Abstract

Organic semiconductors with high-spin ground states are fascinating because they could enable fundamental understanding on the spin-related phenomenon in light element and provide opportunities for organic magnetic and quantum materials. Although high-spin ground states have been observed in some quinoidal type small molecules or doped organic semiconductors, semiconducting polymers with high-spin at their neutral ground state are rarely reported. Here we report three high-mobility semiconducting polymers with different spin ground states. We show that polymer building blocks with small singlet-triplet energy gap (ΔES-T) could enable small ΔES-T gap and increase the diradical character in copolymers. We demonstrate that the electronic structure, spin density, and solid-state interchain interactions in the high-spin polymers are crucial for their ground states. Polymers with a triplet ground state (S = 1) could exhibit doublet (S = 1/2) behavior due to different spin distributions and solid-state interchain spin-spin interactions. Besides, these polymers showed outstanding charge transport properties with high hole/electron mobilities and can be both n- and p-doped with superior conductivities. Our results demonstrate a rational approach to obtain high-mobility semiconducting polymers with different spin ground states.

Semiconducting polymers with high-spin at their neutral ground state are rarely reported. Here the authors synthesize three semiconducting polymers with different spin ground states and high hole/electron mobility, by appropriate choice of the building blocks’ singlet-triplet energy gap, spin distributions and solid-state interchain interactions.

Details

Title
High-mobility semiconducting polymers with different spin ground states
Author
Xiao-Xiang, Chen 1 ; Jia-Tong, Li 2   VIAFID ORCID Logo  ; Yu-Hui, Fang 3 ; Xin-Yu, Deng 2 ; Xue-Qing, Wang 2 ; Liu, Guangchao 2 ; Wang, Yunfei 4   VIAFID ORCID Logo  ; Gu Xiaodan 4   VIAFID ORCID Logo  ; Shang-Da, Jiang 5   VIAFID ORCID Logo  ; Ting, Lei 6   VIAFID ORCID Logo 

 School of Materials Science and Engineering, Peking University, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319); Peking University, College of Chemistry and Molecular Engineering, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 School of Materials Science and Engineering, Peking University, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 Peking University, College of Chemistry and Molecular Engineering, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
 The University of Southern Mississippi, School of Polymer Science and Engineering, Center for Optoelectronic Materials and Devices, Hattiesburg, USA (GRID:grid.267193.8) (ISNI:0000 0001 2295 628X) 
 South China University of Technology, Spin-X Institute, School of Chemistry and Chemical Engineering, Guangzhou, China (GRID:grid.79703.3a) (ISNI:0000 0004 1764 3838) 
 School of Materials Science and Engineering, Peking University, Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319); Peking University, Beijing Key Laboratory for Magnetoelectric Materials and Devices, Beijing, China (GRID:grid.11135.37) (ISNI:0000 0001 2256 9319) 
Publication year
2022
Publication date
2022
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2655335639
Copyright
© The Author(s) 2022. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.