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C. Klewe

Publications and source records attributed to C. Klewe.

7 recordsLinked to original sources

Electronic Structure and Superconductivity in La$_{1.55}$Sr$_{0.45}$CuO$_4$/La$_2$CuO$_4$ Artificial High-$T_c$ Superlattices Probed by Hard and Soft X-ray Spectroscopy

In La$_{1.55}$Sr$_{0.45}$CuO$_4$/La$_2$CuO$_4$ (LSCO/LCO) artificial high-$T_c$ superlattices (AHTS), grown by quantum material design, the superconducting dome can be tuned by varying the geometric ratio $L/d$, where $L$ is the LCO layer thickness and $d$ is the superlattice nanoscale period. Here, we combine hard X-ray photoelectron spectroscopy (HAXPES) and polarization-dependent soft X-ray absorption spectroscopy (XAS) to probe how the electronic structure evolves across the $L/d$-tuned superconducting dome. We observe systematic chemical-potential evolution across the series, together with enhanced spectral weight near the Fermi level, enhanced local and non-local screening signatures, and increased in-plane orbital polarization near the top of the dome. Together, these spectroscopic signatures provide insight into the emergence of Fano-Feshbach resonant superconductivity in the LSCO/LCO AHTS series.

cond-mat.supr-con

Dimensionality-Driven Electronic and Orbital Transitions Mediating Interfacial Magnetism in LaNiO3/CaMnO3 Observed In Situ

Emergent magnetic states at oxide interfaces arise from the interplay of charge transfer, orbital reconstruction, and dimensional confinement, offering a route to engineered correlated-electron behavior in nanoscale spintronic materials. Here, we combine in situ synthesis, polarization-dependent angle-resolved photoelectron spectroscopy, X-ray magnetic circular dichroism, and first-principles electronic-structure calculations to investigate LaNiO3/CaMnO3 superlattices. We show that reducing the LaNiO3 thickness drives a metal-insulator transition accompanied by loss of electronic coherence and an orbital-polarization crossover in the ultrathin limit. These changes weaken charge transfer across the interface and suppress the interfacial Mn magnetic moment in CaMnO3, revealing that the emergent ferromagnetic state is directly governed by electronic confinement in LaNiO3. The insulating state and orbital reconstruction are reproduced by density functional theory combined with dynamical mean-field theory. Together, these results establish a direct and tunable coupling among electronic, orbital, and magnetic degrees of freedom in oxide heterostructures.

cond-mat.str-el

Depth-resolved profile of the interfacial ferromagnetism in $CaMnO_{3}/CaRuO_{3}$ superlattices

Emergent magnetic phenomena at interfaces represent a frontier in materials science, pivotal for advancing technologies in spintronics and magnetic storage. In this letter, we utilize a suite of advanced X-ray spectroscopic and scattering techniques to investigate emergent interfacial ferromagnetism in oxide superlattices comprised of antiferromagnetic CaMnO3 and paramagnetic CaRuO3. Our findings challenge prior theoretical models by demonstrating that the ferromagnetism extends beyond the interfacial layer into multiple unit cells of CaMnO3 and exhibits an asymmetric profile. Complementary density functional calculations reveal that the interfacial ferromagnetism is driven by the double exchange mechanism, facilitated by charge transfer from Ru to Mn ions. Additionally, defect chemistry, particularly the presence of oxygen vacancies, likely plays a crucial role in modifying the magnetic moments at the interface, leading to the observed asymmetry between the top and bottom CaMnO3 interfacial magnetic layers. Our findings underscore the potential of manipulating interfacial ferromagnetism through point defect engineering.

cond-mat.mtrl-sci

Ultrafast terahertz field control of the emergent magnetic and electronic interactions at oxide interfaces

Ultrafast electric-field control of emergent electronic and magnetic states at oxide interfaces offers exciting prospects for the development of new generations of energy-efficient devices. Here, we demonstrate that the electronic structure and emergent ferromagnetic interfacial state in epitaxial LaNiO3/CaMnO3 superlattices can be effectively controlled using intense single-cycle THz electric-field pulses. We employ a combination of polarization-dependent X-ray absorption spectroscopy with magnetic circular dichroism and X-ray resonant magnetic reflectivity to measure a detailed magneto-optical profile and thickness of the ferromagnetic interfacial layer. Then, we use time-resolved and temperature-dependent magneto-optical Kerr effect, along with transient optical reflectivity and transmissivity measurements, to disentangle multiple correlated electronic and magnetic processes driven by ultrafast high-field (~1 MV/cm) THz pulses. These processes include an initial sub-picosecond electronic response, consistent with non-equilibrium Joule heating; a rapid (~270 fs) demagnetization of the ferromagnetic interfacial layer, driven by THz-field-induced nonequilibrium spin-polarized currents; and subsequent multi-picosecond dynamics, possibly indicative of a change in the magnetic state of the superlattice due to the transfer of spin angular momentum to the lattice. Our findings shed light on the intricate interplay of electronic and magnetic phenomena in this strongly correlated material system, suggesting a promising avenue for efficient control of two-dimensional ferromagnetic states at oxide interfaces using ultrafast electric-field pulses.

