English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Robust Magnetic Order Upon Ultrafast Excitation of an Antiferromagnet

MPS-Authors
/persons/resource/persons213525

Lee,  Sang-Eun
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons203272

Windsor,  Yoav William
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22250

Wolf,  Martin
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons104701

Rettig,  Laurenz
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Supplementary Material (public)
There is no public supplementary material available
Citation

Lee, S.-E., Windsor, Y. W., Fedorov, A., Kliemt, K., Krellner, C., Schüßler-Langeheine, C., et al. (2022). Robust Magnetic Order Upon Ultrafast Excitation of an Antiferromagnet. Advanced Materials Interfaces, 9(36): 2201340. doi:10.1002/admi.202201340.


Cite as: https://hdl.handle.net/21.11116/0000-000B-FFA9-8
Abstract
The ultrafast manipulation of magnetic order due to optical excitation is governed by the intricate flow of energy and momentum between the electron, lattice, and spin subsystems. While various models are commonly employed to describe these dynamics, a prominent example being the microscopic three temperature model (M3TM), systematic, quantitative comparisons to both the dynamics of energy flow and magnetic order are scarce. Here, an M3TM was&nbsp;applied to the ultrafast magnetic order dynamics of the layered antiferromagnet GdRh2Si2. The femtosecond dynamics of electronic temperature, surface ferromagnetic order, and bulk antiferromagnetic order were&nbsp;explored at various pump fluences employing time- and angle-resolved photoemission spectroscopy and time-resolved resonant magnetic soft X-ray diffraction, respectively. After optical excitation, both the surface ferromagnetic order and the bulk antiferromagnetic order dynamics exhibit two-step demagnetization behaviors with two similar timescales (<1 ps, ∼10 ps), indicating a strong exchange coupling between localized 4f and itinerant conduction electrons. Despite a good qualitative agreement, the M3TM predicts larger demagnetization than the experimental observation, which can be phenomenologically described by a transient, fluence-dependent increased Néel temperature. The results indicate that effects beyond a mean-field description have to be considered for a quantitative description of ultrafast magnetic order&nbsp;dynamics.