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7123821 
Journal Article 
Temperature-Dependent Charge-Carrier Dynamics in CH3NH3PbI3 Perovskite Thin Films 
Milot, RL; Eperon, GE; Snaith, HJ; Johnston, MB; Herz, LM; , 
2015 
Yes 
Advanced Functional Materials
ISSN: 1616-301X
EISSN: 1616-3028 
WILEY-V C H VERLAG GMBH 
WEINHEIM 
6218-6227 
WOS:000363207000008 
The photoluminescence, transmittance, charge-carrier recombination dynamics, mobility, and diffusion length of CH3NH3PbI3 are investigated in the temperature range from 8 to 370 K. Profound changes in the optoelectronic properties of this prototypical photovoltaic material are observed across the two structural phase transitions occurring at 160 and 310 K. Drude-like terahertz photoconductivity spectra at all temperatures above 80 K suggest that charge localization effects are absent in this range. The monomolecular charge-carrier recombination rate generally increases with rising temperature, indicating a mechanism dominated by ionized impurity mediated recombination. Deduced activation energies E-a associated with ionization are found to increase markedly from the room-temperature tetragonal (E-a approximate to 20 meV) to the higher-temperature cubic (E-a approximate to 200 meV) phase adopted above 310 K. Conversely, the bimolecular rate constant decreases with rising temperature as charge-carrier mobility declines, while the Auger rate constant is highly phase specific, suggesting a strong dependence on electronic band structure. The charge-carrier diffusion length gradually decreases with rising temperature from about 3 m at -93 degrees C to 1.2 m at 67 degrees C but remains well above the optical absorption depth in the visible spectrum. These results demonstrate that there are no fundamental obstacles to the operation of cells based on CH3NH3PbI3 under typical field conditions.