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Title: Molecular Interaction Regulates the Performance and Longevity of Defect Passivation for Metal Halide Perovskite Solar Cells

Journal Article · · Journal of the American Chemical Society
ORCiD logo [1];  [2];  [3];  [3];  [3]; ORCiD logo [3]; ORCiD logo [3];  [4];  [5];  [3];  [3]; ORCiD logo [3]; ORCiD logo [3];  [6];  [3]; ORCiD logo [7]; ORCiD logo [3]
  1. Univ. of California, Los Angeles, CA (United States); University of California, Los Angeles
  2. Univ. of California, Los Angeles, CA (United States); Nanjing Univ. (China)
  3. Univ. of California, Los Angeles, CA (United States)
  4. Hanyang Univ., Seoul (Korea)
  5. Univ. of California, Los Angeles, CA (United States); Sungkyunkwan Univ., Suwon (Korea)
  6. Sungkyunkwan Univ., Suwon (Korea)
  7. Nanjing Univ. (China)

Defect passivation constitutes one of the most commonly used strategies to fabricate highly efficient perovskite solar cells (PSCs). However, the durability of the passivation effects under harsh operational conditions has not been extensively studied regardless of the weak and vulnerable secondary bonding between the molecular passivation agents and perovskite crystals. Here, we incorporated strategically designed passivating agents to investigate the effect of their interaction energies on the perovskite crystals and correlated these with the performance and longevity of the passivation effects. We unraveled that the passivation agents with a stronger interaction energy are advantageous not only for effective defect passivation but also to suppress defect migration. The prototypical PSCs treated with the optimal passivation agent exhibited superior performance and operational stability, retaining 81.9 and 85.3% of their initial performance under continuous illumination or nitrogen at 85 °C after 1008 h, respectively, while the reference device completely degraded during that time. Furthermore, this work provides important insights into designing operationally durable defect passivation agents for perovskite optoelectronic devices.

Research Organization:
Univ. of California, Los Angeles, CA (United States)
Sponsoring Organization:
National Research Foundation of Korea (NRF); Office of Naval Research; USDOE Office of Energy Efficiency and Renewable Energy (EERE), Renewable Power Office. Solar Energy Technologies Office
Grant/Contract Number:
EE0008751
OSTI ID:
1714372
Journal Information:
Journal of the American Chemical Society, Journal Name: Journal of the American Chemical Society Journal Issue: 47 Vol. 142; ISSN 0002-7863
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English

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