Electronic structures at the interface between Au and CH3NH3PbI3

被引:81
作者
Liu, Xiaoliang [1 ]
Wang, Chenggong [2 ]
Lyu, Lu [1 ]
Wang, Congcong [2 ]
Xiao, Zhengguo [3 ,4 ]
Bi, Cheng [3 ,4 ]
Huang, Jinsong [3 ,4 ]
Gao, Yongli [2 ]
机构
[1] Cent S Univ, Coll Phys & Elect, Hunan Key Lab Super Microstruct & Ultrafast Proc, Changsha 410083, Hunan, Peoples R China
[2] Univ Rochester, Dept Phys & Astron, Rochester, NY 14627 USA
[3] Univ Nebraska, Dept Mech & Mat Engn, Lincoln, NE 68588 USA
[4] Univ Nebraska, Nebraska Ctr Mat & Nanosci, Lincoln, NE 68588 USA
基金
美国国家科学基金会; 中国国家自然科学基金;
关键词
PEROVSKITE SOLAR-CELLS; ORGANOMETAL HALIDE PEROVSKITES; THIN-FILM; PHOTOVOLTAIC CELLS; TEMPERATURE; DEPOSITION;
D O I
10.1039/c4cp03842h
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
The electronic properties of interfaces formed between Au and organometal triiodide perovskite (CH3NH3PbI3) are investigated using ultraviolet photoemission spectroscopy (UPS), inverse photoemission spectroscopy (IPES) and X-ray photoemission spectroscopy (XPS). It is found that the CH3NH3PbI3 film coated onto the substrate of poly(3,4-ethylenedioxythiophene) poly(styrenesulfonate) (PEDOT: PSS)/indium tin oxide (ITO) by a two-step method presents n-type semiconductor behavior, with a band gap of 1.7 eV and a valence band (VB) edge of 1.0 eV below the Fermi energy (E-F). An interface dipole of 0.1 eV is observed at the CH3NH3PbI3/Au interface. The energy levels of CH3NH3PbI3 shift upward by ca. 0.4 eV with an Au coverage of 64 angstrom upon it, resulting in band bending, hence a built-in field in CH3NH3PbI3 that encourages hole transport to the interface. Hole accumulation occurs in the vicinity of the interface, facilitating the hole transfer from CH3NH3PbI3 to Au. Furthermore, the shift of the VB maximum of CH3NH3PbI3 toward the EF indicates a decrease of energy loss as holes transfer from CH3NH3PbI3 to Au.
引用
收藏
页码:896 / 902
页数:7
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