Nucleation‐Layer Assisted Quasi‐2D Ruddlesden‐Popper Tin Perovskite Solar Cells with High Oxygen Stability
Authors:
- 8 May 2025
- journal article
- Published by Wiley in Advanced Materials
- Vol. 37 (30) , e2501156
Abstract
Tin (Sn)‐based perovskite solar cells (PSCs) are extremely vulnerable to oxygen. Nevertheless, mechanism understanding and fundamental strategies to achieve oxygen‐stable Sn‐based PSCs are lacking. Here a nucleation‐layer assisted (NLA) strategy by forming nucleation layer at the interface of hole transport layer and perovskite to attain highly oxygen‐stable quasi‐2D Ruddlesden‐Popper (RP) Sn‐based PSCs is reported. The formation process of nucleation layer consists of washing off the prepared perovskite film and annealing the residue on the substrate, which produces a new substrate for perovskite film fabrication. Such nucleation layer can transform the subsequently deposited perovskite film from a small‐n‐value dominated wide phase distribution with random crystal orientation into an intermediate‐n‐value dominated narrow phase distribution with vertical crystal orientation. This nucleation layer also improves the perovskite film morphology with highly coadjacent flake‐like grains, leading to reduced grain boundaries and pinholes. The resultant NLA perovskite film shows more efficient carrier transport capability, lower exciton‐binding energy, weakened electron‐phonon coupling, and significantly decreased oxygen diffusion rate upon oxygen exposure. Consequently, a quasi‐2D RP Sn‐based PSC with a champion efficiency of 11.18% is obtained. The unencapsulated device preserves 95% of its initial efficiency after a 2700‐h oxygen aging test, creating a record oxygen stability for Sn‐based PSCs.Keywords
Funding Information
- Fundamental Research Funds for Central Universities of the Central South University (YJ2021157)
- Natural Science Foundation of Sichuan Province (2022NSFSC1183)
- National Natural Science Foundation of China (62174112, 62104163)
This publication has 71 references indexed in Scilit:
- Crystallization Kinetics Regulation for Strain and Morphology Management Enables Efficient Tin Perovskite Solar CellsAdvanced Functional Materials, 2025
- Host‐Guest Complexation Strategy for Passivating Pb‐Dimer Related Defects in Perovskite PhotovoltaicsAdvanced Functional Materials, 2023
- Dopant‐Free Pyrrolopyrrole‐Based (PPr) Polymeric Hole‐Transporting Materials for Efficient Tin‐Based Perovskite Solar Cells with Stability Over 6000 hAdvanced Materials, 2023
- Highly Efficient and Stable FA‐Based Quasi‐2D Ruddlesden–Popper Perovskite Solar Cells by the Incorporation of β‐Fluorophenylethanamine CationsAdvanced Materials, 2023
- Highly Efficient and Stable Dion−Jacobson Perovskite Solar Cells Enabled by Extended π‐Conjugation of Organic SpacerAdvanced Materials, 2021
- Heterogeneous 2D/3D Tin‐Halides Perovskite Solar Cells with Certified Conversion Efficiency Breaking 14%Advanced Materials, 2021
- Marked Passivation Effect of Naphthalene‐1,8‐Dicarboximides in High‐Performance Perovskite Solar CellsAdvanced Materials, 2021
- Organic‐Salt‐Assisted Crystal Growth and Orientation of Quasi‐2D Ruddlesden–Popper Perovskites for Solar Cells with Efficiency over 19%Advanced Materials, 2020
- Intermolecular π–π Conjugation Self‐Assembly to Stabilize Surface Passivation of Highly Efficient Perovskite Solar CellsAdvanced Materials, 2020
- Oriented Quasi‐2D Perovskites for High Performance Optoelectronic DevicesAdvanced Materials, 2018