Journal article
The impact of the crystallization processes on the structural and optical properties of hybrid perovskite films for photovoltaics
- Abstract:
- We investigate the relationship between structural and optical properties of organo-lead mixed halide perovskite films as a function of the crystallization mechanism. For methylammonium lead tri-iodide, the organic cations rearrange within the inorganic cage, moving from crystals grown in a mesoporous scaffold to larger, oriented crystals grown on a flat substrate. This reduces the strain felt by the bonds forming the cage and affects the motion of the organic cation in it, influencing the electronic transition at the onset of the optical absorption spectrum of the semiconductor. Moreover, we demonstrate that in mixed-halide perovskite, though Cl(-) ions are not present in a detectable concentration in the unit cell, they drive the crystallization dynamics. This induces a preferential order during crystallization, from a molecular, i.e., organic-inorganic moieties arrangement, to a nano-mesoscopic level, i.e., larger crystals with anisotropic shape. Finally, we show that while Cl is mainly expelled from flat films made of large crystals, in the presence of an oxide mesoporous scaffold they are partially retained in the composite.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Accepted manuscript, pdf, 1.2MB, Terms of use)
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- Publisher copy:
- 10.1021/jz501877h
Authors
- Publisher:
- American Chemical Society
- Journal:
- journal of physical chemistry letters More from this journal
- Volume:
- 5
- Issue:
- 21
- Pages:
- 3836-3842
- Publication date:
- 2014-11-01
- DOI:
- EISSN:
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1948-7185
- ISSN:
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1948-7185
- Language:
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English
- Keywords:
- Pubs id:
-
pubs:491166
- UUID:
-
uuid:eb05a653-5bce-4380-bd92-61225bb5e478
- Local pid:
-
pubs:491166
- Source identifiers:
-
491166
- Deposit date:
-
2014-12-12
Terms of use
- Copyright holder:
- American Chemical Society
- Copyright date:
- 2014
- Notes:
-
Copyright © 2014 American Chemical Society. This document is the Accepted Manuscript version of a Published Work that appeared in final form in
Journal of Physical Chemistry Letters, copyright © American Chemical Society after peer review and technical editing by the publisher.
To access the final edited and published work see http://dx.doi.org/10.1021/jz501877h.
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