Efficient and stable perovskite solar cells by introducing organic electrolytes as dual-side passivation layer
Heejoo Kim a c, Ju-Hyun Kim b, Yong-Ryun Kim c, Hongsuk Suh d, Kwanghee Lee b
a Graduate School of Energy Convergence, Institute of Integrated Technology, Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea
b School of Materials Science and Engineering, Heeger Center for Advanced Materials & Research Institute for Solar and Sustainable Energies, Gwangju Institute of Science and Technology
c Research Institute for Solar and Sustainable Energies (RISE), Gwangju Institute of Science and Technology, Gwangju 61005, Republic of Korea
d Department of Chemistry and Chemistry Institute for Functional Materials, Pusan National University (PNU), Busan 46241, Republic of Korea
International Conference on Hybrid and Organic Photovoltaics
Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV23)
London, United Kingdom, 2023 June 12th - 14th
Organizers: Tracey Clarke, James Durrant and Trystan Watson
Oral, Heejoo Kim, presentation 155
DOI: https://doi.org/10.29363/nanoge.hopv.2023.155
Publication date: 30th March 2023

Interface engineering at the interface between the perovskite layer and the charge transport layer (CTL), or CTL and metal electrodes, is critical for demonstrating the efficient and stable perovskite solar cells (PSCs) [1, 2]. Herein, we demonstrate the efficient and stable PSCs by introducing the organic electrolytes (OEs) as a “dual-side passivation layer” in both p-i-n and n-i-p configuration of PSCs. Firstly, a newly synthesized bathocuproine (BCP)-based nonconjugated polyelectrolyte (poly-BCP) is introduced between the tin oxide (SnO2) CTL and the perovskite layer in the n-i-p configuration. Poly-BCP effectively passivate oxygen-vacancy defects of the SnO2 side and simultaneously scavenges ionic defects of perovskite side, suppressing both bulk and interfacial nonradiative recombination in PSCs [3]. As a result, the modified PSCs exhibited a high power conversion efficiency (PCE) of 24.4% and a high open-circuit voltage of 1.21 V. Furthermore, the non-encapsulated PSCs show excellent long-term stability by retaining 93% of the initial PCE after 700 h under continuous 1-sun irradiation in nitrogen atmosphere conditions. Secondly, amine-functionalized small molecule electrolytes (SMEs) are introduced as passivation layer between the PCBM CTL and metal electrode (here, Cu) in the p-i-n configuration [4]. A strong coordination bond of Cu─N forms at the Cu/SMEs interface, leading to the layer–layer growth mode for the dense formation of Cu electrodes with a strong adhesion to the CTL. Thus, this modified electrode prevents the ingress of moisture into the PSCs, resulting in outstanding moisture stability; the efficiency of non-encapsulated PSCs retains 90% of the initial PCE after 200 days of exposure to atmospheric air (25 ℃, relative humidity [RH] ~20–40%). Under harsher conditions (e.g., 25 ℃/RH65%, 25 ℃/RH85% and immersion in water) for a considerable time period, the modified PSCs manifest relatively no degradation compared with the pristine PSCs.

This work was supported by the Korea Government (the Ministry of Science and ICT, MSIT) (NRF-2021R1F1A1061175); by the Technology Development Program to Solve Climate Change of the NRF funded by MSIT (NRF-2020M1A2A2080748); by the GIST Research Institute (GRI), RISE, grant funded by the GIST in 2023.

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