Exciton and Free Charge Dynamics of Methylammonium Lead Iodide Perovskites Are Different in the Tetragonal and Orthorhombic Phases

被引:66
作者
Wang, He [1 ,2 ,3 ,4 ]
Whittaker-Brooks, Luisa [5 ]
Fleming, Graham R. [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Chem, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Kavli Energy NanoSci Inst, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Berkeley, CA 94720 USA
[5] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
基金
美国国家科学基金会;
关键词
SOLAR-CELL; CARRIER MOBILITY; EFFICIENCY; TEMPERATURE; LENGTHS; FILMS; BR;
D O I
10.1021/acs.jpcc.5b04403
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The small exciton binding energy of perovskite suggests that the long-lived photoluminescence and slow recovery of the ground state bleaching of the tetragonal phase at room temperature results primarily from the decay of free charges rather than the decay of the initially created excitons. Here we demonstrate the ground state bleaching recovery of the orthorhombic phase of methylammonium lead iodide (CH3NH3PbI3) is much faster than that of the tetragonal phase using temperature dependent transient absorption spectroscopy. The distribution in orientation of the methylammonium group which is disordered in the tetragonal phase and ordered in the orthorhombic phase results in smaller dielectric constant and larger exciton binding energy in the latter phase. We observe the recovery of the ground state bleaching in the orthorhombic phase to be comprised of decays of both excitons and free charges. Our findings suggest CH3NH3PbI3 behaves like a nonexcitonic semiconductor in the tetragonal phase and an excitonic semiconductor in the orthorhombic phase.
引用
收藏
页码:19590 / 19595
页数:6
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