Ruyan Zhao, Hongde Yu, Heng Zhang, Lei Tao Gao, Arafat Hossain Khan, Congxue Liu, Xiaodong Li, Xingyuan Chu, Yubin Fu, Darius Pohl, Angelika Wrzesińska‐Lashkova, Eike Brunner, Yana Vaynzof, Hai I. Wang, Mischa Bonn, Thomas Heine, Mingchao Wang, Xinliang Feng
Abstract Layered two-dimensional conjugated polymers (2D CPs), or 2D conjugated covalent organic frameworks, are promising semiconductor materials for (opto)electronics and photocatalysis, but their performance is often limited by insufficient in-plane conjugation and poor charge transport. Guided by density functional theory calculations, we report two donor-acceptor-type 2D poly(arylene vinylene)s constructed from thienyl-benzodithiophene and diketopyrrolopyrrole units. These materials are predicted to exhibit strongly dispersive energy bands with ultralow in-plane effective masses (0.036 − 0.159 m 0 ), enabling intrinsic charge mobilities approaching 2000 cm 2 V −1 s −1 . Solid-state Aldol-type 2D polycondensation yields crystalline materials with optical band gaps as narrow as 1.0 eV. Terahertz spectroscopy reveals long charge carrier scattering times of 76 fs and a high room-temperature mobility of 310 cm 2 V −1 s −1 , surpassing previously reported linear and 2D CP powder samples. This work highlights donor-acceptor engineering as an effective strategy to enhance charge transport in 2D CPs.