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Francesco De Angelis

Publications and source records attributed to Francesco De Angelis.

At least 19 recordsLinked to original sources

SERS study of single-live-cell electrical permeabilization dynamics via plasmonic nanotubes

There is a growing demand for minimally invasive methods to analyze intracellular processes and signaling activities in individual living cells, including the identification of tumorigenic cell subpopulations. However, most conventional analytical methods require cell lysis, precluding repeated measurements in the same cell over time, or rely on exogenous labels and reporters that may perturb cellular function. Various applications based on vertical nanotubes have been developed that enable live cell monitoring and analysis by electroporation with low voltages. However, the extent and duration of membrane permeability and kinetics of membrane repair remain elusive. Here, we built a plasmonic platform with the capacity of surface enhanced Raman spectroscopy (SERS) to monitor the electroporation-induced membrane permeability dynamics in individual live cells attached onto 100-nm diameter nanotubes of 2 um height. Fibronectin was employed as extracellular matrix (ECM)-coating to facilitate cell attachment onto nanotubes. Using fluorescent-dye delivery as an independent validation method, we show that the fabricated nanostructures induce localized electrical permeabilization of the plasma membrane and enable monitoring of its subsequent recovery. We further use SERS to track molecular changes at the membrane during permeabilization and resealing. The SERS spectra provide molecular-level insight into changes in membrane-associated components and the ECM during electroporation and subsequent membrane recovery. Real time monitoring of pulse induced molecular changes holds great promise for characterizing intracellular signaling, cellular states, and cellular heterogeneity at the single cell level, including the identification of tumorigenic subpopulations. This capacity could facilitate the development of novel biosensing assay.

physics.app-ph

Microscopic Origin of Random Singlet Behavior in B-site Disordered Spin-1/2 Perovskite BaCu_1/3Nb_2/3O_3 Revealed by EXAFS and Thermodynamics

We report a combined structural and thermodynamic study of the ABO$_3$-type disordered perovskite BaCu$_{1/3}$Nb$_{2/3}$O$_3$ (BCNO), whose B site is jointly occupied by Cu and Nb in the $1:2$ ratio. Using synchrotron powder x-ray diffraction (XRD) and x-ray absorption fine structure (XAFS) spectroscopy, we investigate the microscopic nature of Cu$^{2+}$/Nb$^{5+}$ disorder on the pseudo-cubic B-sublattice and its relation to the emergent random-singlet (RS) behavior evidenced at low temperatures. While XRD reveals no long-range Cu/Nb ordering and average site occupancy consistent with stoichiometry, XAFS reveals a peculiar local chemical order characterized by preferential heteroatomic Cu$:$Nb correlations. This local arrangement strongly suppresses direct Cu$:$Cu linkages, despite the Cu concentration being close to the percolation threshold of a cubic lattice. The resulting exchange network explains the absence of spin-glass freezing or long-range magnetic order in the presence of substantial antiferromagnetic interactions, as indicated by a Curie-Weiss temperature $Θ_{CW}\approx -50$ K. Instead, the magnetic susceptibility $χ(T)$ and specific heat $c_p(T)$ exhibit power-law behavior and characteristic single-parameter $T/H$ scaling over broad temperature and magnetic-field ranges, consistent with random-singlet phenomenology. Notably, at very low temperatures, the specific heat behavior transitions from $T^{1-γ}$ ($γ\approx 0.6$ from the $T/H$ scaling) in zero-field to a T-linear dependence under high field, indicating a crossover to a distinct low-energy regime whose microscopic origin remains to be established.

cond-mat.str-el

Label-free SERS Discrimination of Native Proline Hydroxylation at Single-molecule peptide by Deep Learning-assisted plasmonic nanopore

