Thi, Quyen Vu Nguyen, Quynh H. Choi, Yong-Seok Jeon, Seung-Yeol Boudouris, Bryan W. Joo, Yongho 2024-02-28T00:30:04Z 2024-02-28T00:30:04Z 2024-02-27 2024-02 2691-3704 https://pubs.kist.re.kr/handle/201004/149335 Nonconjugated organic radicals with an open-shell radical active group exhibit unique functionality due to their radical pendant site. Compared with the previously studied doped conjugated polymers, radical polymers reveal superior processability, stability, and optical properties. Despite the success of organic radical polymer conductors based on the TEMPO radicals, it still requires potential design substitutions to meet the fundamental limits of charge transport in the radical polymer. To do so, we demonstrate that the amorphous, nonconjugated radical polymer with backbone？pendant group interaction and low glass transition temperature enables the macromolecules to have rapid charge transport in the solid state, resulting in conductivity higher than 32 S m？1. This charge transport is due to the formation of the local ordered regime with an energetically favored orientation caused by the strong coupling between the backbone and pendant group, which can significantly modulate the polymer packing with active electronic communications. The nonconjugate nature of the radical polymer maintains an optical transparency up to 98% at a 1.5 μm thick film. Thus, this effort will be a dramatically advanced model in the organic radical community for the creation of next-generation polymer conductors. English American Chemical Society Conductive Glassy Nonconjugated Open-Shell Radical Polymer with Organosulfur Backbone for Macroscopic Conductivity Article 10.1021/jacsau.3c00743 1 JACS Au, v.4, no.2, pp.690 - 696 JACS Au 4 2 690 696 Y scopus