TY - JOUR
T1 - [1]Benzothieno[3,2-b][1]benzothiophene-Phthalocyanine Derivatives
T2 - A Subclass of Solution-Processable Electron-Rich Hole Transport Materials
AU - Zanotti, Gloria
AU - Angelini, Nicola
AU - Mattioli, Giuseppe
AU - Paoletti, Anna Maria
AU - Pennesi, Giovanna
AU - Caschera, Daniela
AU - Sobolev, Anatoly Petrovich
AU - Beverina, Luca
AU - Calascibetta, Adiel Mauro
AU - Sanzone, Alessandro
AU - Di Carlo, Aldo
AU - Berionni Berna, Beatrice
AU - Pescetelli, Sara
AU - Agresti, Antonio
N1 - Publisher Copyright:
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
PY - 2020/11/1
Y1 - 2020/11/1
N2 - 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.
AB - 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.
KW - hole transport
KW - organic electronics
KW - perovskite solar cells
KW - photovoltaic devices
KW - phthalocyanines
UR - http://www.scopus.com/inward/record.url?scp=85084601599&partnerID=8YFLogxK
U2 - 10.1002/cplu.202000281
DO - 10.1002/cplu.202000281
M3 - Article
C2 - 32406580
AN - SCOPUS:85084601599
SN - 2192-6506
VL - 85
SP - 2376
EP - 2386
JO - ChemPlusChem
JF - ChemPlusChem
IS - 11
ER -