Post-translational modifications (PTMs) play essential roles in regulating protein structure, function, and cellular signalling. However, peptide level discrimination of hydroxylation at the single-molecule level remains difficult. Here, we report a particle-in-pore single-molecule surface-enhanced Raman spectroscopy (SERS) platform combined with peak occurrence frequency (POF) analysis and a one-dimensional convolutional neural network (1D-CNN) for discriminating hydroxylated and non-hydroxylated HIF peptide fragments. Three peptide pairs containing the Pro-564 hydroxylation site, with lengths of 7, 9, and 15 amino acids (AAs), were investigated. POF analysis revealed reproducible hydroxylation-dependent spectral changes in the 7AA and 9AA peptide pairs, which were attributed to changes in adsorption conformation and surface interactions. CNN-based classification achieved post-evaluation accuracies of 72.98%, 78.55%, and 89.74% for the 7AA, 9AA, and 15AA peptide pairs, respectively, with AUC values above 0.80 for all the pairs, indicating a reliable discrimination. Gradient-weighted feature visualization further showed that CNN-sensitive regions overlapped with recurrent POF features, supporting the chemical relevance of the learned classification patterns. Notably, for the 15AA peptide pair, the enhanced citrate-associated band suggests that hydroxylation can substantially alter peptide-gold nanoparticle adsorption behaviour. This adsorption-mediated effect may amplify hydroxylation-induced spectral differences and contribute to the improved discrimination accuracy despite the increased structural complexity. These results demonstrate that the particle-in-pore sensor, assisted by deep learning, can capture hydroxylation-induced spectral and adsorption changes in peptide fragments, providing a promising strategy for ultrasensitive analysis of weak PTM signatures in peptides.

physics.bio-ph

Emergent Random Spin Singlets in Disordered Spin-1/2 perovskite BaCu$_{1/3}$Ta$_{2/3}$O$_3$

We investigate the disordered perovskite BaCu$_{1/3}$Ta$_{2/3}$O$_3$, where Cu (spin-1/2) and Ta randomly occupy a pseudo-cubic lattice. Synchrotron X-ray diffraction and X-ray absorption spectroscopy establish the local nature of the disorder, revealing the presence of structurally constrained magnetic exchange paths. No magnetic ordering or spin freezing is observed down to 0.1 K. The low-temperature magnetic and thermodynamic behavior is captured by a broad but non-singular distribution $P(J)$ of exchange couplings $J$. These results open the possibility of realizing a disordered quantum ground state where the exchange randomness is broad yet intrinsically bounded, departing from the conventional infinite-randomness fixed point driven random-singlet phase.

cond-mat.str-el

Novel multifunctional plasmonic fiber probe: Enabling plasmonic heating and SERS sensing for biomedical applications

Optical fiber-based platforms are increasingly explored as compact, minimally invasive tools for integrated photonic functionalities in biomedical applications. Among these, the combination of plasmonic heating and optical sensing on a single fiber tip offers compelling opportunities for localized photothermal actuation and in situ molecular detection. In this work, we present a multifunctional plasmonic fiber probe (PFP) that enables spectral multiplexing of thermo-plasmonic heating and surface-enhanced Raman spectroscopy (SERS). This dual capability is achieved by integrating gold nanoislands (AuNIs) onto the flat facet of a multimode optical fiber using a solid-state dewetting process - a straightforward and scalable fabrication method that avoids the complexity of lithographic techniques. We characterize how the morphology of the AuNIs modulates optical extinction, photothermal response, and electromagnetic field enhancement across the visible and near-infrared spectrum. Specifically, we demonstrate efficient, wavelength-dependent heating under visible light and strong SERS signal enhancement under near-infrared excitation, both supported by electromagnetic and thermal simulations. The ability to decouple photothermal stimulation and Raman sensing in a single, fiber-integrated device addresses a current gap in lab-on-fiber technologies, where multifunctional operation is often constrained to a single wavelength.

physics.med-ph

Label-free SERS Discrimination of Proline from Hydroxylated Proline at Single-molecule Level Assisted by a Deep Learning Model

Discriminating the low-abundance hydroxylated proline from hydroxylated proline is crucial for monitoring diseases and eval-uating therapeutic outcomes that require single-molecule sensors. While the plasmonic nanopore sensor can detect the hydrox-ylation with single-molecule sensitivity by surface enhanced Raman spectroscopy (SERS), it suffers from intrinsic fluctuations of single-molecule signals as well as strong interference from citrates. Here, we used the occurrence frequency histogram of the single-molecule SERS peaks to extract overall dataset spectral features, overcome the signal fluctuations and investigate the citrate-replaced plasmonic nanopore sensors for clean and distinguishable signals of proline and hydroxylated proline. By ligand exchange of the citrates by analyte molecules, the representative peaks of citrates decreased with incubation time, prov-ing occupation of the plasmonic hot spot by the analytes. As a result, the discrimination of the single-molecule SERS signals of proline and hydroxylated proline was possible with the convolutional neural network model with 96.6% accuracy.

