arXiv subjects

Harold J. W. Zandvliet

Publications and source records attributed to Harold J. W. Zandvliet.

At least 19 recordsLinked to original sources

arXiv2026

Decorated electronic kagome lattice in twisted bilayer germanene

Artificial kagome lattices provide a route to electronic flat bands, geometric frustration, and correlation driven phases, but their realization in atomically controlled two-dimensional materials remains scarce. Here, we show that commensurate twisted bilayer germanene on Ge2Pt produces two electronically distinct large-angle moiré phases. Scanning tunneling microscopy measurements and density functional theory calculations reveal that commensurate twisted bilayers that are odd under an exchange of sublattices are semiconducting, whereas the twisted bilayers with an even parity are metallic. The twisted bilayers with an even parity host an empty state resonance that exhibits an emergent decorated kagome structure with a C3 symmetry. These results establish large-angle twisted germanene as a platform for engineering kagome-like electronic states in a buckled two-dimensional material.

cond-mat.mes-hall↗

arXiv2026

Topology of honeycomb nanoribbons revisited

We present an in-depth study of end states in honeycomb nanoribbons, focusing on the interplay between nanoribbon termination, chiral symmetry, and complex next-nearest-neighbor hopping in the framework of the Haldane model. Although previous work has identified zero-dimensional end states in such systems, this analysis is incomplete. Here, we systematically investigate zigzag and armchair nanoribbons of various widths, using the multiband Zak phase to characterize the topological properties of the occupied bands. We show that the Zak phase is quantized only for certain ribbon terminations, and we elucidate how this termination dependence governs the existence and robustness of end states. Furthermore, we explore the effect of varying the complex next-nearest-neighbor hopping phase, demonstrating the breakdown of chiral symmetry, the evolution of the bulk gap, and the resulting depinning of end-state energies. Finally, we place our findings in the context of previous studies and discuss connections to the Kane-Mele model, including the role of Rashba spin-orbit coupling. Our work provides a more detailed analysis of topological end states in nanoribbons described by the Haldane and Kane-Mele models and offers a framework for their characterization in related systems.

cond-mat.mes-hall↗

arXiv2025

Electric-field control of zero-dimensional topological states in ultranarrow germanene nanoribbons

Reversible, all-electric control of symmetry-protected zero-dimensional modes has been a long-standing goal. In buckled honeycomb lattices, a perpendicular field couples to the staggered sublattice potential providing the required handle. We combine scanning tunneling microscopy and tight-binding theory to switch zero-dimensional topological end states reversibly on and off in ultranarrow germanene nanoribbons by tuning the electric field in the tunnel junction. Increasing the field switches off the end modes of topological two-hexagon wide ribbons, while the same field switches on zero-dimensional states in initially trivial three- and four-hexagon wide ribbons. This atomic scale platform realizes a proof-of-principle for a zero-dimensional topological field effect device, opening a path for ultrasmall memory, controllable qubits, and neuromorphic architectures.

cond-mat.mtrl-sci↗

arXiv2025

Electric field-induced spin-valley locking in twisted bilayer buckled honeycomb materials

A twisted honeycomb bilayer exhibits a moiré superstructure that is composed of a hexagonal arrangement of AB and BA stacked domains separated by domain boundaries. In the case of twisted bilayer graphene, the application of an electric field normal to the bilayer leads to the opening of inverted band gaps in the AB and BA stacked domains. The inverted band gaps result in the formation of a two-dimensional triangular network of counterpropagating valley protected helical domain boundary states, also referred to as the quantum valley Hall effect. Owing to spin-orbit coupling and buckling, the quantum valley Hall effect in twisted bilayer silicene and germanene is more complex than in twisted bilayer graphene. We found that there is a range of electric fields for which the spin degree of freedom is locked to the valley degree of freedom of the electrons in the quantum valley Hall states, resulting in a stronger topological protection. For electric fields smaller than the aforementioned range the twisted bilayer does not exhibit the quantum valley Hall effect, whereas for larger electric fields the spin-valley locking is lifted and the emergent quantum valley Hall states are only valley-protected.

