Wang Yang, Takimiya Kazuo
Emergent Molecular Function Research Team, RIKEN Center for Emergent Matter Science (CEMS), 2-1 Hirosawa, Wako, Saitama, 351-0198, Japan.
Department of Chemistry, Graduate School of Science, Tohoku University, 6-3 Aoba, Aramaki, Aoba-ku, Sendai, Miyagi, 980-8578, Japan.
Adv Mater. 2020 Jul;32(30):e2002060. doi: 10.1002/adma.202002060. Epub 2020 Jun 22.
The development of n-type conjugated polymers with high electrical conductivity (σ) has continued to pose a massive challenge in organic thermoelectrics (OTEs). New structural insights into the charge-carrier transport are necessitated for the realization of high-performance OTEs. In this study, three new n-type copolymers, named pNB, pNB-Tz, and pNB-TzDP, consisting of naphthodithiophenediimide (NDTI) and bithiopheneimide (BTI) units, are synthesized by direct arylation polymerization. The backbone orientation is altered by incorporating thiazole units into the backbone and tuning the branching point of the side chain. The alteration of the backbone orientation from face-on to bimodal orientation with both face-on and edge-on fractions significantly impacts the σ and the power factors (PFs) of the polymers. As a result, pNB-TzDP, with the bimodal orientation, demonstrates a high σ of up to 11.6 S cm and PF of up to 53.4 µW m K , which are among the highest in solution-processed n-doped conjugated polymers reported so far. Further studies reveal that the bimodal orientation of pNB-TzDP introduces 3D conduction channels and leads to better accommodation of dopants, which should be the key factors for the excellent thermoelectric performance.
在有机热电(OTE)领域,开发具有高电导率(σ)的n型共轭聚合物仍然是一项巨大挑战。为了实现高性能OTE,需要对电荷载流子传输有新的结构见解。在本研究中,通过直接芳基化聚合反应合成了三种新型n型共聚物,分别命名为pNB、pNB-Tz和pNB-TzDP,它们由萘并二噻吩二亚胺(NDTI)和联噻吩亚胺(BTI)单元组成。通过将噻唑单元引入主链并调整侧链的分支点来改变主链取向。主链取向从面对面转变为包含面对面和边缘面对分数的双峰取向,这对聚合物的σ和功率因子(PF)产生了显著影响。结果,具有双峰取向的pNB-TzDP表现出高达11.6 S cm的高σ和高达53.4 µW m K 的PF,这是迄今为止报道的溶液法n掺杂共轭聚合物中最高的之一。进一步研究表明,pNB-TzDP的双峰取向引入了三维传导通道,并导致对掺杂剂的更好容纳,这应该是其优异热电性能的关键因素。