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Plasticity and ductility in graphene oxide through a mechanochemically induced damage tolerance mechanism

Year: 2015

Journal: NATURE COMMUNICATIONS, Vol. 6, p -, 20170208

Authors: Wei, Xiaoding; Mao, Lily; Soler-Crespo, Rafael A.; Paci, Jeffrey T.; Huang, Jiaxing; Nguyen, SonBinh T.; Espinosa, Horacio D.

Organizations: Northwestern Univ, Dept Mech Engn, Evanston, IL 60208 USA; Northwestern Univ, Theoret & Appl Mech Program, Evanston, IL 60208 USA; Northwestern Univ, Dept Chem, Evanston, IL 60208 USA; Univ Victoria, Dept Chem, Victoria, BC V8W 3V6, Canada; Northwestern Univ, Dept Mat Sci & Engn, Evanston, IL 60208 USA

The ability to bias chemical reaction pathways is a fundamental goal for chemists and material scientists to produce innovative materials. Recently, two-dimensional materials have emerged as potential platforms for exploring novel mechanically activated chemical reactions. Here we report a mechanochemical phenomenon in graphene oxide membranes, covalent epoxide-to-ether functional group transformations that deviate from epoxide ring-opening reactions, discovered through nanomechanical experiments and density functional-based tight binding calculations. These mechanochemical transformations in a two-dimensional system are directionally dependent, and confer pronounced plasticity and damage tolerance to graphene oxide monolayers. Additional experiments on chemically modified graphene oxide membranes, with ring-opened epoxide groups, verify this unique deformation mechanism. These studies establish graphene oxide as a two-dimensional building block with highly tuneable mechanical properties for the design of high-performance nanocomposites, and stimulate the discovery of new bond-selective chemical transformations in two-dimensional materials.