We investigate a series of liquid-crystalline phthalocyanines (metal-free and Cu, Zn, Ni, Co complexes) by correlating their vibrational signatures with their electronic performance in organic thin-film transistors (OTFTs). Raman spectroscopy reveals metal-dependent distortions of the phthalocyanine macrocycle, reflected in systematic shifts of the C-N-C and M-N vibrational modes. When integrated into OTFTs, all compounds exhibit markedly enhanced current response under ultrahigh vacuum compared to an N2-rich environment, demonstrating that intrinsic charge transport is strongly suppressed by atmospheric species. Temperature-dependent measurements (100-300 K) show clear threshold-voltage shifts driven by deep interface and bulk traps, while all devices display thermally activated mobility with low activation energies (14-20 meV). These results highlight how mesomorphic order, metal coordination, and environmental conditions collectively govern charge transport in liquid-crystalline phthalocyanines, offering design guidelines for their use as orientable semiconducting materials in organic electronics.
@article{arxiv.2601.03058,
title = {Charge transport in liquid-crystalline phthalocyanine-based thin-film transistors},
author = {L. B. Avila and Zuchong Yang and Ilknur Hatice Eryilmaz and Lilian Skokan and Leonardo N Furini and Andreas Ruediger and H. Bock and I. H. Bechtold and E. Orgiu},
journal= {arXiv preprint arXiv:2601.03058},
year = {2026}
}