ABSTRACT
Using diffraction of femtosecond laser pulses of visible light by a magnetic domain pattern in an iron garnet, we demonstrate a proof of concept of time-resolved measurements of domain pattern movements with nanometer spatial and femtosecond temporal resolution. In this method, a femtosecond laser (pump) pulse initiates magnetization dynamics in a sample that is initially in a labyrinth domain state, while an equally short linearly polarized laser pulse (probe) is diffracted by the domain pattern. The components of the diffracted light that are polarized orthogonally to the incident light generate several concentric diffraction rings. Nanometer small changes in the relative sizes of domains with opposite magnetization result in observable changes in the intensities of the rings. We demonstrate that the signal-to-noise ratio is high enough to detect a 6 nm domain wall displacement with 100 fs temporal resolution using visible light. We also discuss possible artifacts, such as pump-induced changes of optical properties, that can affect the measurements.
ABSTRACT
Using the technique of double high-speed photography, we find that a femtosecond laser pulse is able to change the velocity of a moving domain wall in an yttrium iron garnet. The change depends on the light intensity and the domain wall velocity itself. To explain the results we propose a model in which the domain wall velocity is controlled by photo-induced generation of vertical Bloch lines.
ABSTRACT
A heat-assisted route for subnanosecond magnetic recording is discovered for the dielectric bismuth-substituted yttrium iron garnet, known for possessing small magnetic damping. The experiments and simulations reveal that the route involves nonlinear magnetization precession, triggered by a transient thermal modification of the growth-induced crystalline anisotropy in the presence of a fixed perpendicular magnetic field. The pathway is rendered robust by the damping becoming anomalously large during the switching process. Subnanosecond deterministic magnetization reversal was achieved within just one-half of a precessional period, and this mechanism should be possible to implement in any material with suitably engineered dissimilar thermal derivatives of magnetization and anisotropy.