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Mitigating Stress-Induced Nonphotoactive Phase Transition Through Sodium Sulfonate Engineering for Stable and Efficient Perovskite Solar Cells

Research output: Journal Publications and Reviews › RGC 21 - Publication in refereed journal › peer-review

Abstract

Formamidinium lead triiodide (FAPbI3) perovskite solar cells (PSCs) have attracted significant attention due to their outstanding optoelectronic properties. However, their long-term stability remains limited by lattice strain-induced transition from the photoactive α-phase to the nonphotoactive δ-phase. In this work, first-principles calculations reveal that the incorporation of Na+ into interstitial sites between adjacent FA+ cations significantly reduces the formation energy of the α-phase, thereby promoting its thermodynamic stabilization. Then, experimental results confirm that the introduction of 2 mol% Na+ effectively alleviates lattice strain while simultaneously suppressing δ phase. Moreover, the accompanying sulfonate groups interacting with PbI2 can regulate the crystallization and improve film quality. As a result, the optimized PSC achieved power conversion efficiency (PCE) as high as 26.67% (certificated 26.44%), ranking among the highest reported for the n-i-p structured devices. Notably, the bare device without encapsulation retained over 90% of its initial efficiency after continuous heating at 85°C for 1200 h and maintained 80% after 800 h continuous illumination. This study demonstrates that metal cation doping is an effective strategy for stabilizing the perovskite lattice and enhancing long-term operational stability of perovskite-based optoelectronic devices. © 2026 The Author(s). Angewandte Chemie International Edition published by Wiley-VCH GmbH.
Original languageEnglish
Article numbere2425823
Number of pages13
JournalAngewandte Chemie - International Edition
Online published5 Aug 2026
DOIs
Publication statusOnline published - 5 Aug 2026

Funding

S.L. thanks the support from Key project of National Natural Science Foundation of China (U21A20102); National Natural Science Foundation of China (62174103); the 111 project (B21005). J.Y. thanks the support from Hon Hai (AC-202403-02-9) and Baosteel (BHK2502-03). A.K.Y.J. thanks the sponsorship of the Lee Shau-Kee Chair Professor (Materials Science) and the support from the APRC Grants (9380086, 9610419, 9610440, 9610492, 9610508) of the City University of Hong Kong, the TCFS grant (GHP/121/22SZ) from the Innovation and Technology Commission of Hong Kong, the GRF grants (11304424, 11308625, 11316422) and CRS grants (CRS_CityU104/23, CRS_HKUST203/23) from the Research Grants Council of Hong Kong, and Grant Number. T2541160284 from the National Natural Science Foundation of China. This work was financially supported by City University of Hong Kong for the project ‘Fostering Innovation for Resilience and Sustainable Transformation’ (FIRST), officially endorsed by the United Nations Educational, Scientific and Cultural Organization (UNESCO) under the International Decade of Sciences for Sustainable Development (IDSSD) (2024-2033) via the internal City University of Hong Kong account of 9610739.

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

Research Keywords

  • crystallization kinetics
  • high efficiency
  • lattice geometry
  • perovskite solar cells
  • thermal and light stability

RGC Funding Information

  • RGC-funded

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