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Sabina Caneva

Publications and source records attributed to Sabina Caneva.

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Self-Assembled hBN Wrinkles as Planar Optofluidic Channels

Optically accessible, scalable planar nanofluidic channels are attractive for studying transport and localization under confinement. Two dimensional (2D) materials provide large area, atomically flat interfaces for generating such platforms, yet achieving long range one-dimensional (1D) confinement with top-down nanofabrication remains challenging because it requires reproducible nanoscale feature control over extended distances, high yield, and low nonspecific adsorption of analytes under aqueous conditions. Here we demonstrate that thermally induced wrinkling of exfoliated hexagonal boron nitride (hBN) produces self-assembled, liquid-accessible, channel-like networks through a lithography-free process. By varying flake thickness and substrate choice, we quantify statistical trends in wrinkle density and morphology, thereby establishing a practical fabrication design space. Atomic force microscopy and electron microscopy reveal wrinkle-derived geometries with vertical confinement ranging from <2 nm to >100 nm depending on flake thickness and substrate. We further employ time-sequence optical imaging upon droplet-contact, which together with Raman mapping of the water OH-stretch band and capacitance-gradient mapping (dC/dz) by scanning dielectric microscopy (KPFM-based) measurements, demonstrates liquid infiltration and long-term liquid retention within the wrinkle network for more than 10 h. We finally show a proof-of-concept biomolecule confinement application in which we integrate a graphene overlayer as a background suppression interface, enabling wide-field fluorescence localization of ATTO647N labeled DNA along hBN wrinkle-induced nanochannels. Overall, this work establishes self-assembled hBN wrinkles as a scalable, and optically addressable planar nanofluidic platform for confinement of fluids and biomolecules.

physics.app-ph

Actuation and mapping of SAW-induced high-frequency wavefields on suspended graphene membranes

High frequency acoustic devices based on two-dimensional (2D) materials are unique platforms to design and manipulate the spatiotemporal response of acoustic waves for next-generation sensing and contactless actuation applications. Conventional methods for actuating suspended membranes, however, cannot be applied to all 2D materials, or are limited in frequency. There is, therefore, a need for a universal high-frequency, on-chip actuation technique that can be applied to all types of membranes. Here, we demonstrate that surface acoustic waves (SAWs) can be used to efficiently actuate suspended 2D materials by exciting suspended graphene membranes with high-frequency (375 MHz) Rayleigh surface waves and mapping the resulting vibration field with atomic force acoustic microscopy (AFAM). Acoustic waves travelling from supported to suspended graphene experience a reduction in acoustic wavelength from 10 \mu m to ~2 \mu um due to the decrease in effective bending rigidity, leading to a decrease in wave velocity on suspended graphene. By varying the excitation frequency, we observed a change in phase velocity from ~160 m/s to ~700 m/s. This behavior is consistent with the nonlinear dispersion of acoustic waves, as predicted by plate theory, in suspended graphene membranes. The geometry and bending rigidity of the membrane thus play key roles in modulating the acoustic wave pattern and wavelength. This combined SAW actuation and AFAM visualization scheme can give new insights into the fundamentals of acoustic transport at the nanoscale limit and provides a route towards the manipulation of localized wavefields for on-chip patterning and transport over 2D materials surfaces.

cond-mat.mes-hall

Microsphere-assisted generation of localized optical emitters in 2D hexagonal boron nitride

Crystal defects in hexagonal boron nitride (hBN) are emerging as versatile nanoscale optical probes with a wide application profile, spanning the fields of nanophotonics, biosensing, bioimaging and quantum information processing. However, generating these crystal defects as reliable optical emitters remains challenging due to the need for deterministic defect placement and precise control of the emission area. Here, we demonstrate an approach that integrates microspheres (MS) with hBN optical probes to enhance both defect generation and optical signal readout. This technique harnesses MS to amplify light-matter interactions at the nanoscale through 2 two mechanisms: focused femtosecond (fs) laser irradiation into a photonic nanojet for highly localized defect generation, and enhanced light collection via the whispering gallery mode effect. Our MS-assisted defect generation method reduces the emission area by a factor of 5 and increases the fluorescence collection efficiency by approximately 10 times compared to MS-free samples. These advancements in defect generation precision and signal collection efficiency open new possibilities for optical emitter manipulation in hBN, with potential applications in quantum technologies and nanoscale sensing.

cond-mat.mes-hall

A Mechanically Tunable Quantum Dot in a Graphene Break Junction

Graphene quantum dots (QDs) are intensively studied as platforms for the next generation of quantum electronic devices. Fine tuning of the transport properties in monolayer graphene QDs, in particular with respect to the independent modulation of the tunnel barrier transparencies, remains challenging and is typically addressed using electrostatic gating. We investigate charge transport in back-gated graphene mechanical break junctions and reveal Coulomb blockade physics characteristic of a single, high-quality QD when a nanogap is opened in a graphene constriction. By mechanically controlling the distance across the newly-formed graphene nanogap, we achieve reversible tunability of the tunnel coupling to the drain electrode by five orders of magnitude, while keeping the source-QD tunnel coupling constant. These findings indicate that the tunnel coupling asymmetry can be significantly modulated with a mechanical tuning knob and has important implications for the development of future graphene-based devices, including energy converters and quantum calorimeters.

