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Thermodynamic inhibition of bromine-rich phase nucleation in wide-bandgap perovskites for operationally stable tandem solar cells

  • Xueying Yang
  • , Zhongliang Yan
  • , Shibo Wang
  • , Pengfei Fu
  • , Chunyan Deng
  • , Guang Yang
  • , Yu Lou
  • , Zhaojin Wang
  • , Miao Zeng
  • , You Chen
  • , Zhicong Zhou
  • , Xinyu Ye
  • , Xiaokang Sun
  • , Chengwei Shan
  • , Yuanmiao Sun
  • , Aung Ko Ko Kyaw
  • , Hanlin Hu
  • , Zhifang Shi
  • , Zaiwei Wang
  • , Xinbo Yang
  • Xiaohong Zhang, Gang Li, Yang Bai, Hui Ming Cheng

Research output: Journal article publication › Journal article › Academic research › peer-review

Abstract

Operational instability in wide-bandgap (WBG) perovskites, predominantly caused by light-induced halide phase segregation, remains a major obstacle to the commercialization of perovskite-based tandem solar cells. Current strategies focus on mitigating the consequences of halide migration rather than targeting its fundamental origin. In this study, we reveal that the preferential nucleation of bromine-rich phases during film formation initiates intrinsic compositional inhomogeneity, which subsequently accelerates halide migration and phase segregation under operational stressors. We develop a preemptive inhibition strategy by introducing potassium thiocyanate, which suppresses halide segregation by raising the nucleation energy barrier of bromine-rich phases from the outset, thereby achieving a thermodynamically stabilized halide distribution. This approach enables 1.68 eV single-junction devices to achieve a high power conversion efficiency of 23.50%, with the devices simultaneously demonstrating excellent stability by maintaining 98% of their initial efficiency over 2240 hours of continuous maximum power point tracking. Leveraging this stable absorber, we realize a perovskite-silicon tandem solar cell with a remarkable efficiency of 33.08% (certified 32.52%), which retains its performance over 540 hours of outdoor operation and achieves an extrapolated T90 lifetime exceeding 9700 hours under continuous maximum power point tracking. Furthermore, we demonstrate the broad applicability of this stabilization strategy across WBG perovskites. The 1.68–1.88 eV compositions show exceptional spectral stability with negligible photoluminescence shifts under identical stress conditions, enabling efficient single-junction devices with efficiencies of 20.37% (1.77 eV) and 18.11% (1.88 eV), as well as high-performance all-perovskite (28.18%, certified 28.17%) and perovskite-organic (25.66%) tandem solar cells.

Original languageEnglish
Pages (from-to)2273-2288
Number of pages16
JournalEnergy and Environmental Science
Volume19
Issue number7
DOIs
Publication statusPublished - 14 Apr 2026

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

ASJC Scopus subject areas

  • Environmental Chemistry
  • Renewable Energy, Sustainability and the Environment
  • Nuclear Energy and Engineering
  • Pollution

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