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Franziska Schölzel

Publications and source records attributed to Franziska Schölzel.

4 recordsLinked to original sources

Chiral Spinterfaces as an Overlooked Component of the Chiral-Induced Spin Selectivity Effect

The chiral-induced spin selectivity (CISS) effect is generally attributed to spin-selective transport through chiral molecules, while the role of the molecule-electrode interface remains largely unexplored. Here, we show that adsorption of chiral amino acid derived molecules on ferromagnetic Ni thin films generates a remanent chirality-dependent magneto-optical response that is localized to the molecule-Ni/NiO interface and can be reversibly switched by an external magnetic field, demonstrating its genuine magnetic character. A comprehensive series of control experiments establishes that the response originates from the interfacial region rather than from the molecular layer or the bulk ferromagnet. First-principles calculations reveal that Boc-methionine adsorption proceeds through energetically accessible sulfur- and carboxyl-bound configurations that produce distinct molecular orientations and ligand-p/Ni-d hybridization, thereby defining structurally and electronically distinct interfaces. Together, the experimental and theoretical results support the formation of chiral spinterfaces, identifying the molecule-ferromagnet interface as an active and previously overlooked component of CISS systems. These findings broaden the microscopic picture of CISS beyond the chiral molecule itself and reveals interface electronic structure as a key design parameter for spin-selective molecular devices.

cond-mat.mtrl-sci↗

A step-by-step workflow to extract the genuine circular dichroism of thin films

Circular Dichroism (CD) spectroscopy has evolved from a purely solution based method towards a powerful tool in the analysis of chiral thin films. Although a straightforward technique, the genuine CD signal is often accompanied by artifacts arising from optical anisotropy and instrumental imperfections. This tutorial presents a two-step workflow that reliably isolates the orientation invariant CD response for anisotropic thin films by combining azimuthal sample rotation with sample flipping. For this purpose, a home-built sample stage was developed, which enables systematic suppression of many anisotropy-induced artifacts in commercial CD spectrophotometers. Both a detailed description of the setup itself as well as the needed python script are provided. The reliability of the workflow is demonstrated on two selected samples from different research fields: chiral molecules attached to metallic surfaces as well as metal halide perovskites incorporating chiral spacer molecules

cond-mat.mtrl-sci↗

Microscopic and macroscopic characterization: MBE-grown versus sputter-deposited Au/Co/Au thin films for CISS and MIPAC effect studies

Chirality-induced spin selectivity (CISS) enables spin-dependent transport at chiral molecule/Au(111) interfaces and is used in spintronics when combined with ferromagnetic thin films in spin-valve-type hybrids. However, the influence of substrate microstructure on CISS and the related magnetization induced by the proximity of adsorbed chiral molecules (MIPAC) effect is still not well understood. In this study, we compare the effects of the adsorption of L-chiral alpha-helical alanine-rich peptides on Au/Co/Au ferromagnetic thin films fabricated by molecular beam epitaxy (MBE) and magnetron sputtering. X-ray reflectivity and X-ray diffraction show sharper interfaces and a narrower Au(111) rocking-curve width for the MBE-grown sample. However, atomic force microscopy and scanning tunneling microscopy images reveal that both sample types have locally smooth Au(111) surface regions suitable for peptide adsorption, despite clear differences in larger-scale morphology. Microscopic scanning tunneling spectroscopy after peptide exposure yields similar magnetization-direction-dependent tunneling currents in both sample types, confirming a similar magnitude CISS effect on the molecular scale. In contrast, macroscopic magneto-optical Kerr effect hysteresis loops and effect microscopy reveals that only sputter-deposited samples show slight coercivity enhancements and a consistent reduction in domain wall velocity after peptide exposure. These results suggest that microscopic CISS signatures are robust for both sample types, whereas macroscopic MIPAC-type magnetic responses are more sensitive to the substrate microstructure.

cond-mat.mtrl-sci↗

Chiral-Induced Spin Selectivity Effect in a 1 nm Thin 1,1'-Binaphthyl-2,2'-diyl Hydrogenphosphate Self-Assembled Monolayer on Nickel Oxide

The chiral-induced spin selectivity (CISS) effect describes an observed correlation between the orientation of an electron spin transported or transferred through a molecule and that molecule's chirality. Suitable molecules are usually arranged as self-assembled monolayers (SAMs), and the primary CISS systems are based on multiple nanometer-long biomolecules exhibiting helical chirality. Aside from these typically thiolate-anchored molecules, phosphonic and phosphoric acid SAMs may well become significant for those CISS applications that require a more robust molecular coupling to metal oxide surfaces. In this work, we report on our studies, employing the aromatic, low-molecular-mass, axially chiral organophosphoric acid derivative 1,1'-binaphthyl-2,2'-diyl hydrogenphosphate (BNP). Grown as a roughly 1 nm thin SAM on top of a NiOx/Ni substrate, a strong circular dichroism signal indicates that the thin films preserved chirality. The CISS response exhibits a high magnetoresistance with a spin polarization of 50-80% when measured using magnetic-conductive atomic force microscopy. For biases above 0.5 V, the magnetoresistance curves could be well fitted to the Fowler-Nordheim (FN) tunneling model. Using a minimal FN model, we determined that, depending on the magnetization direction and the handedness of the molecules, electrons of a certain spin direction face an effective tunneling barrier at high bias, which is either 80 % higher or 40 % lower compared to the barrier for electrons of the opposite spin direction. Due to the small size of the molecules, their compatibility with oxide materials, and their commercial availability, they are excellent candidates for the realization of novel (nanoscale) organic spintronic devices.

cond-mat.mtrl-sci↗