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Organic contamination of water results in significant risks to the biosphere and human health. The treatment of organic pollutants found in effluents urgently requires a green, sustainable, and effective approach. Herein, a straightforward one-step procedure was developed to create a photocatalytic mesh using iron mesh as the substrate and the g-C3N4/MIL-101(Fe) heterostructure as the photocatalytic material to activate persulfate (PS) for the removal of methyl orange (MO) from water. Fluorescence stereo microscopy (FSM), scanning electron microscopy (SEM), nitrogen adsorption–desorption, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FT-IR) spectroscopy, and X-ray powder diffraction (XRD) were used to characterize the morphological and physicochemical properties of the synthesized composites, which confirmed the successful growth of g-C3N4/MIL-101(Fe) on the iron mesh. The outstanding PS activation capacity of g-C3N4/MIL-101(Fe) promoted electron transfer and accelerated the generation of SO4˙−, resulting in up to 91.05% MO degradation under 60 min of visible light exposure. The removal mechanisms were investigated by quenching experiments and electron spin resonance (ESR), which proved that ˙OH, ˙O2− and h+ contributed to the removal of MO. Moreover, the degradation pathways of MO and the as-formed intermediates were identified by high-resolution mass spectroscopy (HRMS). This study provides a convenient and economical method to build innovative photocatalytic systems for organic pollutant degradation. [ABSTRACT FROM AUTHOR]

ZnO quantum dots (QDs) supported on porous nitrogen-doped carbon (ZnOQDs/P-NC) exhibited excellent electrochemical performance for the electroreduction of CO2 to CO with a faradaic efficiency of 95.3% and a current density of 21.6 mA cm−2 at −2.2 V vs. Ag/Ag+. [ABSTRACT FROM AUTHOR]

A rapid and highly selective naked-eye detection of hydrochloric acid (HCl) in an aqueous medium was established using HCl-triggered redispersion of gold nanoparticle aggregates. [ABSTRACT FROM AUTHOR]

The triazine‐based covalent organic frameworks (tCOF), an intriguing subtype of COFs, are expected as highly promising photocatalysts for various photocatalytic applications owing to their fully conjugated structures and nitrogen‐rich skeletons. However, the inherent hydrophobicity and fast recombination of photoexcited electron‐hole pairs are two main factors hindering the application of tCOF in practical photocatalytic reactions. Here, a post‐synthetic modification strategy to fabricate superhydrophilic tCOF‐based photocatalysts is demonstrated by in situ growing FeOOH clusters on TaTz COF (TaTz‐FeOOH) for efficient photocatalytic oxidation of various organic pollutants. The strong polar FeOOH endows TaTz‐FeOOH with good hydrophilic properties. The well‐defined heterogeneous interface between FeOOH and TaTz allows the photoelectrons generated by TaTz to be consumed by Fe (III) to transform into Fe (II), synergistically promoting the separation of holes and the generation of free radicals. Compared with the unmodified TaTz, the optimized TaTz‐FeOOH (1%) shows excellent photocatalytic performance, where the photocatalytic degrade rate (k) of rhodamine B is increased by about 12 times, and the degradation rate is maintained at 99% after 5 cycles, thus achieving efficient removal of quinolone antibiotics from water. This study provides a new avenue for the development of COF‐based hydrophilic functional materials for a wide range of practical applications. [ABSTRACT FROM AUTHOR]

The precisely modulated synthesis of programmable light‐emitting materials remains a challenge. To address this challenge, we construct four tetraphenylethylene‐based supramolecular architectures (SA, SB, SC, and SD), revealing that they exhibit higher electrochemiluminescence (ECL) intensities and efficiencies than the tetraphenylethylene monomer and can be classified as highly efficient and precisely modulated intramolecular aggregation–induced electrochemiluminescence (PI‐AIECL) systems. The best‐performing system (SD) shows a high ECL cathodic efficiency exceeding that of the benchmark tris(2,2′‐bipyridyl)ruthenium(II) chloride in aqueous solution by nearly six‐fold. The electrochemical characterization of these architectures in an organic solvent provides deeper mechanistic insights, revealing that SD features the lowest electrochemical band gap. Density functional theory calculations indicate that the band gap of the guest ligand in the SD structure is the smallest and most closely matched to that of the host scaffold. Finally, the SD system is used to realize ECL‐based cysteine detection (detection limit=14.4 nM) in real samples. Thus, this study not only provides a precisely modulated supramolecular strategy allowing chromophores to be controllably regulated on a molecular scale, but also inspires the programmable synthesis of high‐performance aggregation‐induced electrochemiluminescence emitters. [ABSTRACT FROM AUTHOR]

The development of highly selective homogeneous electron transfer reagents is highly desirable for synthetic chemistry. An isolable spirosilole tetra-anion described in this paper has been proved to be a promising soluble electron transfer reagent. The reduction of octaphenyl-1,1′-spirobisilole (1) with lithium resulted in the formation of the isolable spirosilole tetra-anion in good yield. The tetra-anion (2) has been characterized by nuclear magnetic resonance (NMR) and cleanly underwent electron transfer reactions with dioxygen, carbonyl groups, and transition metal halides to yield reduction products with the regeneration of 1.