Affiliation:
1. Frontiers Science Center for Flexible Electronics (FSCFE) Institute of Flexible Electronics (IFE) Ningbo Institute of Northwestern Polytechnical University Northwestern Polytechnical University 127 West Youyi Road Xi'an 710072 P. R. China
2. Qingdao Institute of Bioenergy and Bioprocess Technology Chinese Academy of Sciences Qingdao 266101 P. R. China
3. Shanghai Synchrotron Radiation Facility (SSRF) Zhangjiang Laboratory Shanghai Advanced Research Institute Chinese Academy of Sciences 239 Zhangheng Road Shanghai 201204 P. R. China
Abstract
AbstractOrganometal halide perovskite solar cells (PSCs) have received great attention owing to a rapid increase in power conversion efficiency (PCE) over the last decade. However, the deficit of long‐term stability is a major obstacle to the implementation of PSCs in commercialization. The defects in perovskite films are considered as one of the primary causes. To address this issue, isocyanic acid (HNCO) is introduced as an additive into the perovskite film, in which the added molecules form covalent bonds with FA cations via a chemical reaction. This chemical reaction gives rise to an efficient passivation on the perovskite film, resulting in an improved film quality, a suppressed non‐radiation recombination, a facilitated carrier transport, and optimization of energy band levels. As a result, the HNCO‐based PSCs achieve a high PCE of 24.41% with excellent storage stability both in an inert atmosphere and in air. Different from conventional passivation methods based on coordination effects, this work presents an alternative chemical reaction for defect passivation, which opens an avenue toward defect‐mitigated PSCs showing enhanced performance and stability.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Ningbo Municipality
Fundamental Research Funds for the Central Universities