Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells
Power conversion efficiency (PCE) of the perovskite solar cell in its pristine form is excellent, and its performance increases upon modification with a 3 % concentration of Co2+-MAPbI2Br by the sol–gel spin coating method. X-ray diffraction analysis has attested to the successful integration of Co2...
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2025-01-01
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author | M.I. Khan Saddam Hussain M. Atif J.E. Leal-Perez B.A. García-Grajeda J.M. Mendivil-Escalante |
author_facet | M.I. Khan Saddam Hussain M. Atif J.E. Leal-Perez B.A. García-Grajeda J.M. Mendivil-Escalante |
author_sort | M.I. Khan |
collection | DOAJ |
description | Power conversion efficiency (PCE) of the perovskite solar cell in its pristine form is excellent, and its performance increases upon modification with a 3 % concentration of Co2+-MAPbI2Br by the sol–gel spin coating method. X-ray diffraction analysis has attested to the successful integration of Co2+ ions into the cubic structure of MAPbI2Br. It is worthy of note that 3 % Co2+ doping films exhibited an enlarged grain size that is considered a factor that would raise device performance. Further assessment of the optical properties by UV–Vis analysis reveals that the incorporation of 3 % Co2+ doping into MAPbI2Br reduced the band gap energy to 1.84 eV. All in all, in terms of important solar cell performance metrics, the introduction of 3 % Co2+ doping to MAPbI2Br has led to significant improvements. In particular, FF increased to 0.75, and this was accompanied by enhancements in Jsc to 7.83 mA cm−2, Voc to 1.02 V, and η to 5.85 %. Remarkably, these improvements in important factors bring attention to the advantageous effect of Co2+ doping. We have attempted to contribute our work to the perovskites that are still under development in the organic–inorganic world for solar cell technology. We propose that our findings hold substantial knowledge that will contribute to the improvement and development of perovskite solar cells. |
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language | English |
publishDate | 2025-01-01 |
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spelling | doaj-art-9abd9a3fda7044f989a4c0a57c4cd2252025-01-29T05:00:45ZengElsevierResults in Chemistry2211-71562025-01-0113101974Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cellsM.I. Khan0Saddam Hussain1M. Atif2J.E. Leal-Perez3B.A. García-Grajeda4J.M. Mendivil-Escalante5Department of Physics, The University of Lahore, 53700, PakistanUniversidad Autónoma de Sinaloa. Facultad de Ingeniería Mochis, Fuente de Poseidón y Gral. Ángel Flores S/N, Las Fuentes, 81223 Los Mochis, Sinaloa, Mexico; Corresponding author.Department of Physics and Astronomy, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi ArabiaUniversidad Autónoma de Sinaloa. Facultad de Ingeniería Mochis, Fuente de Poseidón y Gral. Ángel Flores S/N, Las Fuentes, 81223 Los Mochis, Sinaloa, MexicoUniversidad Autónoma de Sinaloa. Facultad de Ingeniería Mochis, Fuente de Poseidón y Gral. Ángel Flores S/N, Las Fuentes, 81223 Los Mochis, Sinaloa, MexicoUniversidad Autónoma de Sinaloa. Facultad de Ingeniería Mochis, Fuente de Poseidón y Gral. Ángel Flores S/N, Las Fuentes, 81223 Los Mochis, Sinaloa, MexicoPower conversion efficiency (PCE) of the perovskite solar cell in its pristine form is excellent, and its performance increases upon modification with a 3 % concentration of Co2+-MAPbI2Br by the sol–gel spin coating method. X-ray diffraction analysis has attested to the successful integration of Co2+ ions into the cubic structure of MAPbI2Br. It is worthy of note that 3 % Co2+ doping films exhibited an enlarged grain size that is considered a factor that would raise device performance. Further assessment of the optical properties by UV–Vis analysis reveals that the incorporation of 3 % Co2+ doping into MAPbI2Br reduced the band gap energy to 1.84 eV. All in all, in terms of important solar cell performance metrics, the introduction of 3 % Co2+ doping to MAPbI2Br has led to significant improvements. In particular, FF increased to 0.75, and this was accompanied by enhancements in Jsc to 7.83 mA cm−2, Voc to 1.02 V, and η to 5.85 %. Remarkably, these improvements in important factors bring attention to the advantageous effect of Co2+ doping. We have attempted to contribute our work to the perovskites that are still under development in the organic–inorganic world for solar cell technology. We propose that our findings hold substantial knowledge that will contribute to the improvement and development of perovskite solar cells.http://www.sciencedirect.com/science/article/pii/S2211715624006702Co2+ dopingMAPbI2BrPerovskite solar cells |
spellingShingle | M.I. Khan Saddam Hussain M. Atif J.E. Leal-Perez B.A. García-Grajeda J.M. Mendivil-Escalante Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells Results in Chemistry Co2+ doping MAPbI2Br Perovskite solar cells |
title | Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells |
title_full | Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells |
title_fullStr | Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells |
title_full_unstemmed | Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells |
title_short | Elevating photovoltaic efficiency: Cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells |
title_sort | elevating photovoltaic efficiency cobalt doping approaches with sustainable transition metal cations in lead halide perovskite solar cells |
topic | Co2+ doping MAPbI2Br Perovskite solar cells |
url | http://www.sciencedirect.com/science/article/pii/S2211715624006702 |
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