During the last decade, perovskite solar technologies underwent an impressive development, with power conversion efficiencies reaching 25.5% for single-junction devices and 29.8% for Silicon-Perovskite tandem configurations. Even though research mainly focused on improving the efficiency of perovskite photovoltaics (PV), stability and scalability remain fundamental aspects of a mature photovoltaics technology. For n-i-p structure perovskite solar cells, using poly-triaryl(amine) (PTAA) as hole transport layer (HTL) allowed to achieve marked improvements in device stability compared with other common hole conductors. For p-i-n structure, poly-triaryl(amine) is also routinely used as dopant-free hole transport layer, but problems in perovskite film growth, and its limited resistance to stress and imperfect batch-to-batch reproducibility, hamper its use for device upscaling. Following previous computational investigations, in this work, we report the synthesis of two small-molecule organic hole transport layers (BPT-1,2), aiming to solve the above-mentioned issues and allow upscale to the module level. By using BPT-1 and methylammonium-free perovskite, max. Power conversion efficiencies of 17.26% and 15.42% on a small area (0.09 cm2) and mini-module size (2.25 cm2), respectively, were obtained, with a better reproducibility than with poly-triaryl(amine). Moreover, BPT-1 was demonstrated to yield more stable devices compared with poly-triaryl(amine) under ISOS-D1, T1, and L1 accelerated life-test protocols, reaching maximum T90 values >1000 h on all tests. © 2022 Zhengzhou University.

Castriotta, L.A., Infantino, R., Vesce, L., Stefanelli, M., Dessì, A., Coppola, C., et al. (2023). Stable methylammonium-free p-i-n perovskite solar cells and mini-modules with phenothiazine dimers as hole-transporting materials. ENERGY & ENVIRONMENT MATERIALS, 6(6), 1-10 [10.1002/eem2.12455].

Stable methylammonium-free p-i-n perovskite solar cells and mini-modules with phenothiazine dimers as hole-transporting materials

Infantino, Rossella;Coppola, Carmen;Sinicropi, Adalgisa;
2023-01-01

Abstract

During the last decade, perovskite solar technologies underwent an impressive development, with power conversion efficiencies reaching 25.5% for single-junction devices and 29.8% for Silicon-Perovskite tandem configurations. Even though research mainly focused on improving the efficiency of perovskite photovoltaics (PV), stability and scalability remain fundamental aspects of a mature photovoltaics technology. For n-i-p structure perovskite solar cells, using poly-triaryl(amine) (PTAA) as hole transport layer (HTL) allowed to achieve marked improvements in device stability compared with other common hole conductors. For p-i-n structure, poly-triaryl(amine) is also routinely used as dopant-free hole transport layer, but problems in perovskite film growth, and its limited resistance to stress and imperfect batch-to-batch reproducibility, hamper its use for device upscaling. Following previous computational investigations, in this work, we report the synthesis of two small-molecule organic hole transport layers (BPT-1,2), aiming to solve the above-mentioned issues and allow upscale to the module level. By using BPT-1 and methylammonium-free perovskite, max. Power conversion efficiencies of 17.26% and 15.42% on a small area (0.09 cm2) and mini-module size (2.25 cm2), respectively, were obtained, with a better reproducibility than with poly-triaryl(amine). Moreover, BPT-1 was demonstrated to yield more stable devices compared with poly-triaryl(amine) under ISOS-D1, T1, and L1 accelerated life-test protocols, reaching maximum T90 values >1000 h on all tests. © 2022 Zhengzhou University.
2023
Castriotta, L.A., Infantino, R., Vesce, L., Stefanelli, M., Dessì, A., Coppola, C., et al. (2023). Stable methylammonium-free p-i-n perovskite solar cells and mini-modules with phenothiazine dimers as hole-transporting materials. ENERGY & ENVIRONMENT MATERIALS, 6(6), 1-10 [10.1002/eem2.12455].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/1218794