Source abstract
Abstract
It is very important to improve the electrical conductivity of polymer nanocomposites (PNCs) which can widen their application. In this work, a coarse-grained molecular dynamics simulation is adopted to investigate the effect of the nanoparticle (NP) functionalization on the formation of the conductive network under the quiescent state or under the shear field, which is denoted by the conductive probability. First, the dispersion state of NPs is characterized which varies from the contact aggregation, the relatively uniform dispersion to the local bridging structure via one polymer layer with the increase of the functionalization degree α. Corresponding to it, the percolation threshold of PNCs exhibits a continuous decrease with the increase of α under the quiescent state which reflects the high conductive probability. However, the percolation threshold shows a weak increase under the shear field. Thus, the α decides whether the conductive probability increases or decreases under the shear field. The smallest change in the percolation threshold appears at the moderate α which reflects the highest conductive stability. Especially, even though the dispersion state of NPs is different for α≥0.2, the percolation threshold is similar under the shear field. The connection mode among NPs is considered to determine the formation of the conductive network. In summary, this work can help to understand how the NP functionalization affects the electrical conductivity of PNCs.
Source: openalex_inverted_index · Quality: baseline
Affiliations
Key Laboratory of Beijing City on Preparation and Processing of Novel Polymer Materials, Beijing University of Chemical Technology, Beijing, China
Key Laboratory of Carbon Fiber and Functional Polymers, Ministry of Education, Beijing University of Chemical Technology, Beijing, People’s Republic of China
Aerospace Research Institute of Materials and Processing Technology, non-metallic material department, Beijing, China
State Key Laboratory of Organic-Inorganic Composites, Beijing University of Chemical Technology, Beijing, China