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Recrystallizing Sputtered NiOx for Improved Hole Extraction in Perovskite/Silicon Tandem Solar Cells.

Authors :
Jin, Yongbin
Feng, Huiping
Li, Yingji
Zhang, Hong
Chen, Xuelin
Zhong, Yawen
Zeng, Qinghua
Huang, Jiarong
Weng, Yalian
Yang, Jinxin
Tian, Chengbo
Zhang, Jinyan
Xie, Liqiang
Wei, Zhanhua
Source :
Advanced Energy Materials. Oct2024, p1. 9p. 5 Illustrations.
Publication Year :
2024

Abstract

Sputtering nickel oxide (NiO<italic>x</italic>) is a production‐line‐compatible route for depositing hole transport layers (HTL) in perovskite/silicon tandem solar cells. However, this technique often results in films with low crystallinity and structural flaws, which can impair electronic conductivity. Additionally, the complex surface chemistry and inadequate Ni3+/Ni2+ ratio impede the effective binding of self‐assembled monolayers (SAMs), affecting hole extraction at the perovskite/HTL interface. Herein, these issues are addressed using a recrystallization strategy by treating sputtered NiO<italic>x</italic> thin films with sodium periodate (NaIO4), an industrially available oxidant. This treatment improved crystallinity and increased the Ni3+/Ni2+ ratio, resulting in a higher content of nickel oxyhydroxide. These enhancements strengthened the SAM's anchoring capability on NiO<italic>x</italic> and improved the hole extraction at the perovskite/HTL interface. Moreover, the NaIO4 treatment facilitated Na+ diffusion within the perovskite layer and minimized phase separation, thus improving device stability. As a result, single‐junction perovskite solar cells with a 1.68 eV bandgap achieve a power conversion efficiency (PCE) of 23.22% for an area of 0.12 cm2. Perovskite/silicon tandem cells with an area of 1 cm2 reached a PCE of 30.48%. Encapsulated tandem devices retained 95% of their initial PCE after 300 h of maximum power point tracking under 1‐sun illumination at 25 °C. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
16146832
Database :
Academic Search Index
Journal :
Advanced Energy Materials
Publication Type :
Academic Journal
Accession number :
180401055
Full Text :
https://doi.org/10.1002/aenm.202403911