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Laetitia Dalstein

Publications and source records attributed to Laetitia Dalstein.

5 recordsLinked to original sources

Terahertz-driven four-wave mixing at glass surfaces: Probing vibrational resonances and structural regimes

Disordered materials such as glasses exhibit complex structural dynamics that are challenging to probe with conventional spectroscopies. We demonstrate that terahertz-driven four-wave mixing (FWM) at glass surfaces provides direct access to low-frequency vibrational modes and structural evolution in amorphous solids. Applied to a compositional series of PbO-silicate glasses (20-54 mol% PbO), this technique resolves distinct contributions from collective Boson-peak excitations and Pb-O / Si-O network stretching modes, and tracks their systematic evolution across structurally distinct compositional regimes. The dominant vibrational frequency blueshifts with PbO content, reflecting the progressive evolution of the Pb$^{2+}$ network role from silicate-modifier to ward network-former. A pronounced enhancement of the FWM signal near 44 mol% PbO coincides with the emergence of medium-range Pb-Pb correlations, while in-plane-to-out-of-plane FWM intensity ratio ($I_{\rm SS}/I_{\rm PS}$) tracks $χ^{(3)}$ tensor anisotropy tied to Pb$^{2+}$ lone-pair spatial correlations. The non-monotonic peak in both observables at 44 mol% PbO - a composition where NMR finds no change in local Pb-O coordination and Pb-O-Pb free-oxide linkages are negligible - provides direct evidence that a collective lone-pair reorganization occurs in the medium-range structure independently of nearest-neighbor bonding. These results establish terahertz-driven FWM as a bulk-sensitive, near-surface depth-confined ($\sim$50 nm) nonlinear spectroscopy sensitive to vibrational and electronic structural fingerprints inaccessible to linear infrared, Raman, and terahertz time-domain probes.

physics.optics

The Prevailing Role of Hotspots in Plasmon-Enhanced Sum-Frequency Generation Spectroscopy

The plasmonic amplification of non-linear vibrational sum frequency spectroscopy (SFG) at the surfaces of gold nanoparticles is systematically investigated by tuning the incident visible wavelength. The SFG spectra of dodecanethiol-coated gold nanoparticles chemically deposited on silicon are recorded for twenty visible wavelengths. The vibrational intensities of thiol methyl stretches extracted from the experimental measurements vary with the visible color of the SFG process and show amplification by coupling to plasmonics. Since the enhancement is maximal in the orange-red region rather than in the green, as expected from the dipolar model for surface plasmon resonances, it is attributed mostly to hotspots created in particle multimers, in spite of their low surface densities.

physics.optics

Intrinsic pH of water/vapor interface revealed by ion-induced water alignment

Protons at the water/vapor interface are relevant for atmospheric and environmental processes, yet to characterize their surface affinity on the quantitative level is still challenging. Here we utilize phase-sensitive sum-frequency vibrational spectroscopy to quantify the surface density of protons (or their hydronium form) at the intrinsic water/vapor interface, through inspecting the surface-field-induced alignment of water molecules in the electrical double layer of ions. With hydrogen halides in water, the surface adsorption of protons is found to be independent of specific proton-halide anion interactions and to follow a constant adsorption free energy, G about -3.74 (+/-0.56) kJ/mol, corresponding to a reduction of the surface pH with respect to the bulk value by 0.66 (+/-0.10), for bulk ion concentrations up to 0.3 M. Our spectroscopic study is not only of importance in atmospheric chemistry, but also offers a microscopic-level basis to develop advanced quantum-mechanical models for molecular simulations.

physics.chem-ph

Direct Quantification of Water Surface Charge by Phase-Sensitive Second Harmonic Spectroscopy

We develop and verify a phase-sensitive second harmonic generation spectroscopic scheme that allows for direct determination of the absolute surface charge density and surface potential of a water interface without need of prior interfacial information. The method relies on selective probing of surface-field-induced reorientation order of water molecules in the electrical double layer and is, hence, independent of the interfacial molecular bonding structure. Application of this technique to a mixed surfactant monolayer on water suggests the manifest effect of the chain-chain interactions among the monolayer on adsorption of soluble ionic surfactants. We also deduce the third-order nonlinear susceptibility of bulk water and prove its applicability to analysis of charges of various water interfaces. In addition, we show that the Debye-Hückle theory should be avoided in the spectroscopic analysis for its potential significant error, as evidenced experimentally and theoretically.

physics.chem-ph

Nonlinear optical response of a gold surface in the visible range: A study by two-color sum-frequency generation spectroscopy. II. Model for metal nonlinear susceptibility

We present a modeling of the nonlinear optical response of a metal surface in order to account for recent experimental results from two-color Sum-Frequency Generation experiments on gold. The model allows calculating the surface and bulk contributions, and explicitly separates free and bound electron terms. Contrary to the other contributions, the perpendicular surface component is strongly model-dependent through the surface electron density profiles. We consider three electron density schemes at the surface, with free and bound electrons overlapping or spilling out of the bulk, for its calculation. The calculated SFG signals from the metal rely only on bulk quantities and do not need an explicit definition of the density profiles. In the particular case of gold, when the free electrons overlap with the bound ones or spill out of the bulk, the free electron response completely dominates through the perpendicular surface terms. When the bound electrons spill out, the situation is more balanced, still in favor of the free electrons, with lower amplitudes and different dispersion lineshapes. As for silver, the free electron contributions dominate, and the calculated slow amplitude growth from blue to red follows the experimental trends.

physics.chem-ph