Order Remains Interior to a Ceramic Ionic Nanocluster Sterically Hindered by Covalently Attached Polymer Segments
摘要
When a ceramic ionic-crystal nanocluster is group-substituted with polymer chain segments to form an ionomeric aggregate, is the ordered structure maintained within the sterically hindered nanocluster? We observed, for Na-salt sulfonated polystyrene ionomer, the electron-diffraction lattice fringes of the nanoclusters, which proved their internal crystalline ordering driven by electrostatic attractions overcoming steric hindrance. Kinetically, the nanoclusters’ enhanced melting endotherm upon aging indicate their quasi-, slow-ordering character. Extended tight binding molecular dynamics simulations provide an insight into the mechanism underlying the ionic-group aggregation during nanoclustering. We hence proposed an uncommon state of order, polymer-bound ceramic quasicrystal, supplementary to the order phenomena in crystalline ceramics.