T132 Environmental Mineralogy
Sunday, 5 October 2008
8:00 AM - 12:00 PM
The Origin of Nano-Scale Stability Reversals in Titanium Oxide Minerals
Paper number: T132-14
Program: Technical Sessions
Time: 11:00 AM – 11:15 AM
Authors
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Peter J. HeaneyPenn State University, University Park, PA
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James D. KubickiThe Pennsylvania State University, University Park, PA
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Jeffrey PostSmithsonian Institution, Washington, DC
Abstract
Density functional theory (DFT) calculations were employed to model the energetics of nano-sized anatase and rutile using our refined structures. The calculated change in free energy between the incipient, surface-strained nanoparticles and the final microcrystals was only ~ 0.5 kJ/mol for each phase, far less than the 6 kJ/mol difference in free energy of formation between the two minerals needed to account for stability reversal. Surface energy calculations of model 1 and 2 nm nanoparticles did yield lower surface energies for anatase than for rutile by ~ 16 kJ/mol for both particle sizes, but these whole-particle surface energies were much higher than the sum of energies of each particle's constituent crystallographic surfaces. We attribute the excess energy to defects associated with the edges and corners of nanoparticles which are not present on a 2-D periodic surface. This previously unreported edge and corner energy may play a dominant role in the stability reversal of nanocrystalline titanium oxides, as well as other mineral systems susceptible to reversals in phase stability at the nano-scale.