Aging effects in interface-engineered perovskite solar cells with 2D nanomaterials: A depth profile analysis

Yan Busby, Antonio Agresti, Sara Pescetelli, Aldo Di Carlo, Céline Noel, Jean-Jacques Pireaux, Laurent Houssiau

Résultats de recherche: Contribution à un journal/une revueArticle

Résumé

The stability of perovskite solar cells (PSCs) is a major factor limiting the market breakthrough of this technology. To understand the aging effects in PSCs is mandatory to rationally design implemented architectures and materials combining a viable deposition process, efficiency and stability. Despite of this
evidence, only few experimental works succeeded in the direct quantitative characterization of aging effects in PSCs. In this work, we apply state-of-the-art X-ray photoelectron spectroscopy (XPS) depth profile analysis and time-of-flight secondary ion mass spectrometry (ToF-SIMS) 3D imaging to investigate the light-induced degradation of layers and interfaces in reference (Au/Spiro-OMeTAD/CH3NH3PbI3/m-TiO2/cTiO2/FTO) and interface-engineered mesoscopic PSCs in which graphene flakes are added into the mesoscopic TiO2
layer and a solution-processed 2H-MoS2 flakes buffer layer is added at the Spiro-OMeTAD/CH3NH3PbI3 interface. Results show that the graphene addition into the mesoscopic TiO2 layer improves the stability of the PSC by reducing the locally-inhomogeneous light-induced back-conversion of the CH3NH3PbI3 layer into PbIxand PbOx species and the consequent release of iodine species, which
diffuse across the interfaces and causes the modifications at the gold electrode (Au-I bonding) and themesoscopic TiO2(Ti-I bonding) interfaces. Moreover, where the CH3NH3PbI3 layer is preserved the gold diffusion across the entire device structure is strongly reduced even after the aging. The 2H-MoS2 flakes
buffer layer allows limiting the localized diffusion of gold and the iodine diffusion in as-prepared PSCs while it is rather ineffective in preventing light-induced aging effects. Overall, thanks to the lower average degradation of the layers and interfaces, interface engineered PSCs could retain ~60% of their
initial PCE after the aging respect to less than ~25% in the reference cells
langue originaleAnglais
Pages (de - à)1-10
Nombre de pages10
journalMaterials Today Energy
Volume9
Les DOIs
étatPublié - 1 sept. 2018

Empreinte digitale

Nanostructured materials
Aging of materials
Gold
Graphite
Iodine
Graphene
Degradation
Buffer layers
Secondary ion mass spectrometry
Perovskite solar cells
X ray photoelectron spectroscopy
Imaging techniques
Electrodes

mots-clés

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    abstract = "The stability of perovskite solar cells (PSCs) is a major factor limiting the market breakthrough of this technology. To understand the aging effects in PSCs is mandatory to rationally design implemented architectures and materials combining a viable deposition process, efficiency and stability. Despite of thisevidence, only few experimental works succeeded in the direct quantitative characterization of aging effects in PSCs. In this work, we apply state-of-the-art X-ray photoelectron spectroscopy (XPS) depth profile analysis and time-of-flight secondary ion mass spectrometry (ToF-SIMS) 3D imaging to investigate the light-induced degradation of layers and interfaces in reference (Au/Spiro-OMeTAD/CH3NH3PbI3/m-TiO2/cTiO2/FTO) and interface-engineered mesoscopic PSCs in which graphene flakes are added into the mesoscopic TiO2layer and a solution-processed 2H-MoS2 flakes buffer layer is added at the Spiro-OMeTAD/CH3NH3PbI3 interface. Results show that the graphene addition into the mesoscopic TiO2 layer improves the stability of the PSC by reducing the locally-inhomogeneous light-induced back-conversion of the CH3NH3PbI3 layer into PbIxand PbOx species and the consequent release of iodine species, whichdiffuse across the interfaces and causes the modifications at the gold electrode (Au-I bonding) and themesoscopic TiO2(Ti-I bonding) interfaces. Moreover, where the CH3NH3PbI3 layer is preserved the gold diffusion across the entire device structure is strongly reduced even after the aging. The 2H-MoS2 flakesbuffer layer allows limiting the localized diffusion of gold and the iodine diffusion in as-prepared PSCs while it is rather ineffective in preventing light-induced aging effects. Overall, thanks to the lower average degradation of the layers and interfaces, interface engineered PSCs could retain ~60{\%} of theirinitial PCE after the aging respect to less than ~25{\%} in the reference cells",
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    Aging effects in interface-engineered perovskite solar cells with 2D nanomaterials : A depth profile analysis. / Busby, Yan; Agresti, Antonio; Pescetelli, Sara; Di Carlo, Aldo; Noel, Céline; Pireaux, Jean-Jacques; Houssiau, Laurent.

    Dans: Materials Today Energy, Vol 9, 01.09.2018, p. 1-10.

    Résultats de recherche: Contribution à un journal/une revueArticle

    TY - JOUR

    T1 - Aging effects in interface-engineered perovskite solar cells with 2D nanomaterials

    T2 - A depth profile analysis

    AU - Busby, Yan

    AU - Agresti, Antonio

    AU - Pescetelli, Sara

    AU - Di Carlo, Aldo

    AU - Noel, Céline

    AU - Pireaux, Jean-Jacques

    AU - Houssiau, Laurent

    PY - 2018/9/1

    Y1 - 2018/9/1

    N2 - The stability of perovskite solar cells (PSCs) is a major factor limiting the market breakthrough of this technology. To understand the aging effects in PSCs is mandatory to rationally design implemented architectures and materials combining a viable deposition process, efficiency and stability. Despite of thisevidence, only few experimental works succeeded in the direct quantitative characterization of aging effects in PSCs. In this work, we apply state-of-the-art X-ray photoelectron spectroscopy (XPS) depth profile analysis and time-of-flight secondary ion mass spectrometry (ToF-SIMS) 3D imaging to investigate the light-induced degradation of layers and interfaces in reference (Au/Spiro-OMeTAD/CH3NH3PbI3/m-TiO2/cTiO2/FTO) and interface-engineered mesoscopic PSCs in which graphene flakes are added into the mesoscopic TiO2layer and a solution-processed 2H-MoS2 flakes buffer layer is added at the Spiro-OMeTAD/CH3NH3PbI3 interface. Results show that the graphene addition into the mesoscopic TiO2 layer improves the stability of the PSC by reducing the locally-inhomogeneous light-induced back-conversion of the CH3NH3PbI3 layer into PbIxand PbOx species and the consequent release of iodine species, whichdiffuse across the interfaces and causes the modifications at the gold electrode (Au-I bonding) and themesoscopic TiO2(Ti-I bonding) interfaces. Moreover, where the CH3NH3PbI3 layer is preserved the gold diffusion across the entire device structure is strongly reduced even after the aging. The 2H-MoS2 flakesbuffer layer allows limiting the localized diffusion of gold and the iodine diffusion in as-prepared PSCs while it is rather ineffective in preventing light-induced aging effects. Overall, thanks to the lower average degradation of the layers and interfaces, interface engineered PSCs could retain ~60% of theirinitial PCE after the aging respect to less than ~25% in the reference cells

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