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Broadband Emission in Hybrid Organic–Inorganic Halides of Group 12 Metals
摘要： We report syntheses, crystal and electronic structures, and characterization of three new hybrid organic?inorganic halides (R)ZnBr3(DMSO), (R)2CdBr4·DMSO, and (R)CdI3(DMSO) (where (R) = C6(CH3)5CH2N(CH3)3, and DMSO = dimethyl sulfoxide). The compounds can be conveniently prepared as single crystals and bulk polycrystalline powders using a DMSO?methanol solvent system. On the basis of the single-crystal X-ray diffraction results carried out at room temperature and 100 K, all compounds have zero-dimensional (0D) crystal structures featuring alternating layers of bulky organic cations and molecular inorganic anions based on a tetrahedral coordination around group 12 metal cations. The presence of discrete molecular building blocks in the 0D structures results in localized charges and tunable room-temperature light emission, including white light for (R)ZnBr3(DMSO), bluish-white light for (R)2CdBr4·DMSO, and green for (R)CdI3(DMSO). The highest photoluminescence quantum yield (PLQY) value of 3.07% was measured for (R)ZnBr3(DMSO), which emits cold white light based on the calculated correlated color temperature (CCT) of 11,044 K. All compounds exhibit fast photoluminescence lifetimes on the timescale of tens of nanoseconds, consistent with the fast luminescence decay observed in π-conjugated organic molecules. Temperature dependence photoluminescence study showed the appearance of additional peaks around 550 nm, resulting from the organic salt emission. Density functional theory calculations show that the incorporation of both the low-gap aromatic molecule R and the relatively electropositive Zn and Cd metals can lead to exciton localization at the aromatic molecular cations, which act as luminescence centers.
关键词： zero-dimensional structures,broadband emission,group 12 metals,exciton localization,photoluminescence quantum yield,hybrid organic?inorganic halides
更新于2025-09-23 15:23:52
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Engineering Tunable Broadband Near-Infrared Emission in Transparent Rare-Earth Doped Nanocrystals-in-Glass Composites via a Bottom-Up Strategy
摘要： Applications of trivalent rare earth (RE3+)-doped light sources in solid-state laser technology, optical communications, biolabeling, and solar energy management have stimulated a growing demand for broadband emission with flexible tunability and high efficiency. Codoping is a conventional strategy for manipulating the photoluminescence of active RE3+ ions. However, energy transfer between sensitizers and activators usually induces nonradiative migration depletion that brings detrimental luminescent quenching. Here, a transparent framework is employed to assemble ordered RE3+-doped emitters to extend the emission spectral range by extracting photons from a variety of RE3+ ions with sequential energy gradient. To block migration-mediated depletion between different RE3+ ions, a nanoscopic heterogeneous architecture is constructed to spatially confine the RE3+ clusters via a 'nanocrystals-in-glass composite' (NGC) structure. This bottom-up strategy endows the obtained RE3+-doped NGC with high emission intensity (nearly one order of magnitude enhancement) and broadband near-infrared emission from 1300 to 1600 nm, which covers nearly the whole low-loss optical communication window. Most crucially, NGC is a versatile approach to design tunable broadband emission for the potential applications in high-performance photonic devices, which also provides new opportunities for engineering multifunctional materials by integration and manipulation of diverse functional building units in a nanoscopic region.
关键词： luminescence,rare earth doping,broadband emission,nanocrystals-in-glass composite,near-infrared emission
更新于2025-09-23 15:22:29
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Broadband light emission induced by laser absorption and optimized by thermal injection in Nd <sup>3+</sup> :Y <sub/>2</sub> SiO <sub/>5</sub> ceramic powder
摘要： Laser induced broadband (white) light emission has been studied in different particle systems for use in light emitting devices. The photoinduced phenomenon occurs above a certain excitation power threshold and it is generally studied under vacuum conditions. In this work, the phenomenon is studied in neodymium doped yttrium silicate ceramic powder synthesized by combustion method. White light is observed when the sample is excited in ambient air with a CW near-infrared (λ = 808 nm) laser powered above 1.3 W. When the temperature of the sample is externally raised above 200 oC, white light is observed above 1.0 W and a large enhancement of the broadband emission intensity is observed.
关键词： broadband emission,up-conversion,neodymium doped yttrium silicate,laser induced,thermal injection
更新于2025-09-11 14:15:04
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Broadband Defects Emission and Enhanced Ligand Raman Scattering in 0D Cs <sub/>3</sub> Bi <sub/>2</sub> I <sub/>9</sub> Colloidal Nanocrystals
摘要： Excitonic 0D and 2D lead-halide perovskites have been recently developed and investigated as new materials for light generation. Here broadband (>1 eV) emission from newly synthesized 0D lead-free colloidal Cs3Bi2I9 nanocrystals (NCs) is reported. The nature of their emissive states as well as the relative dynamics which are currently hotly debated are investigated. In particular, it is found that the broadband emission is made by the coexistence of emissive excitons and sub-bandgap emissive trap-states. Remarkably, evidence of enhanced Raman scattering from the ligands is observed when attached to the NCs surface, an effect that is preliminarily attributed to strong exciton-ligands electronic coupling in these systems.
关键词： trap-states emission,enhanced Raman scattering,broadband emission,lead-free perovskites,0D nanocrystals
更新于2025-09-10 09:29:36
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Pressure-Induced Broadband Emission of 2D Organic-Inorganic Hybrid Perovskite (C <sub/>6</sub> H <sub/>5</sub> C <sub/>2</sub> H <sub/>4</sub> NH <sub/>3</sub> ) <sub/>2</sub> PbBr <sub/>4</sub>
摘要： 2D Ruddlesden–Popper halide perovskites, which incorporate hydrophobic organic interlayers to considerably improve environmental stability and optical properties diversity, have attracted substantial research attention for optoelectronic applications. The burgeoning broad emission arising from exciton self-trapping of 2D perovskites shows a strong dependence on a deformable structure. Here, the pressure-induced broadband emission of layered (001) Pb-Br perovskite with a large Stokes shift in the visible region is observed by finely improving lattice distortion to increase exciton–phonon coupling under hydrostatic pressure. Band gap narrows ≈0.5 eV under modest pressure, mainly due to the large compressibility of the orientational organic layer, confirming that the bulky organic cations notably influence the structure and, in turn, the various properties of materials. Sequential amorphization of the organic and inorganic layer is confirmed by high pressure Raman and X-ray diffraction measurements, suggesting the particularity of layered crystal structures. The mechanism constructed here offers a new route for tuning the optical properties of 2D perovskites.
关键词： broadband emission,band-gap narrowing,pressure,perovskites,amorphization
更新于2025-09-10 09:29:36