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Park, Hyesung
Low-Dimensional Materials & Energy Conversion Lab
Research Interests
  • Nano materials, renewable energy, optoelectronic devices

Two-Step Sequential Blade-Coating Large-Area FA-Based Perovskite Thin Film via a Controlled PbI2 Microstructure

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dc.contributor.author Wen, Yongtao ko
dc.contributor.author Li, Jing ko
dc.contributor.author Gao, Xiaofeng ko
dc.contributor.author Tian, Congcong ko
dc.contributor.author Zhu, Hao ko
dc.contributor.author Yu, Guomu ko
dc.contributor.author Zhang, Xiaoli ko
dc.contributor.author Park, Hyesung ko
dc.contributor.author Huang, Fuzhi ko
dc.date.available 2023-01-06T02:22:11Z -
dc.date.created 2023-01-05 ko
dc.date.issued 2023-01 ko
dc.identifier.citation ACTA PHYSICO-CHIMICA SINICA, v.39, no.2, pp.2203048 ko
dc.identifier.issn 1000-6818 ko
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/60909 -
dc.description.abstract Solar cells, which are excellent alternatives to traditional fossil fuels, can efficiently convert sunlight into electricity. The intensive development of high-performance photovoltaic materials plays an important role in environmental protection and the utilization of renewable energy. Organic– inorganic hybrid perovskite materials, with a formula of ABX3 (A = methylammonium (MA) or formamidinium (FA); B = Pb or Sn; X = Cl, I, or Br), have exhibited remarkable commercial prospects in high-performance photovoltaic devices owing to their long carrier diffusion length, excellent light absorption properties, high charge carrier mobility, and weak exciton binding energy. Recently, perovskite solar cells, fabricated using halide perovskite materials as light-absorbing layers, have achieved remarkable results; their certified power conversion efficiency has continuously improved and reached 25.7%. However, high-performance devices are usually fabricated using spin-coating methods with active areas below 0.1 cm2. Hence, long-term research goals include achieving a large-scale uniform preparation of high-quality photoactive layers. The current one-step preparation of perovskite films involves the nucleation-crystalline growth process of perovskite. Auxiliary processes, such as using an anti-solvent, are often required to increase the nucleation rate and density of the film, which is not suitable for industrial large-area preparation. Additionally, the large-area preparation of perovskite films by spin-coating will result in different film thicknesses in the center and edge regions of the film due to an uneven centrifugal force. This will cause intense carrier recombination in the thicker area of the film and weak light absorption in the thinner area, which will reduce the performance of the device. To address these problems, the development of a large-area fabrication method for high-performance perovskite light-absorbing layers is essential. In this study, a two-step sequential blade-coating strategy was developed to prepare the FA-based perovskite layer. In general, PbI2 easily forms a dense film; therefore, formamidinium iodide (FAI) cannot deeply penetrate to completely react with PbI2. The PbI2 residue is therefore detrimental to charge transportation. To fabricate the desired porous PbI2 film, tetrahydrothiophene 1-oxide (THTO) was introduced into the PbI2 precursor solution. By forming PbI2·THTO complexes, PbI2 crystallization is controlled, resulting in the formation of vertically packed PbI2 flaky crystals. These crystals provide nanochannels for easy FAI penetration. The 5 cm × 5 cm modules fabricated through this strategy achieved a high efficiency of 18.65% with excellent stability. This indicates that the two-step sequential blade-coating strategy has considerable potential for scaling up the production of perovskite solar cells. ko
dc.language 영어 ko
dc.publisher Beijing University Press ko
dc.title Two-Step Sequential Blade-Coating Large-Area FA-Based Perovskite Thin Film via a Controlled PbI2 Microstructure ko
dc.type ARTICLE ko
dc.identifier.scopusid 2-s2.0-85140831450 ko
dc.identifier.wosid 000923293100004 ko
dc.type.rims ART ko
dc.identifier.doi 10.3866/PKU.WHXB202203048 ko
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