Porous Organic Cage Induced Spontaneous Restructuring of Buried Interface Toward High‐Performance Perovskite Photovoltaic

Author:

Gao Feng1,Luo Chao1,Wang Xianjin1,Zhan Changling1,Li Yang1,Li Yiming2,Meng Qingbo2,Yang Miao34,Su Kongzhao34,Yuan Daqiang34,Zhu Rui1,Zhao Qing156ORCID

Affiliation:

1. State Key Lab for Mesoscopic Physics and Frontiers Science Center for Nano‐optoelectronics School of Physics Peking University Beijing 100871 China

2. Key Laboratory for Renewable Energy Institute of Physics Chinese Academy of Sciences Beijing Key Laboratory for New Energy Materials and Devices Beijing 100190 China

3. State Key Laboratory of Structural Chemistry Fujian Institute of Research on the Structure of Matter Chinese Academy of Sciences Fuzhou Fujian 350002 China

4. Fujian Science and Technology Innovation Laboratory for Optoelectronic Information of China Fuzhou Fujian 350108 China

5. Peking University Yangtze Delta Institute of Optoelectronics Nantong Jiangsu 226010 China

6. Collaborative Innovation Center of Quantum Matter Beijing 100084 China

Abstract

AbstractIn perovskite solar cells (PSCs), the buried interface containing high concentrations of defects is critical for efficient charge extraction toward high‐performance device. Herein, porous organic cage (POC) is introduced between tin dioxide and perovskite to spontaneously reconstitute the buried interface. Through the chemical linkage formed by polydentate chelation of POC with SnO2 and perovskite, the buried interface achieves greatly reduced defect density and enhanced carrier extraction. More importantly, it is found that iodide ions in aged devices to migrate down to the electron transport layer and even invade the ITO electrode, changing the work function of ITO. This detrimental effect can be well resolved by POC since the host‐guest interaction of POC can effectively suppress the iodide ions trying to migrate downward. As a result, the PSC fabricated by POC‐restructured strategy yields a superior PCE of 24.13%. Moreover, the unencapsulated PSCs exhibit conspicuous improved long‐term stability and retain 93% of its initial efficiency after 5000 h in ambient condition.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Beijing Municipal Natural Science Foundation

Youth Innovation Promotion Association of the Chinese Academy of Sciences

Publisher

Wiley

Subject

Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials

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