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Jaco Geuchies

Publications and source records attributed to Jaco Geuchies.

3 recordsLinked to original sources

Identifying the Origin of Thermal Modulation of Exchange Bias in MnPS3/Fe3GeTe2 van der Waals Heterostructures

The exchange bias phenomenon, inherent in exchange-coupled ferromagnetic and antiferromagnetic systems, has intrigued researchers for decades. Van der Waals materials, with their layered structure, provide an optimal platform for probing such physical phenomena. However, achieving a facile and effective means to manipulate exchange bias in van der Waals heterostructures remains challenging. In this study, we investigate the origin of exchange bias in MnPS3/Fe3GeTe2 van der Waals heterostructures. Our work demonstrates a method to modulate unidirectional exchange anisotropy, achieving an unprecedented nearly 1000% variation through simple thermal cycling. Despite the compensated interfacial spin configuration of MnPS3, magneto-transport measurements reveal a huge 170 mT exchange bias at 5 K, one of the largest observed in van der Waals antiferromagnet-ferromagnet interfaces. This substantial magnitude of the exchange bias is linked to an anomalous weak ferromagnetic ordering in MnPS3 below 40 K. On the other hand, the tunability of exchange bias during thermal cycling is ascribed to the modified arrangement of interfacial atoms and changes in the vdW gap during field cooling. Our findings highlight a robust and easily adjustable exchange bias in van der Waals antiferromagnetic/ferromagnetic heterostructures, presenting a straightforward approach to enhance other interface-related spintronic phenomena for practical applications. A detailed study of the interface reveals migration of atoms between the layers, leading to the formation of amorphous region on either side of the van der Waals gap, underscoring the importance of precise characterization of interfaces in van der Waals heterostructures, which are often presumed to have pristine interfaces.

cond-mat.mtrl-sci

Signatures of Mode-Resolved, Nonlocal Electron-Phonon Coupling in Two-Dimensional Spectroscopy

Electron-phonon coupling (EPC) is foundational in condensed matter physics, determining intriguing phenomena and properties in both conventional and quantum materials. In this manuscript, we propose and demonstrate a novel two dimensional (2D) EPC spectroscopy which allows for direct extraction of EPC matrix elements for specific phonon modes and different electron energies, simultaneously. Using this technique, we are able to measure the electron-energy dependence of the EPC strength for individual phonon modes. This capability allows us to identify unique signatures distinguishing nonlocal Su-SchriefferHeeger (SSH)-type couplings from local Holstein-type couplings. In application to a methylammonium lead iodide (MAPI) perovskite, we find that two pronounced phonon modes at room temperature exhibit highly distinctive EPC behaviors, concerning strength, anisotropy, and temperature-dependence across the structural phase transition. Our approach paves the way for unraveling the microscopic origin of EPC, the change of the phonon-mode-specific EPC with external conditions, and phonon-mediated ultrafast control of condensed materials.

cond-mat.mtrl-sci

Transiently delocalized states enhance hole mobility in organic molecular semiconductors

There is compelling evidence that charge carriers in organic semiconductors (OSs) self-localize in nano-scale space because of dynamic disorder. Yet, some OSs, in particular recently emerged high-mobility organic molecular crystals, feature reduced mobility at increasing temperature, a hallmark for delocalized band transport. Here we present the temperature-dependent mobility in two record-mobility OSs: DNTT (dinaphtho[2,3-b:2',3'-f]thieno[3,2-b]-thiophene), and its alkylated derivative, C8-DNTT-C8. By combining terahertz photoconductivity measurements with fully atomistic non-adiabatic molecular dynamics simulations, we show that while both crystals display a power-law decrease of the mobility (\mu) with temperature (T, following: \mu \propto T^(-n)), the exponent n differs substantially. Modelling provides n values in good agreement with experiments and reveals that the differences in the falloff parameter between the two chemically closely related semiconductors can be traced to the delocalization of the different states thermally accessible by charge carriers, which in turn depends on the specific electronic band structure of the two systems. The emerging picture is that of holes surfing on a dynamic manifold of vibrationally-dressed extended states with a temperature-dependent mobility that provides a sensitive fingerprint for the underlying density of states.

cond-mat.soft