cond-mat.mes-hall↗

arXiv2024

Realization of a one-dimensional topological insulator in ultrathin germanene nanoribbons

Realizing a one-dimensional (1D) topological insulator and identifying the lower dimensional limit of two-dimensional (2D) behavior are crucial steps toward developing high-density quantum state networks, advancing topological quantum computing, and exploring dimensionality effects in topological materials. Although 2D topological insulators have been experimentally realized, their lower dimensional limit and 1D counterparts remain elusive. Here, we fabricated and characterized arrays of zigzag-terminated germanene nanoribbons, a 2D topological insulator with a large topological bulk gap. The electronic properties of these nanoribbons strongly depend on their width, with topological edge states persisting down to a critical width (approx. 2 nm), defining the limit of 2D topology. Below this threshold, contrary to the tenfold way classification, we observe zero-dimensional (0D) states localized at the ends of the ultrathin nanoribbons. These end states, topologically protected by time-reversal and mirror symmetries, mark the first realization of a 1D topological insulator with strong spin-orbit coupling. Our findings establish germanene nanoribbons as a platform for investigating 1D topology and dimensionality effects in topological materials.

cond-mat.mes-hall↗

arXiv2024

Moiré-modulated band gap and van Hove singularities in twisted bilayer germanene

Twisting bilayers of two-dimensional topological insulators has the potential to create unique quantum states of matter. Here, we successfully synthesized a twisted bilayer of germanene on Ge2Pt(101) with a 21.8$^o$ degrees twist angle, corresponding to a commensurate ($\sqrt{7} \times \sqrt{7}$) structure. Using scanning tunneling microscopy and spectroscopy, we unraveled the structural and electronic properties of this configuration, revealing a moiré-modulated band gap and a well-defined edge state. This band gap opens at AB/BA stacked sites and closes at AA stacked sites, a phenomenon attributed to the electric field induced by the scanning tunneling microscopy tip. Our study further revealed two van Hove singularities at -0.8 eV and +1.04 eV, resulting in a Fermi velocity of $(8 \pm 1) \times 10^5$ m/s. Our tight-binding results uncover a unique quantum state, where the topological properties could be regulated through an electric field, potentially triggering two topological phase transitions.

cond-mat.mes-hall↗

arXiv2022

High-strain-induced local modification of the electronic properties of VO$_2$ thin films

Vanadium dioxide (VO2) is a popular candidate for electronic and optical switching applications due to its well-known semiconductor-metal transition. Its study is notoriously challenging due to the interplay of long and short range elastic distortions, as well as the symmetry change, and the electronic structure changes. The inherent coupling of lattice and electronic degrees of freedom opens the avenue towards mechanical actuation of single domains. In this work, we show that we can manipulate and monitor the reversible semiconductor-to-metal transition of VO2 while applying a controlled amount of mechanical pressure by a nanosized metallic probe using an atomic force microscope. At a critical pressure, we can reversibly actuate the phase transition with a large modulation of the conductivity. Direct tunneling through the VO2-metal contact is observed as the main charge carrier injection mechanism before and after the phase transition of VO2. The tunneling barrier is formed by a very thin but persistently insulating surfacelayer of the VO2. The necessary pressure to induce the transition decreases with temperature. In addition, we measured the phase coexistence line in a hitherto unexplored regime. Our study provides valuable information on pressure-induced electronic modifications of the VO2 properties, as well as on nanoscale metal-oxide contacts, which can help in the future design of oxide electronics.

cond-mat.mtrl-sci↗

arXiv2022

Free energy of domain walls and order-disorder transition in a triangular lattice with anisotropic nearest-neighbor interactions

We have derived exact expressions for the domain wall free energy along the three high-symmetry directions of a triangular lattice with anisotropic nearest-neighbor interactions. The triangular lattice undergoes an orderdisorder phase transition at a temperature Tc given by exp(-(e1+e2)/2kTc)+ exp(-(e2+e3)/2kTc)+ exp(-(e3+e1)/2kTc)= 1, where e1, e2, e3 are the nearest-neighbor interaction energies, and e1+ e2> 0, e2+ e3> 0, e3+ e1> 0. Finally, we have derived expressions for the thermally induced meandering of the domain walls at temperatures below the phase transition temperature. We show how these expressions can be used to extract the interaction energies of two-dimensional systems with a triangular lattice.

