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用于具有超过1000小时运行稳定性的单片硅基串联电池的定向宽带隙钙钛矿。

Oriented wide-bandgap perovskites for monolithic silicon-based tandems with over 1000 hours operational stability.

作者信息

Yao Yuxin, Li Biao, Ding Degong, Kan Chenxia, Hang Pengjie, Zhang Daoyong, Hu Zechen, Ni Zhenyi, Yu Xuegong, Yang Deren

机构信息

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering, Zhejiang University, Hangzhou, Zhejiang, China.

ZJU Hangzhou Global Scientific and Technological Innovation Center, Hangzhou, Zhejiang, China.

出版信息

Nat Commun. 2025 Jan 2;16(1):40. doi: 10.1038/s41467-024-55377-6.

Abstract

The instability of hybrid wide-bandgap (WBG) perovskite materials (with bandgap larger than 1.68 eV) still stands out as a major constraint for the commercialization of perovskite/silicon tandem photovoltaics, yet its correlation with the facet properties of WBG perovskites has not been revealed. Herein, we combine experiments and theoretical calculations to comprehensively understand the facet-dependent instability of WBG perovskites. We find that the (111) facet, which owned higher ion-migration activation energy and lower diffusion constant, endured instability better than the (100) facet in multi-component 1.68 eV perovskites under electron beam or light irradiations, where excess charge carriers facilitate halide migrations and thereafter phase segregations. By introducing trioctylphosphine oxide into the WBG perovskite, a strong oriented growth of the (111) facet for the WBG perovskite film was realized which exhibited enhanced operational stability against light illumination. The fabricated one square centimeter area perovskite/silicon tandems with n-i-p and p-i-n configurations deliver efficiencies of 28.03 % and 30.78 % (certified 30.26 %), respectively, with both configurations exhibiting excellent operational stability at the maximum power point (MPP) with T > 1000 h.

摘要

混合宽带隙(WBG)钙钛矿材料(带隙大于1.68 eV)的不稳定性仍然是钙钛矿/硅串联光伏商业化的主要制约因素,但其与WBG钙钛矿晶面性质的相关性尚未得到揭示。在此,我们结合实验和理论计算,全面了解WBG钙钛矿晶面依赖性不稳定性。我们发现,在电子束或光照下,在多组分1.68 eV钙钛矿中,具有较高离子迁移活化能和较低扩散常数的(111)晶面比(100)晶面更能耐受不稳定性,其中过量的电荷载流子促进卤化物迁移并进而导致相分离。通过将三辛基氧化膦引入WBG钙钛矿中,实现了WBG钙钛矿薄膜(111)晶面的强烈取向生长,其在光照下表现出增强的操作稳定性。制备的面积为1平方厘米的n-i-p和p-i-n结构的钙钛矿/硅串联电池分别实现了28.03%和30.78%的效率(认证效率为30.26%),两种结构在最大功率点(MPP)下均表现出优异的操作稳定性,T>1000小时。

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