钙钛矿(结构)
材料科学
光伏系统
化学工程
光电子学
纳米技术
工程类
电气工程
作者
Xing Zhao,Yujie Qiu,Min Wang,Danxia Wu,Xiaopeng Yue,Huilin Yan,Bing‐Bing Fan,Shuxian Du,Yuqing Yang,Yingying Yang,Danni Li,Peng Cui,Hao Huang,Yingfeng Li,Nam‐Gyu Park,Meicheng Li
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-05-10
卷期号:9 (6): 2659-2669
被引量:7
标识
DOI:10.1021/acsenergylett.4c00386
摘要
The presence of the detrimental PbI2 residue at the buried interface negatively affects the photovoltaic performance of perovskite solar cells (PSCs). However, the underlying mechanism involved in the formation and elimination of residual PbI2 has been rarely investigated, despite its critical significance for high-efficiency and stable PSCs. Here, we investigated the formation and elimination mechanism of residual PbI2 at the buried interface influenced by citric acid (CA) and found that CA can quickly remove the PbI2·DMSO complex through a competitive adsorption mechanism by forming highly crystallized PbI2. This promotes the subsequent intercalation of amine cations into the PbI2 framework by forming a stable perovskite. Consequently, the best-performing target PSC achieves an efficiency of 25.19% (a certified efficiency of 24.64%) and 23% from a 1 cm2 PSC. Additionally, the target PSC also demonstrates improved light stability after 200 h of UV light soaking by maintaining 94.21% of its initial efficiency compared with only 70.76% for the control PSC.
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