| 1. |
- Ke, You, et al.
(författare)
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Defect Passivation for Red Perovskite Light-Emitting Diodes with Improved Brightness and Stability
- 2019
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Ingår i: The Journal of Physical Chemistry Letters. - : AMER CHEMICAL SOC. - 1948-7185. ; 10:3, s. 380-385
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Tidskriftsartikel (refereegranskat)abstract
- Efficient and stable red perovskite light-emitting diodes (PeLEDs) are important for realizing full-color display and lighting. Red PeLEDs can be achieved either by mixed-halide or low-dimensional perovskites. However, the device performance, especially the brightness, is still low owing to phase separation or poor charge transport issues. Here, we demonstrate red PeLEDs based on three-dimensional (3D) mixed-halide perovskites where the defects are passivated by using 5-aminovaleric acid. The red PeLEDs with an emission peak at 690 nm exhibit an external quantum efficiency of 8.7% and a luminance of 1408 cd m(-2). A maximum luminance of 8547 cd m(-2) can be further achieved as tuning the emission peak to 662 nm, representing the highest brightness of red PeLEDs. Moreover, those LEDs exhibit a half-life of up to 8 h under a high constant current density of 100 mA cm(-2), which is over 10 times improvement compared to literature results.
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| 2. |
- Miao, Yanfeng, et al.
(författare)
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Stable and bright formamidinium-based perovskite light-emitting diodes with high energy conversion efficiency
- 2019
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Ingår i: Nature Communications. - : NATURE PUBLISHING GROUP. - 2041-1723. ; 10
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Tidskriftsartikel (refereegranskat)abstract
- Solution-processable perovskites show highly emissive and good charge transport, making them attractive for low-cost light-emitting diodes (LEDs) with high energy conversion efficiencies. Despite recent advances in device efficiency, the stability of perovskite LEDs is still a major obstacle. Here, we demonstrate stable and bright perovskite LEDs with high energy conversion efficiencies by optimizing formamidinium lead iodide films. Our LEDs show an energy conversion efficiency of 10.7%, and an external quantum efficiency of 14.2% without outcoupling enhancement through controlling the concentration of the precursor solutions. The device shows low efficiency droop, i.e. 8.3% energy conversion efficiency and 14.0% external quantum efficiency at a current density of 300 mA cm(-2), making the device more efficient than state-of-the-art organic and quantum-dot LEDs at high current densities. Furthermore, the half-lifetime of device with benzylamine treatment is 23.7 hr under a current density of 100 mA cm(-2), comparable to the lifetime of near-infrared organic LEDs.
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| 3. |
- Wang, Yuming, et al.
(författare)
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High-Efficiency Flexible Solar Cells Based on Organometal Halide Perovskites
- 2016
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 28:22, s. 4532-4540
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Tidskriftsartikel (refereegranskat)abstract
- Flexible and light-weight solar cells are important because they not only supply power to wearable and portable devices, but also reduce the transportation and installation cost of solar panels. High-efficiency organometal halide perovskite solar cells can be fabricated by a low-temperature solution process, and hence are promising for flexible-solar-cell applications. Here, the development of perovskite solar cells is briefly discussed, followed by the merits of organometal halide perovskites as promising candidates as high-efficiency, flexible, and light-weight photovoltaic materials. Afterward, recent developments of flexible solar cells based on perovskites are reviewed.
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| 4. |
- Wang, Yuming, et al.
(författare)
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Light-induced degradation of fullerenes in organic solar cells : a case study on TQ1:PC71BM
- 2018
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Ingår i: Journal of Materials Chemistry A. - : Royal Society of Chemistry. - 2050-7488 .- 2050-7496. ; 6:25, s. 11884-11889
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Tidskriftsartikel (refereegranskat)abstract
- The stability of organic solar cells (OSCs) is critical for practical applications of this emerging technology. Unfortunately, in spite of intensive investigations, the degradation mechanisms in OSCs have not been clearly understood yet. In this report, we employ a range of spectroscopic and transport measurements, coupled with drift-diffusion modelling, to investigate the light-induced degradation mechanisms of fullerene-based OSCs. We find that trap states formed in the fullerene phase under illumination play a critical role in the degradation of the open-circuit voltage (V-OC) in OSCs. Our results indicate that the degradation is intrinsic to the fullerenes in OSCs and that alternative acceptor materials are desired for the development of stable OSCs.
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| 5. |
- Xu, Lei, et al.
(författare)
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The Role of Solution Aggregation Property toward High-Efficiency Non-Fullerene Organic Photovoltaic Cells
- 2024
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095.
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Tidskriftsartikel (refereegranskat)abstract
- In organic photovoltaic cells, the solution-aggregation effect (SAE) is long considered a critical factor in achieving high power-conversion efficiencies for polymer donor (PD)/non-fullerene acceptor (NFA) blend systems. However, the underlying mechanism has yet to be fully understood. Herein, based on an extensive study of blends consisting of the representative 2D-benzodithiophene-based PDs and acceptor-donor-acceptor-type NFAs, it is demonstrated that SAE shows a strong correlation with the aggregation kinetics during solidification, and the aggregation competition between PD and NFA determines the phase separation of blend film and thus the photovoltaic performance. PDs with strong SAEs enable earlier aggregation evolutions than NFAs, resulting in well-known polymer-templated fibrillar network structures and superior PCEs. With the weakening of PDs' aggregation effects, NFAs, showing stronger tendencies to aggregate, tend to form oversized domains, leading to significantly reduced external quantum efficiencies and fill factors. These trends reveal the importance of matching SAE between PD and NFA. The aggregation abilities of various materials are further evaluated and the aggregation ability/photovoltaic parameter diagrams of 64 PD/NFA combinations are provided. This work proposes a guiding criteria and facile approach to match efficient PD/NFA systems. A systematic study of the representative organic photovoltaic systems shows that the aggregation competition between polymer donor (PD) and non-fullerene acceptor (NFA) is a decisive factor in the phase separation of blend film and thus the photovoltaic performance. Based on 64 PD/NFA combinations, the aggregation ability/photovoltaic parameter heatmaps are plotted, providing a new matching rule for developing high-efficiency PD/NFA systems. image
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| 6. |
- Yang, Rong, et al.
