Complex Relationship Between Side-Chain Polarity, Conductivity, And Thermal Stability In Molecularly Doped Conjugated Polymers

Molecularly doped conjugated polymers with polar side chains are an emerging class of conducting materials exhibiting enhanced and thermally stable conductivity. Here, we study the electronic conductivity (sigma) and the corresponding thermal stability of two polythiophene derivatives comprising oligoethylene glycol side chains: one having oxygen attached to the thiophene ring (poly(3-(methoxyethoxyethoxy)thiophene) (P3MEET)) and the other having a methylene spacer between the oxygen and the thiophene ring (poly(3-methoxyethoxyethoxymethyl)thiophene) (P3MEEMT)). Thin films were vapor-doped with fluorinated derivatives of tetracyanoquinodimethane (F(n)TCNQ n = 4, 2, 1) to determine the role of dopant strength (electron affinity) in maximum achievable sigma. Specifically, when vapor doping with F(4)TCNQ, P3MEET achieved a substantially higher a of 37.1 +/- 10.1 S/cm compared to a sigma of 0.82 +/- 0.06 S/cm for P3MEEMT. Structural characterization using a combination of X-ray and optical spectroscopy reveals that the higher degree of conformational order of polymer chains in the amorphous domain upon doping with F(4)TCNQ in P3MEET is a major contributing factor for the higher sigma of P3MEET. Additionally, vapor-doped P3MEET exhibited superior thermal stability compared to P3MEEMT, highlighting that the presence of polar side chains alone does not ensure higher thermal stability. Molecular dynamics simulations indicate that the dopant-side-chain nonbond energy is lower in the P3MEET:F(4)TCNQ mixture, suggesting more favorable dopant-side-chain interaction, which is a factor in improving the thermal stability of a polymer/dopant pair. Our results reveal that additional factors such as polymer ionization energy and side-chain-dopant interaction should be taken into account for the design of thermally stable, highly conductive polymers.