Strong Catalytic Activity Of Iron Nanoparticles On The Surfaces Of Reduced Olivine

It is demonstrated that olivine powders heated to subsolidus temperatures in reducing conditions can develop significant concentrations of 10–50 nm diameter Fe nanoparticles on grain surfaces and that these display strong catalytic activity not observed in powders without Fe nanoparticles. Reduced surfaces were exposed to NH3, CO, and H2, volatiles that may be present on the surfaces of comet and volatile-rich asteroids. In the case of NH3 exposure, rapid decomposition was observed. When exposed to a mixture of CO and H2, significant coking of the mineral surfaces occurred. Analysis of the mineral grains after reaction indicated primarily the presence of graphene or graphitic carbon. The results demonstrate that strong chemical activity can be expected at powders that contain nanophase Fe particles. This suggests space-weathered mineral surfaces may play an important role in the synthesis and processing of organic species. This processing may be part of the weathering processes of volatile-rich but atmosphereless solar-system bodies

Role Of Surface Chemistry In Grain Adhesion And Dissipation During Collisions Of Silica Nanograins

The accretion of dust grains to form larger objects, including planetesimals, is a central problem in planetary science. It is generally thought that weak van der Waals interactions play a role in accretion at small scales where gravitational attraction is negligible. However, it is likely that in many instances, chemical reactions also play an important role, and the particular chemical environment on the surface could determine the outcomes of dust grain collisions. Using atomic-scale simulations of collisional aggregation of nanometer-sized silica (SiO2) grains, we demonstrate that surface hydroxylation can act to weaken adhesive forces and reduce the ability of mineral grains to dissipate kinetic energy during collisions. The results suggest that surface passivation of dangling bonds, which generally is quite complete in an Earth environment, should tend to render mineral grains less likely to adhere during collisions. It is shown that during collisions, interactions scale with interparticle distance in a manner consistent with the formation of strong chemical bonds. Finally, it is demonstrated that in the case of collisions of nanometer-scale grains with no angular momentum, adhesion can occur even for relative velocities of several kilometers per second. These results have significant implications for early planet formation processes, potentially expanding the range of collision velocities over which larger dust grains can form

Atomic-scale simulation of space weathering in olivine and orthopyroxene

Classical molecular dynamics was used to study the annealing of anion and cation Frenkel defects in olivine and orthopyroxene minerals. While it was found that for both minerals, reorganization of the Si-O bonds, often accompanied by large Si displacements, occurs to maintain the fourfold coordination of the SiO4 tetrahedra, important differences are observed in their annealing behavior. Specifically, cation defects are substantially more mobile in olivine than in orthopyroxene leading to rapid annihilation of cation Frenkel defects and formation of extended defects in olivine. By contrast, the diffusion rate of anion defects in orthopyroxene is much higher than that in olivine and also exhibits large anisotropy. Consequently, it was found that diffusion in orthopyroxene occurs without significant annihilation of anion Frenkel defects or trapping of anion interstitials or vacancies into clusters. The results obtained here are discussed in the context of space weathering of olivine and orthopyroxene. Specifically, two important observations are made which may explain previous experimental results. First, ion irradiation experiments that show reduced tolerance for radiation damage in orthopyroxene may be explained by the rapid, one-dimensional anion mobility which prevents healing of the lattice. Second, laser heating experiments which show that orthopyroxene has enhanced tolerance to reduction and the evolution of nanophase Fe inclusions could be due to the observed rapid anion diffusion in orthopyroxene, which might allow the bulk to act as a reservoir for the surface