CsPbBr3 Solar Cells: Controlled Film Growth through Layer-by-Layer Quantum Dot Deposition

被引:169
作者
Hoffmann, Jacob B. [1 ,2 ]
Zaiats, Gary [1 ]
Wappes, Isaac [1 ,2 ]
Kamat, Prashant V. [1 ,2 ,3 ]
机构
[1] Univ Notre Dame, Radiat Lab, Notre Dame, IN 46556 USA
[2] Univ Notre Dame, Dept Chem & Biochem, Notre Dame, IN 46556 USA
[3] Univ Notre Dame, Dept Chem & Biomol Engn, Notre Dame, IN 46556 USA
关键词
EXCITON ABSORPTION-SPECTRUM; CESIUM LEAD HALIDE; PHOTOVOLTAIC CELLS; PEROVSKITE; NANOCRYSTALS; PERFORMANCE; LENGTHS; IODIDE; PHASE; RECOMBINATION;
D O I
10.1021/acs.chemmater.7b03751
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
All inorganic cesium lead bromide (CsPbBr3) perovskite is a more stable alternative to methylammonium lead bromide (MAPbBr(3)) for designing high open-circuit voltage solar cells and display devices. Poor solubility of CsBr in organic solvents makes typical solution deposition methods difficult to adapt for constructing CsPbBr3 devices. Our layer-by-layer methodology, which makes use of CsPbBr3 quantum dot (QD) deposition followed by annealing, provides a convenient way to cast stable films of desired thickness. The transformation from QDs into bulk during thermal annealing arises from the resumption of nanoparticle growth and not from sintering as generally assumed. Additionally, a large loss of organic material during the annealing process is mainly from 1-octadecene left during the QD synthesis. Utilizing this deposition approach for perovskite photovoltaics is examined using typical planar architecture devices. Devices optimized to both QD spin-casting concentration and overall CsPbBr3 thickness produce champion devices that reach power conversion efficiencies of 5.5% with a V-oc value of 1.4 V. The layered QD deposition demonstrates a controlled perovskite film architecture for developing efficient, high open-circuit photovoltaic devices.
引用
收藏
页码:9767 / 9774
页数:8
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