arXiv subjects

Elisa Riedo

Publications and source records attributed to Elisa Riedo.

14 recordsLinked to original sources

arXiv2026

Laser-written reconfigurable energy landscapes and programmable Moir\'e spin textures

Magnetic textures are central to emerging spintronic and unconventional computing technologies due to their rich dynamics, topological properties and nanoscale dimensions. A major challenge remains achieving tunable, reversible, and spatially resolved control over these textures and their evolution as a function of external stimuli, by spatially reprogramming the magnetic energy landscape that governs their nucleation and stability. Here, we exploit a focused laser-assisted local field cooling technique that establishes a fast, non-contact and scalable platform for grayscale spin texture engineering. By non-destructively controlling the exchange-bias anisotropy with nanoscale resolution in thin-film heterostructures, this approach enables grayscale, reprogrammable control of the local energy profile, which we use to create magnetic patterns with highly controlled hysteresis, field-dependent readability and tunable switching thresholds. Leveraging this capability, we demonstrate information encoding with magnetic field-gated readability, and artificial spin metamaterials, stabilizing spin lattices with field-reconfigurable symmetries and creating artificial Moir\'e spin textures via the geometric superposition of twisted magnetic potentials. These results establish a versatile, reprogrammable platform that bridges the gap between application-oriented magnetic memory and fundamental studies of emergent order in artificial lattices.

cond-mat.mtrl-sci↗

arXiv2019

Nonreciprocal nano-optics with spin-waves in synthetic antiferromagnets

Integrated optically-inspired wave-based processing is envisioned to outperform digital architectures in specific tasks, such as image processing and speech recognition. In this view, spin-waves represent a promising route due to their nanoscale wavelength in the GHz frequency range and rich phenomenology. Here, we realize a versatile optically-inspired platform using spin-waves, demonstrating the wavefront engineering, focusing, and robust interference of spin-waves with nanoscale wavelength. In particular, we use magnonic nanoantennas based on tailored spin-textures for launching spatially shaped coherent wavefronts, diffraction-limited spin-wave beams, and generating robust multi-beam interference patterns, which spatially extend for several times the spin-wave wavelength. Furthermore, we show that intriguing features, such as resilience to back-reflection, naturally arise from the spin-wave nonreciprocity in synthetic antiferromagnets, preserving the high quality of the interference patterns from spurious counterpropagating modes. This work represents a fundamental step towards the realization of nanoscale optically-inspired devices based on spin-waves.

cond-mat.mes-hall↗

arXiv2019

Layer dependence of graphene-diamene phase transition in epitaxial and exfoliated few-layer graphene using machine learning

The study of the nanomechanics of graphene $-$ and other 2D materials $-$ has led to the discovery of exciting new properties in 2D crystals, such as their remarkable in-plane stiffness and out of plane flexibility, as well as their unique frictional and wear properties at the nanoscale. Recently, nanomechanics of graphene has generated renovated interest for new findings on the pressure-induced chemical transformation of a few-layer thick epitaxial graphene into a new ultra-hard carbon phase, named diamene. In this work, by means of a machine learning technique, we provide a fast and efficient tool for identification of graphene domains (areas with a defined number of layers) in epitaxial and exfoliated films, by combining data from Atomic Force Microscopy (AFM) topography and friction force microscopy (FFM). Through the analysis of the number of graphene layers and detailed Å-indentation experiments, we demonstrate that the formation of ultra-stiff diamene is exclusively found in 1-layer plus buffer layer epitaxial graphene on silicon carbide (SiC) and that an ultra-stiff phase is not observed in neither thicker epitaxial graphene (2-layer or more) nor exfoliated graphene films of any thickness on silicon oxide (SiO$_{2}$).

cond-mat.mtrl-sci↗

arXiv2019

$Å$-Indentation for non-destructive elastic moduli measurements of supported ultra-hard ultra-thin films and nanostructures

During conventional nanoindentation measurements, the indentation depths are usually larger than 1-10 nm, which hinders the ability to study ultra-thin films ($<$ 10 nm) and supported atomically thin two-dimensional (2D) materials. Here, we discuss the development of modulated Å-indentation to achieve sub-Å indentation depths during force-indentation measurements while also imaging materials with nanoscale resolution. Modulated nanoindentation (MoNI) was originally invented to measure the radial elasticity of multi-walled nanotubes. Now, by using extremely small amplitude oscillations ($\ll$ 1 Å) at high frequency, and stiff cantilevers, we show how modulated nano/Å-indentation (MoNI/ÅI) enables non-destructive measurements of the contact stiffness and indentation modulus of ultra-thin ultra-stiff films, including CVD diamond films (modulus $\sim$ 1000 GPa), as well as the transverse modulus of 2D materials. Our analysis demonstrates that in presence of a standard laboratory noise floor, the signal to noise ratio of MoNI/ÅI implemented with a commercial atomic force microscope (AFM) is such that a dynamic range of 80 dB $-$ achievable with commercial Lock-in amplifiers $-$ is sufficient to observe superior indentation curves, having indentation depths as small as 0.3 Å, resolution in indentation $<$ 0.05 Å, and in normal load $<$ 0.5 nN. Being implemented on a standard AFM, this method has the potential for a broad applicability.

