硫化
能量转换效率
异质结
材料科学
钙钛矿(结构)
原位
化学工程
化学
纳米技术
结晶学
光电子学
有机化学
硫黄
工程类
冶金
作者
Xuemin Guo,Chunyan Lu,Wenxiao Zhang,Haobo Yuan,Hui Yang,H. Liu,Zhengbo Cui,Wen J. Li,Yuyang Hu,Xiaodong Li,Junfeng Fang
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-01-03
卷期号:9 (1): 329-335
被引量:21
标识
DOI:10.1021/acsenergylett.3c01855
摘要
Inverted CsPbI3 commonly exhibits a more p-type surface than bulk, which induces severe interfacial recombination and, thus, limits the device's Voc and efficiency in inverted perovskite solar cells (PSCs). Here, a gradual CsPbI3/PbS heterojunction is constructed to inhibit such recombination through in situ chemical sulfidation with N,N′-diphenylthiourea (DPhTA). DPhTA can directly react with CsPbI3 to form PbS and induce a p- to n-type transition at the CsPbI3 surface, which leads to the energy level bending downward and establishing a gradual CsPbI3/PbS heterojunction at the top of the surface region. PSCs with DPhTA exhibit a high Voc of 1.20 V and reach over 20% efficiency (stabilized efficiency of 19.5%), which is among the highest efficiencies of inverted CsPbI3 PSCs. In addition, the strong Pb–S bond and well-matched crystal lattice of PbS will protect and stabilize the CsPbI3 layer beneath, thereby greatly improving the device's stability. Resulting PSCs retain over 95% of the initial efficiency whether after maximum power point (MPP) tracking for 1200 h or N2 storage for 300 days.
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