| Literature DB >> 35648576 |
Yuhang Che1, Zhike Liu1, Yuwei Duan1, Jungang Wang1, Shaomin Yang1, Dongfang Xu1, Wanchun Xiang1, Tao Wang1, Ningyi Yuan2, Jianning Ding2, Shengzhong Frank Liu1,3.
Abstract
All-inorganic CsPbI3 perovskite presents preeminent chemical stability and a desirable band gap as the front absorber for perovskite/silicon tandem solar cells. Unfortunately, CsPbI3 perovskite solar cells (PSCs) still show low efficiency due to high density of defects in solution-prepared CsPbI3 films. Herein, three kinds of hydrazide derivatives (benzoyl hydrazine (BH), formohydrazide (FH) and benzamide (BA)) are designed to reduce the defect density and stabilize the phase of CsPbI3 . Calculation and characterization results corroborate that the carboxyl and hydrazine groups in BH form strong chemical bonds with Pb2+ ions, resulting in synergetic double coordination. In addition, the hydrazine group in the BH also forms a hydrogen bond with iodine to assist the coordination. Consequently, a high efficiency of 20.47 % is achieved, which is the highest PCE among all pure CsPbI3 -based PSCs reported to date. In addition, an unencapsulated device showed excellent stability in ambient air.Entities:
Keywords: CsPbI3; Defect Passivation; Hydrazide; Perovskite; Solar Cells
Year: 2022 PMID: 35648576 DOI: 10.1002/anie.202205012
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 16.823