Transporting holes stably under iodide invasion in efficient perovskite solar cells

Author:

Wang Tao123ORCID,Zhang Yao1ORCID,Kong Weiyu123,Qiao Liang123,Peng Bingguo123,Shen Zhichao1,Han Qifeng1,Chen Han1,Yuan Zhiliang4ORCID,Zheng Rongkun5ORCID,Yang Xudong123ORCID

Affiliation:

1. State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, Shanghai 200240, China.

2. Center of Hydrogen Science, School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.

3. Zhangjiang Institute for Advanced Study, Shanghai Jiao Tong University, Shanghai 201210, China.

4. Beijing Academy of Quantum Information Sciences, Beijing 100193, China.

5. School of Physics, Sydney Nano Institute, The University of Sydney, Sydney, NSW 2006, Australia.

Abstract

Highly efficient halide perovskite solar cells generally rely on lithium-doped organic hole transporting layers that are thermally and chemically unstable, in part because of migration of iodide anions from the perovskite layer. We report a solution strategy to stabilize the hole transport in organic layers by ionic coupling positive polymer radicals and molecular anions through an ion-exchange process. The target layer exhibited a hole conductivity that was 80 times higher than that of the conventional lithium-doped layer. Moreover, after extreme iodide invasion caused by light-soaking at 85°C for 200 hours, the target layer maintained high hole conductivity and well-matched band alignment. This ion-exchange strategy enabled fabrication of perovskite solar cells with a certified power conversion efficiency of 23.9% that maintained 92% under standard illumination at 85°C after 1000 hours.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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