physics.app-ph↗

arXiv2018

Ultrahard carbon film from epitaxial two-layer graphene

Atomically thin graphene exhibits fascinating mechanical properties, although its hardness and transverse stiffness are inferior to those of diamond. To date, there hasn't been any practical demonstration of the transformation of multi-layer graphene into diamond-like ultra-hard structures. Here we show that at room temperature and after nano-indentation, two-layer graphene on SiC(0001) exhibits a transverse stiffness and hardness comparable to diamond, resisting to perforation with a diamond indenter, and showing a reversible drop in electrical conductivity upon indentation. Density functional theory calculations suggest that upon compression, the two-layer graphene film transforms into a diamond-like film, producing both elastic deformations and sp2-to-sp3 chemical changes. Experiments and calculations show that this reversible phase change is not observed for a single buffer layer on SiC or graphene films thicker than 3 to 5 layers. Indeed, calculations show that whereas in two-layer graphene layer-stacking configuration controls the conformation of the diamond-like film, in a multilayer film it hinders the phase transformation.

cond-mat.mtrl-sci↗

arXiv2017

Nanomagnonic waveguides based on reconfigurable spin-textures for spin computing

Magnonics is gaining momentum as an emerging technology for information processing. The wave character and Joule heating-free propagation of spin-waves hold promises for highly efficient analog computing platforms, based on integrated magnonic circuits. Miniaturization is a key issue but, so far, only few examples of manipulation of spin-waves in nanostructures have been demonstrated, due to the difficulty of tailoring the nanoscopic magnetic properties with conventional fabrication techniques. In this Letter, we demonstrate an unprecedented degree of control in the manipulation of spin-waves at the nanoscale by using patterned reconfigurable spin-textures. By space and time-resolved scanning transmission X-ray microscopy imaging, we provide direct evidence for the channeling and steering of propagating spin-waves in arbitrarily shaped nanomagnonic waveguides based on patterned domain walls, with no need for external magnetic fields or currents. Furthermore, we demonstrate a prototypic nanomagnonic circuit based on two converging waveguides, allowing for the tunable spatial superposition and interaction of confined spin-waves modes.

cond-mat.mes-hall↗

arXiv2015

Imaging thermal conductivity with nanoscale resolution using a scanning spin probe

The ability to probe nanoscale heat flow in a material is often limited by lack of spatial resolution. Here, we use a diamond-nanocrystal-hosted nitrogen-vacancy centre attached to the apex of a silicon thermal tip as a local temperature sensor. We apply an electrical current to heat up the tip and rely on the NV to monitor the thermal changes the tip experiences as it is brought into contact with surfaces of varying thermal conductivity. With the aid of a combined AFM/confocal setup, we image phantom microstructures with nanoscale resolution, and attain excellent agreement between the thermal conductivity and topographic maps. The small mass and high thermal conductivity of the diamond host make the time response of our technique short, which we demonstrate by monitoring the tip temperature upon application of a heat pulse. Our approach promises multiple applications, from the investigation of phonon dynamics in nanostructures to the characterization of heterogeneous phase transitions and chemical reactions in various solid-state systems.

cond-mat.mes-hall↗

arXiv2015

Advanced scanning probe lithography

The nanoscale control afforded by scanning probe microscopes has prompted the development of a wide variety of scanning probe-based patterning methods. Some of these methods have demonstrated a high degree of robustness and patterning capabilities that are unmatched by other lithographic techniques. However, the limited throughput of scanning probe lithography has prevented their exploitation in technological applications. Here, we review the fundamentals of scanning probe lithography and its use in materials science and nanotechnology. We focus on the methods and processes that offer genuinely lithography capabilities such as those based on thermal effects, chemical reactions and voltage-induced processes.

