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Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) in the absorption mode has a superior performance over the conventional magnitude mode. However, this improved performance for the analysis of dissolved organic matter (DOM) in negative-ion and positive-ion modes of electrospray ionization [ESI(-) and ESI(+), respectively] remains unknown. This study systemically compared the improved performance by the absorption mode for DOM FT-ICR MS spectra acquired with the low-field and high-field magnet instruments between two charge modes. The absorption mode enhanced the resolution and signal-to-noise ratio values of DOM peaks with factors of 1.88-1.94 and 1.60-1.72, respectively. The significantly higher improvement of mass resolution for the ESI(+) mode than that for the ESI(-) mode could resolve the extensive occurrence of mass doublets in the ESI(+) mode, yielding some formulas exclusively identified in the ESI(+) mode. The findings of this study have systemically demonstrated the superiority of the absorption mode in improving the spectra quality during the routine FT-ICR MS postdata analysis and highlighted its great potential in characterizing the molecular composition of DOM using the FT-ICR MS technique in both ESI(-) and ESI(+) modes.
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http://dx.doi.org/10.1021/acs.analchem.3c04651 | DOI Listing |
Spectrochim Acta A Mol Biomol Spectrosc
September 2025
Department of Chemistry, University of Copenhagen, Universitetsparken 5, Copenhagen-Ø, DK-2100, Denmark. Electronic address:
Absorption spectra of neopentyl alcohol and pinacolyl alcohol are recorded in the gas phase at room temperature and equilibrium conditions. A combination of conventional Fourier transform spectroscopy and cavity ringdown spectroscopy is used to cover the spectral OH-stretching regions, Δv=1-5. The conformer distributions of the alcohols are determined from the recorded spectra combined with transition intensities calculated with a reduced dimensional local mode model.
View Article and Find Full Text PDFLangmuir
September 2025
Biophysical Chemistry Laboratory, Physical Chemistry Section, Department of Chemistry, Jadavpur University, Raja S. C. Mullick Road, Jadavpur, Kolkata 700032, India.
Photophysical studies on the interaction of small molecules with various forms of nucleic acids are attracting attention nowadays in order to delineate the molecular level mechanism of various biological processes occurring in vivo. Herein, we employed vivid steady-state and time-resolved spectroscopic techniques to elucidate the detailed characterization of the binding interaction of a biologically active cationic dye thioflavin T (ThT) with double and triple helical forms of RNA - A.U duplex and U.
View Article and Find Full Text PDFAnal Chem
September 2025
Department of Chemistry, Korea University, Seoul 02841, Korea.
The incidence of cancer has escalated at a distressing pace, creating an urgent demand for advancements and breakthroughs in medical interventions. Amidst the multitude of approaches for diagnosing and managing cancer, fluorescence imaging, photodynamic therapy, and photothermal therapy have emerged as key approaches due to their unique advantages. Herein, two new xanthene-based probes, namely, and , with D-π-A conjugated structures, are reported.
View Article and Find Full Text PDFLight Sci Appl
September 2025
State Key Lab for Mesoscopic Physics and Frontiers Science Center for Nano-optoelectronics, School of Physics, Peking University, 100871, Beijing, China.
The fiber-based saturable absorber (SA) that enables mode-locking within a ring cavity serves as the core component of the ultrafast all-fiber lasers. However, the integration of SAs onto fibers with high compactness suffers from imbalanced saturable absorption properties and unstable mode-locking performance. Here, we present a robust mode-locking SA by integrating a nanocavity composed of a two-dimensional graphene heterostructure on the fiber end facet.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Institute of Semiconductor Electronics (IHT), RWTH Aachen University, 52074 Aachen, Germany.
Hard entropy limits of impurity doping prevent further miniaturization of low nanoscale silicon-based very large scale integration (VLSI) devices, thereby obstructing the path toward more energy-efficient VLSI designs with higher yield in compute power. As demonstrated here by synchrotron UV photoelectron spectroscopy (UPS) and X-ray absorption spectroscopy in total fluorescence yield mode (XAS-TFY), intrinsic Si at the bottom of the nanoscale (i-nano-Si) turns into strong p- or n-Si by embedding in silicon nitride (SiN) or silicon dioxide (SiO), respectively. The associated Nanoscale Electronic Structure Shift Induced by Anions at Surfaces (NESSIAS) creates a p/n junction in i-nano-Si by the quantum-chemical impact of SiN- vs SiO-coating, providing energy landscapes to accumulate electrons (holes) when SiO- (SiN-) coated, with free charge carriers provided by metallic interconnects.
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