Issue 19, 2021

Overcoming the carrier transport limitation in Ruddlesden–Popper perovskite films by using lamellar nickel oxide substrates

Abstract

Quasi two-dimensional (2D) Ruddlesden–Popper perovskites films fabricated by a solution process are composed of multiple 2D perovskite phases, and carrier transportation is limited by low-n-value 2D perovskite phases (n = 1 and n = 2). Systematic characterization shows that BA based 2D perovskites do not form low-n-value phases, while PEA and FPEA based 2D perovskites have strong n = 1, 2 signals when excited from the bottom of the perovskite films. To solve this problem, a lamellar nickel oxide substrate (lamellar-NiOx) fabricated by the hydrothermal method is employed as a hole transporting layer, forming a vertical charge transport pathway at the bottom of perovskite films, thus bypassing the charge trapping and recombination centers of the low-n-value regions of PEA and FPEA based 2D perovskites. As a result, both fill factor and open-circuit voltage are greatly enhanced for PEA and FPEA based 2D perovskite solar cells and a champion power conversion efficiency of 15.2% is achieved with a composition of FPEA2MA3Pb4I13. Furthermore, 2D perovskite films on lamellar-NiOx show enlarged grain size, improved out-of-plane orientation, and enhanced carrier transport efficiency between different n-value 2D perovskite phases. These findings suggest that lamellar-NiOx is an ideal substrate candidate to help overcome the carrier transport limitation of low-n-value 2D perovskite phases near the bottom of perovskite films.

Graphical abstract: Overcoming the carrier transport limitation in Ruddlesden–Popper perovskite films by using lamellar nickel oxide substrates

Supplementary files

Article information

Article type
Paper
Submitted
03 Feb 2021
Accepted
14 Apr 2021
First published
15 Apr 2021

J. Mater. Chem. A, 2021,9, 11741-11752

Overcoming the carrier transport limitation in Ruddlesden–Popper perovskite films by using lamellar nickel oxide substrates

J. Liang, Z. Zhang, Y. Zheng, X. Wu, J. Wang, Z. Zhou, Y. Yang, Y. Huang, Z. Chen and C. Chen, J. Mater. Chem. A, 2021, 9, 11741 DOI: 10.1039/D1TA01038G

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