physics.chem-ph

Local electronic properties of La3Ni2O7 under pressure

The recent discovery of superconductivity in $\rm La_3Ni_2O_7$ has attracted significant attention due to its high critical temperature and analogy to cuprate oxides. The oxidation and spin states of Ni ions are among the most important local properties in this compound, extensively discussed in the context of its superconductivity. Despite their direct link to the electron filling configurations of the relevant $\rm 3d_{x^2-y^2}$ and $\rm 3d_{z^2}$ orbitals, these local electronic properties of $\rm La_3Ni_2O_7$ yet to be systematically investigated. In this work, we address this issue using x-ray absorption spectroscopy (XAS) and x-ray emission spectroscopy (XES) measurements under pressure. Comparison of Ni \textit{K}-edge XAS and $\rm Kβ$ XES with the reference spectra of $\rm NiO$ and $\rm LaNiO_3$ shows that Ni ions, with an average valence of $\sim 2.53+$, are in a low-spin ($\rm S = 1/2$) ground state under ambient conditions. High pressure XAS and XES data clearly show that the oxidation ($\sim 2.5+$) and spin ($\rm S = 1/2$) states of Ni ions remain stable across the investigated pressure (up to 30 GPa) and temperature (down to 10 K) ranges, ruling out previously proposed spin transition scenarios.

cond-mat.supr-con

SAPNet: a deep learning model for identification of single-molecule peptide post-translational modifications with surface enhanced Raman spectroscopy

Nanopore resistive pulse sensors are emerging technologies for single-molecule protein sequencing. But they can hardly detect small post-translational modifications (PTMs) such as hydroxylation in single-molecule level. While a combination of surface enhanced Raman spectroscopy (SERS) with plasmonic nanopores can detect the small PTMs, the blinking Raman peaks in the single-molecule SERS spectra leads to a big challenge in data analysis and PTM identification. Herein, we developed and validated a one-dimensional convolutional neural network (1D-CNN) for amino acids and peptides identification from their PTMs including hydroxylation and phosphorylation by their single-molecule SERS spectra, named Single Amino acid and Peptide Network (SAPNet). Our work combines cutting-edge plasmonic nanopore technology for SERS signal acquisition and deep learning for fully automated extraction of information from the SERS signals. The SAPNet model achieved an overall accuracy of 99.66% for the identification of amino acids from their modification, and 98.38% for the identification of peptides from their PTM translation. We also evaluated the model with out-of-sample examples with good performance. Our work can be beneficial for early detection of diseases such as cancers and Alzheimer's disease.

q-bio.QM

Nanofluidic trapping and enhanced Raman detection of single biomolecules in plasmonic bowl-shaped nanopore

Solid-state nanopores are emerging platforms for single-molecule protein sequencing due to their tolerance to hash physiology environment and compatibility with different electrical and optical detection methods. However, they suffer from poor molecular manipulations that were twisted with and thus limited by the detection methods. Here, we report a bowl-shaped plasmonic gold nanopore on silicon nitride with hydrogel to demonstrate near-field nanofluidic manipulation of DNA translocation for plasmon-enhanced Raman spectroscopic detection. The hydrogel linearized the DNA, and the linear DNA was trapped in the nanopore for tens of seconds due assumably to bipolar effect of the nanopore that generate electroosmotic sheath flow and bipolar surface charge distribution. Their combination led to a near-field confinement of the DNA in the nanopore hot spot to allow stable Raman detection. We envision that a combination of Raman spectroscopy with the bowl-shaped nanopores can succeed in single-molecule protein sequencing in a label-free way

physics.app-ph

High sensitivity nanoporous gold metamaterials for plasmonic sensing

Surface Plasmon Resonance sensors are a well-established class of sensors which includes a very large variety of materials and detection schemes. However, the development of portable devices is still challenging as due to the intrinsic complexity of the optical excitation/detection schemes. In this work we show that Nanoporous gold (NPG) films may overcome these limitations by providing excellent sensitivity without the need of sophisticated fabrication approaches and/or optical setup. The sensing mechanism is related the co-localization of optical energy and analytes into the pores that promote an enhanced light-matter coupling. As result, when molecules are adsorbed into the pores, the NPG film shows a significant spectral shift of the effective plasma frequency and then an abrupt change of the reflectivity. By monitoring the reflectivity in the spectral region close to the plasma frequency (namely the plasma edge) is then possible to detect the analyte. Through a set of experiments we demonstrated a sensitivity exceeding 15.000 nm/RIU in the Near Infrared Range that is comparable with the state of the art of plasmonic metamaterials.

