An isomerism strategy to optimize electrochromic performance: a small orientation change of S atoms in thiophene makes a big difference
Author:
Affiliation:
1. School of Applied Physics and Materials, Wuyi University, Jiangmen, 529020, China
2. School of Pharmacy and Food Engineering, Wuyi University, Jiangmen 529020, China
Abstract
Funder
Department of Education of Guangdong Province
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/2024/PY/D4PY00659C
Reference34 articles.
1. Recent Advances in Bulk Heterojunction Polymer Solar Cells
2. Chalcogenodiazolo[3,4-c]pyridine based donor–acceptor–donor polymers for green and near-infrared electrochromics
3. Electrochromic and photovoltaic properties of benzothiadiazole-based donor-acceptor conjugated polymers with oligo(ethylene glycol) side chains
4. Benzothiadiazole, hexylthiophen and alkoxy benzene based solution processable copolymer: Effect of the electron withdrawing substituents (fluorine atoms) on electrochemical, optical and electrochromic properties
5. Synthesis, Characterization and Application of Four Novel Electrochromic Materials Employing Nitrotriphenylamine Unit as the Acceptor and Different Thiophene Derivatives as the Donor
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