Abstract

Herein we report the design and synthesis of two new naphthalenediimide (NDI) chromophores; (2Z,2′Z)-3,3′-(5,5′-(2,7-dioctyl-1,3,6,8-tetraoxo-1,2,3,6,7,8-hexahydrobenzo [lmn][3,8]phenanthroline-4,9-diyl)bis (thiophene-5,2-diyl))bis(2-(4-(trifluoromethyl)phenyl) acrylonitrile) (F1) and (2Z,2′Z)-3,3′-(5,5′-(2,7-dioctyl-1,3,6,8-tetraoxo-1,2,3,6,7,8-hexahydrobenzo[lmn][3,8] phenanthroline-4,9-diyl)bis(thiophene-5,2-diyl))bis(2-(3,5-bis(trifluoroomethyl)phenyl) acrylonitrile) (F2). Both compounds are thermally stable as confirmed by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), and are employed in perovskite solar cells (PSCs), making F1 and F2 promising candidates as electron transfer layers (ETL). Further, F1 and F2 were utilized as electron transport layers (ETLs) in inverted PSC assemblies. The overall power conversion efficiency (PCE) of inverted PSC devices constructed using F1 layer was 10.2 %, with circuit current density (Jsc) of 24.17 mAcm−2 and open circuit voltage (Voc) of 0.81 V, and fill factor (FF) of 52 %, while PSCs constructed using F2 had 9.1 % PCE, Jsc of 24.35 mAcm−2, Voc of 0.83 V, and FF of 45.4 %. The performance of PSCs are mainly attributed to the presence of -CF3 functional groups in F1 and F2.

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.