Aging effects in interface-engineered perovskite solar cells with 2D nanomaterials: A depth profile analysis. (September 2018)

• Record Type: Journal Article
• Authors: Busby, Yan; Agresti, Antonio; Pescetelli, Sara; Di Carlo, Aldo; Noel, Celine; Pireaux, Jean-Jacques; Houssiau, Laurent
• Is Part Of: Materials today energy. Volume 9(2018)
• Page Start: 1
• Page End: 10
• Publication Date: 2018-09
• Subjects: Perovskite solar cells -- Interface engineering -- XPS -- ToF-SIMS -- Depth profiling -- Interface analysis -- Aging effects; Energy development -- Periodicals; Energy industries -- Periodicals; Power resources -- Periodicals; Energy policy -- Periodicals; Energy development; Energy industries; Energy policy; Power resources; Electronic journals; Periodicals; 621.042
• DOI: 10.1016/j.mtener.2018.04.005
• Languages: English
• ISSNs: 2468-6069

Abstract

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 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/CH3 NH3 PbI3 /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/CH3 NH3 PbI3 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 CH3 NH3 PbI3 layer into PbIx and PbO x 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 the mesoscopic TiO2 (Ti-I bonding) interfaces. Moreover, where the CH3 NH3 PbI3 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. Graphical abstract: Highlights: Light-induced aging effects in interface engineered PSC are characterized by depth profiling. ToF-SIMS depth profiles of the full hybrid device stack is performed by low-energy Cs+. Graphene addition into the m-TiO2 is improves the average light stability of the perovskite. The light-induced aging is correlated by specific indicators in XPS and ToF-SIMS profiles.