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Naji, M. |
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Motta, Antonella |
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Aletan, Dirar |
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Mohamed, Tarek |
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Ertürk, Emre |
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Taccardi, Nicola |
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Kononenko, Denys |
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Petrov, R. H. | Madrid |
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Alshaaer, Mazen | Brussels |
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Bih, L. |
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Casati, R. |
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Muller, Hermance |
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Kočí, Jan | Prague |
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Šuljagić, Marija |
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Kalteremidou, Kalliopi-Artemi | Brussels |
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Azam, Siraj |
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Ospanova, Alyiya |
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Blanpain, Bart |
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Ali, M. A. |
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Popa, V. |
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Rančić, M. |
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Ollier, Nadège |
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Azevedo, Nuno Monteiro |
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Landes, Michael |
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Rignanese, Gian-Marco |
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Abdi-Jalebi, Mojtaba
University College London
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (29/29 displayed)
- 2024Doping Up the Light: A Review of A/B-Site Doping in Metal Halide Perovskite Nanocrystals for Next-Generation LEDs.
- 2023Recent development in metal halide perovskites synthesis to improve their charge-carrier mobility and photocatalytic efficiencycitations
- 2023Champion Device Architectures for Low-Cost and Stable Single-Junction Perovskite Solar Cells.
- 2023Champion Device Architectures for Low-Cost and Stable Single-Junction Perovskite Solar Cells
- 2023The race between complicated multiple cation/anion compositions and stabilization of FAPbI3 for halide perovskite solar cells
- 2021Beyond 17% stable perovskite solar module via polaron arrangement of tuned polymeric hole transport layercitations
- 2021Highly absorbing lead-free semiconductor Cu2AgBiI6 for photovoltaic applications from the quaternary CuI-AgI-BiI3 phase spacecitations
- 2020Performance-limiting nanoscale trap clusters at grain junctions in halide perovskites.
- 2020A general approach for hysteresis-free, operationally stable metal halide perovskite field-effect transistors.
- 2020A general approach for hysteresis-free, operationally stable metal halide perovskite field-effect transistors.
- 2020Photodoping through local charge carrier accumulation in alloyed hybrid perovskites for highly efficient luminescencecitations
- 2020Bandgap lowering in mixed alloys of Cs2Ag(SbxBi1−x)Br6 double perovskite thin filmscitations
- 2019Charge extraction via graded doping of hole transport layers gives highly luminescent and stable metal halide perovskite devices.
- 2019Lattice Strain Causes Non-Radiative Losses in Halide Perovskitescitations
- 2019Reversible Removal of Intermixed Shallow States by Light Soaking in Multication Mixed Halide Perovskite Films.
- 2019Back-Contact Perovskite Solar Cells
- 2018Maximizing and stabilizing luminescence from halide perovskites with potassium passivationcitations
- 2018Maximizing and stabilizing luminescence from halide perovskites with potassium passivationcitations
- 2018Local Strain Heterogeneity Influences the Optoelectronic Properties of Halide Perovskites
- 2018Potassium- and Rubidium-Passivated Alloyed Perovskite Films: Optoelectronic Properties and Moisture Stability.
- 2018Dedoping of Lead Halide Perovskites Incorporating Monovalent Cations.
- 2018Probing buried recombination pathways in perovskite structures using 3D photoluminescence tomography.
- 2018In situ simultaneous photovoltaic and structural evolution of perovskite solar cells during film formationcitations
- 2017Vapour-Deposited Cesium Lead Iodide Perovskites: Microsecond Charge Carrier Lifetimes and Enhanced Photovoltaic Performancecitations
- 2017Vapour-Deposited Cesium Lead Iodide Perovskitescitations
- 2017Impact of microstructure on the electron-hole interaction in lead halide perovskitescitations
- 2017Vapour-Deposited Cesium Lead Iodide Perovskites: Microsecond Charge Carrier Lifetimes and Enhanced Photovoltaic Performance.
- 2016Photon recycling in lead iodide perovskite solar cells.
- 2015Influence of an Inorganic Interlayer on Exciton Separation in Hybrid Solar Cells.
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article
Dedoping of Lead Halide Perovskites Incorporating Monovalent Cations.
Abstract
We report significant improvements in the optoelectronic properties of lead halide perovskites with the addition of monovalent ions with ionic radii close to Pb2+. We investigate the chemical distribution and electronic structure of solution processed CH3NH3PbI3 perovskite structures containing Na+, Cu+, and Ag+, which are lower valence metal ions than Pb2+ but have similar ionic radii. Synchrotron X-ray diffraction reveals a pronounced shift in the main perovskite peaks for the monovalent cation-based films, suggesting incorporation of these cations into the perovskite lattice as well as a preferential crystal growth in Ag+ containing perovskite structures. Furthermore, the synchrotron X-ray photoelectron measurements show a significant change in the valence band position for Cu- and Ag-doped films, although the perovskite bandgap remains the same, indicating a shift in the Fermi level position toward the middle of the bandgap. Such a shift infers that incorporation of these monovalent cations dedope the n-type perovskite films when formed without added cations. This dedoping effect leads to cleaner bandgaps as reflected by the lower energetic disorder in the monovalent cation-doped perovskite thin films as compared to pristine films. We also find that in contrast to Ag+ and Cu+, Na+ locates mainly at the grain boundaries and surfaces. Our theoretical calculations confirm the observed shifts in X-ray diffraction peaks and Fermi level as well as absence of intrabandgap states upon energetically favorable doping of perovskite lattice by the monovalent cations. We also model a significant change in the local structure, chemical bonding of metal-halide, and the electronic structure in the doped perovskites. In summary, our work highlights the local chemistry and influence of monovalent cation dopants on crystallization and the electronic structure in the doped perovskite thin films. ; Cambridge Materails Limited, Nava Technology Limited