Publications by authors named "Deying Luo"

Tin halide perovskite (THP) has emerged as a promising lead-free material for high-performance solar cells, attracting significant attention for their potential use for energy conversion. However, the rapid crystallization of THP due to its high Lewis acidity and easy oxidation of Sn leads to poor morphology and rampant defects in the resulting perovskite films. These strongly hamper the advances in efficiency and stability in THP solar cells.

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Continuous breakthroughs have been achieved in the photoelectric conversion efficiency (PCE) of tin-based perovskite solar cells (TPSCs) in recent years. Inspired by performance improvements observed during device storage, we identified beneficial light-induced interface doping (LIID) in the TPSCs. In situ analyses using X-ray photoelectron spectroscopy and ultraviolet photoelectron spectroscopy reveal that ion migration and oxidation at the interface induce beneficial doping effects, enhancing carrier transport and significantly boosting device performance.

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Obtaining micron-thick perovskite films of high quality is key to realizing efficient and stable positive (p)-intrinsic (i)-negative (n) perovskite solar cells, but it remains a challenge. Here we report an effective method for producing high-quality, micron-thick formamidinium-based perovskite films by forming coherent grain boundaries, in which high-Miller-index-oriented grains grow on the low-Miller-index-oriented grains in a stabilized atmosphere. The resulting micron-thick perovskite films, with enhanced grain boundaries and grains, showed stable material properties and outstanding optoelectronic performances.

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Article Synopsis
  • Inverted perovskite solar cells (PSCs) are being studied a lot because they are really stable, efficient, cheap, and can be made at low temperatures, which helps them work well in future solar tech.
  • The best single-junction PSCs have reached over 26% efficiency, while a combination of PSCs and silicon can reach nearly 34%, making them great for real-world use.
  • To make these solar cells even better, scientists are looking into different methods of improving their design and figuring out how to make them more environmentally friendly and cost-effective.
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  • Pb-Sn solar cells use a special layer called PEDOT:PSS to help move electricity, but it has some problems that make it less efficient.
  • A new molecule called 2-fluoro benzylammonium iodide (FBI) helps fix these problems and makes the solar cells work better.
  • With this new molecule, scientists were able to create solar cells that have a higher efficiency of 20.5% and can produce more energy.
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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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Article Synopsis
  • Interest in halide perovskites for photovoltaics (PVs) has surged due to their excellent properties and potential for efficient production.
  • Formamidinium lead triiodide (FAPbI) is leading in commercialization efforts, but its stability issues hinder long-term use, especially under operational conditions.
  • The text reviews current understanding of these instabilities, discusses strategies for enhancement, and suggests future pathways for improving perovskite PV technology and exploring new applications.
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The tunable bandgaps and facile fabrication of perovskites make them attractive for multi-junction photovoltaics. However, light-induced phase segregation limits their efficiency and stability: this occurs in wide-bandgap (>1.65 electron volts) iodide/bromide mixed perovskite absorbers, and becomes even more acute in the top cells of triple-junction solar photovoltaics that require a fully 2.

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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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There exists a considerable density of interaggregate grain boundaries (GBs) and intra-aggregate GBs in polycrystalline perovskites. Mitigation of intra-aggregate GBs is equally notable to that of interaggregate GBs as intra-aggregate GBs can also cause detrimental effects on the photovoltaic performances of perovskite solar cells (PSCs). Here, we demonstrate full-scale GB mitigation ranging from nanoscale intra-aggregate to submicron-scale interaggregate GBs, by modulating the crystallization kinetics using a judiciously designed brominated arylamine trimer.

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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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Halide perovskites are a compelling candidate for the next generation of clean-energy-harvesting technologies owing to their low cost, facile fabrication and outstanding semiconductor properties. However, photovoltaic device efficiencies are still below practical limits and long-term stability challenges hinder their practical application. Current evidence suggests that strain in halide perovskites is a key factor in dictating device efficiency and stability.

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Objective: To investigate the effects of epidural labor analgesia and natural delivery without analgesia on labor duration, pain, uterine continuous contraction time, abnormal labor process and complications.

