Spatial and temporal imaging of long-range charge transport in perovskite thin films by ultrafast microscopy

被引:321
作者
Guo, Zhi [1 ]
Manser, Joseph S. [1 ,2 ]
Wan, Yan [3 ]
Kamat, Prashant V. [1 ,2 ,4 ]
Huang, Libai [1 ,3 ]
机构
[1] Univ Notre Dame, Radiat Lab, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
[3] Purdue Univ, Dept Chem, W Lafayette, IN 47907 USA
[4] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
关键词
LEAD IODIDE PEROVSKITE; SOLAR-CELLS; HALIDE PEROVSKITES; CARRIER MOBILITY; RECOMBINATION; ELECTRON; DYNAMICS; DIFFUSION; LENGTHS; ABSORPTION;
D O I
10.1038/ncomms8471
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Charge carrier diffusion coefficient and length are important physical parameters for semiconducting materials. Long-range carrier diffusion in perovskite thin films has led to remarkable solar cell efficiencies; however, spatial and temporal mechanisms of charge transport remain unclear. Here we present a direct measurement of carrier transport in space and in time by mapping carrier density with simultaneous ultrafast time resolution and similar to 50-nm spatial precision in perovskite thin films using transient absorption microscopy. These results directly visualize long-range carrier transport of similar to 220nm in 2 ns for solution-processed polycrystalline CH3NH3PbI3 thin films. Variations of the carrier diffusion coefficient at the mm length scale have been observed with values ranging between 0.05 and 0.08 cm(2) s(-1). The spatially and temporally resolved measurements reported here underscore the importance of the local morphology and establish an important first step towards discerning the underlying transport properties of perovskite materials.
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页数:8
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