Dopant‐free Starlike Molecular Hole Conductor with Ordered Packing for Durable all‐Inorganic Perovskite Solar Cells

Author:

Duan Chenghao12,Zou Feilin1,Li Shiang2,Zhu Qiliang1,Li Jiong1,Chen Honggang1,Zhang Zheng1,Chen Chang1,Guo Huan1,Qiu Jianhang3,Wang Ke1,Dong Yuyan1,Qiu Yongcai1,Ding Liming4,Lu Xinhui2ORCID,Luo Hongze5,Yan Keyou1ORCID

Affiliation:

1. School of Environment and Energy State Key Laboratory of Luminescent Materials and Devices Guangdong Provincial Key Laboratory of Solid Wastes Pollution Control and Recycling South China University of Technology Guangzhou 510000 China

2. Department of Physics Chinese University of Hong Kong Shatin Hong Kong China

3. Shenyang National Laboratory for Materials Science Institute of Metal Research Chinese Academy of Sciences Shenyang 110016 China

4. Center of Excellence in Nanoscience (CAS) Key Laboratory of Nanosystem and Hierarchical Fabrication (CAS) National Center for Nanoscience and Technology Beijing 100190 China

5. Energy Centre Council for Scientific and Industrial Research (CSIR) P O Box 395 Pretoria 0001 South Africa

Abstract

AbstractAll‐inorganic n‐i‐p perovskite solar cells (PSCs) using doped Spiro‐OMeTAD as hole transport material (HTM) suffer from photothermal stability due to ionic diffusion and radical‐induced degradation by the dopants. In this article, dopant‐free starlike molecule (N2, N2‐bis(4‐(bis(4‐methoxyphenyl)amino)phenyl)‐N5,N5‐bis(4‐methoxyphenyl)pyridine‐2,5‐diamine (BD)) is synthesized to engineer the stacking properties and delivered higher hole mobility than doped Spiro‐OMeTAD (3.2 × 10−4 versus 1.76 × 10−4 cm2 V−1 s−1) as dopant‐free HTM. Starlike BD HTM has a twisted acceptor unit and strong dipole, forming crystalline and ordered packing film to ensure intramolecular charge transfer and improve mobility. The BD CsPbI3 PSCs deliver the maximum efficiency of 19.19%, which is the highest performance for all‐inorganic PSCs based on dopant‐free HTMs. Meanwhile, the ordered molecules‐packing blocks the migration channel of I ions to metal electrodes and improves the device stability. BD‐based devices maintain more than 93% and 80% of the initial efficiency after 85 °C storage for 35 days and maximum power point (MPP) tracking at 85 °C for 1000 h, respectively.

Funder

National Natural Science Foundation of China

National Basic Research Program of China

Publisher

Wiley

Subject

General Materials Science,Renewable Energy, Sustainability and the Environment

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