Ultrafast transient increase of oxygen octahedral rotations in a perovskite

التفاصيل البيبلوغرافية
العنوان: Ultrafast transient increase of oxygen octahedral rotations in a perovskite
المؤلفون: Porer, M., Fechner, M., Kubli, M., Neugebauer, M. J., Parchenko, S., Esposito, V., Narayan, A., Spaldin, N. A., Huber, R., Radovic, M., Bothschafter, E. M., Glownia, J. M., Sato, T., Song, S., Johnson, S. L., Staub, U.
المصدر: Phys. Rev. Research 1, 012005 (2019)
سنة النشر: 2019
المجموعة: Condensed Matter
مصطلحات موضوعية: Condensed Matter - Strongly Correlated Electrons
الوصف: The ability to control the structure of a crystalline solid on ultrafast timescales bears enormous potential for information storage and manipulation or generating new functional states of matter [1]. In many materials where the ultrafast control of crystalline structures has been explored, optical excitation pushes materials towards their less ordered high temperature phase [2{9] as electronically driven ordered phases melt and possible concomitant structural modifications relax. Nonetheless, for a few select materials it has been shown that photoexcitation can slightly enhance the amplitude of an electronic ordering phenomenon (i.e. its electronic order parameter) [9{13]. Here we show via femtosecond hard X-ray diffraction that photodoping of the perovskite EuTiO3 transiently increases the order parameter associated with a purely structural [14] phase transition represented by the antiferrodistortive rotation of the oxygen octahedra. This can be understood from an ultrafast charge-transfer induced reduction of the Goldschmidt tolerance factor [15], which is a fundamental control parameter for the properties of perovskites
Comment: 11 pages, 3 figures
نوع الوثيقة: Working Paper
DOI: 10.1103/PhysRevResearch.1.012005
URL الوصول: http://arxiv.org/abs/1901.08388
رقم الأكسشن: edsarx.1901.08388
قاعدة البيانات: arXiv
الوصف
DOI:10.1103/PhysRevResearch.1.012005