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    Evolution of Chemical Composition, Morphology, and Photovoltaic Efficiency of CH 3 NH 3 PbI 3 Perovskite under Ambient Conditions

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    Type
    Article
    Authors
    Huang, Weixin
    Manser, Joseph S.
    Kamat, Prashant V.
    Ptasinska, Sylwia
    KAUST Grant Number
    OCRF-2014-CRG3-2268
    Date
    2015-12-23
    Online Publication Date
    2015-12-23
    Print Publication Date
    2016-01-12
    Permanent link to this record
    http://hdl.handle.net/10754/598259
    
    Metadata
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    Abstract
    © 2015 American Chemical Society. The surface composition and morphology of CH3NH3PbI3 perovskite films stored for several days under ambient conditions were investigated by X-ray photoelectron spectroscopy, scanning electron microscopy, and X-ray diffraction techniques. Chemical analysis revealed the loss of CH3NH3 + and I- species from CH3NH3PbI3 and its subsequent decomposition into lead carbonate, lead hydroxide, and lead oxide. After long-term storage under ambient conditions, morphological analysis revealed the transformation of randomly distributed defects and cracks, initially present in the densely packed crystalline structure, into relatively small grains. In contrast to PbI2 powder, CH3NH3PbI3 exhibited a different degradation trend under ambient conditions. Therefore, we propose a plausible CH3NH3PbI3 decomposition pathway that explains the changes in the chemical composition of CH3NH3PbI3 under ambient conditions. In addition, films stored under such conditions were incorporated into photovoltaic cells, and their performances were examined. The chemical changes in the decomposed films were found to cause a significant decrease in the photovoltaic efficiency of CH3NH3PbI3.
    Citation
    Huang W, Manser JS, Kamat PV, Ptasinska S (2016) Evolution of Chemical Composition, Morphology, and Photovoltaic Efficiency of CH 3 NH 3 PbI 3 Perovskite under Ambient Conditions . Chem Mater 28: 303–311. Available: http://dx.doi.org/10.1021/acs.chemmater.5b04122.
    Sponsors
    This material is based upon work supported by the U.S. Department of Energy Office of Science, Office of Basic Energy Sciences under Award Number DE2FC02204ER15533. This is contribution number NDRL 5076 from the Notre Dame Radiation Laboratory. The authors thank the cSEND Materials Characterization Facility for the use of the PHI VersaProbe II XPS and the use of the Bruker pXRD. Joseph Manser acknowledges the support of King Abdullah University of Science and Technology (KAUST) through the award OCRF-2014-CRG3-2268.
    Publisher
    American Chemical Society (ACS)
    Journal
    Chemistry of Materials
    DOI
    10.1021/acs.chemmater.5b04122
    ae974a485f413a2113503eed53cd6c53
    10.1021/acs.chemmater.5b04122
    Scopus Count
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