arXiv subjects

Kees Flipse

Publications and source records attributed to Kees Flipse.

7 recordsLinked to original sources

arXiv2026

The interplay between topology, defects and chiral order in the nearly-commensurate charge density wave of 1T-TaS2

In 1T-TaS2, the nearly-commensurate charge density wave (NC-CDW) exhibits emergent chirality, a property of interest for technological applications such as memory. We study the relationship between chirality and topological defects using holographic analysis of scanning tunneling microscopy data. By characterizing the CDW order parameter, we uncover distinct topological defects and define a chiral order parameter that connects directly to them. Our analysis distinguishes between vortex pairs in high-strain areas and glass-like soliton or discommensurations networks. We propose that perturbations, such as strain, drive vortex nucleation and annihilation, leaving solitons or discommensurations pinned by disorder. Electric fields induce soliton and discommensurations movement, causing chiral switching via localized order parameter melting, enabling controllable room-temperature chirality

cond-mat.mtrl-sci↗

arXiv2024

Order in disorder: oxygen vacancy driven electronic phase separation of LaNiO3-x epitaxial thin film surface investigated by scanning probe microscopy

Oxygen vacancies in nickelates are known to introduce a variety of emergent phenomena and are considered to significantly affect conductivity. Few studies have examined real-space evidence for oxygen vacancies on the surface, particularly using scanning probe microscopy. Understanding the surface composition, both structurally and chemically, is crucial for the application of nickelates, such as in electrochemical water splitting reactions as catalysts. In this study, we investigate a 20 nm epitaxial LaNiO3-x(LNO) film grown on SrTiO3 (STO) via pulsed laser deposition. We examine the surface of this film using scanning tunneling microscopy (STM) and reveal a complex surface morphology composed of densely packed crystalline nanometer-sized circular features with radius ranging from 10 to 20 nm. Scanning tunneling spectroscopy revealed an electronic inhomogeneity, or phase separation, in nanoscale islands of semi-conductive nature embedded within a metallic matrix. This change in the electronic density of the states was associated with increased concentration of oxygen vacancies. Further evidence for significant oxygen vacancies at the surface was inferred by examining scanning tunneling tip-induced surface degradation. The strong electric field between the tip and sample likely facilitates oxygen removal in a vacuum environment, increasing the formation of vacancies, which can lead to the breakdown of the crystal structure. This provides insight into the possible origin of the chemical surface transformation during the electrochemical water splitting reaction of this nickelate.

cond-mat.mtrl-sci↗

arXiv2023

A complementary experimental study of epitaxial La0.67Sr0.33MnO3 to identify morphological and chemical disorder

Gaining insight into the characteristics of epitaxial complex oxide films is essential to control the behavior of devices and catalytic processes. It is known that substrate induced strain, doping, and layer growth can affect the electronic and magnetic properties of the film's bulk. In this study, we demonstrate a clear distinction between the bulk and surface of thin films of La0.67Sr0.33MnO3 in terms of chemical composition, electronic disorder, and surface morphology. We employed a combined experimental approach of X-ray based characterization methods and scanning probe microscopy. X-ray diffraction and resonant X-ray reflectivity revealed surface non-stochiometry in the strontium and lanthanum, as well as an accumulation of oxygen vacancies. Scanning tunneling microscopy showed a staggered growth surface morphology accompanied by an electronic phase separation (EPS) related to this non-stochiometry. The EPS is likely responsible for the temperature-dependent resistivity transition and is a cause of a proposed mixed-phase ferromagnetic and paramagnetic state near room temperature in these thin films.

cond-mat.mtrl-sci↗

arXiv2023

Beyond domain alignment: Revealing the effect of intrinsic magnetic order on electrochemical water splitting

