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The contamination of natural basins by agricultural or industrial activities, and the growing need for potable water due to climate changes accelerate the drive to find versatile, fast, practical, and easy-to-use methods for water analysis. A potentially versatile technique suitable for water analysis is Raman Spectroscopy (RS). Featured by good resolution but low sensitivity, RS detects molecular vibrational modes of an analyte in water. Nitrate is an indicator of chemical and/or biological pollution, it displays Raman active vibrational modes affected by the interaction with other systems in solution, allowing a wide range of applications. Concerning Nitrate analysis in water, a general introduction to the Raman effect and the basic instrumentation were herein discussed. RS is a potential solution to wastewater analysis. This review first reports the theoretical background of the technique and its basic working principles, then, the state-of-the-art scientific contributions related to Nitrate detection are investigated with a particular interest in the instrumental setup and the chemometric techniques employed to improve its sensitivity. In the studies hereby considered, instrumental setup (for example, laser frequency, laser power, acquisition times) and different technical solutions (for example, micro- versus macro-Raman instruments) to increase the technique's sensitivity on Nitrate detection are described. Concisely, the use of deep-UV lasers, optically active Surface-Enhanced Raman Spectroscopy (SERS) or Fiber-Enhanced Raman spectroscopy (FERS) equipment, coupled with instrumental settings, i.e. acquisition time, variable temperature of acquisition, use of special sampling apparatus (cuvettes or immersion probes), or with ion exchange resins for analyte enrichment, have been reported. Remarkably, examples of large data correction of unwanted fluorescence by mathematical processing or chemical quenching were reported too, suggesting solutions for the Raman analysis of wastewaters. Finally, a short digression on Machine Learning (ML) applied to RS is proposed, showing the promising results reported in other fields. Data-driven methods could be a solution to improve the low sensitivity of the RS for Nitrate detection. Hence, an approach of ML methods for the typical RS spectra processing (spike removal, baseline correction, fluorescence curve elimination, instrumental noise correction) was hereby mentioned, suggesting an improvement in the detection capability of Nitrate ion in water.
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http://dx.doi.org/10.1021/acsmeasuresciau.5c00016 | DOI Listing |
J Phys Chem B
September 2025
National Research Institute of Chinese Medicine, Ministry of Health and Welfare, Taipei 11221, Taiwan, ROC.
The synthesis of -tetrakis(3,4,5-trimethoxyphenyl)porphyrin [HT(3,4,5-OCH)PP] and cobalt(II) -tetrakis(3,4,5-trimethoxyphenyl)porphyrin [Co(T(3,4,5-OCH)PP)] has been successfully accomplished. The oxidation properties of [Co(T(3,4,5-OCH)PP)] have been assessed through UV-vis, NMR, and EPR techniques. It can be seen in the UV-vis spectrum that adding SbCl caused extra peaks to appear at 674 nm, which means that a π-cation radical was formed.
View Article and Find Full Text PDFJ Phys Chem Lett
September 2025
Department of Chemistry, Oregon State University, 153 Gilbert Hall, Corvallis, Oregon 97331, United States.
Carbon dots (CDs) represent a new class of nontoxic and sustainable nanomaterials with increasing applications. Among them, bright and large Stokes-shift CDs are highly desirable for display and imaging, yet the emission mechanisms remain unclear. We obtained structural signatures for the recently engineered green and red CDs by ground-state femtosecond stimulated Raman spectroscopy (FSRS), then synthesized orange CDs with similar size but much higher nitrogen dopants than red CDs.
View Article and Find Full Text PDFInorg Chem
September 2025
Synthesis and Characterization of Innovative Materials, TUM School of Natural Sciences, Department of Chemistry, Technical University of Munich, Lichtenbergstraße 4, Garching b. München 85748, Germany.
Semiconductors with one-dimensional (1D) substructures are promising for next-generation optical and electronic devices due to their directional transport and flexibility. Representatives of this class include HgPbP-type materials. This study investigates the related semiconductors AgGeP and AgSnP.
View Article and Find Full Text PDFSmall
September 2025
Nanochemistry Department, Max Planck Institute for Solid State Research, Heisenbergstraße 1, 70569, Stuttgart, Germany.
Flexible metal-organic frameworks (MOFs) have emerged as a new generation of porous materials and are considered for various applications such as sensing, water or gas capture, and water purification. MIL-88 A (Fe) is one of the earliest and most researched flexible MOFs, but to date, there is a lack in the structural aspects that govern its dynamic behaviour. Here, we report the first crystal structure of DMF-solvated MIL-88 A and investigate the impact of real structure effects on the dynamic behaviour of MIL-88 A (Fe), particularly upon water adsorption.
View Article and Find Full Text PDFSmall
September 2025
School of Materials Science and Engineering, State Key Laboratory of Silicon and Advanced Semiconductor Materials, Zhejiang University, Hangzhou, 310027, P. R. China.
High-concentration electrolytes (HCEs) face inherent challenges such as high viscosity and diminished ionic conductivity caused by the formation of three-dimensional (3D) anion networks, which limit their practical applications. In this study, it is demonstrated that encapsulating HCEs within metal-organic frameworks (MOFs) effectively disrupts these 3-D networks, resulting in significantly enhanced ionic conductivity. Raman spectroscopy, nuclear magnetic resonance (NMR), and molecular dynamics (MD) simulations reveal a significant reduction in aggregates (AGGs)-state anion within MOF-confined electrolytes, confirming the reconstruction of the solvation environment.
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