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Updated: Mar 8, 2026

Monovalent Cation Doping of CH3NH3PbI3 for Efficient Perovskite Solar Cells
Published on: March 19, 2017
Cesium power: low Cs+ levels impart stability to perovskite solar cells
Melepurath Deepa1, Manuel Salado2, Laura Calio2
1Department of Chemistry, Indian Institute of Technology Hyderabad, Kandi-502285, Sangareddy, Telangana, India.
Abstract:
Towards increasing the stability of perovskite solar cells, the addition of Cs+ is found to be a rational approach. Recently triple cation based perovskite solar cells were found to be more effective in terms of stability and efficiency. Heretofore they were unexplored, so we probed the Cs/MA/FA (cesium/methyl ammonium/formamidinium) cation based perovskites by X-ray photoelectron spectroscopy (XPS) and correlated their compositional features with their solar cell performances. The Cs+ content was found to be optimum at 5%, when incorporated in the (MA0.15FA0.85)Pb(I0.85Br0.15)3 lattice, because the corresponding device yielded the highest fill factor compared to the perovskite without Cs+ and with 10% Cs+. XPS studies distinctly reveal how Cs+ aids in maintaining the expected stoichiometric ratios of I : Pb2+, I : N and Br : Pb2+ in the perovskites, and how the valence band (VB) edge is dependent on the Cs+ proportion, which in turn governs the open circuit voltage. Even at a low content of 5%, Cs+ resides deep within the absorber layer, and ensures minimum distortion of the VB level (compared to 0% and 10% Cs+ perovskites) upon Ar+ sputtering, thus allowing the formation of a stable robust material that delivers excellent solar cell response. This study which brings out the role of Cs+ is anticipated to be of paramount significance to further engineer the composition and improve device performances.
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