Transparent 3 nm-thick MoS2 counter electrodes for bifacial dye-sensitized solar cells

[Display omitted] Molybdenum disulfide (MoS2) counter electrode (CE) is considered one of the most viable alternatives to Pt CE in dye-sensitized solar cells (DSSCs) owing to its abundance, low cost, and superior electrocatalytic activity. However, mostly, MoS2 CEs for DSSCs are prepared by conventi...

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Published inJournal of industrial and engineering chemistry (Seoul, Korea) Vol. 80; pp. 106 - 111
Main Authors Jeong, Taehee, Ham, So-Yeon, Koo, Bonkee, Lee, Phillip, Min, Yo-Sep, Kim, Jae-Yup, Ko, Min Jae
Format Journal Article
LanguageEnglish
Published Elsevier B.V 25.12.2019
한국공업화학회
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Summary:[Display omitted] Molybdenum disulfide (MoS2) counter electrode (CE) is considered one of the most viable alternatives to Pt CE in dye-sensitized solar cells (DSSCs) owing to its abundance, low cost, and superior electrocatalytic activity. However, mostly, MoS2 CEs for DSSCs are prepared by conventional chemical reactions and annealing at a high temperature. By these conventional processes, deposition of sufficiently thin and transparent MoS2 layers is challenging; therefore, bifacial DSSCs employing transparent MoS2 CEs have not been studied. Here, we report transparent few-nanometer-thick MoS2 CEs prepared by atomic layer deposition at a relatively low temperature (98°C) for bifacial DSSC applications. MoS2 nanofilms with precisely controlled thicknesses of 3–16nm are conformally coated on transparent conducting oxide glass substrates. With increase in the MoS2 nanofilm thickness, the MoS2 CE electrocatalytic activity for the iodide/triiodide redox couple enhances, but its transparency decreases. Notably, the application of a thinner MoS2 nanofilm in a bifacial DSSC leads to lower conversion efficiency under front-illumination, but higher conversion efficiency under back-illumination. In particular, only the 3nm-thick MoS2 nanofilm shows reasonable photovoltaic performances under both front- and back-illumination conditions.
ISSN:1226-086X
1876-794X
DOI:10.1016/j.jiec.2019.07.037