Jinyong Jung

Improvement of the interfacial Dzyaloshinskii-Moriya interaction by introducing a Ta buffer layer

We report systematic measurements of the interfacial Dzyaloshinskii-Moriya interaction (iDMI) by employing Brillouin light scattering in Pt/Co/AlOx and Ta/Pt/Co/AlOx structures. By introducing a tantalum buffer layer, the saturation magnetization and the interfacial perpendicular magnetic anisotropy are significantly improved due to the better interface between heavy metal and ferromagnetic layer. From the frequency shift between Stokes- and anti-Stokes spin-waves, we successively obtain considerably larger iDM energy densities (Dmax = 1.65 ± 0.13 mJ/m2 at tCo = 1.35 nm) upon adding the Ta buffer layer, despite the nominally identical interface materials. Moreover, the energy density shows an inverse proportionality with the Co layer thickness, which is the critical clue that the observed iDMI is indeed originating from the interface between the Pt and Co layers.

Role of top and bottom interfaces of a Pt/Co/AlOx system in Dzyaloshinskii-Moriya interaction, interface perpendicular magnetic anisotropy, and magneto-optical Kerr effect

We investigate the role of top and bottom interfaces in inversion symmetry-breaking Pt/Co/AlOx systems by inserting ultra-thin Cu layers. Wedge-type ultrathin Cu layers (0-0.5 nm) are introduced between Pt/Co or Co/AlOx interfaces. Interface sensitive physical quantities such as the interfacial Dzyaloshinskii-Moriya interaction (iDMI) energy density, the interfacial perpendicular magnetic anisotropy (iPMA), and the magneto-optical Kerr effects (MOKE) are systematically measured as a function of Cu-insertion layer thickness. We find that the Cu-insertion layer in the bottom interface (Pt/Co) plays a more important role in iDMI, PMA, and MOKE. In contrast, the top interface (Co/AlOx) noticeably contributes to only PMA, while its contributions to iDMI and MOKE enhancement are less significant. Although the PMA mainly comes from the bottom interface (Pt/Co), the Cu-insertion layers of all interfaces (Pt/Co, Co/AlOx) influence PMA. For iDMI, only the Cu-insertion layer in the bottom interface exerts SOC suppre...

Study of spin dynamics and damping on the magnetic nanowire arrays with various nanowire widths

Abstract We investigate the spin dynamics including Gilbert damping in the ferromagnetic nanowire arrays. We have measured the ferromagnetic resonance of ferromagnetic nanowire arrays using vector-network analyzer ferromagnetic resonance (VNA-FMR) and analyzed the results with the micromagnetic simulations. We find excellent agreement between the experimental VNA-FMR spectra and micromagnetic simulations result for various applied magnetic fields. We find that the same tendency of the demagnetization factor for longitudinal and transverse conditions, N z ( N y ) increases (decreases) as increasing the nanowire width in the micromagnetic simulations while N x is almost zero value in transverse case. We also find that the Gilbert damping constant increases from 0.018 to 0.051 as the increasing nanowire width for the transverse case, while it is almost constant as 0.021 for the longitudinal case.

Solvent-dependent self-assembly of two dimensional layered perovskite (C6H5CH2CH2NH3)2MCl4 (M = Cu, Mn) thin films in ambient humidity

Two dimensional layered organic-inorganic halide perovskites offer a wide variety of novel functionality such as solar cell and optoelectronics and magnetism. Self-assembly of these materials using solution process (ex. spin coating) makes crystalline thin films synthesized at ambient environment. However, flexibility of organic layer also poses a structure stability issue in perovskite thin films against environment factors (ex. moisture). In this study, we investigate the effect of solvents and moisture on structure and property in the (C6H5(CH2)2NH3)2(Cu, Mn)Cl4 (Cu-PEA, Mn-PEA) perovskite thin films spin-coated on Si wafer using three solvents (H2O, MeOH, MeOH + H2O). A combination of x-ray diffraction (XRD) and x-ray absorption spectroscopy (XAS) show that relative humidity (RH) has a profound effect on perovskite thin films during sample synthesis and storage, depending on the kind of solvent used. The ones prepared using water (Cu-PEA:H2O, Mn-PEA:H2O) show quite different behavior from the other cases. According to time-dependent XRD, reversible crystalline-amorphous transition takes place depending on RH in the former cases, whereas the latter cases relatively remain stable. It also turns out from XAS that Mn-PEA thin films prepared with solvents such as MeOH and MeOH + H2O are disordered to the depth of about 4 nm from surface.