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S. G. Jeong

Publications and source records attributed to S. G. Jeong.

2 recordsLinked to original sources

Disentangling Strain and Ti3+ Contributions to the Anomalous Hall Effect in Epitaxial RuO2 Films

The anomalous Hall effect (AHE) reported in epitaxial RuO2/TiO2 has been attributed to a strain-stabilized magnetic state, but strain can be entangled with Ru-Ti intermixing and interfacial charge redistribution, which can produce Ti3+ and potentially localized moments. Here, we disentangle these contributions using Ti-alloyed RuO2 heterostructures in which abundant Ti3+ states are retained while epitaxial strain is independently changed. The strained and relaxed films have nearly identical Ti/Ru compositions and comparable Ti3+ fractions, yet a pronounced nonlinear AHE appears only in the coherently strained film, while the relaxed heterostructure exhibits an almost linear Hall response. Spectroscopic ellipsometry further shows that the AHE-active strained state is accompanied by a reconstruction of the itinerant electronic response, including enhanced metallicity and longer carrier relaxation times. These results show that Ti3+ formation alone is insufficient to generate the anomalous Hall state and identify epitaxial strain, through its modification of the itinerant RuO2 electronic structure, as the dominant control parameter.

cond-mat.mtrl-sci↗

Anisotropic Strain Relaxation-Induced Directional Ultrafast Carrier Dynamics in RuO2 Films

Ultrafast light-matter interactions inspire potential functionalities in picosecond optoelectronic applications. However, achieving directional carrier dynamics in metals remains challenging due to strong carrier scattering within a multiband environment, typically expected to isotropic carrier relaxation. In this study, we demonstrate epitaxial RuO2/TiO2 (110) heterostructures grown by hybrid molecular beam epitaxy to engineer polarization-selectivity of ultrafast light-matter interactions via anisotropic strain engineering. Combining spectroscopic ellipsometry, X-ray absorption spectroscopy, and optical pump-probe spectroscopy, we revealed the strong anisotropic transient optoelectronic response of strain-engineered RuO2/TiO2 (110) heterostructures along both in-plane [001] and [1-10] crystallographic directions. Theoretical analysis identifies strain-induced modifications in band nesting as the underlying mechanism for enhanced anisotropic carrier relaxation. These findings establish epitaxial strain engineering as a powerful tool for tuning anisotropic optoelectronic responses in metallic systems, paving the way for next-generation polarization-sensitive ultrafast optoelectronic devices.

cond-mat.mtrl-sci↗