Metallic contamination was key to the discovery of semiconductor nanowires, but today it stands in the way of their adoption by the semiconductor industry. This is because many of the metallic catalysts required for nanowire growth are not compatible
with standard CMOS (complementary metal oxide semiconductor) fabrication processes. Nanowire synthesis with those metals which are CMOS compatible, such as aluminium and copper, necessitate temperatures higher than 450 C, which is the maximum temperature allowed in CMOS processing. Here, we demonstrate that the synthesis temperature of silicon nanowires using copper based catalysts is limited by catalyst preparation. We show that the appropriate catalyst can be produced by chemical means at temperatures as low as 400 C. This is achieved by oxidizing the catalyst precursor, contradicting the accepted wisdom that oxygen prevents metal-catalyzed nanowire growth. By simultaneously solving material compatibility and temperature issues, this catalyst synthesis could represent an important step towards real-world applications of semiconductor nanowires.
An unusual increase of the conductance with temperature is observed in clean quantum point contacts for conductances larger than 2e^2/h. At the same time a positive magnetoresistance arises at high temperatures. A model accounting for electron-electr
on interactions mediated by bound- aries (scattering on Friedel oscillations) qualitatively describes the observation. It is supported by numerical simulation at zero magnetic field.
Pressure solution creep rates and interface structures have been measured by two methods on calcite single crystals. In the first kind of experiments, calcite monocrystals were indented at 40 degrees C for six weeks using ceramic indenters under stre
sses in the 50-200 MPa range in a saturated solution of calcite and in a calcite-saturated aqueous solution of NH4Cl. The deformation (depth of the hole below the indenter) is measured ex-situ at the end of the experiment. In the second type of experiment, calcite monocrystals were indented by spherical glass indenters for 200 hours under stresses in the 0-100 MPa range at room temperature in a saturated aqueous solution of calcite. The displacement of the indenter was continuously recorded using a specially constructed differential dilatometer. The experiments conducted in a calcite-saturated aqueous solution of NH4Cl show an enhanced indentation rate owing to the fairly high solubility of calcite in this solution. In contrast, the experiments conducted in a calcite-saturated aqueous solution show moderate indentation rate and the dry control experiments did not show any measurable deformation. The rate of calcite indentation is found to be inversely proportional to the indenter diameter, thus indicating that the process is diffusion-controlled. The microcracks in the dissolution region under the indenter dramatically enhance the rate of calcite indentation by a significant reduction of the distance of solute transport in the trapped fluid phase. This result indicates that care should be taken in extrapolating the kinetic data of pressure solution creep from one mineral to another.
Stylolites are spectacular rough dissolution surfaces that are found in many rock types. Despite many studies, their genesis is still debated, particularly the time scales of their formation and the relationship between this time and their morphology
. We developed a new discrete simulation technique to explore the dynamic growth of the stylolite roughness, starting from an initially flat dissolution surface. We demonstrate that the typical steep stylolite teeth geometry can accurately be modelled and reproduce natural patterns. The growth of the roughness takes place in two successive time regimes: i) an initial non-linear increase in roughness amplitude that follows a power-law in time up to ii) a critical time where the roughness amplitude saturates and stays constant.
The formation of solid calcium carbonate (CaCO3) from aqueous solutions or slurries containing calcium and carbon dioxide (CO2) is a complex process of considerable importance in the ecological, geochemical and biological areas. Moreover, the demand
for powdered CaCO3 has increased considerably recently in various fields of industry. The aim of this study was therefore to synthesize fine particles of calcite with controlled morphology by hydrothermal carbonation of calcium hydroxide at high CO2 pressure (initial PCO2=55 bar) and at moderate and high temperature (30 and 90 degrees C). The morphology of precipitated particles was identified by transmission electron microscopy (TEM/EDS) and scanning electron microscopy (SEM/EDS). In addition, an X-ray diffraction analysis was performed to investigate the carbonation efficiency and purity of the solid product. Carbonation of dispersed calcium hydroxide in the presence of supercritical (PT=90 bar, T=90 degrees C) or gaseous (PT=55 bar, T=30 degrees C) CO2 led to the precipitation of sub-micrometric isolated particles (<1$mu$m) and micrometric agglomerates (<5$mu$m) of calcite. For this study, the carbonation efficiency (Ca(OH)2-CaCO3 conversion) was not significantly affected by PT conditions after 24 h of reaction. In contrast, the initial rate of calcium carbonate precipitation increased from 4.3 mol/h in the 90bar-90 degrees C system to 15.9 mol/h in the 55bar-30 degrees C system. The use of high CO2 pressure may therefore be desirable for increasing the production rate of CaCO3, carbonation efficiency and purity, to approximately 48 kg/m3h, 95% and 96.3%, respectively in this study. The dissipated heat for this exothermic reaction was estimated by calorimetry to be -32 kJ/mol in the 90bar-90 degrees C system and -42 kJ/mol in the 55bar-30 degrees C system.
