4.6 Article

Photoinduced transient states of antiferromagnetic orderings in La1/3Sr2/3FeO3 and SrFeO3-δ thin films observed through time-resolved resonant soft x-ray scattering

Journal

NEW JOURNAL OF PHYSICS
Volume 24, Issue 4, Pages -

Publisher

IOP Publishing Ltd
DOI: 10.1088/1367-2630/ac5f31

Keywords

synchrotron radiation; time-resolved resonant soft x-ray scattering; antiferromagnetic ordering

Funding

  1. Photon Factory Program Advisory Committee [2016PF-BL-19B, 2015G556, 2015S2-007, 2013G058, 2013G661]
  2. MEXT Quantum Leap Flagship Program (MEXT Q-LEAP) Grant [JPMXS0118068681]
  3. ALPS program of the University of Tokyo
  4. [19H05824]
  5. [19H01816]
  6. [19K23430]
  7. [17K14334]

Ask authors/readers for more resources

The relationship between the magnetic interaction and photoinduced dynamics in antiferromagnetic perovskites is investigated in this study. The findings show that time-resolved resonant soft x-ray scattering can be used to observe the ultrafast quenching of magnetic ordering and the efficient channel for spin-order manipulation through optically induced charge transfer.
The relationship between the magnetic interaction and photoinduced dynamics in antiferromagnetic perovskites is investigated in this study. In La1/3Sr2/3FeO3 thin films, commensurate spin ordering is accompanied by charge disproportionation, whereas SrFeO3-delta thin films show incommensurate helical antiferromagnetic spin ordering due to increased ferromagnetic coupling compared to La1/3Sr2/3FeO3. To understand the photoinduced spin dynamics in these materials, we investigate the spin ordering through time-resolved resonant soft x-ray scattering. In La1/3Sr2/3FeO3, ultrafast quenching of the magnetic ordering within 130 fs through a nonthermal process is observed, triggered by charge transfer between the Fe atoms. We compare this to the photoinduced dynamics of the helical magnetic ordering of SrFeO3-delta . We find that the change in the magnetic coupling through optically induced charge transfer can offer an even more efficient channel for spin-order manipulation.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available