-doped LiNbO 3 crystal growth is treated by investigating both steady-state and initial transient solute redistribution based on the concept of a field-modified partition coefficient and an effective growth velocity. The magnitude of these electric field effects is dominated not only by the strength of the field but also by the solute diffusion coefficient in the phase considered. The high diffusion coefficient of Cr 3+ in the liquid and the very low diffusion coefficient of Cr 3+ in the solid combined with the electric field operating in the liquid leads to a strong pulling force on the Cr 3+ from the solid through the interface into the liquid. This generates a deep solute depletion region in the solid behind the interface. An analytical solution to this depletion phenomena is given for a specific case.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.