材料科学
塞贝克系数
热电效应
掺杂剂
共轭体系
聚合物
热电材料
兴奋剂
分子内力
轨道能级差
混溶性
接受者
高分子化学
结晶学
有机化学
光电子学
分子
凝聚态物理
化学
热力学
复合材料
热导率
物理
作者
Changshuai Dong,Bin Meng,Jun Liu,Lixiang Wang
标识
DOI:10.1021/acsami.9b21527
摘要
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.
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