(författare)
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Inhomogeneous degradation in metal halide perovskites
- 2017
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Ingår i: Applied Physics Letters. - : AMER INST PHYSICS. - 0003-6951 .- 1077-3118. ; 111:7
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Tidskriftsartikel (refereegranskat)abstract
- Although the rapid development of organic-inorganic metal halide perovskite solar cells has led to certified power conversion efficiencies of above 20%, their poor stability remains a major challenge, preventing their practical commercialization. In this paper, we investigate the intrinsic origin of the poor stability in perovskite solar cells by using a confocal fluorescence microscope. We find that the degradation of perovskite films starts from grain boundaries and gradually extend to the center of the grains. Firmly based on our findings, we further demonstrate that the device stability can be significantly enhanced by increasing the grain size of perovskite crystals. Our results have important implications to further enhance the stability of optoelectronic devices based on metal halide perovskites. Published by AIP Publishing.
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| 7. |
- Yang, Rong, et al.
(författare)
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Oriented Quasi-2D Perovskites for High Performance Optoelectronic Devices
- 2018
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Ingår i: Advanced Materials. - : WILEY-V C H VERLAG GMBH. - 0935-9648 .- 1521-4095. ; 30:51
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Tidskriftsartikel (refereegranskat)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 approximate to 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 approximate to 96 h at a high current density of 200 mA cm(-2) in air.
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| 8. |
- Bao, Chunxiong, et al.
(författare)
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A multifunctional display based on photo-responsive perovskite light-emitting diodes
- 2024
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Ingår i: NATURE ELECTRONICS. - : NATURE PORTFOLIO. - 2520-1131.
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Tidskriftsartikel (refereegranskat)abstract
- Current display screens are typically only used for information display, but can have a range of different sensors integrated into them for functions such as touch control, ambient light sensing and fingerprint sensing. Photo-responsive light-emitting diodes (LEDs), which can display information and respond to light excitation, could be used to develop future ultra-thin and large screen-to-body ratio screens. However, photo-response is difficult to achieve with conventional display technologies. Here, we report a multifunctional display that uses photo-responsive metal halide perovskite LEDs as pixels. The perovskite LED display can be simultaneously used as a touch screen, ambient light sensor and image sensor (including for fingerprint drawing) without integrating any additional sensors. The light-to-electricity conversion efficiency of the pixels also allow the display to act as a photovoltaic device that can charge the equipment. Photo-responsive metal halide perovskite light-emitting diodes can be used to create a multifunctional display that can function as a touch screen, ambient light sensor and image sensor.
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| 9. |
- Kuang, Chaoyang, et al.
(författare)
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Critical role of additive-induced molecular interaction on the operational stability of perovskite light-emitting diodes
- 2021
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Ingår i: Joule. - : Cell Press. - 2542-4351. ; 5:3, s. 618-630
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Tidskriftsartikel (refereegranskat)abstract
- Despite rapid improvements in efficiency and brightness of perovskite light-emitting diodes (PeLEDs), the poor operational stability remains a critical challenge hindering their practical applications. Here, we demonstrate greatly improved operational stability of high-efficiency PeLEDs, enabled by incorporating dicarboxylic acids into the precursor for perovskite depositions. We reveal that the dicarboxylic acids efficiently eliminate reactive organic ingredients in perovskite emissive layers through an in situ amidation process, which is catalyzed by the alkaline zinc oxide substrate. The formed stable amides prohibit detrimental reactions between the perovskites and the charge injection layer underneath, stabilizing the perovskites and the interfacial contacts and ensuring the excellent operational stability of the resulting PeLEDs. Through rationally optimizing the amidation reaction in the perovskite emissive layers, we achieve efficient PeLEDs with a peak external quantum efficiency of 18.6% and a long half-life time of 682 h at 20 mA cm(-2), presenting an important breakthrough in PeLEDs.
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| 10. |
- Wang, Kang, et al.
(författare)
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Luminescent metal-halide perovskites: fundamentals, synthesis, and light-emitting devices
- 2024
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Ingår i: Science in China Series B. - : SCIENCE PRESS. - 1674-7291 .- 1869-1870. ; 67:6, s. 1776-1838
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Forskningsöversikt (refereegranskat)abstract
- Metal-halide perovskites have garnered considerable research attention as highly efficient light emitters in recent years due to their outstanding optoelectronic properties with remarkable tunability and excellent solution processabilities. Substantial advancements have been achieved in the development of novel halide perovskites, and the exploitations of these materials in light-emitting devices. This review comprehensively outlines recent breakthroughs in metal-halide perovskites, encompassing the rational design of perovskite materials with tunable light emission properties, the controllable growth of single crystal for a deeper understanding of their structure-property relationships, as well as the fundamental insights into the photophysics and carrier dynamics in perovskite systems. Additionally, it provides an overview of recent applications of perovskite materials in high-performance light-emitting diodes (LEDs) and lasers.
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