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Zuchong Yang

Publications and source records attributed to Zuchong Yang.

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Role of structure and charge trapping on the bipolaron formation and magnetic-field response of gated conjugated polymers

Conjugated polymers exhibit unique spin-dependent phenomena arising from weak yet critical hyperfine interactions. Understanding these spin effects, particularly the spin-dependent formation and decay of correlated spin pairs, is important for advancing both organic electronics and polymer-based spintronics. Intrinsic magnetic-field responses such as magnetoresistance have primarily been investigated in diode architectures, where electrons and holes coexist. However, such systems are less suitable for probing bipolaron formation in unipolar transport, and the relationship between polymer structure and bipolaron formation in lightly doped polymers remains unclear. Here, we systematically investigate intrinsic magnetoresistance in representative conjugated polymers using field-effect transistors and observe a generally positive magnetoresistance. First-principles simulations reveal that bipolarons preferentially form on short conjugated segments associated with amorphous regions. Moreover, comparisons across these polymers show that enhanced charge trapping correlates with stronger magnetoresistance, implying promoted bipolaron formation. Bipolaron-incorporated energylevel-alignment modeling near metal/polymer interfaces suggests that charge traps can increase the bipolaron density.

cond-mat.mtrl-sci

Charge Transport in Thin-Film Transistors Based on Liquid-Crystalline Phthalocyanines

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.

cond-mat.mtrl-sci