Interfacial engineering of a ZnO electron transporting layer using self-assembled monolayers for high performance and stable perovskite solar cells

Authors
Han, JinyoungKwon, HannahKim, EunahKim, Dong-WookSon, Hae JungKim, Dong Ha
Issue Date
2020-01-28
Publisher
ROYAL SOC CHEMISTRY
Citation
JOURNAL OF MATERIALS CHEMISTRY A, v.8, no.4, pp.2105 - 2113
Abstract
We developed perovskite solar cells (PSCs) with a ZnO electron-transporting layer (ETL) of which the surface was passivated with methoxybenzoic acid self-assembled monolayers (SAMs). The self-assembled monolayer (SAM) simultaneously improved the photovoltaic performance and device stability. First, the methoxybenzoic acid, which is noncovalently bonded to the methylammonium of the perovskite layer, effectively induced dipole moments; in particular, 3,4,5-trimethoxybenzoic acid (TMBA) gave a larger workfunction shift of ZnO ETL compared with 4-methoxybenzoic acid (MBA) and 3,4-dimethoxybenzoic acid (DMBA) owing to its strong dipole moment and hydrogen-bonding between the methoxy group and ammonium. This effectively enhanced the built-in voltage of the perovskite solar cell (PSC) device, which resulted in an improved electron transfer from the active layer to the ETL and a higher open-circuit voltage. Secondly, the SAM layer controlled the wettability of the perovskite precursor solution on the ZnO ETL and significantly improved the crystalline properties of the perovskite layer. Moreover, the ZnO/SAM ETL remarkably increased the PSC device stability under ambient conditions by preventing the proton transfer reaction between the perovskite layer and the ZnO ETL. As a result, the TMBA-SAM based PSC device achieved a significantly enhanced efficiency of 13.75% compared to 1.44% for the bare ZnO with high long-term stability.
Keywords
ZINC-OXIDE; EFFICIENT; STABILITY; ENHANCEMENT; TEMPERATURE; EXTRACTION; FILMS; ZINC-OXIDE; EFFICIENT; STABILITY; ENHANCEMENT; TEMPERATURE; EXTRACTION; FILMS; 페로브스카이트 태양전지; 계면; 광전 변환효율
ISSN
2050-7488
URI
https://pubs.kist.re.kr/handle/201004/119068
DOI
10.1039/c9ta12750j
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KIST Article > 2020
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