Enhancing the photovoltaic performance of planar heterojunction perovskite solar cells by doping the perovskite layer with alkali metal ions

被引:151
作者
Chang, Jingjing [1 ,2 ]
Lin, Zhenhua [1 ]
Zhu, Hai [3 ]
Isikgor, Furkan Halis [2 ]
Xu, Qing-Hua [3 ]
Zhang, Chunfu [1 ]
Hao, Yue [1 ]
Ouyang, Jianyong [1 ]
机构
[1] Xidian Univ, Sch Microelect, State Key Lab Wide Band Gap Semicond Technol, 2 South Taibai Rd, Xian 710071, Peoples R China
[2] Natl Univ Singapore, Dept Mat Sci & Engn, 7 Engn Dr 1, Singapore 117574, Singapore
[3] Natl Univ Singapore, Dept Chem, 3 Sci Dr 3, Singapore 117543, Singapore
关键词
HOLE-CONDUCTOR-FREE; HALIDE PEROVSKITES; DOPED ZNO; EFFICIENT; CH3NH3PBI3; CRYSTALLIZATION; HYSTERESIS; PASSIVATION; DEPOSITION; STABILITY;
D O I
10.1039/c6ta06851k
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
Perovskite solar cells (PSCs) have attracted much attention due to their impressive photovoltaic performance and low fabrication cost. The perovskite layer plays a critical role in light-to-electricity conversion. Here we study the effects of alkali metal ion dopants on the growth, structure and properties of perovskite films and the photovoltaic performance of PSCs. At a low doping level, the alkali metal ions can significantly affect the formation and properties of the perovskite films. They can enhance the short-circuit current density (J(sc)) and power conversion efficiency (PCE) significantly. The J(sc) increases significantly from 19.2 mA cm(-2) to 21.0 mA cm(-2) and 20.3 mA cm(-2) for the PSCs with a methylammonium lead triode layer doped with 0.5 mol% K+ and 0.25 mol% Na+, respectively, and the fill factor (FF) increases from 0.74 to 0.79 for the devices with both doping ions. Correspondingly, the PCE increases from 13.7% to 15.3% and 14.6% for the PSCs, respectively. The efficiency improvement by K+ or Na+ doping is attributed to their effect in increasing the crystallinity and crystallite size of the perovskite films.
引用
收藏
页码:16546 / 16552
页数:7
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