Proceedings of International Conference on Hybrid and Organic Photovoltaics (HOPV22)
DOI: https://doi.org/10.29363/nanoge.hopv.2022.080
Publication date: 20th April 2022
Engineering interfaces in perovskite solar cells is nowadays paramount in the optimization of multilayer perovskite device stack. This stem true for multi-dimensional (2D/3D) perovskite based solar cells, where high efficiency can be combined with promising device durability. However, the exact function of the 2D/3D interface in controlling the device behaviour and the the role of the 2D cations are still vague.
Here I will discuss the 2D/3D functions which can simultaneously act as surface passivant, electron blocking layer, and driving efficient and selective charge extraction. In particular, I will demonstrate that the exact knowledge on the interface energetics is crucial to obtain for a smart interface engineering. As an example, I will discuss the case of thiophene-based 2D perovskite/ 3D perovskite interfaces forming a p-n junction. This leads to a reduction of the electron density at the hole transport layer interface and ultimately suppress the interfacial recombination. As a consequence, we demonstrate that photovoltaic devices with enhanced fill factor (FF) and open-circuit voltage (VOC) of 1.19V which approaches the potential internal Quasi-Fermi Level Splitting (QFLS) voltage of the perovskite absorber, nullifying the interfacial losses. We thus identify the essential parameters and energetic alignment scenario required for 2D/3D perovskite systems in order to surpass the current limitations of hybrid perovskite solar cell performances. This knowledge turns fundamental for device design, opening a new avenue for perovskite interface optimization.
I acknowledge the HY-NANO project that has received funding from the European Research Council (ERC) Starting Grant 2018 under the European Union’s Horizon 2020 research and innovation programme (Grant agreement No. 802862).