Soluble tetratriphenylamine Zn phthalocyanine as Hole Transporting Material for Perovskite Solar Cells

被引:41
|
作者
Nouri, Esmaiel [1 ,4 ]
Krishna, Jonnadula Venkata Suman [2 ]
Kumar, Challuri Vijay [3 ,5 ]
Dracopoulos, Vassilios [3 ]
Giribabu, Lingamallu [2 ]
Mohammadi, Mohammad Reza [4 ]
Lianos, Panagiotis [1 ]
机构
[1] Univ Patras, Dept Chem Engn, Patras 26500, Greece
[2] Indian Inst Chem Technol, Inorgan & Phys Chem Div, Hyderabad 500007, Andhra Pradesh, India
[3] FORTH ICE HT, POB 1414, Patras 26504, Greece
[4] Sharif Univ Technol, Dept Mat Sci & Engn, Azadi Str, Tehran, Iran
[5] Univ Picardie Jules Verne, CNRS UMR 7314, Lab React & Chim Solides, 33 Rue St Leu, F-80039 Amiens, France
基金
美国国家科学基金会;
关键词
Perovskite; Solar cells; Hole transport material; Phthalocyanine; COPPER PHTHALOCYANINE; PERFORMANCE; STABILITY; EFFICIENT; LAYER;
D O I
10.1016/j.electacta.2016.11.052
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Perovskite solar cells have been constructed under the standard procedure by employing soluble tetratriphenylamine-substituted Zn phthalocyanine as hole transporting material. Solution processed device construction was carried out under ambient conditions of 50-60% ambient humidity. Triphenylamine substitution played the double role of imparting solubility to the core metal phthalocyanine as well as to introduce electron-rich ligands, which could enhance the role of Zn phthalocyanine as hole transporter. Indeed, the obtained material was functional. The present data highlight tetratriphenylamine-substituted Zn phthalocyanine as hole transporting material but also highlight the importance of the presence of a buffer layer between the perovskite layer and the hole transporting layer. Thus the efficiency of the cells was 9.0% in the absence but increased to 13.65% in the presence of Al2O3 buffer layer. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:875 / 880
页数:6
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