Order Remains Interior to a Ceramic Ionic Nanocluster Sterically Hindered by Covalently Attached Polymer Segments
Leiyu Jia , Junji Wu , Zixin Yu , Yuan Chen , Yao Xu , Jie Wang , Zhen Hu , Chuanqun Hu , Dachuan Ding , Bin Yang , Tao Hu , Xinghou Gong , Juan Wang , Jan-Michael Albina , Chonggang Wu , Masanori Hara
Journal of Wuhan University of Technology Materials Science Edition ›› 2026, Vol. 41 ›› Issue (2) : 537 -546.
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.
ceramic ionic nanocluster / polymer chain segment / morphology / order / molecular dynamics simulation
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Wuhan University of Technology and Springer-Verlag GmbH Germany, Part of Springer Nature
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