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Effect of Water Addition during Preparation on the Early‐Time Photodynamics of CH 3 NH 3 PbI 3 Perovskite Layers
Author(s) -
Aphrham S.,
Pan Q.,
Zaccarine S. F.,
Felter K. M.,
Thieme J.,
van den Nieuwenhuijzen K. J. H.,
ten Elshof J. E.,
Huijser A.
Publication year - 2017
Publication title -
chemphyschem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.016
H-Index - 140
eISSN - 1439-7641
pISSN - 1439-4235
DOI - 10.1002/cphc.201700896
Subject(s) - chemistry , perovskite (structure) , aqueous solution , thermalisation , chemical physics , femtosecond , absorption (acoustics) , ultrafast laser spectroscopy , isomerization , molecule , charge (physics) , dipole , inorganic chemistry , photochemistry , analytical chemistry (journal) , catalysis , crystallography , materials science , atomic physics , laser , organic chemistry , quantum mechanics , physics , optics , composite material
The effect of water addition during preparation of a CH 3 NH 3 PbI 3 layer on the photodynamics is studied by femtosecond transient absorption. Both the regular perovskite and the aqueous analogue show charge thermalisation on a timescale of about 500 fs. This process is, however, less pronounced in the latter layer. The spectral feature associated with hot charges does not fully decay on this timescale, but also shows a long‐lived (sub‐ns) component. As water molecules may interfere with the hydrogen bonding between the CH 3 NH 3 + cations and the inorganic cage, this effect is possibly caused by immobilisation of cation motion, suggesting a key role of CH 3 NH 3 + dipole reorientation in charge thermalisation. This effect shows the possibility of controlling hot charge carrier cooling to overcome the Shockley–Queisser limit.