physics.app-ph↗

arXiv2022

On the mystery of the absence of a spin-orbit gap in scanning tunneling microscopy spectra of germanene

Germanene, the germanium analogue of graphene, shares many properties with its carbon counterpart. Both materials are two-dimensional materials that host Dirac fermions. There are, however, also a few important differences between these two materials: (1) graphene has a planar honeycomb lattice, whereas germanene's honeycomb lattice is buckled and (2) the spin-orbit gap in germanene is predicted to be about three orders of magnitude larger than the spin-orbit gap in graphene (24 meV for germanene versus 20 $μ$eV for graphene). Surprisingly, scanning tunneling spectra recorded on germanene layers synthesized on different substrates do not show any sign of the presence of a spin-orbit gap in germanene. To date the exact origin of the absence of this spin-orbit gap in the scanning tunneling spectra of germanene has remained a mystery. In this work we show that the absence of the spin-orbit can be explained by germanene's exceptionally low work function of only 3.8 eV. The difference in work function between germanene and the scanning tunneling microscopy tip (the work functions of most commonly used STM tips are in the range of 4.5 to 5.5 eV) gives rise to an electric field in the tunnel junction. This electric field results in a strong suppression of the size of the spin-orbit gap.

cond-mat.mes-hall↗

arXiv2022

Droplet dissolution driven by emerging thermal gradients and Marangoni flow

The lifetime $τ$ of an isothermal and purely diffusively dissolving droplet in a host liquid scales as $τ\sim R_0^2$ with its initial radius $R_0$ [Langmuir, Phys. Rev. 12, 368 (1919)]. For a droplet dissolving due to natural convection driven by density differences, its lifetime scales as $τ\sim R_0^{5/4}$ [Dietrich et al., J. Fluid Mech. 794, 45 (2016)]. In this paper we experimentally find and theoretically derive yet another droplet dissolution behavior, resulting in $τ\sim R_0^4$. It occurs when the dissolution dynamics is controlled by local heating of the liquid, leading to a modified solubility and a thermal Marangoni flow around the droplet. The thermal gradient is achieved by plasmonic heating of a gold nanoparticle decorated sample surface, on which a sessile water droplet immersed in water-saturated 1-butanol solution is sitting. The resulting off-wall thermal Marangoni flow and the temperature dependence of the solubility determine the droplet dissolution rate, resulting in a shrinkage $R(t) \sim (τ-t )^{1/4}$ of the droplet radius and thus in $τ\sim R_0^{4}$.

physics.flu-dyn↗

arXiv2021

Droplet plume emission during plasmonic bubble growth in ternary liquids

Plasmonic bubbles are of great relevance in numerous applications, including catalytic reactions, micro/nanomanipulation of molecules or particles dispersed in liquids, and cancer therapeutics. So far, studies have been focused on bubble nucleation in pure liquids. Here we investigate plasmonic bubble nucleation in ternary liquids consisting of ethanol, water, and trans-anethole oil which can show the so-called ouzo-effect. We find that oil (trans-anethole) droplet plumes are produced around the growing plasmonic bubbles. The nucleation of the microdroplets and their organization in droplet plumes is due to the symmetry breaking of the ethanol concentration field during the selective evaporation of ethanol from the surrounding ternary liquids into the growing plasmonic bubbles. Numerical simulations show the existence of a critical Marangoni number Ma (the ratio between solutal advection rate and the diffusion rate), above which the symmetry breaking of the ethanol concentration field occurs, leading to the emission of the droplet plumes. The numerical results agree with the experimental observation that more plumes are emitted with increasing ethanol-water relative weight ratios and hence Ma. Our findings on the droplet plume formation reveal the rich phenomena of plasmonic bubble nucleation in multicomponent liquids and help to pave the way to achieve enhanced mixing in multicomponent liquids in chemical, pharmaceutical, and cosmetic industries.

physics.flu-dyn↗

arXiv2021

Periodic bouncing of a plasmonic bubble in a binary liquid by competing solutal and thermal Marangoni forces

