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Silver nanoparticles (Ag NPs) are extensively used as an antibacterial additive in commercial products and their release has caused environmental risk. However, conventional methods for the toxicity detection of Ag NPs are very time consuming and the mechanisms of action are not clear. We developed a new, in situ, rapid, and sensitive fingerprinting approach, using surface-enhanced Raman spectroscopy (SERS), to study the antibacterial activity and mechanism of Ag NPs of 80 and 18 nm (Ag80 and Ag18, respectively), by using the strong electromagnetic enhancement generated by Ag NPs. Sensitive spectra changes representing various biomolecules in bacteria were observed with increasing concentrations of Ag NPs. They not only allowed SERS to monitor the antibacterial activity of Ag NPs of different sizes in different water media but also to study the antibacterial mechanism at the molecular level. Ag18 were found to be more toxic than Ag80 in water, but their toxicity declined to a similar level in the PBS medium. The antibacterial mechanism was proposed on the basis of a careful identification of the chemical origins by comparing the SERS spectra with model compounds. The dramatic change in protein, hypoxanthine, adenosine, and guanosine bands suggested that Ag NPs have a significant impact on the protein and metabolic processes of purine. Finally, by adding nontoxic and SERS active Au NPs, SERS was successfully utilized to study the action mode of the NPs unable to produce an observable SERS signal. This work opens a window for the future extensive SERS studies of the antibacterial mechanism of a great variety of non-SERS-active NPs.

The design of nanosheets interlayer between the substrate and polyamide layer has attracted growing attention to improve the performance of thin-film composite membranes. However, the membrane size is limited by current fabrication methods such as vacuum filtration. Herein, a high-performance MXene (Ti3C2T x ) interlayered polyamide forward osmosis (FO) membrane is fabricated based on a combination of a facile and scalable brush-coating of MXene on nylon substrates and the interfacial polymerization process. The as-prepared FO membrane shows high water permeability of 31.8 L m–2 h–1 and low specific salt flux of 0.27 g L–1 using 2.0 mol L–1 sodium chloride as the draw solution. This is attributed to the adjustment of substrate properties and the polyamide layer by coating of MXene as well as the facilitation of water transportation by the interlayer distances between Ti3C2T x . The membrane also exhibits a good organic solvent forward osmosis performance with high ethanol flux as 9.5 L m–2 h–1 and low specific salt flux of 0.4 g L–1 using 2.0 mol L–1 lithium chloride as the draw solution. Moreover, the MXene interlayered FO membrane demonstrates a feasible application in real seawater desalination and industrial textile wastewater treatment. This work presents an effective approach to fabricating nanomaterials interlayered FO membranes with superior performance for both desalination and organic solvent recovery.