Publications by authors named "Alban Jonchere"

Second Harmonic Generation (SHG) today represents one of the most powerful techniques to selectively probe all types of interfaces. However, the origin of the SHG signal at a molecular level is still debated since the local dipole contribution, which is strongly correlated to the molecular orientation can be counterbalanced by non-local quadrupole contributions. Here, we propose a method to simulate the SHG signal of a model water/air interface from the molecular response of each contribution.

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Article Synopsis
  • Second harmonic generation (SHG) is a technique that helps monitor surface dynamics and reactions, especially at interfaces, but its molecular origins are not well understood.
  • A new method has been developed to predict and interpret SHG signals at an atomic level without relying on traditional concepts, revealing that bulk quadrupole contributions are more significant than previously thought.
  • This breakthrough aligns simulated SHG responses with experimental data and emphasizes the importance of bulk effects over interface-specific characteristics, potentially changing how SHG signals are interpreted in various contexts.
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Hypothesis: Weakly hydrated nanometric ions, called superchaotropes, were recently shown to adsorb strongly to non-ionic surfaces affecting drastically the surface's physical-chemical properties due to a charging effect. Superchaotropic ions could serve as stabilizing agents for non-ionic colloidal systems, such as non-ionic surfactant foams.

Experiments: We study foams of the non-ionic surfactant BrijO10 (CE) without and in presence of the superchaotropic Keggin-ion SiWO (SiW).

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Metalla-bis-dicarbollides, such as the cobalta-bis-dicarbollide (COSAN) anion [Co(C B H ) ] , have attracted much attention in biology but a deep understanding of their interactions with cell components is still missing. For this purpose, we studied the interactions of COSAN with the glucose moiety, which is ubiquitous at biological interfaces. Octyl-glucopyranoside surfactant (C8G1) was chosen as a model as it self-assembles in water and creates a hydrated glucose-covered interface.

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Owing to their multiple charges and their nanometric size, polyoxometalates (POMs) are at the frontier between ions and charged colloids. We investigated here the effect of POM-POM electrostatics repulsions on their self-diffusion in water by varying POM and supporting salt concentrations. The self-diffusion coefficients of two Keggin's POMs [silicotungstate (SiWO) and phosphotungstate (PWO)] were determined by dynamic light scattering (DLS) and H/P DOSY NMR, whereas POM-POM electrostatic repulsions were investigated by the determination of the static structure factors using small-angle X-ray scattering (SAXS).

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Three different liquid interfaces, water/air, thiophene/air, and water/thiophene, were probed using the second harmonic generation (SHG) technique. Thiophene and water have been chosen because the hyperpolarizability of these molecules has already been measured or calculated and the different values can be found in literature. We have studied the microscopic structure of these interfaces by comparing the components of the second order susceptibility tensor determined from the SHG polarization curve analysis with those determined via a molecular dynamics (MD) simulation of these interfaces.

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Because of their amphiphilic structure, surfactants adsorb at the water-air interface with their hydrophobic tails pointing out of the water and their polar heads plunging into the liquid phase. Unlike classical surfactants, metallabisdicarbollides (MCs) do not have a well-defined amphiphilic structure. They are nanometer-sized inorganic anions with an ellipsoidal shape composed of two carborane semicages sandwiching a metal ion.

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