cond-mat.mtrl-sci↗

arXiv2013

Sliding on a Nanotube: Interplay of Friction, Deformations and Structure

The frictional properties of individual carbon nanotubes (CNTs) are studied by sliding an atomic force microscopy tip across and along its principle axis. This direction-dependent frictional behavior is found to correlate strongly with the presence of structural defects, surface chemistry, and CNT chirality. This study shows that it is experimentally possible to tune the frictional/adhesion properties of a CNT by controlling the CNT structure and surface chemistry, as well as use friction force to predict its structural and chemical properties.

cond-mat.mtrl-sci↗

arXiv2013

Morphology dependence of radial elasticity in multiwalled boron nitride nanotubes

We report on the measurement of the effective radial modulus of multiwalled Boron Nitride nanotubes with external radii in the range 3.7 to 36 nm and number of layers in between 5 and 48. These Boron Nitride nanotubes are radially much stiffer than previously reported thinner and smaller Boron Nitride nanotubes. Here, we show the key role of the morphology of the nanotubes in determining their radial rigidity, in particular we find that the external and internal radii, R_ext and R_int, have a stronger influence on the radial modulus than the NT's thickness, t. We find that the effective radial modulus decreases nonlinearly with 1/R_ext until reaching, for a large number of layers and a large radius, the transverse elastic modulus of bulk hexagonal-Boron Nitride.

cond-mat.mtrl-sci↗

arXiv2013

Adhesion and size dependent friction anisotropy in boron nitride nanotubes

The frictional properties of individual multiwalled boron nitride nanotubes (BN-NTs) synthesized by chemical vapor deposition (CVD) and deposited on a silicon substrate are investigated using an atomic force microscope tip sliding along (longitudinal sliding) and across (transverse sliding) the tube's principal axis. Because of the tube transverse deformations during the tip sliding, a larger friction coefficient is found for the transverse sliding as compared to the longitudinal sliding. Here, we show that the friction anisotropy in BN-NTs, defined as the ratio between transverse and longitudinal friction forces per unit area, increases with the nanotube-substrate contact area. Larger contact area denotes stronger surface adhesion, resulting in a longitudinal friction coefficient closer to the value expected in absence of transverse deformations. Compared to carbon nanotubes (C-NT), BN-NTs display a friction coefficient in each sliding direction with intermediate values between CVD and arc discharge C-NTs. CVD BN-NTs with improved tribological properties and higher oxidation temperature might be a better candidate than CVD C-NTs for applications in extreme environments.

cond-mat.mtrl-sci↗

arXiv2012

Hindered rolling and friction anisotropy in supported carbon nanotubes

Carbon nanotubes (CNTs) are well known for their exceptional thermal, mechanical and electrical properties. For many CNT applications it is of the foremost importance to know their frictional properties. However, very little is known about the frictional forces between an individual nanotube and a substrate or tip. Here, we present a combined theoretical and experimental study of the frictional forces encountered by a nanosize tip sliding on top of a supported multiwall CNT along a direction parallel or transverse to the CNT axis. Surprisingly, we find a higher friction coefficient in the transverse direction compared with the parallel direction. This behaviour is explained by a simulation showing that transverse friction elicits a soft 'hindered rolling' of the tube and a frictional dissipation that is absent, or partially absent for chiral CNTs, when the tip slides parallel to the CNT axis. Our findings can help in developing better strategies for large-scale CNT assembling and sorting on a surface.

cond-mat.mtrl-sci↗

arXiv2012

Radial elasticity of multi-walled carbon nanotubes

We report an experimental and a theoretical study of the radial elasticity of multi-walled carbon nanotubes as a function of external radius. We use atomic force microscopy and apply small indentation amplitudes in order to stay in the linear elasticity regime. The number of layers for a given tube radius is inferred from transmission electron microscopy, revealing constant ratios of external to internal radii. This enables a comparison with molecular dynamics results, which also shed some light onto the applicability of Hertz theory in this context. Using this theory, we find a radial Young modulus strongly decreasing with increasing radius and reaching an asymptotic value of 30 +/- 10 GPa.

cond-mat.mtrl-sci↗

arXiv2007

Nonlinear viscoelastic dynamics of nano-confined water

The viscoelastic dynamics of nano-confined water is studied by means of atomic force microscopy (AFM). We observe a nonlinear viscoelastic behavior remarkably similar to that widely observed in metastable complex fluids. We show that the origin of the measured nonlinear viscoelasticity in nano-confined water is a strain rate dependent relaxation time and slow dynamics. By measuring the viscoelastic modulus at different frequencies and strains, we find that the intrinsic relaxation time of nano-confined water is in the range 0.1-0.0001 s, orders of magnitude longer than that of bulk water, and comparable to the dielectric relaxation time measured in supercooled water at 170-210 K.

cond-mat.soft↗