The [1]benzothieno[3,2-b][1]benzothiophene (BTBT) planar system was used to functionalize the phthalocyanine ring aiming at synthesizing novel electron-rich pi-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.
Zanotti, G., Angelini, N., Mattioli, G., Paoletti, A.m., Pennesi, G., Caschera, D., et al. (2020). [1]Benzothieno[3,2-b][1]benzothiophene-phthalocyanine derivatives: a subclass of solution-processable electron-rich hole transport materials. CHEMPLUSCHEM, 85(11), 2376-2386 [10.1002/cplu.202000281].
[1]Benzothieno[3,2-b][1]benzothiophene-phthalocyanine derivatives: a subclass of solution-processable electron-rich hole transport materials
Zanotti, G.;Di Carlo, A.;Berionni Berna, B.;Pescetelli, S.;Agresti, A.
2020-01-01
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 pi-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.| File | Dimensione | Formato | |
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