Chuanyi Huang, Xianyong Zhou, Yintai Xu, Kai Yuan, Minhang Liu, Kaixin Huang, Yuanwei Wang, Guo Ding, Zhiwei Deng, Yuhan Chen, Jiacheng Zhan, Yizhou Qian, Hu Shen, Bin Tian, Jinbo Chen, Binbin Yu, Jing Li, Hanjian Lai, Zhixin Liu, Lei Yan, Baomin Xu, Xingzhu Wang, Chang Liu
{"title":"Phase Separation Suppression by Guanidine Phosphate Enables 21.54% Wide-Bandgap Perovskite Cells for All-Perovskite Tandem Solar Cells","authors":"Chuanyi Huang, Xianyong Zhou, Yintai Xu, Kai Yuan, Minhang Liu, Kaixin Huang, Yuanwei Wang, Guo Ding, Zhiwei Deng, Yuhan Chen, Jiacheng Zhan, Yizhou Qian, Hu Shen, Bin Tian, Jinbo Chen, Binbin Yu, Jing Li, Hanjian Lai, Zhixin Liu, Lei Yan, Baomin Xu, Xingzhu Wang, Chang Liu","doi":"10.1002/cnl2.70189","DOIUrl":null,"url":null,"abstract":"<p>Wide-bandgap perovskite materials with high bromine content (> 1.7 eV) suffer from severe light‑induced phase separation, leading to irreversible device degradation—yet effective suppression strategies remain scarce. Here, we introduce guanidine phosphate (GP) as a bifunctional additive that simultaneously passivates defects and regulates crystal orientation. The Gua<sup>+</sup> and PO<sub>4</sub><sup>3−</sup> ions act cooperatively: Gua<sup>+</sup> passivates undercoordinated Pb<sup>2+</sup> and reacts with excess surface Pb<sup>2+</sup>, while PO<sub>4</sub><sup>3−</sup> stabilizes iodide vacancies through strong Pb–O–P bonds. This dual passivation suppresses ion migration and promotes (100)-oriented crystallization, thereby improving film quality. Consequently, GP‑modified 1.78 eV perovskite solar cells achieve a champion power conversion efficiency (PCE) of 21.54% (control: 19.72%)—the highest reported for devices in the 1.74–1.79 eV range. Unencapsulated devices retain 90.64% of their initial efficiency after 1400 h in N<sub>2</sub> atmosphere. The strategy also yields 19.64% efficiency for 1.85 eV perovskites, demonstrating its generality. Furthermore, all‑perovskite tandem cells incorporating this approach achieve a PCE of 28.72%.</p>","PeriodicalId":100214,"journal":{"name":"Carbon Neutralization","volume":"5 4","pages":""},"PeriodicalIF":12.0000,"publicationDate":"2026-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/cnl2.70189","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbon Neutralization","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cnl2.70189","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Wide-bandgap perovskite materials with high bromine content (> 1.7 eV) suffer from severe light‑induced phase separation, leading to irreversible device degradation—yet effective suppression strategies remain scarce. Here, we introduce guanidine phosphate (GP) as a bifunctional additive that simultaneously passivates defects and regulates crystal orientation. The Gua+ and PO43− ions act cooperatively: Gua+ passivates undercoordinated Pb2+ and reacts with excess surface Pb2+, while PO43− stabilizes iodide vacancies through strong Pb–O–P bonds. This dual passivation suppresses ion migration and promotes (100)-oriented crystallization, thereby improving film quality. Consequently, GP‑modified 1.78 eV perovskite solar cells achieve a champion power conversion efficiency (PCE) of 21.54% (control: 19.72%)—the highest reported for devices in the 1.74–1.79 eV range. Unencapsulated devices retain 90.64% of their initial efficiency after 1400 h in N2 atmosphere. The strategy also yields 19.64% efficiency for 1.85 eV perovskites, demonstrating its generality. Furthermore, all‑perovskite tandem cells incorporating this approach achieve a PCE of 28.72%.