Methods: A total of 220 primiparas in our hospital were selected and divided into two groups according to whether they accepted epidural labor analgesia, including 146 cases in the study group and 74 cases in the blank group. Primiparas in the study group received epidural block analgesia, and those in the blank group received routine labor without analgesia.

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  • Surfaces and interfaces in perovskite semiconductors significantly influence charge-carrier dynamics, which are essential for improving optoelectronic devices like solar cells and LEDs.
  • The report highlights various defects on common perovskite surfaces that create deep-level charge-carrier traps, negatively impacting device performance by disrupting band alignment.
  • Strategies to enhance surface and interface quality include using specific buffer layers, surface passivation, catalysts for microstructure improvements, and optimal heterojunction designs to reduce defects and optimize device efficiency.
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  • Perovskite solar cells can lose their power over time because of problems like ion movement and metal corrosion.
  • Scientists created a new layer using boron chloride subphthalocyanine and fullerene to help fix these issues and improve the solar cells' performance.
  • With this new approach, the solar cells reached an efficiency level of 22%, lasted much longer than before, and showed great results under different testing conditions, which could help them become commercially available.
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The performance of perovskite photovoltaics is fundamentally impeded by the presence of undesirable defects that contribute to non-radiative losses within the devices. Although mitigating these losses has been extensively reported by numerous passivation strategies, a detailed understanding of loss origins within the devices remains elusive. Here, we demonstrate that the defect capturing probability estimated by the capture cross-section is decreased by varying the dielectric response, producing the dielectric screening effect in the perovskite.

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Understanding the fundamental properties of buried interfaces in perovskite photovoltaics is of paramount importance to the enhancement of device efficiency and stability. Nevertheless, accessing buried interfaces poses a sizeable challenge because of their non-exposed feature. Herein, the mystery of the buried interface in full device stacks is deciphered by combining advanced in situ spectroscopy techniques with a facile lift-off strategy.

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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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Article Synopsis
  • Organometal halide perovskite solar cells (OHPSCs) have significantly improved in efficiency over the past decade but face sustainability issues due to the use of toxic lead components.
  • Many teams have explored chemical methods to reduce lead usage, but low-lead alternatives haven't matched the performance of traditional lead-based solar cells.
  • The proposed physical lead reduction (PLR) concept suggests reducing the perovskite film thickness, achieving a 70% reduction in lead while maintaining 96% of the solar cell's original performance through strategic design adjustments.
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Metal halide perovskite films are endowed with the nature of ions and polycrystallinity. Formamidinium iodide (FAI)-based perovskite films, which include large cations (FA) incorporated into the crystal lattice, are most likely to induce local defects due to the presence of the unreacted FAI species. Here, a diboron-assisted strategy is demonstrated to control the defects induced by the unreacted FAI both inside the grain boundaries and at the surface regions.

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The highest power conversion efficiencies (PCEs) reported for perovskite solar cells (PSCs) with inverted planar structures are still inferior to those of PSCs with regular structures, mainly because of lower open-circuit voltages (). Here we report a strategy to reduce nonradiative recombination for the inverted devices, based on a simple solution-processed secondary growth technique. This approach produces a wider bandgap top layer and a more n-type perovskite film, which mitigates nonradiative recombination, leading to an increase in by up to 100 millivolts.

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Hybrid lead halide perovskites have emerged as high-performance photovoltaic materials with their extraordinary optoelectronic properties. In particular, the remarkable device efficiency is strongly influenced by the perovskite crystallinity and the film morphology. Here, we investigate the perovskites crystallisation kinetics and growth mechanism in real time from liquid precursor continually to the final uniform film.

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In many optoelectronic applications, patterning is required for functional and/or aesthetic purposes. However, established photolithographic technique cannot be applied directly to the hybrid perovskites, which are considered as promising candidates for optoelectronic applications. In this work, a wettability-assisted photolithography (WAP) process, which employs photolithography and one-step solution process to deposit hybrid perovskite, was developed for fabricating patterned hybrid perovskite films.

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