Affiliation: | 1. Instituto de Macromoléculas Professora Eloisa Mano (IMA), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil
Contribution: Formal analysis (equal), Methodology (lead), Writing - original draft (equal);2. Instituto de Macromoléculas Professora Eloisa Mano (IMA), Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil;3. Laboratório de Nanotecnologia e Energia Solar (LNES), Instituto de Química, Universidade de Campinas (UNICAMP), Campinas, São Paulo, Brazil
Contribution: Formal analysis (equal), Methodology (equal), Validation (equal), Writing - review & editing (equal);4. Laboratório de Nanotecnologia e Energia Solar (LNES), Instituto de Química, Universidade de Campinas (UNICAMP), Campinas, São Paulo, Brazil |
Abstract: | Polymeric semiconductors offer the dual advantages of lightness and flexibility, facilitating the large-scale production of organic electronic devices. In the present research, electron donor polymers were synthesized incorporating high electron density aromatic units, specifically benzodithiophene (BDT) and thiophene (Th), to explore their efficacy in organic electronics. This systematic study focused on evaluating the impact of varying side chains on the material properties of these polymers. It was found that polymers with Th side chains exhibited significantly enhanced thermal stability, approximately 100°C higher than their alkoxide side chain counterparts. For the polymer PEHO-BDT3HT, a bandgap value of around 1.6 eV was obtained. Furthermore, binary devices were developed using these novel copolymers, among which PDT-BDT3HT demonstrated superior photovoltaic performance, achieving a power conversion efficiency of 1.56% without any optimization. This work not only sheds light on the influence of side chain variations in polymer properties but also showcases the potential of BDT and Th-based copolymers in the field of organic electronics. |