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Perovskite (structure)

About: Perovskite (structure) is a research topic. Over the lifetime, 51482 publications have been published within this topic receiving 1541750 citations.


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Journal ArticleDOI
TL;DR: In this paper, a two-step technique for preparing thin films of the organic−inorganic perovskites (RNH3)2(CH3NH3n-1MnI3n+1 (R = butyl, phenethyl; M = Pb, Sn; n = 1, 2, ∞) has been achieved.
Abstract: A convenient two-step technique for preparing thin films of the organic−inorganic perovskites (RNH3)2(CH3NH3)n-1MnI3n+1 (R = butyl, phenethyl; M = Pb, Sn; n = 1, 2, ∞) has been achieved. Films of the metal halide, MI2, were first deposited onto ash glass or quartz disks using vacuum evaporation or spin-coating. By dipping these inorganic films, at room temperature, into an organic ammonium iodide solution for a short period of time (1−5 min for the layered perovskites), single-phase samples of the corresponding organic−inorganic perovskite thin films were formed. While a variety of solvents can be used for the dipping process, toluene/2-propanol mixtures have been shown to work well for many of the present compounds. The layered organic−inorganic perovskite films exhibited uniform surfaces and strong photoluminescence at wavelengths that were consistent with the corresponding materials made by single-crystal growth from solution. However, dipped organic−inorganic films made from evaporated PbI2 exhibited ...

563 citations

Journal ArticleDOI
Lijian Zuo1, Zhuowei Gu1, Tao Ye1, Weifei Fu1, Gang Wu1, Hanying Li1, Hongzheng Chen1 
TL;DR: A facile but efficient method of modifying the ZnO-coated substrates with 3-aminopropanioc acid (C3-SAM) to direct the crystalline evolution and achieve the optimal morphology of CH3NH3PbI3 perovskite film is developed.
Abstract: Morphology control is critical to achieve high efficiency CH3NH3PbI3 perovskite solar cells (PSC). The surface properties of the substrates on which crystalline perovskite thin films form are expected to affect greatly the crystallization and, thus, the resulting morphology. However, this topic is seldom examined in PSC. Here we developed a facile but efficient method of modifying the ZnO-coated substrates with 3-aminopropanioc acid (C3-SAM) to direct the crystalline evolution and achieve the optimal morphology of CH3NH3PbI3 perovskite film. With incorporation of the C3-SAM, highly crystalline CH3NH3PbI3 films were formed with reduced pin-holes and trap states density. In addition, the work function of the cathode was better aligned with the conduction band minimum of perovskite for efficient charge extraction and electronic coupling. As a result, the PSC performance remarkably increased from 9.81(±0.99)% (best 11.96%) to 14.25(±0.61)% (best 15.67%). We stress the importance of morphology control through ...

562 citations

Journal ArticleDOI
TL;DR: In this article, a low temperature route for compact TiO2, tailored for perovskite MSSC operation, was realized, and the optimized formulation was shown to achieve full sun solar power conversion efficiencies of up to 15.9% in an all low temperature processed solar cell.
Abstract: The ability to process amorphous or polycrystalline solar cells at low temperature (<150 °C) opens many possibilities for substrate choice and monolithic multijunction solar cell fabrication. Organometal trihalide perovskite solar cells have evolved rapidly over the last two years, and the CH3NH3PbX3 (X = Cl, I or Br) material is processed at low temperature. However the first embodiments of the solar cell were composed of high temperature processed (500 °C) compact and mesoporous layers of TiO2. The sintering of the mesoporous TiO2 has been negated by replacing this with a mesoporous insulating scaffold in the meso-superstructured solar cell (MSSC), yet the high temperature processed compact TiO2 layer still persists in the most efficient devices. Here we have realised a low temperature route for compact TiO2, tailored for perovskite MSSC operation. With our optimized formulation we demonstrate full sun solar power conversion efficiencies of up to 15.9% in an all low temperature processed solar cell.

559 citations

Journal ArticleDOI
TL;DR: The p-i-n structure of perovskite solar cells has shown efficiencies as high as 18%, lower temperature processing, flexibility, and, furthermore, negligible J-V hysteresis effects.
Abstract: ConspectusInorganic–organic hybrid perovskite solar cells research could be traced back to 2009, and initially showed 3.8% efficiency. After 6 years of efforts, the efficiency has been pushed to 20.1%. The pace of development was much faster than that of any type of solar cell technology. In addition to high efficiency, the device fabrication is a low-cost solution process. Due to these advantages, a large number of scientists have been immersed into this promising area. In the past 6 years, much of the research on perovskite solar cells has been focused on planar and mesoporous device structures employing an n-type TiO2 layer as the bottom electron transport layer. These architectures have achieved champion device efficiencies. However, they still possess unwanted features. Mesoporous structures require a high temperature (>450 °C) sintering process for the TiO2 scaffold, which will increase the cost and also not be compatible with flexible substrates. While the planar structures based on TiO2 (regular s...

558 citations

Journal ArticleDOI
TL;DR: In this paper, the combination of a layered perovskite compound (C6H5C2H4NH3)2PbI4 (PAPI), which forms a stable exciton with a large binding energy owing to its low-dimensional semiconductor nature and exhibits sharp and strong photoluminescence from the exciton band, and an electron-transporting oxadiazole derivative, was used to construct an organic-inorganic heterostructure electroluminescent (EL) device.
Abstract: Using the combination of a layered perovskite compound (C6H5C2H4NH3)2PbI4 (PAPI), which forms a stable exciton with a large binding energy owing to its low‐dimensional semiconductor nature and exhibits sharp and strong photoluminescence from the exciton band, and an electron‐transporting oxadiazole derivative, we fabricated an organic–inorganic heterostructure electroluminescent (EL) device. The EL spectrum of the device corresponded well to the photoluminescence spectrum of the PAPI film; the emission was peaking at 520 nm and half‐width of the emission was about 10 nm at liquid‐nitrogen temperature. Further, highly intense EL of more than 10 000 cd m−2 was performed at 2 A cm−2 at liquid‐nitrogen temperature in the device.

557 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20235,193
20229,857
20216,144
20205,859
20195,498
20184,741