Highly efficient and stable perovskite solar cells via a multifunctional hole transporting material

被引:262
|
作者
Zhou, Junjie [1 ]
Tan, Liguo [1 ]
Liu, Yue [1 ]
Li, Hang [1 ]
Liu, Xiaopeng [1 ]
Li, Minghao [1 ]
Wang, Siyang [1 ]
Zhang, Yu [1 ]
Jiang, Chaofan [1 ]
Hua, Ruimao [2 ]
Tress, Wolfgang [3 ]
Meloni, Simone [4 ]
Yi, Chenyi [1 ]
机构
[1] Tsinghua Univ, Dept Elect Engn, State Key Lab Power Syst Operat & Control, Beijing 100084, Peoples R China
[2] Tsinghua Univ, Dept Chem, Beijing 100084, Peoples R China
[3] Zurich Univ Appl Sci, Inst Computat Phys, CH-8401 Winterthur, Switzerland
[4] Univ Ferrara, Dept Chem Pharmaceut & Agr Sci, Via Luigi Borsari 46, I-44121 Ferrara, Italy
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
LOW-COST; INTERLAYERS; INTERFACE;
D O I
10.1016/j.joule.2024.02.019
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 hole -transporting material (HTM) plays a crucial role in the performance and stability of perovskite solar cells (PSCs). Ideally, it facilitates lossless charge transfer and suppresses charge recombination and ion migration between the perovskite and electrode. These bulk and interface functionalities require tailored electronic, structural, and chemical properties of the material and film. Here, we report a multifunctional organic HTM T2 based on a thiomethylsubstituted fluorene arm and spiro-[fluorene-9,9 0 -xanthene] core exhibiting enhanced hole extraction and reduced interface recombination compared with the benchmark HTM spiro-OMeTAD. T2 exhibits strong interactions with adjacent layers, which effectively inhibit interlayer ion migration, leading to enhanced stability. In combination with thermally evaporated perovskite films, power conversion efficiencies of 26.41% (26.21% certified) and 24.88% (certified) have been achieved for 0.1 and 1.0 cm 2 PSCs. The excellent performance together with a scalable and low-cost synthesis laid a solid foundation for the future large-scale application of PSCs.
引用
收藏
页码:1691 / 1706
页数:17
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