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Highly Durable Inverted Inorganic Perovskite/Organic Tandem Solar Cells Enabled by Multifunctional Additives

  • Yanxun Li
  • , Yichao Yan
  • , Yuang Fu
  • , Wenlin Jiang
  • , Ming Liu
  • , Mingqian Chen
  • , Xiaofeng Huang
  • , Guanghao Lu
  • , Xinhui Lu
  • , Jun Yin
  • , Shengfan Wu
  • , Alex K.Y. Jen
  • City University of Hong Kong
  • Nanjing University
  • Chinese University of Hong Kong
  • Hong Kong Polytechnic University
  • University of Washington

科研成果: 期刊稿件文章同行评审

29 引用 (Scopus)

摘要

Inverted perovskite/organic tandem solar cells (P/O TSCs) suffer from poor long-term device stability due to halide segregation in organic–inorganic hybrid wide-band gap (WBG) perovskites, which hinders their practical deployment. Therefore, developing all-inorganic WBG perovskites for incorporation into P/O TSCs is a promising strategy because of their superior stability under continuous illumination. However, these inorganic WBG perovskites also face some critical issues, including rapid crystallization, phase instability, and large energy loss, etc. To tackle these issues, two multifunctional additives based on 9,10-anthraquinone-2-sulfonic acid (AQS) are developed to regulate the perovskite crystallization by mediating the intermediate phases and suppress the halide segregation through the redox-shuttle effect. By coupling with organic cations having the desirable functional groups and dipole moments, these additives can effectively passivate the defects and adjust the alignment of interface energy levels. Consequently, a record Voc approaching 1.3 V with high power conversion efficiency (PCE) of 18.59 % could be achieved in a 1.78 eV band gap single-junction inverted all-inorganic PSC. More importantly, the P/O TSC derived from this cell demonstrates a T90 lifetime of 1000 h under continuous operation, presenting the most stable P/O TSCs reported so far.

源语言英语
文章编号e202412515
期刊Angewandte Chemie - International Edition
63
52
DOI
出版状态已出版 - 20 12月 2024

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