A conformally bonded molecular interface retarded iodine migration for durable perovskite solar cells

被引:51
作者
Yuan, Ligang [1 ]
Zhu, Weiya [1 ]
Zhang, Yiheng [1 ]
Li, Yuan [1 ]
Chan, Christopher C. S. [2 ,3 ]
Qin, Minchao [4 ]
Qiu, Jianhang [5 ]
Zhang, Kaicheng [6 ]
Huang, Jiaxing [1 ]
Wang, Jiarong [1 ]
Luo, Huiming [1 ]
Zhang, Zheng [1 ]
Chen, Ruipeng [1 ]
Liang, Weixuan [1 ]
Wei, Qi [1 ]
Wong, Kam Sing [2 ,3 ]
Lu, Xinhui [4 ]
Li, Ning [1 ]
Brabec, Christoph J. [6 ,7 ]
Ding, Liming [8 ]
Yan, Keyou [1 ]
机构
[1] South China Univ Technol, Inst Polymer Optoelect Mat & Devices, AIE Inst,State Key Lab Luminescent Mat & Devices,G, Guangdong Prov Key Lab Luminescence Mol Aggregates, Guangzhou 510000, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Phys, Clearwater Bay, Hong Kong, Peoples R China
[3] Hong Kong Univ Sci & Technol, William Mong Inst Nano Sci & Technol, Clearwater Bay, Hong Kong, Peoples R China
[4] Chinese Univ Hong Kong, Dept Phys, Shatin, Hong Kong 999077, Peoples R China
[5] Chinese Acad Sci, Inst Met Res, Shenyang Natl Lab Mat Sci, Shenyang 110016, Peoples R China
[6] Friedrich Alexander Univ Erlangen Nuremberg, Inst Mat Elect & Energy Technol I MEET, Martensstr 7, D-91058 Erlangen, Germany
[7] Forschungszentrum Julich, Helmholtz Inst Erlangen Nurnberg Renewable Energy, D-91058 Erlangen, Germany
[8] Natl Ctr Nanosci & Technol, Ctr Excellence Nanosci CAS, Key Lab Nanosyst & Hierarch Fabricat CAS, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
HOLE-TRANSPORTING MATERIALS; LOW-COST; EFFICIENT; PERFORMANCE; INDACENODITHIOPHENE; STABILITY; DESIGN;
D O I
10.1039/d2ee03565k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
State-of-the-art n-i-p perovskite solar cells (PSCs) suffer from stability issues due to ionic interdiffusion. Herein, by enlarging the indacenodithiophene pi-bridge donor (D ') to combine with the methoxy triphenylamine donor (D) and benzothiadiazole acceptor (A), three linear molecules termed L1, L2 and L3 with a D-A-D '-A-D structure are developed as dopant-free hole transport materials (HTMs). The pi-bridge extension with active sites for coordination leverages the intramolecular dipole effect and intermolecular packing effect, resulting in a conformally bonded ultrathin interface with compact and uniform coverage (similar to 60 nm) to retard iodine migration and protect the buried perovskite. The unencapsulated L3-PSC (ITO/SnO2/perovskite/L3/MoO3/Au) achieved an impressive PCE of 22.61% (certified 21.79%, 0.0525 cm(2)). Ultrafast laser spectroscopy reveals that L-series molecules have a sequential reduction of photoexcited energy disorder to illustrate the structure-performance-stability relationship. L3-PSC maintains over 85% of the initial efficiency after 500 h at 85 degrees C maximum power point tracking (MPP) and enables the possibility of using small molecules to stabilize n-i-p PSCs.
引用
收藏
页码:1597 / 1609
页数:13
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