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Mass Transfer in a Nanoscale Material Enhanced by an Opposing Flux

Source: Phys. Rev. Lett. 104, 085902 (2010); doi:10.1103/PhysRevLett.104.085902

Published 25 February 2010

PACS
  • 66.30.Pa
    Diffusion in nanoscale solids
  • 68.43.Jk
    Diffusion of adsorbates, kinetics of coarsening and aggregation
  • YEAR: 2010
PUBLICATION DATA
ISSN:
1553-9644 (online)
Publisher:
AIP is a member of CrossRef APS
Christian Chmelik,1 Helge Bux,2 Jürgen Caro,2 Lars Heinke,1,3 Florian Hibbe,1 Tobias Titze,1 and Jörg Kärger1
1Leipzig University, Faculty of Physics and Geosciences, Linnéstrasse 5, D-04103 Leipzig, Germany
2Leibniz University Hannover, Institute of Physical Chemistry and Electrochemistry, Callinstrasse 3a, D-30167 Hannover, Germany
3Fritz-Haber-Institute of the Max-Planck-Society, Faradayweg 4-6, D-14195 Berlin, Germany

Diffusion is known to be quantified by measuring the rate of molecular fluxes in the direction of falling concentration. In contrast with intuition, considering methanol diffusion in a novel type of nanoporous material (MOF ZIF-8), this rate has now been found to be enhanced rather than slowed down by an opposing flux of labeled molecules. In terms of the key quantities of random particle movement, this result means that the self-diffusivity exceeds the transport diffusivity. It is rationalized by considering the strong intermolecular interaction and the dominating role of intercage hopping in mass transfer in the systems under study. ©2010 The American Physical Society
History: Received 16 November 2009; published 25 February 2010
Permalink: http://link.aps.org/abstract/PRL/v104/e085902
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