Abstract
Nanoporous glasses are inherently brittle materials that become increasingly fragile with increasing porosity. We show that remarkable increases in fracture energy can be obtained from remnants of the porogen molecules used to create the nanoscale pores. The interfacial fracture energy of ∼2.6 J m−2 for dense methylsilsesquioxane glass films is shown to increase by over one order of magnitude to >30 J m−2 for glasses containing 50 vol.% porosity. The increased fracture resistance is related to a powerful molecular-bridging mechanism that was modelled using bridging mechanics. The study demonstrates that significant increases in interfacial fracture energy may be obtained using strategies involving controlled decomposition of the porogen molecule during processing of nanoporous glasses. The implications are important for a range of emerging optical, electronic and biological technologies that use nanoporous thin films, but are limited by the degradation of mechanical properties with increasing porosity.
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Acknowledgements
Work was supported primarily by a seed grant from the Stanford-CPIMA MRSEC Program of the National Science Foundation under Award Number DMR -0213618.
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Maidenberg, D., Volksen, W., Miller, R. et al. Toughening of nanoporous glasses using porogen residuals. Nature Mater 3, 464–469 (2004). https://doi.org/10.1038/nmat1153
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DOI: https://doi.org/10.1038/nmat1153
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