Maidenberg Daniel A, Volksen Willi, Miller Robert D, Dauskardt Reinhold H
Department of Materials Science and Engineering, Stanford University, 416 Escondido Mall, Stanford, California 94305-2205, USA.
Nat Mater. 2004 Jul;3(7):464-9. doi: 10.1038/nmat1153. Epub 2004 Jun 27.
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 approximately 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.
纳米多孔玻璃本质上是脆性材料,随着孔隙率的增加,其脆性会越来越大。我们发现,用于制造纳米级孔隙的致孔剂分子残余物能够显著提高断裂能。对于致密的甲基倍半硅氧烷玻璃薄膜,其界面断裂能约为2.6 J m(-2),而对于孔隙率为50体积%的玻璃,其界面断裂能增加了一个多数量级,达到>30 J m(-2)。断裂阻力的增加与一种强大的分子桥接机制有关,该机制是用桥接力学建模的。该研究表明,在纳米多孔玻璃的加工过程中,采用涉及致孔剂分子可控分解的策略,可以显著提高界面断裂能。这对于一系列新兴的光学、电子和生物技术具有重要意义,这些技术使用纳米多孔薄膜,但受到随着孔隙率增加而导致的机械性能退化的限制。