π-Extended Poly(benzimidazoanthradiisoquinolinedione) Ladder-type Conjugated Polymer.

Since the 1960s, poly(benzobisimidazobenzophenathrolinedione) (BBL) has been the only n-type ladder-type conjugated polymer (LCP) that is utilized in thin film electronic devices. Its high electrochemical and thermal stabilities make it a promising candidate for organic electrochemical transistors (OECTs) and thermoelectrics (OTEs) applications. Here we report the synthesis and characterization of a new π-extended poly(benzimidazoanthradiisoquinolinedione) (BAL). The tetrachlorinated BAL (Cl4-BAL) is fully soluble in methanesulfonic acid (MSA) and can be spin-coated into good quality thin films, enabling the fabrication and characterization of OTEs. Doping of Cl4-BAL films using our in-house benzyl viologen radical cation (BV●+) n-dopant shows better electrical air-stability as compared to BBL due to its very low LUMO value (-4.83 eV), making it a promising material toward air-stable n-doped conducting polymers.

Polaron Delocalization Dependence of the Conductivity and the Seebeck Coefficient in Doped Conjugated Polymers.

Conjugated polymers are promising materials for thermoelectrics as they offer good performances at near ambient temperatures. The current focus on polymer thermoelectric research mainly targets a higher power factor (PF; a product of the conductivity and square of the Seebeck coefficient) through improving the charge mobility. This is usually accomplished via structural modification in conjugated polymers using different processing techniques and doping. As a result, the structure-charge transport relationship in conjugated polymers is generally well-established. In contrast, the relationship between the structure and the Seebeck coefficient is poorly understood due to its complex nature. A theoretical framework by David Emin (Phys. Rev. B, 1999, 59, 6205-6210) suggests that the Seebeck coefficient can be enhanced via carrier-induced vibrational softening, whose magnitude is governed by the size of the polaron. In this work, we seek to unravel this relationship in conjugated polymers using a series of highly identical pro-quinoid polymers. These polymers are ideal to test Emin's framework experimentally as the quinoid character and polaron delocalization in these polymers can be well controlled even by small atomic differences (<10 at. % per repeating unit). By increasing the polaron delocalization, that is, the polaron size, we demonstrate that both the conductivity and the Seebeck coefficient (and hence PF) can be increased simultaneously, and the latter is due to the increase in the polaron's vibrational entropy. By using literature data, we also show that this phenomenon can be observed in two closely related diketopyrrolopyrrole-conjugated polymers as well as in p-doped P3HT and PANI systems with an increasing molecular order.