Kyosuke Yonezawa

Annealing effects on CsPbI3-based planar heterojunction perovskite solar cells formed by vacuum deposition method

Cesium iodide (CsI) is attracting attention as a substitute for organic materials such as CH3NH3I. In this work, we fabricated sequential-vacuum-deposited planar heterojunction (PHJ) cesium lead iodide (CsPbI3) perovskite solar cells with enhanced efficiencies by varying the annealing time (0.5, 1, 5, and 10 min). The effect of performance enhancement was investigated as a function of varying annealing time at 350 °C employing a hot plate. The best-performing device was obtained with an annealing time of 1 min, delivered photocurrent density (J SC) of 12.06 mA/cm2, voltage (V OC) of 0.71 V, and fill factor (FF) of 0.67, leading to a power conversion efficiency (PCE) of 5.71% at standard AM 1.5G solar illumination.

Improved Reproducibility and Intercalation Control of Efficient Planar Inorganic Perovskite Solar Cells by Simple Alternate Vacuum Deposition of PbI2 and CsI

Vacuum deposition is a simple and controllable approach that aims to form higher-quality perovskite films compared with those formed using solution-based deposition processes. Herein, we demonstrate a novel method to promote the intercalation control of inorganic cesium lead iodide (CsPbI3) perovskite thin films via alternate vacuum deposition. We also investigated the effect of layer-by-layer deposition of PbI2/CsI to fabricate efficient planar heterojunction CsPbI3 thin films and solar cells. This procedure is comparatively simple when compared with commonly used coevaporation techniques; further, precise intercalation control of the CsPbI3 thin films can be achieved by increasing the number of layers in the layer-by-layer deposition of PbI2/CsI. The best control and the highest reproducibility were achieved for the deposition of four double layers owing to the precise intercalation control during the deposition of the CsPbI3 thin film. A power conversion efficiency of 6.79% was obtained via alternating vacuum deposition of two double layers with a short-circuit current density (Jsc) of 12.06 mA/cm2, an open-circuit voltage (Voc) of 0.79 V, and a fill factor (FF) of 0.72. Our results suggest a route for inorganic precursors to be used for efficient perovskite solar cells via alternating vacuum deposition.