Publications by authors named "Yuanzhi Jiang"

Pure-halide reduced-dimensional perovskites, featuring large exciton binding energy and tunable bandgap, show great potential for high-efficiency deep-blue perovskite light-emitting diodes (PeLEDs). However, their efficiency, particularly in the low n-value phase domain ("n" represents the number of octahedral sheets), lags behind analogous perovskite emitters. Herein, it is demonstrated that the vibration of edge-dangling octahedra in the low n-value phase activates notorious exciton-phonon (EP) coupling, thereby deteriorating efficiency.

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α-FACsPbI is a promising absorbent material for efficient and stable perovskite solar cells (PSCs). However, the most efficient α-FACsPbI PSCs require the inclusion of the additive methylammonium chloride, which generates volatile organic residues (methylammonium) that limit device stability at elevated temperatures. Previously, the highest certified power-conversion efficiency of α-FACsPbI PSCs without methylammonium chloride was only approximately 24% (refs.

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Metal halide perovskites are promising candidates for gamma-ray (γ-ray) spectrum detectors. However, achieving high-resolution energy spectra in single-photon pulse-height analysis mode remains challenging, due to the inevitable leakage currents degrade the recognizable fingerprint energies which is critical for resolving γ-ray spectroscopy. We demonstrate under high bias voltage, a deficient contact barrier can lead to excessive surface charge injection, thereby increasing leakage current from electrodes to perovskites.

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Full-Stokes polarization detection, with high integration and portability, offers an efficient path toward next-gen multi-information optoelectronic systems. Nevertheless, current techniques relying on optical filters create rigid and bulky configurations, limiting practicality. Here, a flexible, filter-less full-Stokes polarimeter featuring a uniaxial-oriented chiral perovskite film is first reported.

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Hybrid organic-inorganic perovskites with diverse lattice structures and chemical composition provide an ideal material platform for novel functionalization, including chirality transfer. Chiral perovskites combine organic and inorganic sublattices, therefore encoding the structural asymmetry into the electronic structures and giving rise to the spin-splitting effect. From a structural chemistry perspective, the magnitude of the spin-splitting effect crucially depends on the noncovalent and electrostatic interaction within the chiral perovskite, which induces the local site and long-range bulk inversion symmetry breaking.

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Tailoring bandgap by mixed-halide strategy in perovskites has attracted extraordinary attention due to the flexibility of halide ion combinations and has emerged as the most direct and effective approach to precisely tune the emission wavelength throughout the entire visible light spectrum. Mixed-halide perovskites, yet, still suffered from several problems, particularly phase segregation under external stimuli because of ions migration. Understanding the essential cause and finding sound strategies, thus, remains a challenge for stable and efficient mixed-halide perovskite light-emitting diodes (PeLEDs).

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Lead halide perovskite nanocrystals (LHP NCs) have rapidly emerged as one of the most promising materials for optical sources, photovoltaics, and sensor fields. The controlled synthesis of LHP NCs with high monodispersity and precise size tunability has been a subject of intensive research in recent years. However, due to their ionic nature, LHP NCs are usually formed instantaneously, and the corresponding nucleation and growth are difficult to monitor and regulated.

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Mixed-halide perovskites enable precise spectral tuning across the entire spectral range through composition engineering. However, mixed halide perovskites are susceptible to ion migration under continuous illumination or electric field, which significantly impedes the actual application of perovskite light-emitting diodes (PeLEDs). Here, we demonstrate a novel approach to introduce strong and homogeneous halogen bonds within the quasi-two-dimensional perovskite lattices by means of an interlayer locking structure, which effectively suppresses ion migration by increasing the corresponding activation energy.

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Mixed-halide perovskites show tunable emission wavelength across the visible-light range, with optimum control of the light color. However, color stability remains limited due to the notorious halide segregation under illumination or an electric field. Here, a versatile path toward high-quality mixed-halide perovskites with high emission properties and resistance to halide segregation is presented.

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Article Synopsis
  • Mixed-halide perovskites are promising candidates for blue light-emitting diodes (PeLEDs), but they face issues with halide migration, especially in those with high chloride content.
  • Researchers found that by adjusting the degree of local lattice distortion (LLD), they could increase the energy barrier for halide migration, improving stability.
  • Using "A-site" cation engineering, they optimized LLD, leading to blue PeLEDs with a maximum external quantum efficiency (EQE) of 14.2% and impressive spectral stability during operation.
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Perovskite quantum dots are a competitive candidate for next-generation solar cells owing to their superior phase stability and multiple exciton generation effects. However, given the voltage loss in perovskite quantum dot solar cells (PQDSCs) is mainly caused by various surface and interfacial defects and the energy band mismatch in the devices, tremendous achievements have been made to mitigate the loss of PQDSCs. Herein, we elucidate the potential threats that hinder the high of PQDSCs.

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Despite the rapid progress in perovskite light-emitting diodes (PeLEDs), the electroluminescence performance of large-area perovskite devices lags far behind that of laboratory-size ones. Here, we report a 3.5 cm × 3.

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Perovskite light-emitting diodes (PeLEDs) with an external quantum efficiency exceeding 20% have been achieved in both green and red wavelengths; however, the performance of blue-emitting PeLEDs lags behind. Ultrasmall CsPbBr quantum dots are promising candidates with which to realize efficient and stable blue PeLEDs, although it has proven challenging to synthesize a monodispersed population of ultrasmall CsPbBr quantum dots, and difficult to retain their solution-phase properties when casting into solid films. Here we report the direct synthesis-on-substrate of films of suitably coupled, monodispersed, ultrasmall perovskite QDs.

