Overcoming ionic migration in perovskite solar cells through alkali metals

被引:36
作者
Aranda, Clara A. [1 ,3 ]
Alvarez, Agustin O. [2 ,3 ]
Chivrony, Vladimir S. [4 ]
Das, Chittaranjan [1 ]
Rai, Monika [1 ]
Saliba, Michael [1 ,2 ]
机构
[1] Univ Stuttgart, Inst Photovolta ipv, D-70569 Stuttgart, Germany
[2] Forschungszentrum Julich, IEK5 Photovolta, D-52425 Julich, Germany
[3] Univ Jaume 1, Inst Adv Mat, Ave Vicent Sos Baynat S-N, Castellon de La Plana 12006, Spain
[4] Univ Valencia, Inst Ciencia Mat ICMUV, C-Catedrat Jose Beltran 2, Valencia 46980, Spain
基金
欧盟地平线“2020”;
关键词
HYSTERESIS; POLARIZATION; IMPEDANCE; CATIONS;
D O I
10.1016/j.joule.2023.11.011
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Alkali metals, as additives in perovskite solar cells (PSCs), have been extensively investigated for their impact on performance enhancement. This performance is sensitive to ion -driven interfacial recombination processes that lead to voltage losses and perform with negative capacitance features in impedance spectroscopy (IS). In this study, we exploited negative capacitance as a tool to systematically investigate the influence of Li, Na, and K on the photovoltage of the wide band -gap material MAPbBr3, known for historical photovoltage losses. Sodium cations were found to mitigate adverse interfacial recombination pathways, yielding a remarkable stabilized open -circuit potential of 1.65 V. Impedance measurements indicated sodium significant influence within the material's bulk, corroborated by time -of -flight secondary ion mass spectrometry and X-ray photoelectron spectroscopy. These techniques confirmed the ability of Na to decrease ionic migration in perovskite materials. X-ray photoelectron spectroscopy (XPS) revealed the underlying mechanism by which Na accomplishes this task: through an electrostatic interaction with the organic compounds.
引用
收藏
页码:241 / 254
页数:15
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