Topology-Mediated Enhanced Polaron Coherence in Covalent Organic Frameworks

We employ the Holstein model for polarons to investigate the relationship among defects, topology, Coulomb trapping, and polaron delocalization in covalent organic frameworks (COFs). We find that intrasheet topological connectivity and pi-column density can override disorder-induced deep traps and significantly enhance polaron migration by several orders of magnitude in good agreement with recent experimental observations. The combination of percolation networks and micropores makes trigonal COFs ideally suited for charge transport followed by kagome/tetragonal and hexagonal structures. By comparing the polaron spectral signatures and coherence numbers of large three-dimensional frameworks having a maximum of 180 coupled chromophores, we show that controlling nanoscale defects and the location of the counteranion is critical for the design of new COF-based materials yielding higher mobilities. Our analysis establishes design strategies for enhanced conductivity in COFs that can be readily generalized to other classes of conductive materials such as metal-organic frameworks and perovskites.

Automated summary

The Holstein model for polarons was used to investigate the relationship among defects, topology, Coulomb trapping, and polaron delocalization in COFs, showing that intrasheet topological connectivity and pi-column density can enhance polaron migration significantly. Trigonal COFs are ideal for charge transport, and controlling nanoscale defects and the location of the counteranion is critical for designing new COF-based materials with higher mobilities. Design strategies for enhanced conductivity in COFs can be generalized to other conductive materials such as metal-organic frameworks and perovskites.