physics.app-ph

Nonlinear Hall effect as a local probe of plasmonic magnetic hot spots

Recently developed plasmonic nanostructures are able to generate intense and localized magnetic hot spots in a large spectral range from the terahertz to the visible. However, a direct measurement of the magnetic field at the hot spot has not been performed yet, due to the absence of magnetic field detectors that work at those high frequencies and that fit the hot-spot area. We propose to place a graphene ribbon in the hot spot of a plasmonic nanostructure driven by a laser beam, such that a current is generated due to both the magnetic field at the hot spot and the electric field of the laser. We demonstrate that a nonlinear Hall voltage, which can be measured by standard electrical means, builds up across the ribbon, making it possible to directly probe the magnetic field at the hot spot.

cond-mat.mes-hall

X-ray study of krypton and xenon under pressure reveals the mechanism of martensitic transformations

The martensitic transformation is a fundamental physical phenomenon at the origin of important industrial applications. However, the underlying microscopic mechanism, which is of critical importance to explain the outstanding mechanical properties of martensitic materials, is still not fully understood. This is because for most martensitic materials the transformation is a fast process that makes in situ studies extremely challenging. Noble solids krypton and xenon undergo a progressive pressure induced fcc to hcp martensitic transition with a very wide coexistence domain. Here, we took advantage of this unique feature to study the detailed mechanism of the transformation by employing in situ X-ray diffraction and absorption. We evidenced a four stages mechanism where the lattice mismatch between the fcc and hcp forms plays a key role in the generation of strain. We also determined precisely the effect of the transformation on the compression behavior of these materials.

cond-mat.mtrl-sci

Magnetic Circular Dichroism in Hyperbolic Metamaterial Nanoparticles

The optical properties of some nanomaterials can be controlled by an external magnetic field, providing active functionalities for a wide range of applications, from single-molecule sensing to nanoscale nonreciprocal optical isolation. Materials with broadband tunable magneto-optical response are therefore highly desired for various components in next-generation integrated photonic nanodevices. Concurrently, hyperbolic metamaterials received a lot of attention in the past decade since they exhibit unusual properties that are rarely observed in nature and provide an ideal platform to control the optical response at the nanoscale via careful design of the effective permittivity tensor, surpassing the possibilities of conventional systems. Here, we experimentally study magnetic circular dichroism in a metasurface made of type-II hyperbolic nanoparticles on a transparent substrate. Numerical simulations confirm the experimental findings, and an analytical model is established to explain the physical origin of the observed magneto-optical effects, which can be described in terms of the coupling of fundamental electric and magnetic dipole modes with an external magnetic field. Our system paves the way for the development of nanophotonic active devices combining the benefits of sub-wavelength light manipulation in hyperbolic metamaterials supporting a large density of optical states with the ability to freely tune the magneto-optical response via control over the anisotropic permittivity of the system.

physics.optics

Enhanced nonlinear optical response of single metal-dielectric nanocavities resonating in the near-infrared

Harmonic generation mechanisms are of great interest in nanoscience and nanotechnology, since they allow generating visible light by using near-infrared radiation, which is particularly suitable for its endless applications in bio-nanophotonics and opto-electronics. In this context, multilayer metal-dielectric nanocavities are widely used for light confinement and waveguiding at the nanoscale. They exhibit intense and localized resonances that can be conveniently tuned in the near-infrared and are therefore ideal for enhancing nonlinear effects in this spectral range. In this work, we experimentally investigate the nonlinear optical response of multilayer metal-dielectric nanocavities. By engineering their absorption efficiency and exploiting their intrinsic interface-induced symmetry breaking, we achieve one order of magnitude higher second-harmonic generation efficiency compared to gold nanostructures featuring the same geometry and resonant behavior. In particular, while the third order nonlinear susceptibility is comparable with that of bulk Au, we estimate a second order nonlinear susceptibility of the order of 1 pm/V, which is comparable with that of typical nonlinear crystals. We envision that our system, which combines the advantages of both plasmonic and dielectric materials, might enable the realization of composite and multi-functional nano-systems for an efficient manipulation of nonlinear optical processes at the nanoscale.

physics.optics

Hyperbolic Metamaterial Nanoparticles for Efficient Hyperthermia in the II and III Near-Infrared Windows

