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Engineering ligand reactivity enables high-temperature operation of stable perovskite solar cells

  • So Min Park
  • , Mingyang Wei
  • , Jian Xu
  • , Harindi R. Atapattu
  • , Felix T. Eickemeyer
  • , Kasra Darabi
  • , Luke Grater
  • , Yi Yang
  • , Cheng Liu
  • , Sam Teale
  • , Bin Chen
  • , Hao Chen
  • , Tonghui Wang
  • , Lewei Zeng
  • , Aidan Maxwell
  • , Zaiwei Wang
  • , Keerthan R. Rao
  • , Zhuoyun Cai
  • , Shaik M. Zakeeruddin
  • , Jonathan T. Pham
  • Chad M. Risko, Aram Amassian, Mercouri G. Kanatzidis, Kenneth R. Graham*, Michael Grätzel*, Edward H. Sargent*
*此作品的通讯作者
  • University of Toronto
  • Swiss Federal Institute of Technology Lausanne
  • University of Kentucky
  • North Carolina State University
  • Northwestern University

科研成果: 期刊稿件文章同行评审

摘要

Perovskite solar cells (PSCs) consisting of interfacial two- and three-dimensional heterostructures that incorporate ammonium ligand intercalation have enabled rapid progress toward the goal of uniting performance with stability. However, as the field continues to seek ever-higher durability, additional tools that avoid progressive ligand intercalation are needed to minimize degradation at high temperatures. We used ammonium ligands that are nonreactive with the bulk of perovskites and investigated a library that varies ligand molecular structure systematically. We found that fluorinated aniliniums offer interfacial passivation and simultaneously minimize reactivity with perovskites. Using this approach, we report a certified quasi-steady-state power-conversion efficiency of 24.09% for inverted-structure PSCs. In an encapsulated device operating at 85°C and 50% relative humidity, we document a 1560-hour T85 at maximum power point under 1-sun illumination.

源语言英语
页(从-至)209-215
页数7
期刊Science
381
6654
DOI
出版状态已出版 - 14 7月 2023
已对外发布

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