B ← N Unit Enables n‑Doping of Conjugated Polymers for Thermoelectric Application

• Published in: ACS applied materials & interfaces 2020-03, Vol.12 (9), p.10428-10433
• Main Authors: Dong, Changshuai, Meng, Bin, Liu, Jun, Wang, Lixiang
• Format: Article
• Language: English
• ISSN: 1944-8244; 1944-8252
• DOI: 10.1021/acsami.9b21527

Only very few conjugated polymers can be n-doped for thermoelectric applications. In this work, for the first time, we report that incorporation of Boron–Nitrogen coordination bond (B ← N unit) to a donor–acceptor (D–A) type conjugated polymer enable n-doping for thermoelectric application. The incorporation of B ← N unit into the polymer backbone leads to not only a downshift of LUMO/HOMO energy levels by 0.27 eV/0.33 eV, but also diminished intramolecular D–A character of the polymer backbone. As a result, while the control polymer cannot be n-doped, the polymer containing B ← N unit (PI-BN) can be n-doped by 4-(1,3-dimethyl-2,3-dihydro-1H-benzoimidazol-2-yl)-N,N-dimethylaniline (N-DMBI). Finally, PI-BN exhibits an electrical conductivity (σ) of 0.97 × 10–3 S cm–1, Seebeck coefficient (S) of −453.8 μV K–1, and power factor (PF) of 0.02 μW m–1 K–2 when doped with 5 wt % N-DMBI. A great advantage of PI-BN is its excellent miscibility with the n-dopant because of its amorphous nature and large pendent substituents. This work indicates that organoboron polymers can be n-doped and can be used for thermoelectrics.