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In this work, we demonstrate that an external pressure of 15–30 kPa can significantly improve metal halide perovskite (MHP) film thermal stability. We demonstrate this through the application of weight on top of an MHP film during thermal aging in preserving the perovskite phase and the mobile ion concentration, an effect which we hypothesize reduces the extent to which volatile species can escape from the MHP lattice. This method is shown to be effective for a more scalable approach by only applying the weight to a cover glass during the lamination of an epoxy-based resin, after which the weight is removed. The amount of pressure applied during lamination is shown to correlate with stability in both 1 sun illumination and damp heat testing. Lastly, the performance of MHP photovoltaic devices is improved using pressure during lamination, an effect which is attributed to improved interfacial contact between the MHP and the adjacent charge transport layers and healing of any voids or defects that may exist at the buried interface after processing. As such, there are implications for tuning the amount of pressure that is applied during lamination to enable the durability of MHP solar modules toward manufacturing-scale deployment. 

Air-processed carbon-based perovskite solar cells (C-PSCs) offer scalable and cost-effective photovoltaic manufacturing but face efficiency loss compared to metal-contact perovskite solar cells. 

Abstract Hybrid metal halide perovskite (MHP) materials, while being promising for photovoltaic technology, also encounter challenges related to material stability. Combining 2D MHPs with 3D MHPs offers a viable solution, yet there is a gap in the understanding of the stability among various 2D materials. The mechanical, ionic, and environmental stability of various 2D MHP ligands are reported, and an improvement with the use of a quater‐thiophene‐based organic cation (4TmI) that forms an organic‐semiconductor incorporated MHP structure is demonstrated. It is shown that the best balance of mechanical robustness, environmental stability, ion activation energy, and reduced mobile ion concentration under accelerated aging is achieved with the usage of 4TmI. It is believed that by addressing mechanical and ion‐based degradation modes using this built‐in barrier concept with a material system that also shows improvements in charge extraction and device performance, MHP solar devices can be designed for both reliability and efficiency. 

We report on an examination of mobile ion concentration (N₀) in perovskite solar cells (PSCs) as a function of temperature and device architecture.