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Serious performance decline arose for perovskite light-emitting diodes (PeLEDs) once the active area was enlarged. Here we investigate the failure mechanism of the widespread active film fabrication method; and ascribe severe phase-segregation to be the reason. We thereby introduce L-Norvaline to construct a COO-coordinated intermediate phase with low formation enthalpy.

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Quasi-two-dimensional (quasi-2D) perovskites have attracted extraordinary attention due to their superior semiconducting properties and have emerged as one of the most promising materials for next-generation light-emitting diodes (LEDs). The outstanding optical properties originate from their structural characteristics. In particular, the inherent quantum-well structure endows them with a large exciton binding energy due to the strong dielectric- and quantum-confinement effects; the corresponding energy transfer among different n-value species thus results in high photoluminescence quantum yields (PLQYs), particularly at low excitation intensities.

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Quasi-two-dimensional (quasi-2D) perovskites, demonstrating excellent radiative efficiency and facile processability, have been considered as next-generation materials for light-emitting applications. Quasi-2D perovskites with a unique energy-funneling process offer an approach to achieve not only high photoluminescence quantum yields at low excitation but also tunable emission induced by dielectric and quantum confinement. In this Perspective, we highlight the mechanism of the energy-funneling process and discuss the salient position of it in quasi-2D perovskite materials for light-emitting applications; we then present the significance of component and molecular engineering strategies for the energy-funneling process to meet the requirements of stable emission and display technologies.

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Quasi-two-dimensional (quasi-2D) Ruddlesden-Popper (RP) perovskites such as BACsPbBr (BA = butylammonium, n > 1) are promising emitters, but their electroluminescence performance is limited by a severe non-radiative recombination during the energy transfer process. Here, we make use of methanesulfonate (MeS) that can interact with the spacer BA cations via strong hydrogen bonding interaction to reconstruct the quasi-2D perovskite structure, which increases the energy acceptor-to-donor ratio and enhances the energy transfer in perovskite films, thus improving the light emission efficiency. MeS additives also lower the defect density in RP perovskites, which is due to the elimination of uncoordinated Pb by the electron-rich Lewis base MeS and the weakened adsorbate blocking effect.

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Rapid Auger recombination represents an important challenge faced by quasi-2D perovskites, which induces resulting perovskite light-emitting diodes' (PeLEDs) efficiency roll-off. In principle, Auger recombination rate is proportional to materials' exciton binding energy (E). Thus, Auger recombination can be suppressed by reducing the corresponding materials' E.

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Quasi-two-dimensional (quasi-2D) Ruddlesden-Popper perovskites (RPPs) have been reported recently as laser media. The carrier dynamics of lasing in quasi-2D RPP films is still controversial. This work presents the amplified spontaneous emission (ASE) at room temperature based on the solution-processed quasi-2D (PEA)CsPbBr (⟨⟩ = 3-5) thin films.

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Organic-inorganic hybrid lead-halide perovskite materials (ABX ) have attracted widespread attention in the field of photovoltaics owing to their impressive optical and electrical properties. However, obstacles still exist in the commercialization of perovskite photovoltaics, such as poor stability, hysteresis, and human toxicity. A-site cation engineering is considered to be a powerful tool to tune perovskite structures and the resulting optoelectronic properties.

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Reduced-dimensional (quasi-2D) perovskite materials are widely applied for perovskite photovoltaics due to their remarkable environmental stability. However, their device performance still lags far behind traditional three dimensional perovskites, particularly high open circuit voltage (V) loss. Here, inhomogeneous energy landscape is pointed out to be the sole reason, which introduces extra energy loss, creates band tail states and inhibits minority carrier transport.

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Fermented dairy products have been recognized as the best carriers for the administration of probiotics. Because one of the potential probiotic strains, Lactobacillus plantarum, has poor proteolytic ability and weak acidifying capacity in milk fermentation, the aim of this study was to preliminarily investigate the stimulation effect of plant-based meals on L. plantarum CCFM8661 growth in milk, and subsequently develop a yogurt or yogurt drinks containing probiotic strain L.

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Metal halide perovskites have emerged as a new generation of X-ray detector materials. However, large-sized MAPbI single crystals (SCs) still exhibit lower performance than MAPbBr SCs in X-ray detection. DFT (density functional theory) simulations suggest the problem could be overcome by alloying large-sized cations at the A site.

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Device performance and in particular device stability for blue perovskite light-emitting diodes (PeLEDs) remain considerable challenges for the whole community. In this manuscript, we conceive an approach by tuning the 'A-site' cation composition of perovskites to develop blue-emitters. We herein report a Rubidium-Cesium alloyed, quasi-two-dimensional perovskite and demonstrate its great potential for pure-blue PeLED applications.

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A multi-functional fluorescent probe based on PzDPM (10-ethyl-3,7-di(pyrimidin-4-yl)-10H-phenothiazine) for Hg(2+), Cu(2+) and ClO(-) has been synthesized and characterized. The probe comprises an electron-donating fluorophore core of 10-ethylphenothiazine and two Hg(2+)-specific chelating arms of pyrimidin-4-yl. The 10-ethylphenothiazine also acts as a Cu(2+)/ClO(-)-specific reactive moiety.

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