Robust Imidazole‐Linked Covalent Organic Framework Enabling Crystallization Regulation and Bulk Defect Passivation for Highly Efficient and Stable Perovskite Solar Cells

Author:

He Zhengyan123,Luan Tianxiang12,Zhang Shufang4,Wei Qilin123,Huang Dan5,Wang Lingyun6,Wang Yu7,Li Peizhou12,Yu William W.123ORCID

Affiliation:

1. School of Chemistry and Chemical Engineering Shandong University Jinan 250100 China

2. Shandong Provincial Key Laboratory for Science of Material Creation and Energy Conversion Science Center for Material Creation and Energy Conversion Qingdao 266237 China

3. Ministry of Education Key Laboratory of Special Functional Aggregated Materials Shandong Key Laboratory of Advanced Organosilicon Materials and Technologies Shandong University Jinan 250100 China

4. School of Physics and Photoelectronic Engineering Ludong University Yantai 264025 China

5. State Key Laboratory of Featured Metal Materials and Life‐cycle Safety for Composite Structures School of Physical Science and Technology Guangxi University Nanning 530004 China

6. School of Integrated Circuits Shandong University Jinan 250101 China

7. School of Light Industry and Chemical Engineering Dalian Polytechnic University Dalian 116034 China

Abstract

AbstractThe low crystallinity of the perovskite layers and many defects at grain boundaries within the bulk phase and at interfaces are considered huge barriers to the attainment of high performance and stability in perovskite solar cells (PSCs). Herein, a robust photoelectric imidazole‐linked porphyrin‐based covalent organic framework (PyPor‐COF) is introduced to precisely control the perovskite crystallization process and effectively passivate defects at grain boundaries through a sequential deposition method. The 1D porous channels, abundant active sites, and high crystallization orientation of PyPor‐COF offer advantages for regulating the crystallization of PbI2 and eliminating defects. Moreover, the intrinsic electronic characteristics of PyPor‐COF endow a more closely matched energy level arrangement within the perovskite layer, which promotes charge transport and thereby suppresses the recombination of photogenerated carriers. The champion PSCs containing PyPor‐COF achieved power conversion efficiencies of 24.10% (0.09 cm2) and 20.81% (1.0 cm2), respectively. The unpackaged optimized device is able to maintain its initial efficiency of 80.39% even after being exposed to air for 2000 h. The device also exhibits excellent heating stability and light stability. This work gives a new impetus to the development of highly efficient and stable PSCs via employing COFs.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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