Efficiency Potential and Voltage Loss of Inorganic CsPbI<sub>2</sub>Br Perovskite Solar Cells
Max Grischek, Pietro Caprioglio, Jiahuan Zhang, Francisco Peña‐Camargo, Kári Sveinbjörnsson, Fengshuo Zu, Dorothee Menzel, Jonathan Warby, Jinzhao Li, Norbert Koch, Eva Unger, Lars Korte, Dieter Neher, Martin Stolterfoht, Steve Albrecht
Abstract
Inorganic perovskite solar cells show excellent thermal stability, but the reported power conversion efficiencies are still lower than for organic–inorganic perovskites. This is mainly caused by lower open‐circuit voltages ( V OC s). Herein, the reasons for the low V OC in inorganic CsPbI 2 Br perovskite solar cells are investigated. Intensity‐dependent photoluminescence measurements for different layer stacks reveal that n–i–p and p–i–n CsPbI 2 Br solar cells exhibit a strong mismatch between quasi‐Fermi level splitting (QFLS) and V OC . Specifically, the CsPbI 2 Br p–i–n perovskite solar cell has a QFLS– e · V OC mismatch of 179 meV, compared with 11 meV for a reference cell with an organic–inorganic perovskite of similar bandgap. On the other hand, this study shows that the CsPbI 2 Br films with a bandgap of 1.9 eV have a very low defect density, resulting in an efficiency potential of 20.3% with a MeO–2PACz hole‐transporting layer and 20.8% on compact TiO 2 . Using ultraviolet photoelectron spectroscopy measurements, energy level misalignment is identified as a possible reason for the QFLS– e · V OC mismatch and strategies for overcoming this V OC limitation are discussed. This work highlights the need to control the interfacial energetics in inorganic perovskite solar cells, but also gives promise for high efficiencies once this issue is resolved.