All-inorganic halide perovskites for air-processed "n-i-p" monolithic perovskite/organic hybrid tandem solar cells exceeding 23% efficiency

被引:17
|
作者
Mali, Sawanta S. [1 ]
Patil, Jyoti V. [1 ,2 ]
Steele, Julian A. [3 ,4 ]
Nazeeruddin, Mohammad Khaja [5 ]
Kim, Jin Hyeok [6 ]
Hong, Chang Kook [1 ,2 ]
机构
[1] Chonnam Natl Univ, Polymer Energy Mat Lab, Sch Chem Engn, Gwangju 61186, South Korea
[2] Chonnam Natl Univ, Optoelect Convergence Res Ctr, Sch Chem Engn, Gwangju 61186, South Korea
[3] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld 4072, Australia
[4] Univ Queensland, Sch Math & Phys, Brisbane, Qld 4072, Australia
[5] Swiss Fed Inst Technol, Inst Chem Sci & Engn, Grp Mol Engn Funct Mat, EPFL VALAI, CH-1951 Sion, Switzerland
[6] Chonnam Natl Univ, Dept Mat Sci & Engn, Gwangju 61186, South Korea
基金
新加坡国家研究基金会; 澳大利亚研究理事会;
关键词
PHOTOVOLTAICS; LAYER;
D O I
10.1039/d3ee02763e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
All-perovskite tandem solar cells recently surpassed 26% power conversion efficiency using a Sn(ii)-based halide perovskite rear subcell, which introduces several issues related to the chemical instability and the effectiveness of common, inexpensive interconnecting layers. Adopting an all-organic blend as the rear subcell, we report here efficient "n-i-p" monolithic hybrid tandem solar cells based on metal-ion doped all-inorganic gamma-CsPb(I1-xBrx)(3), perovskite front subcells and a solution-processed ternary organic blend rear subcell. Dynamic hot-air deposition of the perovskite films allowed devices to be made and tested entirely in the open air, and passivation of the perovskite layer and the zinc oxide electron selection layer suppressed interfacial recombination and minimized the open-circuit voltage loss (0.025 V). Our devices achieved a maximum efficiency of 23.07% with an open-circuit voltage of 2.110 V, retaining >90% of the initial efficiency over 600 h at maximum power tracking under continuous illumination.
引用
收藏
页码:1046 / 1060
页数:16
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