The physicochemical hydrodynamics of bubbles and droplets out of equilibrium, in particular with phase transitions, displays surprisingly rich and often counterintuitive phenomena. Here we experimentally and theoretically study the nucleation and early evolution of plasmonic bubbles in a binary liquid consisting of water and ethanol. Remarkably, the submillimeter plasmonic bubble is found to be periodically attracted to and repelled from the nanoparticle-decorated substrate, with frequencies of around a few kHz. We identify the competition between solutal and thermal Marangoni forces as origin of the periodic bouncing. The former arises due to the selective vaporization of ethanol at the substrate's side of the bubble, leading to a solutal Marangoni flow towards the hot substrate, which pushes the bubble away. The latter arises due to the temperature gradient across the bubble, leading to a thermal Marangoni flow away from the substrate which sucks the bubble towards it. We study the dependence of the frequency of the bouncing phenomenon from the control parameters of the system, namely the ethanol fraction and the laser power for the plasmonic heating. Our findings can be generalized to boiling and electrolytically or catalytically generated bubbles in multicomponent liquids.

physics.flu-dyn↗

arXiv2021

Plasmonic Microbubble Dynamics in Binary Liquids

The growth of surface plasmonic microbubbles in binary water/ethanol solutions is experimentally studied. The microbubbles are generated by illuminating a gold nanoparticle array with a continuous wave laser. Plasmonic bubbles exhibit ethanol concentration-dependent behaviors. For low ethanol concentrations (f_e) of < 67.5%, bubbles do not exist at the solid-liquid interface. For high f_e values of >80%, the bubbles behave as in pure ethanol. Only in an intermediate window of 67.5% < f_e < 80% do we find sessile plasmonic bubbles with a highly nontrivial temporal evolution, in which as a function of time three phases can be discerned. (1) In the first phase, the microbubbles grow, while wiggling. (2) As soon as the wiggling stops, the microbubbles enter the second phase in which they suddenly shrink, followed by (3) a steady reentrant growth phase. Our experiments reveal that the sudden shrinkage of the microbubbles in the second regime is caused by a depinning event of the three phase contact line. We systematically vary the ethanol concentration, laser power, and laser spot size to unravel water recondensation as the underlying mechanism of the sudden bubble shrinkage in phase 2.

cond-mat.soft↗

arXiv2020

Giant plasmonic bubbles nucleation under different ambient pressures

Water-immersed gold nanoparticles irradiated by a laser can trigger the nucleation of plasmonic bubbles after a delay time of a few microseconds [Wang et al., Proc. Natl. Acad. Sci. USA 122, 9253,(2018)]. Here we systematically investigated the light-vapor conversion efficiency, η, of these plasmonic bubbles as a function of the ambient pressure. The efficiency of the formation of these initial-phase and mainly water-vapor containing bubbles, which is defined as the ratio of the energy that is required to form the vapor bubbles and the total energy dumped in the gold nanoparticles before nucleation of the bubble by the laser, can be as high as 25%. The amount of vaporized water first scales linearly with the total laser energy dumped in the gold nanoparticles before nucleation, but for larger energies the amount of vaporized water levels off. The efficiency η decreases with increasing ambient pressure. The experimental observations can be quantitatively understood within a theoretical framework based on the thermal diffusion equation and the thermal dynamics of the phase transition.

physics.optics↗

arXiv2020

Gas-Vapor Interplay in Plasmonic Bubble Shrinkage

The understanding of the shrinkage dynamics of plasmonic bubbles formed around metallic nanoparticles immersed in liquid and irradiated by a resonant light source is crucial for the usage of these bubbles in numerous applications. In this paper we experimentally show and theoretically explain that a plasmonic bubble during its shrinkage undergoes two different phases: first, a rapid partial bubble shrinkage governed by vapor condensation and, second, a slow diffusion-controlled bubble dissolution. The history of the bubble formation plays an important role in the shrinkage dynamics during the first phase, as it determines the gas-vapor ratio in the bubble composition. Higher laser powers lead to more vaporous bubbles, while longer pulses and higher dissolved air concentrations lead to more gaseous bubbles. The dynamics of the second phase barely depends on the history of bubble formation, i.e. laser power and pulse duration, but strongly on the dissolved air concentration, which defines the concentration gradient at the bubble interface. Finally, for the bubble dissolution in the second phase, with decreasing dissolved air concentration, we observe a gradual transition from a $R(t) \propto (t_0 - t) ^{1/3}$ scaling law to a $R(t) \propto (t_0 - t) ^{1/2}$ scaling law, where $t_0$ is the lifetime of the bubble and theoretically explain this transition.

