White-light emission (WLE) materials based on organic-inorganic hybrid lead halides have drawn considerable attention because of their applications in light-emission equipment. Despite considerable efforts, there is still a lack of two-dimensional (2D) lead-chlorine white-light emitting halides with high photoluminescence quantum efficiency (PLQE). Herein, we report the preparation of a new 2D layered hybrid halide, [DTHPE]PbCl, which exhibits bright wide-band WLE, a high PLQE of 8.86% and high anti-water stability. To the best of our knowledge, the PLQE of [DTHPE]PbCl exceeds that of most 2D lead chlorides. Furthermore, the emission intensity is unchanged even after continuous immersion in water for 7 days. Photoluminescence measurements indicate that the WLE originates from self-trapped excitons. [DTHPE]PbCl is a promising visible-blind UV hybrid halide owing to its excellent photoelectric response. [DTHPE]PbCl is an effective white-light emitting material for display applications. The coexistence of a high performance visible-blind UV response and high efficiency white-light emission provides attractive possibilities for potential applications in the multifunctional photoelectronic field.
Induction of systemic acquired resistance (SAR) in plants to control bacterial diseases has become an effective solution to the problems of agrochemical resistance and ecological environment damage caused by long-term and large-scale use of traditional bactericides. However, current SAR-inducing compounds are often unable to rapidly eliminate pathogenic bacteria in infected plant tissues to prevent further spread of the disease, severely restraining the potential for extensive application in agriculture. Herein, we address the limitations by developing a series of visible-light-absorbing aggregation-induced emission photosensitizers suitable for agricultural use.
In recent years, researchers studying fluorogenic samples have steadily shifted from using large, expensive, poorly soluble fluorophores with complex synthetic sequences to smaller, simpler p scaffolds with low molecular weight. This research article presents an in-depth study of the photophysical properties of five bridged single-benzene-based fluorophores (SBBFs) investigated for their solution and solid-state emission (SSSE) properties. The compounds O4, N1O3, N2O2, N3O1, and N4 are derived from a central terephthalonitrile core and vary in the amount of oxygen and nitrogen bridging atoms.
A chiral agent, TPE-ASP, incorporating aspartic acid as the chiral source and tetraphenylene derivatives as chromophores, was designed and synthesized. The chiral agent was self-assembled into regular spherical nanoparticles with a maximum luminescence asymmetry factor of |2.41 × 10| at 460 nm which is attributed to TPE-ASP.
The construction of single-component, white-light-emitting, conjugated polymers always utilizes fluorescence resonance energy transfer (FRET) for efficient emission. However, the main challenges in developing such materials primarily come from the effects of aggregation states during solution processing and the precise structural control required for the synthesis of compounds. Both aspects can affect the FRET between different lumophores in white-light-emitting materials.
In the present research work, a solid-state reaction method was employed to synthesize a series of CaGdSbWO:SmEu (x = 1, 1.5, 2, 3 and 4 mol%) phosphors. The phase purity, crystallinity, morphological and compositional studies were analysed via X-ray diffraction (XRD), scanning electron microscopy (SEM) imaging, and energy dispersive spectroscopy (EDS) analysis.
