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Dedoping of Lead Halide Perovskites Incorporating Monovalent Cations

Abdi-Jalebi, Mojtaba (författare)
Univ Cambridge, Dept Phys, Cavendish Lab, JJ Thomson Ave, Cambridge, England
Pazoki, Meysam (författare)
Uppsala universitet,Fasta tillståndets fysik
Philippe, Bertrand, Dr. 1986- (författare)
Uppsala universitet,Molekyl- och kondenserade materiens fysik
visa fler...
Dar, M. Ibrahim (författare)
Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Lab Photon & Interfaces, Lausanne, Switzerland
Alsari, Mejd (författare)
Univ Cambridge, Dept Phys, Cavendish Lab, JJ Thomson Ave, Cambridge, England
Sadhanala, Aditya (författare)
Univ Cambridge, Dept Phys, Cavendish Lab, JJ Thomson Ave, Cambridge, England
Diyitini, Giorgio (författare)
Univ Cambridge, Dept Mat Sci & Met, Charles Babbage Rd, Cambridge, England
Imani, Roghayeh (författare)
Uppsala universitet,Strukturkemi
Lilliu, Samuele (författare)
Univ Sheffield, Dept Phys & Astron, Sheffield, S Yorkshire, England; UAE Ctr Crystallog, Dubai, U Arab Emirates
Kullgren, Jolla, 1978- (författare)
Uppsala universitet,Strukturkemi
Rensmo, Håkan (författare)
Uppsala universitet,Molekyl- och kondenserade materiens fysik
Gratzel, Michael (författare)
Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, Lab Photon & Interfaces, Lausanne, Switzerland
Friend, Richard H. (författare)
Univ Cambridge, Dept Phys, Cavendish Lab, JJ Thomson Ave, Cambridge, England
visa färre...
 (creator_code:org_t)
2018-06-28
2018
Engelska.
Ingår i: ACS Nano. - : American Chemical Society (ACS). - 1936-0851 .- 1936-086X. ; 12:7, s. 7301-7311
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • 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.

Ämnesord

NATURVETENSKAP  -- Kemi -- Materialkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Materials Chemistry (hsv//eng)

Nyckelord

monovalent cations
dedoped perovskite thin films
enhanced optoelectronic quality
substitutional doping
interstitial doping

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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  • ACS Nano (Sök värdpublikationen i LIBRIS)

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