Ambient-air-stable inorganic Cs2SnI6 double perovskite thin films via aerosol-assisted chemical vapour deposition

被引:96
|
作者
Ke, Jack Chun-Ren [1 ,2 ]
Lewis, David J. [3 ]
Walton, Alex S. [2 ,4 ]
Spencer, Ben F. [3 ]
O'Brien, Paul [3 ,4 ]
Thomas, Andrew G. [2 ,3 ]
Flavell, Wendy R. [1 ,2 ]
机构
[1] Univ Manchester, Sch Phys & Astron, Manchester M13 9PL, Lancs, England
[2] Univ Manchester, Photon Sci Inst, Manchester M13 9PL, Lancs, England
[3] Univ Manchester, Sch Mat, Manchester M13 9PL, Lancs, England
[4] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; SOLAR-CELLS; CH3NH3PBI3; PEROVSKITE; HALIDE; EFFICIENT; TIN; INTERFACE; STABILITY; CVD; PRECURSORS;
D O I
10.1039/c8ta03133a
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
Air-stable caesium tin iodide double perovskite (Cs2SnI6) thin films have been fabricated via aerosol-assisted chemical vapour deposition (AACVD). We compare the properties of the double perovskite films made using AACVD with those made by the widely used spin-coating method. Films with purer crystalline phase (less CsI impurity) and far better stability in ambient air can be obtained by AACVD compared with spin coating. The AACVD-grown Cs2SnI6 films retain high phase purity for at least approximate to 100 days aging in air with negligible CsI impurities detected over this time, as determined by X-ray diffraction. The films exhibit an optical band gap energy (E-g) of ca. 1.3 eV and a homogeneous morphology with the expected nominal stoichiometry within error, as probed by energy-dispersive X-ray spectroscopy. Overall, the characteristics of the Cs2SnI6 films are highly process-dependent, e.g. they are influenced by the presence of hydroiodic acid (HI) in the precursor solution. Without HI addition, an iodine-deficient film with more CsI is produced, which also exhibits a larger E-g of ca. 1.6 eV. In addition to bulk properties, we utilise X-ray photoelectron spectroscopy (XPS) to scrutinise the surface characteristics in detail. We find excess Sn and I located at the surfaces. This can be attributed to the presence of SnI4 from the deposition precursor vapour. Furthermore, following aging in air, an increase in CsI impurity for the AACVD (+HI)-grown film is observed, along with a reduction in SnI4 at the surfaces. Near-ambient pressure XPS (NAP-XPS) is used to examine the surface stability of AACVD (+HI)-grown films on exposure to O-2 and H2O. No enhancement in the amount of CsI impurity is observed after both H2O vapour (9 mbar) and O-2 (5 mbar) exposure. Nevertheless, the concentrations of tin and iodine change after exposure, suggesting that SnI4 protects Cs2SnI6 from degradation. This passivation effect of SnI4 on Cs2SnI6 surfaces is proposed to explain the additional stability of Cs2SnI6 fabricated via AACVD.
引用
收藏
页码:11205 / 11214
页数:10
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