Efficient Two-Dimensional Perovskite Solar Cells Realized by Incorporation of Ti3C2Tx MXene as Nano-Dopants

被引:55
|
作者
Jin, Xin [1 ]
Yang, Lin [1 ]
Wang, Xiao-Feng [1 ]
机构
[1] Jilin Univ, Coll Phys, Minist Educ, Key Lab Phys & Technol Adv Batteries, Changchun 130012, Peoples R China
基金
中国国家自然科学基金;
关键词
2D perovskite solar cells; Ti3C2Tx nanosheets; Trap densities; Vertical orientation; Charge transport; SYNTHETIC CONTROL; ELECTRON; TRANSPORT; MIGRATION; LENGTHS;
D O I
10.1007/s40820-021-00602-w
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Highlights2D Ti3C2T MXene nanosheets with high electrical conductivity and mobility were employed as a nanosized additive to prepare 2D perovskite films.xDoping of Ti3C2T nanosheets can passivate the defects on the perovskite films surface and accelerate charge transfer process in vertical direction.xEnhanced crystallinity and orientation of the perovskite films result in a significant increase in short-circuit current density and power conversion efficiency. AbstractTwo-dimensional (2D) perovskites solar cells (PSCs) have attracted considerable attention owing to their excellent stability against humidity; however, some imperfectness of 2D perovskites, such as poor crystallinity, disordered orientation, and inferior charge transport still limit the power conversion efficiency (PCE) of 2D PSCs. In this work, 2D Ti3C2Tx MXene nanosheets with high electrical conductivity and mobility were employed as a nanosized additive to prepare 2D Ruddlesden-Popper perovskite films. The PCE of solar cells was increased from 13.69 (without additive) to 15.71% after incorporating the Ti3C2Tx nanosheets with an optimized concentration. This improved performance is attributed to the enhanced crystallinity, orientation, and passivated trap states in the 3D phase that result in accelerated charge transfer process in vertical direction. More importantly, the unencapsulated cells exhibited excellent stability under ambient conditions with 555% relative humidity.
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页数:13
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