Publications by authors named "Maotao Yu"

Perovskite light-emitting diodes (PeLEDs) are the next promising display technologies because of their high color purity and wide color gamut, while two classical emitter forms, i.e., polycrystalline domains and quantum dots, are encountering bottlenecks.

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Perovskite solar cells (PSCs) comprise a solid perovskite absorber sandwiched between several layers of different charge-selective materials, ensuring unidirectional current flow and high voltage output of the devices. A 'buffer material' between the electron-selective layer and the metal electrode in p-type/intrinsic/n-type (p-i-n) PSCs (also known as inverted PSCs) enables electrons to flow from the electron-selective layer to the electrode. Furthermore, it acts as a barrier inhibiting the inter-diffusion of harmful species into or degradation products out of the perovskite absorber.

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Blue perovskite light-emitting diodes (PeLEDs) are essential in pixels of perovskite displays, while their progress lags far behind their red and green counterparts. Here, we focus on recent advances of blue PeLEDs and systematically review the noteworthy strategies, which are categorized into compositional engineering, dimensional control, and size confinement, on optimizing microstructures, energy landscapes, and charge behaviors of wide-bandgap perovskite emitters (bandgap >2.5 eV).

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Inverted-structure metal halide perovskite solar cells (PSCs) have attractive advantages like low-temperature processability and outstanding device stability. The two-step sequential deposition method shows the benefits of easy fabrication and decent performance repeatability. Nevertheless, it is still challenging to achieve high-performance inverted PSCs with similar or equal power conversion efficiencies (PCEs) compared to the regular-structure counterparts via this deposition method.

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Article Synopsis
  • Multifunctional solar cells have been developed that can harvest light during the day and emit light at night, showcasing versatile applications.
  • Researchers improved the performance of halide perovskite solar cells by refining the heterojunction interfaces, achieving stable and efficient operation.
  • The enhanced design allows these devices to function effectively as both solar cells and ultra-low-voltage LEDs, potentially benefiting multifunctional harvesting-storage-utilization systems.
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A prerequisite for commercializing perovskite photovoltaics is to develop a swift and eco-friendly synthesis route, which guarantees the mass production of halide perovskites in the industry. Herein, a green-solvent-assisted mechanochemical strategy is developed for fast synthesizing a stoichiometric δ-phase formamidinium lead iodide (δ-FAPbI ) powder, which serves as a high-purity precursor for perovskite film deposition with low defects. The presynthesized δ-FAPbI precursor possesses high concentration of micrometer-sized colloids, which are in favor of preferable crystallization by spontaneous nucleation.

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Lead halide perovskite films have witnessed rapid progress in optoelectronic devices, whereas polycrystalline heterogeneities and serious native defects in films are still responsible for undesired recombination pathways, causing insufficient utilization of photon-generated charge carriers. Here, radiation-enhanced polycrystalline perovskite films with ultralong carrier lifetimes exceeding 6 μs and single-crystal-like electron-hole diffusion lengths of more than 5 μm are achieved. Prolongation of charge-carrier activities is attributed to the electronic structure regulation and the defect elimination at crystal boundaries in the perovskite with the introduction of phenylmethylammonium iodide.

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Perovskite solar cells (PSCs) toward practical application relies on high efficiency, long lifetime, low toxicity, and device up-scaling. To realize large-area PSCs, a green solution-bathing strategy is delivered to prepare high-performance PSCs. By utilizing 2-pentanol as a green solvent and formamidinium chloride (FACl) as a solute in the green solution-bathing process, perovskite films with enlarged grain sizes, improved crystallinity, and alleviated defect state density were obtained, resulting in the enhancement in the power conversion efficiency of PSCs.

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To explore new constituents in two-dimensional (2D) materials and to combine their best in van der Waals heterostructures is in great demand as being a unique platform to discover new physical phenomena and to design novel functionalities in interface-based devices. Herein, PbI crystals as thin as a few layers are synthesized, particularly through a facile low-temperature solution approach with crystals of large size, regular shape, different thicknesses, and high yields. As a prototypical demonstration of band engineering of PbI -based interfacial semiconductors, PbI crystals are assembled with several transition metal dichalcogenide monolayers.

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