Elevating Charge Transport Layer for Stable Perovskite Light‐Emitting Diodes

Author:

Yi Chang1,Wang Airu1,Cao Chensi1,Kuang Zhiyuan1,Tao Xiangru1,Wang Zekun1,Zhou Fuyi1,Zhang Guolin1,Liu Ziping1,Huang Heyong2,Cao Yu34,Li Renzhi1,Wang Nana1,Huang Wei135,Wang Jianpu136ORCID

Affiliation:

1. Key Laboratory of Flexible Electronics (KLOFE) School of Flexible Electronics (Future Technologies) and Institute of Advanced Materials (IAM) Nanjing Tech University (NanjingTech) 30 South Puzhu Road Nanjing 211816 China

2. Center of Analysis and Testing Nanjing Normal University Nanjing 210023 China

3. Strait Laboratory of Flexible Electronics (SLoFE) Fuzhou Fujian 350117 China

4. Strait Institute of Flexible Electronics (SIFE, Future Technologies) Fujian Normal University Fuzhou Fujian 350117 China

5. Shaanxi Institute of Flexible Electronics (SIFE) Xi'an Institute of Biomedical Materials and Engineering (IBME) Northwestern Polytechnical University (NPU) 127 West Youyi Road Xi'an 710072 China

6. School of Materials Science and Engineering & School of Microelectronics and Control Engineering Changzhou University Changzhou Jiangsu 213164 China

Abstract

AbstractIon migration is a major factor affecting the long term stability of perovskite light‐emitting diodes (LEDs), which limits their commercialization potential. The accumulation of excess halide ions at the grain boundaries of perovskite films is a primary cause of ion migration in these devices. Here, it is demonstrated that the channels of ion migrations can be effectively impeded by elevating the hole transport layer between the perovskite grain boundaries, resulting in highly stable perovskite LEDs. The unique structure is achieved by reducing the wettability of the perovskites, which prevents infiltration of the upper hole‐transporting layer into the spaces of perovskite grain boundaries. Consequently, nanosized gaps are formed between the excess halide ions and the hole transport layer, effectively suppressing ion migration. With this structure, perovskite LEDs with operational half‐lifetimes of 256 and 1774 h under current densities of 100 and 20 mA cm−2 respectively are achieved. These lifetimes surpass those of organic LEDs at high brightness. It is further found that this approach can be extended to various perovskite LEDs, showing great promise for promoting perovskite LEDs toward commercial applications.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

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