| Literature DB >> 29271198 |
Weiran Zhou1, Pengcheng Zhou1, Xunyong Lei2, Zhimin Fang1, Mengmeng Zhang1, Qing Liu1, Tao Chen1, Hualing Zeng2, Liming Ding3, Jun Zhu4, Songyuan Dai5, Shangfeng Yang1.
Abstract
Organometal halide CH3NH3PbI3 (MAPbI3) has been commonly used as the light absorber layer of perovskite solar cells (PSCs), and, especially, another halide element chlorine (Cl) has been often incorporated to assist the crystallization of perovskite film. However, in most cases, a predominant MAPbI3 phase with trace of Cl- is obtained ultimately and the role of Cl involvement remains unclear. Herein, we develop a low-cost and facile method, named hydrochloric acid vapor annealing (HAVA) post-treatment, and realize a rapid conversion of MAPbI3 to phase-pure MAPbCl3, demonstrating a new concept of phase engineering of perovskite materials toward efficiency enhancement of PSCs for the first time. The average grain size of perovskite film after HAVA post-treatment increases remarkably through an Ostwald ripening process, leading to a denser and smoother perovskite film with reduced trap states and enhanced crystallinity. More importantly, the generation of MAPbCl3 secondary phase via phase engineering is beneficial for improving the carrier mobility with a more balanced carrier transport rate and enlarging the band gap of perovskite film along with optimized energy level alignment. As a result, under the optimized HAVA post-treatment time (2 min), we achieved a significant enhancement of the power conversion efficiency (PCE) of the MAPbI3-based planar heterojunction-PSC device from 14.02 to 17.40% (the highest PCE reaches 18.45%) with greatly suppressed hysteresis of the current-voltage response.Entities:
Keywords: gas−solid reaction; organometal halide; perovskite solar cells; phase engineering; vapor annealing
Year: 2018 PMID: 29271198 DOI: 10.1021/acsami.7b15008
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229