physics.flu-dyn↗

arXiv2020

Plasmonic Bubble Nucleation and Growth in Water: Effect of Dissolved Air

Under continuous laser irradiation, noble metal nanoparticles immersed in water can quickly heat up, leading to the nucleation of so-called plasmonic bubbles. In this work, we want to further understand the bubble nucleation and growth mechanism. In particular, we quantitatively study the effect of the amount of dissolved air on the bubble nucleation and growth dynamics, both for the initial giant bubble, which forms shortly after switching on the laser and is mainly composed of vapor, and for the final life phase of the bubble, during which it mainly contains air expelled from water. We found that the bubble nucleation temperature depends on the gas concentration: the higher the gas concentration, the lower the bubble nucleation temperature. Also, the long-term diffusiondominated bubble growth is governed by the gas concentration. The radius of the bubbles grows as R(t)~t^1/3 for airequilibrated and air-oversaturated water. In contrast, in partially degassed water, the growth is much slower since, even for the highest temperature we achieve, the water remains undersaturated.

physics.flu-dyn↗

arXiv2020

Entrapment and Dissolution of Microbubbles Inside Microwells

The formation and evolution of immersed surface micro- and nanobubbles are essential in various practical applications, such as the usage of superhydrophobic rematerials, drug delivery, and mineral flotation. In this work, we investigate the entrapment of microbubbles on a hydrophobic surface, structured with microwells, when water flow passes along, and the subsequent microbubble dissolution. At entrapment, the microbubble is initially pinned at the edge of the microwell. At some point, the three-phase contact line detaches from one side of the edge and separates from the wall, after which it further recedes. We systematically investigate the evolution of the footprint diameter and the contact angle of the entrapped microbubbles, which reveals that the dissolution process is in the constant contact angle mode. By varying the gas undersaturation level, we quantify how a high gas undersaturation enhances the dissolution process, and compare with simplified theoretical predictions for dissolving bubbles on a plane surface. We find that geometric partial blockage effects of the diffusive flux out of the microbubble trapped in the microwell lead to reduced dissolution rates.

physics.flu-dyn↗

arXiv2019

Evaporation of dilute sodium dodecyl sulfate droplets on a hydrophobic substrate

Evaporation of surfactant laden sessile droplets is omnipresent in nature and industrial applications such as inkjet printing. Soluble surfactants start to form micelles in an aqueous solution for surfactant concentrations exceeding the critical micelle concentration (CMC). Here, the evaporation of aqueous sodium dodecyl sulfate (SDS) sessile droplets on hydrophobic surfaces were experimentally investigated for SDS concentrations ranging from 0.025 to 1 CMC. In contrast to the constant contact angle of an evaporating sessile water droplet, we observed that, at the same surface the contact angle of an SDS laden droplet with a concentration below 0.5 CMC first decreases, then increases, and finally decreases resulting in a local contact angle minimum. Surprisingly, the minimum contact angle was found to be substantially lower than the static receding contact angle and it decreased with decreasing initial SDS concentration. Furthermore, the bulk SDS concentration at the local contact angle minimum was found to decrease with a decrease in the initial SDS concentration. The location of the observed contact angle minimum relative to the normalized evaporation time and its minimum value proved to be independent of both the relative humidity and the droplet volume and thus, of the total evaporation time. We discuss the observed contact angle dynamics in terms of the formation of a disordered layer of SDS molecules on the substrate at concentrations below 0.5 CMC. The present work underlines the complexity of the evaporation of sessile liquid-surfactant droplets and the influence of surfactant-substrate interactions on the evaporation process.

cond-mat.soft↗