The use of gold nanoparticles for hyperthermia therapy in near infrared (NIR) spectral regions has catalysed substantial research efforts due to the potential impact in clinical therapy applications. However, the photoscattering effect scaling with the square of the nanoparticle volume leads to a low absorption efficiency, which has hindered the utility of gold nanoparticles in NIR II regions above 1000 nm. Here, we conquer this limit by introducing hyperbolic metamaterial nanoparticles that are made of multi-layered gold/dielectric nanodisks and exhibit >70% absorption efficiency in the NIR II and III regions. Their high light-to-heat conversion is demonstrated by a much larger temperature increase than that of gold nanodisks with the same amount of gold. Efficient in vitro hyperthermia of living cells with negligible cytotoxicity shows the potential of our approach for next-generation bio-medical applications.

physics.app-ph

lambda DNA through a plasmonic nanopore What can be detected by means of Surface Enhanced Raman Scattering?

Engineered electromagnetic fields in plasmonic nanopores enable enhanced optical detection and their use in single molecule sequencing. Here, a plasmonic nanopore prepared in a thick nanoporous film is used to investigate the interaction between the metal and a long-chain double strand DNA molecule. We discuss how the matrix of nanoporous metal can interact with the molecule thanks to: i) transient aspecific interactions between the porous surface and DNA and ii) optical forces exerted by the localized field in a metallic nanostructure. A duration of interaction up to tens of milliseconds enables to collect high signal-to-noise Raman vibrations allowing an easy label-free reading of information from the DNA molecule. Moreover, in order to further increase the event of detection rate, we tested a polymeric porous hydrogel placed beneath the solid-state membrane. This approach enables a slowdown of the molecule diffusion, thus increasing the number of detected interactions by a factor of about 20.

physics.app-ph

Designer Bloch Plasmon Polariton Dispersion in Hyperbolic Meta-Gratings

Hyperbolic metamaterials (HMMs) represent a novel class of fascinating anisotropic plasmonic materials, supporting highly confined propagating plasmon polaritons in addition to surface plasmon polaritons. However, it is very challenging to tailor and excite these modes at optical frequencies by prism coupling because of the intrinsic difficulties in engineering non-traditional optical properties with artificial nanostructures and the unavailability of high refractive index prisms for matching the momentum between the incident light and the guided modes. Here, we report the mechanism of excitation of high-k Bloch-like Plasmon Polariton (BPPs) modes with ultrasmall modal volume using a meta-grating, which is a combined structure of a metallic diffraction grating and a type II HMM. We show how a 1D plasmonic grating without any mode in the infrared spectral range, if coupled to a HMM supporting high-k modes, can efficiently enable the excitation of these modes via coupling to far-field radiation. Our theoretical predictions are confirmed by reflection measurements as a function of angle of incidence and excitation wavelength. We introduce design principles to achieve a full control of high-k modes in meta-gratings, thus enabling a better understanding of light-matter interaction in this type of hybrid meta-structures. The proposed spectral response engineering is expected to find potential applications in bio-chemical sensors, integrated optics and optical sub-wavelength imaging.

physics.optics

SERS discrimination of single amino acid residue in single peptide by plasmonic nanocavities

Surface-enhanced Raman spectroscopy (SERS) is a sensitive label-free optical method that can provide fingerprint Raman spectra of biomolecules such as DNA, amino acids and proteins. While SERS of single DNA molecule has been recently demonstrated, Raman analysis of single protein sequence was not possible because the SERS spectra of proteins are usually dominated by signals of aromatic amino acid residues. Here, we used electroplasmonic approach to trap single gold nanoparticle in a nanohole for generating a plasmonic nanocavity between the trapped nanoparticle and the nanopore wall. The giant field generated in the nanocavity was so sensitive and localized that it enables SERS discrimination of 10 distinct amino acids at single-molecule level. The obtained spectra are used to analyze the spectra of 2 biomarkers (Vasopressin and Oxytocin) made of a short sequence of 9 amino-acids. Significantly, we demonstrated identification of single non-aromatic amino acid residues in a single short peptide chain as well as discrimination between two peptides with sequences distinguishable in 2 specific amino-acids. Our result demonstrate the high sensitivity of our method to identify single amino acid residue in a protein chain and a potential for further applications in proteomics and single-protein sequencing.

q-bio.QM