Fluorination Position: A Study of the Optoelectronic Properties of Two Regioisomers Using Spectroscopic and Computational Techniques
Author:
Affiliation:
1. Department of Chemistry, University of Otago, Dunedin and MacDiarmid Institute, Dunedin 9016, New Zealand
2. Department of Chemistry, College of Science, Korea University, Seoul 02841, Republic of Korea
Funder
MacDiarmid Institute for Advanced Materials and Nanotechnology
National Research Foundation of Korea
University of Otago
Dodd-Walls Centre
Publisher
American Chemical Society (ACS)
Subject
Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.jpca.0c05210
Reference29 articles.
1. Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells
2. Organic fluorine compounds: a great opportunity for enhanced materials properties
3. Tuning of the electronic and photophysical properties of ladder-type quaterphenyl by selective methylene-bridge fluorination
4. The fluorine effect: photophysical properties of borondipyrromethene (bodipy) dyes appended at the meso position with fluorinated aryl groups
5. Fluorinated conjugated polymers in organic bulk heterojunction photovoltaic solar cells
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