Low-temperature processed SnO is a promising electron transporting layer in perovskite solar cells (PSCs) due to its optoelectronic advantage. Atomic layer deposition (ALD) is suitable for forming a conformal SnO layer on a high-haze substrate. However, oxygen vacancy formed by the conventional ALD process using HO might have a detrimental effect on the efficiency and stability of PSCs. Here, we report on the photovoltaic performance and stability of PSCs based on the ALD-SnO layer with low oxygen vacancies fabricated HO. Compared to the ALD-SnO layer formed using HO vapors, the ALD-SnO layer prepared HO shows better electron extraction due to a reduced oxygen vacancy associated with the highly oxidizing nature of HO. As a result, the power conversion efficiency (PCE) is enhanced from 21.42% for HO to 22.34% for HO mainly due to an enhanced open-circuit voltage. Operational stability is simultaneously improved, where 89.3% of the initial PCE is maintained after 1000 h under an ambient condition for the HO-derived ALD SnO as compared to the control device maintaining 72.5% of the initial PCE.
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http://dx.doi.org/10.1039/d2nr06884b | DOI Listing |
ACS Appl Energy Mater
January 2021
Department of Materials Science, Uppsala University, Uppsala 75103, Sweden.
High-end organic-inorganic lead halide perovskite semitransparent p-i-n solar cells for tandem applications use a phenyl-C-butyric acid methyl ester (PCBM)/atomic layer deposition (ALD)-SnO electron transport layer stack. Omitting the PCBM would be preferred for manufacturing, but has in previous studies on (FA,MA)Pb(Br,I) and (Cs,FA)Pb(Br,I) and in this study on CsFAMAPbBrI (perovskite) led to poor solar cell performance because of a bias-dependent light-generated current. A direct ALD-SnO exposure was therefore suggested to form a nonideal perovskite/SnO interface that acts as a transport barrier for the light-generated current.
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