Interfacial engineering by p-methylphenylmethylammonium iodide for efficient carbon counter electrode (CE)-based 2D/3D hybrid perovskite solar cells

被引:5
作者
Cao, Duoling [1 ]
Li, Zuhong [1 ]
Xu, Ya [1 ]
Li, Wenbo [1 ]
Zhong, Hang [1 ]
Huang, Yin [1 ]
Zhang, Xu [1 ]
Wan, Li [1 ,3 ]
Zhang, Xiuhua [1 ]
Li, Yuebin [1 ]
Ren, Xiaoming [1 ]
Wang, Xianbao [1 ]
Eder, Dominik [2 ]
Wang, Shimin [1 ]
机构
[1] Hubei Univ, Fac Mat Sci & Engn, Hubei Collaborat Innovat Ctr Adv Organ Chem Mat, Key Lab Green Preparat & Applicat Funct Mat,Hubei, Wuhan 430062, Peoples R China
[2] Tech Univ Wien, Inst Mat Chem, Getreidemarkt 9-165, A-1060 Vienna, Austria
[3] Hubei Univ, Fac Mat Sci & Engn, Wuhan 430062, Peoples R China
关键词
perovskite Solar cells; Interfacial engineering; P-methylphenylmethylammonium iodide; 2D layered perovskites; Carbon counter electrode; Stability; HALIDE PEROVSKITES; PASSIVATION; AMMONIUM;
D O I
10.1016/j.orgel.2022.106699
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Defects at the surface and grain boundaries of three-dimensional (3D) organic-inorganic metal halide perovskite films lead to the non-radiative recombination of charge carriers and accelerate perovskite decomposition. In turn, this deteriorates the power conversion efficiency (PCE) and stability of perovskite solar cells (PSCs). Herein, pmethylphenylmethylammonium iodide (p-MePMAI) was reacted with a 3D perovskite to in-situ form a twodimensional (2D) perovskite upper layer. This upper layer passivated the surface and grain boundary defects of the 3D perovskite film, improving its surface hydrophobicity. As a result, a carbon counter electrode (CE)based 2D/3D PSC achieved a maximum PCE of up to 15.63%, which was much higher than that of an unmodified 3D MAPbI3 PSC (12.16%). Moreover, the unencapsulated 2D/3D device maintained 80% of its initial PCE after exposure to air for 700 h with a relative humidity (RH) of 40 +/- 5%. This research opens a new pathway for the successful construction of stable and efficient 2D/3D PSCs with organic ammonium salts.
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页数:8
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