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    Enhancing the triiodide reduction activity of a perovskite-based electrocatalyst for dye-sensitized solar cells through exsolved silver nanoparticles

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    Fulltext not available
    Authors
    Xu, M.
    Wang, Wei
    Zhong, Yijun
    Xu, Xiaomin
    Wang, J.
    Zhou, W.
    Shao, Zongping
    Date
    2019
    Type
    Journal Article
    
    Metadata
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    Citation
    Xu, M. and Wang, W. and Zhong, Y. and Xu, X. and Wang, J. and Zhou, W. and Shao, Z. 2019. Enhancing the triiodide reduction activity of a perovskite-based electrocatalyst for dye-sensitized solar cells through exsolved silver nanoparticles. Journal of Materials Chemistry A. 7 (29): pp. 17489-17497.
    Source Title
    Journal of Materials Chemistry A
    DOI
    10.1039/c9ta05005a
    ISSN
    2050-7488
    Faculty
    Faculty of Science and Engineering
    School
    WASM: Minerals, Energy and Chemical Engineering
    Funding and Sponsorship
    http://purl.org/au-research/grants/arc/DP150104365
    http://purl.org/au-research/grants/arc/DP160104835
    URI
    http://hdl.handle.net/20.500.11937/91953
    Collection
    • Curtin Research Publications
    Abstract

    Research on the efficient synthesis and application of nanostructured perovskite oxides is attracting intensive attention nowadays. Herein, a silver (Ag) nanoparticle decorated A-site deficient perovskite is prepared using a facile exsolution method and used as a cathode in dye-sensitized solar cells (DSSCs). The Ag nanoparticle modified (La0.8Sr0.2)0.95MnO3-δ composite (e-LSAM) prepared by the exsolution method displays exceptional activity for the electrocatalytic triiodide (I3-) reduction reaction (IRR) in DSSCs, which is much superior to that of the Ag/perovskite hybrids synthesized by physical mixing and impregnation methods due to the strong interfacial interaction and small Ag particle size. DSSC with this newly developed heteroelectrocatalyst shows a high photovoltaic efficiency of 12.4%, surpassing that of the expensive platinum (Pt)-based control cell (9.93%) with an enhancement factor of 25%, which is among the highest performances of Pt-free cathodes reported to date. Moreover, this new composite cathode shows a much superior IRR durability to Pt, indicating its great potential for replacing Pt. This study paves the way for the rational design of active and durable perovskite electrocatalysts for various energy conversion and storage systems.

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