Published April 24, 2023 | Version v1
Journal article

Managing secondary phase lead iodide in hybrid perovskites via surface reconstruction for high-performance perovskite solar cells with robust environmental stability

  • 1. State Key Laboratory of Solidification Processing, Center for Nano Energy Materials, School of Materials Science and Engineering, Northwestern Polytechnical University and Shaanxi Joint Laboratory of Graphene (NPU), Xi'an, 710071 (China)
  • 2. Chongqing Innovation Center, Northwestern Polytechnical University, Chongqing, 401135 (China)
  • 3. School of Microelectronics, State Key Discipline Lab of Wide Band Gap Semiconductor Technology, Shaanxi Joint Key Lab of Graphene, Advanced Interdisciplinary Research Center for Flexible Electronics, Xidian University, Xi'an, 710071 (China)

Description

Rationally managing the secondary-phase excess lead iodide (PbI2) in hybrid perovskite is of significance for pursuing high performance perovskite solar cells (PSCs), while the challenge remains on its conversion to a homogeneous layer that is robust stable against environmental stimuli. We herein demonstrate an effective strategy of surface reconstruction that converts the excess PbI2 into a gradient lead sulfate-silica bi-layer, which substantially stabilizes the perovskite film and reduces interfacial charge transfer barrier in the PSCs device. The perovskite films with such bi-layer could bear harsh conditions such as soaking in water, light illumination at 70 % relative humidity, and the damp-thermal (85 °C and 30 % humidity) environment. The resulted PSCs deliver a champion efficiency up to 24.09 %, as well as remarkable environmental stability, e.g., retaining 78 % of their initial efficiency after 5500 h of shelf storage, and 82 % after 1000 h of operational stability testing. (© 2023 Wiley‐VCH GmbH)

Availability note (English)

Available from: http://dx.doi.org/10.1002/anie.202300678

Additional details

Identifiers

Publishing Information

Journal Title
Angewandte Chemie (International Edition)
Journal Volume
62
Journal Issue
18
Journal Page Range
p. 1-10
ISSN
1433-7851
CODEN
ACIEF5

Optional Information

Notes
AID: e202300678