cond-mat.mtrl-sci

Direct experimental evidence of tunable charge transfer at the $LaNiO_{3}/CaMnO_{3}$ ferromagnetic interface

Interfacial charge transfer in oxide heterostructures gives rise to a rich variety of electronic and magnetic phenomena. Designing heterostructures where one of the thin-film components exhibits a metal-insulator transition opens a promising avenue for controlling such phenomena both statically and dynamically. In this letter, we utilize a combination of depth-resolved soft X-ray standing-wave and hard X-ray photoelectron spectroscopies in conjunction with polarization-dependent X-ray absorption spectroscopy to investigate the effects of the metal-insulator transition in $LaNiO_{3}$ on the electronic and magnetic states at the $LaNiO_{3}/CaMnO_{3}$ interface. We report on a direct observation of the reduced effective valence state of the interfacial Mn cations in the metallic superlattice with an above-critical $LaNiO_{3}$ thickness (6 u.c.) due to the leakage of itinerant Ni 3d $e_{g}$ electrons into the interfacial $CaMnO_{3}$ layer. Conversely, in an insulating superlattice with a below-critical $LaNiO_{3}$ thickness of 2 u.c., a homogeneous effective valence state of Mn is observed throughout the $CaMnO_{3}$ layers due to the blockage of charge transfer across the interface. The ability to switch and tune interfacial charge transfer enables precise control of the emergent ferromagnetic state at the $LaNiO_{3}/CaMnO_{3}$ interface and, thus, has far-reaching consequences on the future strategies for the design of next-generation spintronic devices.

cond-mat.mtrl-sci

Observation of Coherently Coupled Cation Spin Dynamics in an Insulating Ferrimagnetic Oxide

Many technologically useful magnetic oxides are ferrimagnetic insulators, which consist of chemically distinct cations. Here, we examine the spin dynamics of different magnetic cations in ferrimagnetic NiZnAl-ferrite (Ni$_{0.65}$Zn$_{0.35}$Al$_{0.8}$Fe$_{1.2}$O$_4$) under continuous microwave excitation. Specifically, we employ time-resolved x-ray ferromagnetic resonance to separately probe Fe$^{2+/3+}$ and Ni$^{2+}$ cations on different sublattice sites. Our results show that the precessing cation moments retain a rigid, collinear configuration to within $\approx$2$^\circ$. Moreover, the effective spin relaxation is identical to within $<$10% for all magnetic cations in the ferrite. We thus validate the oft-assumed ``ferromagnetic-like'' dynamics in resonantly driven ferrimagnetic oxides, where the magnetic moments from different cations precess as a coherent, collective magnetization.

cond-mat.mtrl-sci

Coherent ac spin current transmission across an antiferromagnetic CoO insulator

The recent discovery of spin-current transmission through antiferromagnetic (AFM) insulating materials opens up unprecedented opportunities for fundamental physics and spintronics applications. The great mystery currently surrounding this topic is: how could THz AFM magnons mediate a GHz spin current? This mis-match of frequencies becomes particularly critical for the case of coherent ac spin-current, raising the fundamental question of whether a GHz ac spin-current can ever keep its coherence inside an AFM insulator and so drive the spin precession of another FM layer coherently? Utilizing element- and time-resolved x-ray pump-probe measurements on Py/Ag/CoO/Ag/Fe75Co25/MgO(001) heterostructures, we demonstrate that a coherent GHz ac spin current pumped by the permalloy (Py) ferromagnetic resonance (FMR) can transmit coherently across an antiferromagnetic CoO insulating layer to drive a coherent spin precession of the FM Fe75Co25 layer. Further measurement results favor thermal magnons rather than evanescent spin waves as the mediator of the coherent ac spin current in CoO.

physics.app-ph