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Comparative study demonstrates matrix-dependent electrical percolation and transport dynamics in carbon nanotube polymer composites, highlighting chitosan for flexible electronics.
This study presents a systematic comparative investigation of large‐diameter (100–110 nm) multi‐walled carbon nanotube (MWCNT) reinforced composites utilizing three structurally distinct polymer matrices: chitosan (CS), epoxy (EP), and polypropylene (PP). Synthesized via aerosol‐assisted chemical vapor deposition, the MWCNTs were incorporated at concentrations ranging from 0.5 to 3 wt.%. The composite properties were evaluated through a comprehensive suite of analytical techniques, including SEM for morphology, FTIR and Raman spectroscopy for structural/chemical characterization, thermogravimetric analysis for thermal stability, laser flash analysis for thermal conductivity, and detailed DC/AC electrical characterization to assess charge transport dynamics. Experimental results demonstrate that the percolation threshold lies at approximately 1.0 wt.% for the EP and PP systems, while the CS‐based composite exhibits enhanced charge transport at this concentration. At 3 wt.% loading, all composites demonstrate ohmic, quasi‐metallic behavior. While all composites achieve a robust percolative network at 3 wt.% filler loading, the AC electrical characterization highlights distinct matrix‐dependent charge transport dynamics. These findings underscore the critical role of polymer‐filler interfacial interactions in governing functionality, positioning the MWCNT/CS composite as a promising candidate for eco‐friendly biomedical interfaces and advanced flexible electronics.
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Gahramanova et al. (2026) studied this question.
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