| Literature DB >> 34369106 |
Qingwei Zhou1, Jialong Duan1, Jian Du1, Qiyao Guo1, Qiaoyu Zhang1, Xiya Yang1, Yanyan Duan2, Qunwei Tang1.
Abstract
The crystal distortion such as lattice strain and defect located at the surfaces and grain boundaries induced by soft perovskite lattice highly determines the charge extraction-transfer dynamics and recombination to cause an inferior efficiency of perovskite solar cells (PSCs). Herein, the authors propose a strategy to significantly reduce the superficial lattice tensile strain by means of incorporating an inorganic 2D Cl-terminated Ti3 C2 (Ti3 C2 Clx ) MXene into the bulk and surface of CsPbBr3 film. Arising from the strong interaction between Cl atoms in Ti3 C2 Clx and the under-coordinated Pb2+ in CsPbBr3 lattice, the expanded perovskite lattice is compressed and confined to act as a lattice "tape", in which the PbCl bond plays a role of "glue" and the 2D Ti3 C2 immobilizes the lattice. Finally, the defective surface is healed and a champion efficiency as high as 11.08% with an ultrahigh open-circuit voltage up to 1.702 V is achieved on the best all-inorganic CsPbBr3 PSC, which is so far the highest efficiency record for this kind of PSCs. Furthermore, the unencapsulated device demonstrates nearly unchanged performance under 80% relative humidity over 100 days and 85 °C over 30 days.Entities:
Keywords: Ti3C2 MXene; all-inorganic CsPbBr3 perovskite solar cells; interface solidification; long-term stability; strain release
Year: 2021 PMID: 34369106 DOI: 10.1002/advs.202101418
Source DB: PubMed Journal: Adv Sci (Weinh) ISSN: 2198-3844 Impact factor: 16.806