To reach a long term viable green hydrogen economy, rational design of active oxygen evolution reaction (OER) catalysts is critical. An important hurdle in this reaction originates from the fact that the reactants are singlet molecules, whereas the oxygen molecule has a triplet ground state with parallel spin alignment, implying that magnetic order in the catalyst is essential. Accordingly, multiple experimentalists reported a positive effect of external magnetic fields on OER activity of ferromagnetic catalysts. However, it remains a challenge to investigate the influence of the intrinsic magnetic order on catalytic activity. Here, we tuned the intrinsic magnetic order of epitaxial La$_{0.67}$Sr$_{0.33}$MnO$_{3}$ thin film model catalysts from ferro- to paramagnetic by changing the temperature in-situ during water electrolysis. Using this strategy, we show that ferromagnetic ordering below the Curie temperature enhances OER activity. Moreover, we show a slight current density enhancement upon application of an external magnetic field and find that the dependence of magnetic field direction correlates with the magnetic anisotropy in the catalyst film. Our work thus suggests that both the intrinsic magnetic order in La$_{0.67}$Sr$_{0.33}$MnO$_{3}$ films and magnetic domain alignment increase their catalytic activity. We observe no long-range magnetic order at the catalytic surface, implying that the OER enhancement is connected to the magnetic order of the bulk catalyst. Combining the effects found with existing literature, we propose a unifying picture for the spin-polarized enhancement in magnetic oxide catalysts.

cond-mat.mtrl-sci↗

arXiv2023

Charge transport modulation by a redox supramolecular spin-filtering chiral crystal

The chirality induced spin selectivity (CISS) effect is a fascinating phenomena correlating molecular structure with electron spin-polarisation in excited state measurements. Experimental procedures to quantify the spin-filtering magnitude relies generally on averaging data sets, especially those from magnetic field dependent conductive-AFM. We investigate the underlying observed disorder in the IV spectra and the origin of spikes superimposed. We demonstrate and explain that a dynamic, voltage sweep rate dependent, phenomena can give rise to complex IV curves for chiral crystals of coronene bisimide. The redox group, able to capture localized charge states, acts as an impurity state interfering with a continuum, giving rise to Fano resonances. We introduce a novel mechanism for the dynamic transport which might also provide insight into the role of spin-polarization. Crucially, interference between charge localisation and delocalisation during transport may be important properties into understanding the CISS phenomena.

cond-mat.mtrl-sci↗

arXiv2023

Switchable-magnetisation planar probe MFM sensor

We present an alternative switching-magnetization magnetic force microscopy (SM- MFM) method using planar tip-on-chip probes. Unlike traditional needle-like tips, the planar probe approach integrates a microdevice near the tip apex with dedicated functionality. Its 1 mm x 1 mm planar surface paves the way for freedom in ultra thin-film engineering and micro-/nano-tailoring for application-oriented tip functionalization. Here, we form a microscale current pathway near the tip end to control tip magnetisation. The chip like probe or planar probe, was applied to study the complex magnetic behaviour of epitaxial transition metal oxide perovskite LaMnO3, which was previously shown to behave as complex material with domains associated with superpara-, antiferro- and ferromagnetism. To this end we successfully imaged an inhomogeneous distribution of weak ferromagnetic islands with a resolution better than 10 nm.

physics.ins-det↗

arXiv2022

Enhancing sensitivity in atomic force microscopy for planar tip-on-chip probes

We present a new approach to tuning fork-based atomic force microscopy for utilizing advanced "tip-on-chip" probes with high sensitivity and broad compatibility. Usually, such chip-like probes with a size reaching 2 mm x 2 mm drastically perturb the oscillation of the tuning fork, resulting in poor performance in its intrinsic force sensing. Therefore, restoring initial oscillatory characteristics is necessary for regaining high sensitivity. To this end, we developed a new approach consisting of three basic steps: tuning fork rebalancing, revamping holder-sensor fixation, and electrode reconfiguration. Mass rebalancing allows the tuning fork to recover the frequency and regain high Q-factor values up to 10E4 in air and up to 4 x 10E4 in ultra-high vacuum conditions. The floating-like holder-fixation using soft wires significantly reduces energy dissipation from the mounting elements. Combined with the soft wires, reconfigured electrodes provide electrical access to the chip-like probe without intervening in the force-sensing signal. Finally, our easy-to-implement approach allows converting the atomic force microscopy-tip from a passive tool to a dedicated microdevice with extended functionality.

physics.ins-det↗