Abstract
Perovskite solar cells (PSCs) have already achieved efficiencies of over 25%; however, their instability and degradation in the operational environment have prevented them from becoming commercially viable. Understanding the degradation mechanism, as well as improving the fabrication technique for achieving high-quality perovskite films, is crucial to overcoming these shortcomings. In this study, we investigated details in the changes of physical properties associated with the degradation and/or decomposition of perovskite films and solar cells using XRD, FESEM, EDX, UV-Vis, Hall-effect, and current-voltage (I-V) measurement techniques. The dissociation, as well as the intensity of perovskite peaks, have been observed as an impact of film degradation by humidity. The decomposition rate of perovskite film has been estimated from the structural and optical changes. The performance degradation of novel planner structure PSCs has been investigated in detail. The PSCs were fabricated in-room ambient using candle soot carbon and screen-printed Ag electrode. It was found that until the perovskite film decomposed by 30%, the film properties and cell efficiency remained stable.
Highlights
The organic-inorganic perovskite solar cells (PSCs) are considered a major recent discovery in the field of photovoltaics, which has attracted much attention recently
We focused on the effect of humidity and heat for understanding the perovskite films, as well as Perovskite solar cells (PSCs) degradation rate
Water molecules (H2 O) from the ambient first diffused into the perovskite film and formed CH3 NH3 PbI3 ·H2 O (Equation (6)), which initiated the slow degradation of Jsc [35]
Summary
The organic-inorganic perovskite solar cells (PSCs) are considered a major recent discovery in the field of photovoltaics, which has attracted much attention recently. Kim et al [11] proposed that the lifetime of PSC could increase via the incorporation of materials that had water-splitting capability within the adjacent layers (ETL or HTL) of the perovskite film. Guo et al have been investigating the impact of light on the degradation of PSC operated under vacuum and a nitrogen ambient [12] They reported that whereas lightinduced phase segregation, morphological deformation, and lattice shrinkage occur in a vacuum, only lattice shrinkage occurs when solar cells are operated in a nitrogen ambient, resulting in improved device stability. Despite the scientific community’s best attempts to prevent the penetration of water molecules into the perovskite layers from the environment, device lifetimes, and stability remains yet to be critical, and certainly, novel disruptive approaches are necessary to move forward with PSC commercialization. The complete PSCs with novel planner structures have been fabricated and their performance and stability have further been investigated in this study for similar environmental conditions and similar time duration
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