| Literature DB >> 32406580 |
Gloria Zanotti1, Nicola Angelini1, Giuseppe Mattioli1, Anna Maria Paoletti1, Giovanna Pennesi1, Daniela Caschera2, Anatoly Petrovich Sobolev3, Luca Beverina4, Adiel Mauro Calascibetta4, Alessandro Sanzone4, Aldo Di Carlo1,5,6, Beatrice Berionni Berna5, Sara Pescetelli5, Antonio Agresti5,6.
Abstract
The [1]benzothieno[3,2-b][1]benzothiophene (BTBT) planar system was used to functionalize the phthalocyanine ring aiming at synthesizing novel electron-rich π-conjugated macrocycles. The resulting ZnPc-BTBT and ZnPc-(BTBT)4 derivatives are the first two examples of a phthalocyanine subclass having potential use as solution-processable p-type organic semiconductors. In particular, the combination of experimental characterizations and theoretical calculations suggests compatible energy level alignments with mixed halide hybrid perovskite-based devices. Furthermore, ZnPc-(BTBT)4 features a high aggregation tendency, a useful tool to design compact molecular films. When tested as hole transport materials in perovskite solar cells under 100 mA cm-2 standard AM 1.5G solar illumination, ZnPc-(BTBT)4 gave power conversion efficiencies as high as 14.13 %, irrespective of the doping process generally required to achieve high photovoltaic performances. This work is a first step toward a new phthalocyanine core engineerization to obtain robust, yet more efficient and cost-effective materials for organic electronics and optoelectronics.Entities:
Keywords: hole transport; organic electronics; perovskite solar cells; photovoltaic devices; phthalocyanines
Year: 2020 PMID: 32406580 DOI: 10.1002/cplu.202000281
Source DB: PubMed Journal: Chempluschem ISSN: 2192-6506 Impact factor: 2.863