材料科学
钙钛矿(结构)
降级(电信)
光伏系统
限制
钝化
太阳能电池
光电子学
硅
光伏
太阳能
载流子寿命
化学工程
能量转换效率
钙钛矿太阳能电池
晶体硅
纳米技术
晶体缺陷
作者
Qiu Xiong,C Y Wang,Xiaofeng Huang,Abd. Rashid bin Mohd Yusoff,Pingping Sun,Weichun Pan,Zilong Zhang,Qin Zhou,Lusheng Liang,Jinbo Zhao,Yong Gang,Chunming Liu,Yao Wang,Jihuai Wu,Yongguang Tu,Meng Li,Xin Li,Binghui Wu,Nanfeng Zheng,Su‐Yuan Xie
摘要
ABSTRACT The unclear mechanisms and dominant types of defects causing degradation hinder the stability of perovskite solar cells, leading to increased operating costs and limiting their commercialization. In this study, we identify deep‐level I FA and I Pb defects as the primary cause of device degradation based on quantitative analysis of capacitance‐frequency spectra combined with detailed balance theory, although the concentrations are lower than those of commonly believed shallow‐level defects by three orders of magnitude. To mitigate these issues, we design a non‐intercalary ligand coordination strategy through dual‐end electropositive 3TU 2+ ions, which effectively passivated the degradation‐induced deep‐level defects. This approach results in a significant improvement in quasi‐Fermi level splitting alignment, reducing energy loss at the rear interface by an order of magnitude (from 1.46% to 0.62%). In addition to achieving a certified efficiency of 25.56%, our devices demonstrate an extrapolated T 80 lifetime exceeding 10 years, as per the ISOS‐LC‐1 protocol. This improvement reduces the levelized cost of energy to 0.148$ kWh −1 , on par with silicon photovoltaics, thus enhancing the commercial viability of perovskite solar cells.
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