The electrochemical doping/dedoping kinetics, and the organic electrochemical transistor (OECT) performance of a series polythiophene homopolymers with ethylene glycol units in their side chains using both kosmotropic and chaotropic anion...
We study the organic electrochemical transistor (OECT) performance of the ladder polymer poly-(benzimidazobenzophenanthroline) (BBL) in an attempt to better understand how an apparently hydrophobic side-chain-free polymer is able to operate as an OECT with favorable redox kinetics in an aqueous environment. We examine two BBLs of different molecular masses from different sources. Regardless of molecular mass, both BBLs show significant film swelling during the initial reduction step. By combining electrochemical quartz crystal microbalance gravimetry, in-operando atomic force microscopy, and both ex-situ and in-operando grazing incidence wideangle X-ray scattering (GIWAXS), we provide a detailed structural picture of the electrochemical charge injection process in BBL in the absence of any hydrophilic side-chains. Compared with ex-situ measurements, in-operando GIWAXS shows both more swelling upon electrochemical doping than has previously been recognized and less contraction upon dedoping. The data show that BBL films undergo an irreversible hydration driven by the initial electrochemical doping cycle with significant water retention and lamellar expansion that persists across subsequent oxidation/ reduction cycles. This swelling creates a hydrophilic environment that facilitates the subsequent fast hydrated ion transport in the absence of the hydrophilic side-chains used in many other polymer systems. Due to its rigid ladder backbone and absence of hydrophilic side-chains, the primary BBL water uptake does not significantly degrade the crystalline order, and the original dehydrated, unswelled state can be recovered after drying. The combination of doping induced hydrophilicity and robust crystalline order leads to efficient ionic transport and good stability.
Unlike
naphthalene diimides, perylene diimides, and other classes
of n-type conjugated polymers with numerous derivatives that enable
understanding of structure–property relationships, the electronic
structure and properties have not been reported for any derivative
of ladder poly(benzimidazobenzophenanthroline) (BBL). Herein, we report
the synthesis and properties of BBL-P, a phenazine derivative of BBL.
In acid solution, BBL-P has a broad absorption spectrum with a lowest
energy absorption peak at 840 nm due to protonation-enhanced intramolecular
charge transfer. Compared to BBL, BBL-P thin films have decreased
crystallinity with face-on molecular orientations on substrates, resulting
in a substantially decreased field-effect electron mobility of 1.2
× 10–4 cm2/V s. BBL-P films have
excellent mechanical properties exemplified by a Young modulus of
11 GPa. The results demonstrate that BBL-P is a promising n-type semiconducting
polymer and provide new insights into the effects of backbone structure
on electronic structure, thin film microstructure, and charge transport
properties of conjugated ladder polymers.
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