TY - JOUR
T1 - Lattice matching propels customized-dimensionality 2D/3D perovskite heterojunctions for high-performance photovoltaics
AU - Liang, Yuncai
AU - Xia, Junmin
AU - Fan, Baojin
AU - Liang, Chao
AU - Yuan, Fangfang
AU - Peng, Sihui
AU - Sun, Qihang
AU - Zhao, Rudai
AU - Miao, Zhipeng
AU - Zhang, Ting
AU - Zhu, He
AU - Liang, Wenlong
AU - Xie, Yunhang
AU - Chen, Shufen
AU - Hu, Xiaotian
AU - Zhang, Yiqiang
AU - Li, Pengwei
AU - Song, Yanlin
N1 - Publisher Copyright:
© 2024 Elsevier Ltd
PY - 2024/12
Y1 - 2024/12
N2 - 2D/3D perovskite heterojunctions typically yield mixed-phase 2D perovskites, generating multiple quantum wells that impede charge transfer, thereby limiting the potential enhancement of solar cell efficiency. Here, we successfully fabricated phase-pure 2D (n = 2)/3D perovskite heterojunctions via introducing the γ-aminobutyric acid (GABA) ligand, which minimized energetic inhomogeneity, thus favoring interfacial charge transfer through optimized energy band alignment. The ligation between the oxygen atoms in the ligand and the uncoordinated lead in the 3D perovskite triggered a structural transition from cubic to tetragonal at the 3D perovskite surface, ensuring a seamless lattice matching with the 2D perovskite (n = 2), resulting in this optimized configuration. Utilizing this innovative structural configuration, the carrier properties of 2D/3D perovskite thin films have been significantly enhanced, exhibiting diffusion lengths exceeding 1000 nm and a mobility of 3.35 cm² V⁻¹ s⁻¹. Consequently, the fabricated small-area perovskite solar cells exhibited an impressive power conversion efficiency (PCE) of 25.06 %, while the mini-modules (10 cm × 10 cm) attained a maximum PCE of 17.27 %. Furthermore, the passivation of the 2D perovskite layers, coupled with their inherent superior resistance, enabled the unencapsulated target device to maintain outstanding long-term stability, even under challenging environmental conditions of light, heat, and humidity.
AB - 2D/3D perovskite heterojunctions typically yield mixed-phase 2D perovskites, generating multiple quantum wells that impede charge transfer, thereby limiting the potential enhancement of solar cell efficiency. Here, we successfully fabricated phase-pure 2D (n = 2)/3D perovskite heterojunctions via introducing the γ-aminobutyric acid (GABA) ligand, which minimized energetic inhomogeneity, thus favoring interfacial charge transfer through optimized energy band alignment. The ligation between the oxygen atoms in the ligand and the uncoordinated lead in the 3D perovskite triggered a structural transition from cubic to tetragonal at the 3D perovskite surface, ensuring a seamless lattice matching with the 2D perovskite (n = 2), resulting in this optimized configuration. Utilizing this innovative structural configuration, the carrier properties of 2D/3D perovskite thin films have been significantly enhanced, exhibiting diffusion lengths exceeding 1000 nm and a mobility of 3.35 cm² V⁻¹ s⁻¹. Consequently, the fabricated small-area perovskite solar cells exhibited an impressive power conversion efficiency (PCE) of 25.06 %, while the mini-modules (10 cm × 10 cm) attained a maximum PCE of 17.27 %. Furthermore, the passivation of the 2D perovskite layers, coupled with their inherent superior resistance, enabled the unencapsulated target device to maintain outstanding long-term stability, even under challenging environmental conditions of light, heat, and humidity.
KW - 2D/3D perovskite heterojunctions
KW - Customized-dimensionality
KW - Perovskite solar cells
UR - https://www.scopus.com/pages/publications/85203191524
U2 - 10.1016/j.nantod.2024.102479
DO - 10.1016/j.nantod.2024.102479
M3 - 文章
AN - SCOPUS:85203191524
SN - 1748-0132
VL - 59
JO - Nano Today
JF - Nano Today
M1 - 102479
ER -