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Mesoscopic structural phase progression in photo-excited VO(2) revealed by time-resolved x-ray diffraction microscopy

Dynamical phase separation during a solid-solid phase transition poses a challenge for understanding the fundamental processes in correlated materials. Critical information underlying a phase transition, such as localized phase competition, is difficult to reveal by measurements that are spatially a...

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Detalles Bibliográficos
Autores principales: Zhu, Yi, Cai, Zhonghou, Chen, Pice, Zhang, Qingteng, Highland, Matthew J., Jung, Il Woong, Walko, Donald A., Dufresne, Eric M., Jeong, Jaewoo, Samant, Mahesh G., Parkin, Stuart S. P., Freeland, John W., Evans, Paul G., Wen, Haidan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4768076/
https://www.ncbi.nlm.nih.gov/pubmed/26915398
http://dx.doi.org/10.1038/srep21999
Descripción
Sumario:Dynamical phase separation during a solid-solid phase transition poses a challenge for understanding the fundamental processes in correlated materials. Critical information underlying a phase transition, such as localized phase competition, is difficult to reveal by measurements that are spatially averaged over many phase separated regions. The ability to simultaneously track the spatial and temporal evolution of such systems is essential to understanding mesoscopic processes during a phase transition. Using state-of-the-art time-resolved hard x-ray diffraction microscopy, we directly visualize the structural phase progression in a VO(2) film upon photoexcitation. Following a homogenous in-plane optical excitation, the phase transformation is initiated at discrete sites and completed by the growth of one lattice structure into the other, instead of a simultaneous isotropic lattice symmetry change. The time-dependent x-ray diffraction spatial maps show that the in-plane phase progression in laser-superheated VO(2) is via a displacive lattice transformation as a result of relaxation from an excited monoclinic phase into a rutile phase. The speed of the phase front progression is quantitatively measured, and is faster than the process driven by in-plane thermal diffusion but slower than the sound speed in VO(2). The direct visualization of localized structural changes in the time domain opens a new avenue to study mesoscopic processes in driven systems.