4.2 Article

Beyond Conformational Control: Effects of Noncovalent Interactions on Molecular Electronic Properties of Conjugated Polymers

期刊

JACS AU
卷 1, 期 12, 页码 2182-2187

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jacsau.1c00284

关键词

noncovalent interactions; conjugated polymers; resonance effect; hole transfer; constrained density functional theory

资金

  1. PROCORE-France/Hong Kong Joint Research Scheme - Research Grants Council of Hong Kong
  2. Consulate General of France in Hong Kong [46911XA, F-HKUST603/20]
  3. COMETE project (COnception in silico de Materiaux pour l'EnvironnemenT et l'Energie)
  4. European Union under the program FEDERFSE Lorraine et Massif des Vosges 2014-2020
  5. Croucher Foundation
  6. National Natural Science Foundation of China
  7. Energy Institute in Hong Kong University of Science and Technology

向作者/读者索取更多资源

It has been found that the sulfur-nitrogen noncovalent interaction may reduce the band gaps of polymers and enhance charge transfer more significantly than other noncovalent interactions, a discovery consistent with experimental data. This interaction may further influence the electronic structure of coplanar conjugated polymers beyond just improving molecular planarity, suggesting a new mechanism for manipulating the electronic properties of polymers for high-performance solar cells.
Tuning the electronic properties of polymers is of great importance in designing highly efficient organic solar cells. Noncovalent intramolecular interactions have been often used for conformational control to enhance the planarity of polymers or molecules, which may reduce band gaps and promote charge transfer. However, it is not known if noncovalent interactions may alter the electronic properties of conjugated polymers through some mechanism other than the conformational control. Here, we studied the effects of various noncovalent interactions, including sulfur-nitrogen, sulfur-oxygen, sulfur-fluorine, oxygen-nitrogen, oxygen-fluorine, and nitrogen-fluorine, on the electronic properties of polymers with planar geometry using unconstrained and constrained density functional theory. We found that the sulfur-nitrogen intramolecular interaction may reduce the band gaps of polymers and enhance the charge transfer more obviously than other noncovalent interactions. Our findings are also consistent with the experimental data. For the first time, our study shows that the sulfur-nitrogen noncovalent interaction may further affect the electronic structure of coplanar conjugated polymers, which cannot be only explained by the enhancement of molecular planarity. Our work suggests a new mechanism to manipulate the electronic properties of polymers to design high-performance small-molecule-polymer and all-polymer solar cells.

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