Journal
DYES AND PIGMENTS
Volume 216, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2023.111349
Keywords
Perovskite solar cells; Hole -transport materials; Conjugated polymers; Triisopropylsilyl chains; Benzodithiophene
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Conjugated polymers based on benzodithiophene (BDT) and thiophene-flanked thiazolothiazole block (Tz) were designed and studied as promising hole-transport materials (HTMs) for perovskite solar cells (PSCs). The position of side chain greatly affects their performance, and the polymer in-BDTTz showed higher power conversion efficiency and stable operation compared to aus-BDTTz and poly(triarylamine) (PTAA). These alkylsilyl-substituted benzodithiophene-based polymers could be potential dopant-free hole-transport materials for efficient and stable perovskite photovoltaics.
Conjugated polymers are promising hole-transport materials (HTMs) for designing efficient and stable perovskite solar cells (PSCs). The structure of polymer backbone and position of side substituents greatly influences their electronic properties, film morphology, and hence, the charge extraction and charge transport characteristics of HTMs. Herein, we design two novel donor-acceptor conjugated polymers based on benzodithiophene (BDT) bearing triisopropylsilyl substituents and thiophene-flanked thiazolothiazole block (Tz) with different side chain position. In polymer in-BDTTz alkyl chains are placed toward to the Tz moiety, while in aus-BDTTz outward to the Tz block. Polymeric HTM in-BDTTz enables 18.7% power conversion efficiency in devices outperforming that of PSCs with aus-BDTTz and reference devices employing poly(triarylamine) (PTAA). Furthermore, PSCs with in-BDTTz as HTM demonstrates stable operation comparable to that of PTAA-based devices. These findings feature alkylsilyl-substituted benzodithiophene-based polymers as promising dopant-free hole-transport mate-rials for efficient and stable perovskite photovoltaics.
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