Theories of polyaniline nanostructure self-assembly: Towards an expanded, comprehensive Multi-Layer Theory (MLT)

• Published in: Progress in polymer science 2010-12, Vol.35 (12), p.1403-1419
• Main Authors: Laslau, Cosmin, Zujovic, Zoran, Travas-Sejdic, Jadranka
• Format: Article
• Language: English
• Subjects: Agglomeration; Applied sciences; Conducting polymers; Exact sciences and technology; Morphology; Nanocomposites; Nanomaterials; Nanostructure; Nanotube; Organic polymers; Physicochemistry of polymers; Polyaniline; Polyanilines; Polymers with particular properties; Preparation, kinetics, thermodynamics, mechanism and catalysts; Self assembly; Theory
• ISSN: 0079-6700; 1873-1619
• DOI: 10.1016/j.progpolymsci.2010.08.002

Nanostructured conducting polymeric materials are of exceptional interest due to their potential applications in sensors, actuators, transistors and displays. Arguably the most promising method for synthesizing polyaniline nanostructures is self-assembly, which is very advantageous in its simplicity and volume. However, this self-assembly remains only partly understood, with a number of already established models (a “micelle theory” and a “phenazine theory”) at odds with more recent discoveries (nanosheet curling and nanoparticle agglomeration), leading to a fragmented understanding of this important topic. In this paper we address this problem in two ways. First, we review the aforementioned older models and recent discoveries. Second, we propose an expanded polyaniline nanostructure self-assembly model – “Multi-Layer Theory” – that goes beyond the scope of existing theories, thereby accommodating the more recent discoveries. The expanded synthesis framework we present is based on a multi-layered approach incorporating intrinsic morphologies. The three proposed intrinsic morphologies underpinning our model are nanofibrils, nanosheets and nanoparticles; the forces driving their subsequent self-assembly interactions are mainly π–π stacking, hydrogen bonding and charge–charge repulsion from protonation. These interactions between the three intrinsic morphologies give rise to observed growth, agglomeration and curling behaviours that ultimately generate complex multi-layered nanostructures such as double-walled conducting polymer nanotubes.