Publications by authors named "Hou Jingshan"

Organic-inorganic hybrid ferroelectrics have attracted considerable attention due to their outstanding piezoelectricity, mechanical flexibility, and robust nonlinear optical properties. But the species with above room-temperature (RT) ferroelectricity, visible-light bandgap, and high photoelectric performance are still scarce. Herein, a novel organic-inorganic hybrid ferroelectric [CNH][SbI] has been synthesized hydrothermally and employed as a light-absorbing layer in organic-inorganic hybrid solar cells.

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The heteroepitaxy of 2D materials with engineered bandgaps are crucial to broaden the spectral response for their integrated optoelectronic devices. However, it is a challenge to achieve the high-oriented epitaxy and integration of multicomponent 2D materials with varying lattice constants on the same substrate due to the limitation of lattice matching. Here, in-plane adaptive heteroepitaxy of a series of high-oriented 2D cesium bismuth halide (CsBiX X = I, Br, Cl) single crystals with varying lattice constants from 8.

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Non-toxic molecular ferroelectrics have attracted significant interest due to their unique flexibility, low costs, and environmental friendliness. However, such materials with narrow bandgaps and ferroelectricity above room temperature (RT) are still scarce. Herein, we present a brand-new lead-free molecular ferroelectric [CNH][BiI] synthesized hydrothermally.

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Cyan-emitting phosphors are urgently needed to address the "cyan gap" in artificial full-spectrum lighting. In this research, a series of SrBaYLa(SiO)O:Eu (0.005 ≤ ≤ 0.

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Hybrid organic-inorganic molecular ferroelectrics (HOIMFs) have garnered significant attention for their potential applications in nonvolatile memory and spintronic devices. However, few efforts have been devoted to the photoelectric properties of lead halide molecular ferroelectrics, despite the fact that robust ferroelectricity and flexibility are desirable for thin-film photoelectric devices. Herein, we present a novel lead halide molecular ferroelectric [CNH][PbI] () synthesized hydrothermally.

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Hybrid organic-inorganic molecular ferroelectrics (HOIMFs) have garnered significant attention owing to their potential applications in optoelectronic and spintronic devices. However, HOIMFs with high Curie temperature (), narrow bandgap (), excellent stability, and high breakdown voltage are still very rare. Herein, we present a novel lead-halide molecular ferroelectric, (1,4-butanediammonium)PbI (), synthesized hydrothermally.

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Lead-free molecular ferroelectrics have garnered considerable attention for their promising potential, but such species with narrow band gap and sensitive photoelectric response are yet inadequate. Herein, we demonstrated the bulk ferroelectric photovoltaic effect in a novel lead-free molecular ferroelectric [CNH][BiI] with a Curie temperature () of 366 K and a narrow band gap () of 1.92 eV.

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The inherent poor stability of CsPbI nanocrystals hinders the practical application of this material. Therefore, it is still a challenge to improve the stability of CsPbI nanocrystals and realize their large-scale continuous preparation. In this work, we report the preparation of CsPbI/TiO nanocomposites with high stability by a microfluidic method.

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Coxsackievirus B1 (CVB1), an enterovirus with multiple clinical presentations, has been associated with potential long-term consequences, including hand, foot, and mouth disease (HFMD), in some patients. However, the related animal models, transmission dynamics, and long-term tissue tropism of CVB1 have not been systematically characterized. In this study, we established a model of CVB1 respiratory infection in rhesus macaques and evaluated the clinical symptoms, viral load, and immune levels during the acute phase (0-14 days) and long-term recovery phase (15-30 days).

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Single-component white-light luminescent materials are considered an economical and facile choice for phosphor-converted white light-emitting diodes (pc-WLEDs). Here, a new single-component white-light-emitting material CsMnCl:Eu based on the combination of a lead-free halide structure and a rare-earth ion is first reported. Benefiting from the smart dilution-sensitization design strategy, white light composed of dual broad emission originating from Eu (blue light, 444 nm, 4f5d → 4f) and Mn (yellow light, 566 nm, T → A) was successfully realized under near-ultraviolet light (404 nm) radiation with a high photoluminescence quantum yield of 66%.

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Phosphor-in-glass represents a promising avenue for merging the luminous efficiency of high-quality phosphor and the thermal stability of a glass matrix. Undoubtedly, the glass matrix system and its preparation are pivotal factors in achieving high stability and preserving the original performance of embedded phosphor particles. In contrast to the well-established commercial YAlO:Ce oxide phosphor, red nitride phosphor, which plays a critical role in high-quality lighting, exhibits greater structural instability during the high-temperature synthesis of inorganic glasses.

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Heterojunction semiconductors have been extensively applied in various optoelectronic devices due to their unique carrier transport characteristics. However, it is still a challenge to construct heterojunctions based on colloidal quantum dots (CQDs) due to stress and lattice mismatch. Herein, HgSe/CsPbBrI heterojunctions with type I band alignment are acquired that are derived from minor lattice mismatch (~1.

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Cyan phosphors are urgently needed to fill the cyan gap and improve the spectral continuity of white light-emitting diodes (LEDs) to cater to the high demand for high-quality lighting. Here, a series of new Eu-activated LaSiAlNO (LSANO) cyan phosphors were prepared, and their luminescence properties and color centers were analyzed through fluorescence spectral measurements from 7 K to 475 K. At 300 K, the photoluminescence excitation (PLE) spectrum monitored at 483 nm presents a broadband of 200-460 nm with a peak at 398 nm, matching well with commercial violet LED chips.

