| Literature DB >> 30345566 |
Rong Yang1, Renzhi Li1, Yu Cao1, Yingqiang Wei1, Yanfeng Miao1, Wen Liang Tan2, Xuechen Jiao2,3, Hong Chen1, Liangdong Zhang1, Qing Chen1, Huotian Zhang4, Wei Zou1, Yuming Wang4, Ming Yang1, Chang Yi1, Nana Wang1, Feng Gao4, Christopher R McNeill2, Tianshi Qin1, Jianpu Wang1, Wei Huang1,5.
Abstract
Quasi-2D layered organometal halide perovskites have recently emerged as promising candidates for solar cells, because of their intrinsic stability compared to 3D analogs. However, relatively low power conversion efficiency (PCE) limits the application of 2D layered perovskites in photovoltaics, due to large energy band gap, high exciton binding energy, and poor interlayer charge transport. Here, efficient and water-stable quasi-2D perovskite solar cells with a peak PCE of 18.20% by using 3-bromobenzylammonium iodide are demonstrated. The unencapsulated devices sustain over 82% of their initial efficiency after 2400 h under relative humidity of ≈40%, and show almost unchanged photovoltaic parameters after immersion into water for 60 s. The robust performance of perovskite solar cells results from the quasi-2D perovskite films with hydrophobic nature and a high degree of electronic order and high crystallinity, which consists of both ordered large-bandgap perovskites with the vertical growth in the bottom region and oriented small-bandgap components in the top region. Moreover, due to the suppressed nonradiative recombination, the unencapsulated photovoltaic devices can work well as light-emitting diodes (LEDs), exhibiting an external quantum efficiency of 3.85% and a long operational lifetime of ≈96 h at a high current density of 200 mA cm-2 in air.Entities:
Keywords: multiple quantum wells; perovskites; solar cells; stability; two dimension
Year: 2018 PMID: 30345566 DOI: 10.1002/adma.201804771
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849