Theoretical models of compaction processes, such as for example intergranular pressure-solution (IPS), focus on deformation occurring at the contacts between spherical grains that constitute an aggregate. In order to investigate the applicability of
such models, and to quantify the deformation of particles within an aggregate, isostatic experiments were performed in cold-sealed vessels on glass sphere aggregates at 200 MPa confining pressure and 350 degrees C with varying amounts of fluid.
In order to better understand the interaction between pore-fluid overpressure and failure patterns in rocks we consider a porous elasto-plastic medium in which a laterally localized overpressure line source is imposed at depth below the free surface.
We solve numerically the fluid filtration equation coupled to the gravitational force balance and poro-elasto-plastic rheology equations. Systematic numerical simulations, varying initial stress, intrinsic material properties and geometry, show the existence of five distinct failure patterns caused by either shear banding or tensile fracturing. The value of the critical pore-fluid overpressure at the onset of failure is derived from an analytical solution that is in excellent agreement with numerical simulations. Finally, we construct a phase-diagram that predicts the domains of the different failure patterns and at the onset of failure.
We are currently measuring the dissolution kinetics of albite feldspar at 100 deg C in the presence of high levels of dissolved CO_2 (pCO_2 = 9 MPa) as a function of the saturation state of the feldspar (Gibbs free energy of reaction, Delta G). The e
xperiments are conducted using a flow through reactor, thereby allowing the dissolution reactions to occur at a fixed pH and at constant, but variable saturation states. Preliminary results indicate that at far-from-equilibrium conditions, the dissolution kinetics of albite are defined by a rate plateau, with R approx 5.0 x 10^{-10} mol m^{-2} s^{-1} at -70 < Delta G < -40 kJ mol^{-1}. At Delta G > -40 kJ mol^{-1}, the rates decrease sharply, revealing a strong inverse relation between the dissolution rate and free energy. Based on the experiments carried out to date, the dissolution rate-free energy data correspond to a highly non-linear and sigmoidal relation, in accord with recent studies.
The surface roughness of several stylolites in limestones was measured using high resolution laser profilometry. The 1D signals obtained were statistically analyzed to determine the scaling behavior and calculate a roughness exponent, also called Hur
st exponent. Statistical methods based on the characterization of a single Hurst exponent imply strong assumptions on the mathematical characteristics of the signal: the derivative of the signal (or local increments) should be stationary and have finite variance. The analysis of the measured stylolites show that these properties are not always verified simultaneously. The stylolite profiles show persistence and jumps and several stylolites are not regular, with alternating regular and irregular portions. A new statistical method is proposed here, based on a non-stationary but Gaussian model, to estimate the roughness of the profiles and quantify the heterogeneity of stylolites. This statistical method is based on two parameters: the local roughness (H) which describes the local amplitude of the stylolite, and the amount of irregularities on the signal (mu), which can be linked to the heterogeneities initially present in the rock before the stylolite formed. Using this technique, a classification of the stylolites in two families is proposed: those for which the morphology is homogeneous everywhere and those with alternating regular and irregular portions.
Hydraulic tension fractures were produced in porous limestones using a specially designed hydraulic cell. The 3D geometry of the samples was imaged using X-ray computed microtomography before and after fracturation. Using these data, it was possible
to estimate the permeability tensor of the core samples, extract the path of the rupture and compare it to the heterogeneities initially present in the rock.