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Atomically thin two-dimensional (2D) bismuth oxychalcogenides have been considered as promising candidates for high-speed and low-power photoelectronic devices due to their high charge carrier mobility and excellent environmental stability. However, the photoelectric performance of their bulk materials still falls short of expectations. Herein, a novel BiOS/SnS composite film with a type-II heterojunction was successfully prepared by combining hydrothermal and knife-coating techniques.

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A green phosphor Sr ZnGe O :Mn with a melilite structure was prepared using a high-temperature solid-state reaction. When the 535 nm emission was monitored, the excitation spectrum of the Sr ZnGe O :Mn was found to contain two excitation bands in the ultraviolet (UV) region. When excited by UV light, the sample shows bright green emission at 535 nm, which corresponds to the distinctive transition of Mn ( T → A ).

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Layered bismuth oxychalcogenides have been demonstrated as potential candidates for high-speed and low-power electronics due to their outstanding environmental stability and high carrier mobility, but the photoelectric performance of bulk species is still far from satisfactory. Herein, a novel BiOS/CdS composite film with a type-II heterojunction has been successfully prepared by combining chemical bath deposition (CBD) and spin-coating technologies. The structure, morphology, optical and photoelectric properties of the samples were investigated systematically.

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A novel quaternary oxysulfide, FeOCuS has been successfully synthesized with a tetragonal anti-PbO-type structure and a visible-light bandgap of about 1.37 eV. Driven by only a 0.

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In this work, a novel red-emitting oxyfluoride phosphor NaNbOF:Mn with an ultra-intense zero-phonon line (ZPL) was successfully synthesized by hydrothermal method. The phase composition and luminescent properties of NaNbOF:Mn were studied in detail. The photoluminescence excitation spectrum contains two intense excitation bands centered at 369 and 470 nm, which match well with commercial UV and blue light-emitting diode (LED) chips.

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The synthesis of highly luminescent colloidal CsSnX (X = halogen) perovskite nanocrystals (NCs) remains a long-standing challenge due to the lack of a fundamental understanding of how to rationally suppress the formation of structural defects that significantly influence the radiative carrier recombination processes. Here, we develop a theory-guided, general synthetic concept for highly luminescent CsSnX NCs. Guided by density functional theory calculations and molecular dynamics simulations, we predict that, although there is an opposing trend in the chemical potential-dependent formation energies of various defects, highly luminescent CsSnI NCs with narrow emission could be obtained through decreasing the density of tin vacancies.

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Pulsed laser deposition on 3-dimensional micro-objects of complex morphology is demonstrated by the paradigmatic growth of cellulose and polymer/YAlO:Ce phosphor composite nanolayers. Congruent materials transfer is a result of multicomponent ablation performed by relatively low fluence (<200 mJ cm) ArF excimer laser pulses (λ = 193 nm). Films grown on optical and engineering components, having a thickness from ~50 nm to more than ~300 nm, are durable, well adherent and maintain the structural and functional properties of the parent solids.

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Recently, all-inorganic halide perovskite (CsPbX , (X = Cl, Br, and I)) nanocrystals (NCs) based hybrid architectures have attracted extensive attention owing to their distinct luminescence characteristics. However, due to stress and lattice mismatch, it is still a challenge to construct heterojunctions between perovskite NCs and the nanostructures with different lattice parameters and non-cubic contour. In this work, a room temperature mechanochemical method is presented to construct TiO @CsPbBr hybrid architectures, in which TiO nanoparticles (NPs) with a hard lattice as nano "balls" mill off the angles and anchor to the CsPbBr NCs with a soft lattice.

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The presence of labile bulky insulating hydrocarbon ligands in halide perovskite nanocrystals (NCs) passivates surface traps but concurrently makes charge transport difficult in optoelectronic devices. Early efforts routinely rely on the replacement of long-chain ligands with short-chain cousins, leading to notable changes in NC's sizes and photophysical properties and thus making it hard to obtain devices with nearly designed emissions. Here we report a general solution-phase ligand-exchange strategy to produce organic-ligand-lacking halide perovskite NCs with high photoluminescence (PL) quantum yields and good stability in ambient air.

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Recently, CsPbX (X = Cl, Br, and I) perovskite quantum dots (QDs) have exhibited significant potential for application in the field of lighting. However, their self-absorption and agglomeration significantly decrease their photoluminescence when their solution is centrifuged to form a powder; this hinders their applications in the field of solid-state lighting. Currently, there is lack of efficient solutions to overcome the self-absorption issue for CsPbX QDs.

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Doping of semiconductors by introducing foreign atoms enables their widespread applications in microelectronics and optoelectronics. We show that this strategy can be applied to direct bandgap lead-halide perovskites, leading to the realization of ultrawide photoluminescence (PL) at new wavelengths enabled by doping bismuth (Bi) into lead-halide perovskites. Structural and photophysical characterization reveals that the PL stems from one class of Bi doping-induced optically active center, which is attributed to distorted [PbI6] units coupled with spatially localized bipolarons.

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Objective: To investigate the impact of diameter of needles on the effect of dry needling treatment of chronic lumbar myofascial pain syndrome.

Design: Forty-eight patients with chronic lumbar myofascial pain syndrome were randomly allocated to 3 groups. They received dry needling with needles of diameter 0.

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