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The detection of highly toxic chemicals such as phosgene is crucial for addressing the severe threats to human health and public safety posed by terrorist attacks and industrial mishaps. However, timely and precise monitoring of phosgene at a low cost remains a significant challenge. This work is the first to report a novel fluorescent system based on the Intramolecular Charge Transfer (ICT) effect, which can rapidly detect phosgene in both solution and gas phases with high sensitivity by integrating a benzo[1,2-b:6,5-b’]dithiophene-4,5-diamine (BDTA) probe. Among existing detecting methods, this fluorescent system stands out as it can respond to phosgene within a mere 30 s and has a detection limit as low as 0.16 μM in solution. Furthermore, the sensing mechanism was rigorously validated through high-resolution mass spectrometry (HRMS) and density functional theory (DFT) calculations. As a result, this fluorescent probing system for phosgene can be effectively adapted for real-time, high-sensitivity sensing and used as a test strip for visual monitoring without the need for specific equipment, which will also provide a new strategy for the fluorescent detection of other toxic materials.

Aqueous zinc-ion batteries (ZIBs) are regarded as one of the most promising electrical energy-storage systems for their eco-friendliness, low cost and high-safety. Although there have been a lot of studies recently on the Zn metal anode, little attention has been paid to its initial nucleation and growth behavior, which is critical to the understanding of fundamental mechanisms of the Zn plating. Herein, the digital holographic surface imaging (DHSI) method, combined synchronously with electrochemical tests, is employed to in-situ observe the non-uniform concentration changes on the surface of the copper substrate caused by the Zn nucleation and growth at the early stage. It is the first time to observe the early uneven depositions from a perspective of solution concentration changes in a symmetrical battery system. Results show that the later dendritic growth of Zn is closely related to the nucleation and earlier deposition process. Based on the phase maps obtained with in-situ DHSI technique, the nucleation and growth during the Zn electrodeposition can be closely investigated and vividly demonstrated, offering a promising avenue towards the understanding of the interfacial electrochemistry in all aqueous metal-ion batteries.