cond-mat.mes-hall

Non-equilibrium properties of graphene probed by superconducting tunnel spectroscopy

We report on non-equilibrium properties of graphene probed by superconducting tunnel spectroscopy. A hexagonal boron nitride (hBN) tunnel barrier in combination with a superconducting Pb contact is used to extract the local energy distribution function of the quasiparticles in graphene samples in different transport regimes. In the cases where the energy distribution function resembles a Fermi-Dirac distribution, the local electron temperature can directly be accessed. This allows us to study the cooling mechanisms of hot electrons in graphene. In the case of long samples (device length $L$ much larger than the electron-phonon scattering length $l_{e-ph}$), cooling through acoustic phonons is dominant. We find a cross-over from the dirty limit with a power law $~T^3$ at low temperature to the clean limit at higher temperatures with a power law $~T^4$ and a deformation potential of 13.3 eV. For shorter samples, where $L$ is smaller than $l_{e-ph}$ but larger than the electron-electron scattering length $l_{e-e}$, the well-known cooling through electron out-diffusion is found. Interestingly, we find strong indications of an enhanced Lorenz number in graphene. We also find evidence of a non-Fermi-Dirac distribution function, which is a result of non-interacting quasiparticles in very short samples.

cond-mat.mes-hall

Mechanically Controlled Quantum Interference in Graphene Break Junctions

The ability to detect and distinguish quantum interference signatures is important for both fundamental research and for the realization of devices including electron resonators, interferometers and interference-based spin filters. Consistent with the principles of subwavelength optics, the wave nature of electrons can give rise to various types of interference effects, such as Fabry-Pérot resonances, Fano resonances and the Aharonov-Bohm effect. Quantum-interference conductance oscillations have indeed been predicted for multiwall carbon nanotube shuttles and telescopes, and arise from atomic-scale displacements between the inner and outer tubes. Previous theoretical work on graphene bilayers indicates that these systems may display similar interference features as a function of the relative position of the two sheets. Experimental verification is, however, still lacking. Graphene nanoconstrictions represent an ideal model system to study quantum transport phenomena due to the electronic coherence and the transverse confinement of the carriers. Here, we demonstrate the fabrication of bowtie-shaped nanoconstrictions with mechanically controlled break junctions (MCBJs) made from a single layer of graphene. We find that their electrical conductance displays pronounced oscillations at room temperature, with amplitudes that modulate over an order of magnitude as a function of sub-nanometer displacements. Surprisingly, the oscillations exhibit a period larger than the graphene lattice constant. Charge-transport calculations show that the periodicity originates from a combination of quantum-interference and lattice-commensuration effects of two graphene layers that slide across each other. Our results provide direct experimental observation of Fabry-Pérot-like interference of electron waves that are partially reflected/transmitted at the edges of the graphene bilayer overlap region.

cond-mat.mes-hall

Massively parallel fabrication of crack-defined gold break junctions featuring sub-3 nm gaps for molecular devices

Break junctions provide tip-shaped contact electrodes that are fundamental components of nano and molecular electronics. However, the fabrication of break junctions remains notoriously time-consuming and difficult to parallelize. Here we demonstrate true parallel fabrication of gold break junctions featuring sub-3 nm gaps on the wafer-scale, by relying on a novel self-breaking mechanism based on controlled crack formation in notched bridge structures. We achieve fabrication densities as high as 7 million junctions per cm$^{2}$, with fabrication yields of around 7% for obtaining crack-defined break junctions with sub-3 nm gaps of fixed gap width that exhibit electron tunneling. We also form molecular junctions using dithiol-terminated oligo(phenylene ethynylene) (OPE3) to demonstrate the feasibility of our approach for electrical probing of molecules down to liquid helium temperatures. Our technology opens a whole new range of experimental opportunities for nano and molecular electronics applications, by enabling very large-scale fabrication of solid-state break junctions.

physics.app-ph

Imaging of optically active defects with nanometer resolution

Point defects significantly influence the optical and electrical properties of solid-state materials due to their interactions with charge carriers, which reduce the band-to-band optical transition energy. There has been a demand for developing direct optical imaging methods that would allow in-situ characterization of individual defects with nanometer resolution. Here, we demonstrate the localization and quantitative counting of individual optically active defects in monolayer hexagonal boron nitride using single molecule localization microscopy. By exploiting the blinking behavior of defect emitters to temporally isolate multiple emitters within one diffraction limited region, we could resolve two defect emitters with a point-to-point distance down to ten nanometers. The results and conclusion presented in this work add unprecedented dimensions towards future applications of defects in quantum information processing and biological imaging.

cond-mat.mes-hall