Direct Visualization of Single Ions in the Stern Layer of Calcite

Calcite is among the most abundant minerals on earth and plays a central role in many environmental and geochemical processes. Here we used amplitude modulation atomic force microscopy (AFM) operated in a particular regime to visualize single ions close to the (10 (1) over bar4) surface of calcite in solution. The results were acquired at equilibrium, in aqueous solution containing different concentrations of NaCl, RbCl, and CaCl2. The AFM images provide a direct and atomic-level picture of the different cations adsorbed preferentially at certain locations of the calcite water interface. Highly ordered water layers at the calcite surface prevent the hydrated ions from directly interacting with calcite due to the energy penalty incurred by the necessary restructuring of the ions' solvation shells. Controlled removal of the adsorbed ions from the interface by the AFM tip provides indications about the stability of the adsorption site. The AFM results show the familiar "row pairing" of the carbonate oxygen atoms, with the adsorbed monovalent cations located adjacent to the most prominent oxygen atoms. The location of adsorbed cations near the surface appears better defined for monovalent ions than for Ca2+, consistent with the idea that Ca2+ ions remain further away from the surface of calcite due to their larger hydration shell. The precise distance between the different hydrated ions and the surface of calcite is quantified using MD simulation. The preferential adsorption sites found by MD as well as the ion residence times close to the surface support the AFM findings, with Na+ ions dwelling substantially longer and closer to the calcite surface than Ca2+. The results also bring new insights into the problem of the Stern and electrostatic double layer at the surface of calcite, showing that parameters such as the thickness of the Stern layer can be highly ion dependent.

Characterization of Solid-Liquid Interfaces with High-Resolution Atomic Force Microscop

Maria Ricci

Solid-liquid interfaces are ubiquitous. Despite the unquestioned relevance, many scientific research fields rely on simplified or macroscopic descriptions, discarding the molecular nature of the constituents. However, it is the specific molecular interactions and the complex chemistry in the interfacial region that are fundamental in phenomena such as heterogeneous catalysis, electrochemistry, crystal growth, membrane transport and body-antibody recognition. In particular, the models used to describe the so-called electrical double layer of ionic distributions at charged surfaces in liquid, are based on continuum assumptions. For example, the Gouy-Chapman-Stern model assumes that a dense, homogenously distributed layer with a thickness of a hydrated ion (referred to as the "Stern layer"), is adsorbed onto the charged surface, proceeded by an exponentially decaying diffuse ionic cloud, in which ions are point charges in a continuous dielectric media. In this thesis, I will first illustrate how the assumption of a homogeneous ion lateral density in the Stern Layer fails to describe the actual solid-water interface of several relevant surfaces. Then I will show how the lateral organization of the ions indeed plays a role as important as the vertical modulation of the charge distribution. This is because the molecular nature of the ions, the surface, and the water molecules themselves each contribute to the precise lateral organization of the constituents. As result, the ions can reside on discrete surface sites, defined both laterally and vertically in space. Moreover, the water-mediated interaction can impart a correlation in the reciprocal lateral distribution of the ions. To achieve this level of description, high-resolution atomic force microscopy (AFM) is used. Unlike most of other experimental techniques, AFM is able to characterize interfaces locally at the atomic/molecular level. In fact, in the AFM small-amplitude regime, detection of even single ions adsorbed at the surface of the solid is possible by measuring the perturbation they induce on the local solvation environment. This capability represents an invaluable tool for the exploration of phenomena occurring at the Stern layer of solid-liquid interfaces. Following, I will investigate the properties of several solid-aqueous interfaces in the presence of different ionic concentrations and species, ranging from hard (mica) to soft systems such as organic self-assembled monolayers, lipid bilayers, and the dynamic surface restructuring of calcite when covered with fatty acid molecules. The experimental study, combined with molecular dynamic simulations, reveals a water-induced ion-ion attractive interaction for some ionic species. These results show that water alone is the driving force to induce order within the Stern layer, creating hydration-correlation effects on mica, self-assembled monolayers and possibly lipid bilayers. The local modulation of the hydration properties of the surface is fundamental to highly dynamic systems such as calcite, where steps act as nucleating points for the processes of dissolution and growth. The specific interaction of foreign ions and fatty acids modify these processes as well as the equilibrium between the crystal and the solution. This thesis provides clear experimental evidence of new mechanisms developing at solid-liquid interfaces paving the way for a deeper and more conscious understanding of the colloidal properties of materials.

EPFL2015

Atomic force microscopy studies of nanotribology and nanomechanics

Ismaël Palaci

This thesis comes within the scope of tribology studies at the nanometer scale. The experimental techniques used in this work are essentially related to atomic force microscopy, which gives a direct access to the topography and forces of the studied systems. Two principal aspects of the nanotribology have kept our attention. They are the nanofriction and the nanomechanics. These two domains divide the thesis in two main parts that remain however intimately bound. The first experimental part of the thesis describes the friction of a nanoscopic tip sliding on hydrophilic surfaces. The dependence of the friction force on the sliding velocity is studied for various applied normal loads and surrounding relative humidity levels. We found a logarithmic dependence of the friction force on both the scanning velocity and the relative humidity. For the first time, a transition from a positive to a negative slope of the friction force versus the logarithm of the sliding velocity has been observed for the very same tip-surface contact, by varying the relative humidity. The role of the relative humidity on the friction force has then been studied more deeply, leading to a two-thirds power law dependence of the capillary force on the normal load. Finally, analytical expressions for the friction phenomenon and the capillary condensation between the asperities of the tip and the surface have been developed to explain the phenomenological behaviors. The second experimental part describes themechanics of carbon nanotubes and tobacco mosaic viruses. In order to stay in the linear elasticity regime, small indentation amplitudes have been applied in the radial direction of multiwalled carbon nanotubes adsorbed on a silicon oxide surface. Using a theory based on the Hertz model, the radial stiffness has been evaluated and compared to molecular dynamics simulations. We found a radial Young modulus strongly decreasing with increasing radius and reaching an asymptotic value of 30 ± 10 GPa. The tobacco mosaic viruses have been adsorbed on a polyimide porous membrane. Evidence for the softness of the viruses has been obtained by imaging the tubes with the atomic force microscope in non-contact mode. Viruses hanging like ropes over the pores of the surface served as basis to measure their bending Young modulus. Using a model of a clamped beam loaded by a discrete gradient of van der Waals forces, we found a bending Young modulus of 3.1 ± 0.1 MPa.

EPFL2007

Atomic force microscopy studies of nanotribology and nanomechanics

Ismaël Palaci

EPFL2007

Characterization of Solid-Liquid Interfaces with High-Resolution Atomic Force Microscop

Maria Ricci

EPFL2015