Search Results (135)

Herein, we propose a simple and cost-effective method for fabricating moderate-sensitivity surface-enhanced Raman scattering (SERS) substrates using Cu-plasma polymer fluorocarbon (Cu-PPFC) nanocomposite films fabricated through RF sputtering. The use of a composite target composed of carbon nanotube (CNT), Cu, and polytetrafluoroethylene (PTFE) powders (5:60–80:35–15 wt%) offers the advantage of the simple fabrication of moderate-sensitivity SERS substrates with a single cathode compared to co-sputtering. X-ray photoelectron spectroscopy (XPS) revealed that the film surface was partially composed of metallic Cu with Cu-F bonds and Cu–O bonds, confirming the coexistence of the conducting and plasmon-active domains. UV-VIS spectroscopy revealed a distinct absorption peak at approximately 680 nm, indicating the excitation of localized surface plasmon resonances in the Cu nanoclusters embedded in the plasma polymer fluorocarbon (PPFC) matrix. Atomic force microscopy and grazing incidence small-angle X-ray scattering analyses confirmed that the Cu nanoparticles were uniformly distributed with interparticle distances of 20–35 nm. The Cu-PPFC nanocomposite film with the highest Cu content (80 wt%) exhibited a Raman enhancement factor of 2.18 × 10⁴ for rhodamine 6G, demonstrating its potential as a moderate-sensitivity SERS substrate. Finite-difference time-domain (FDTD) simulations confirmed the strong electromagnetic field localization at the Cu-Cu nanogaps separated by the PPFC matrix, corroborating the experimentally observed SERS enhancement. These results suggest that a Cu-PPFC nanocomposite film, easily fabricated using a composite target, provides an efficient and scalable route for fabricating reproducible, inexpensive, and moderate-sensitivity SERS substrates suitable for practical sensing applications. Full article

We investigate how grain growth, strain relaxation, and vacancy chemistry shape the near-edge optical response of nanocrystalline Ce${\mathrm{O}}_{2-\delta }$ prepared by a chymosin-assisted Pechini route from nitrate–citrate precursors. Rietveld line-profile analysis shows that phase-pure Ce${\mathrm{O}}_{2-\delta }$ forms after calcination between 400 and 1000 °C. Over this range, the average crystallite size increases from ≈3.4 to ≈57 nm, while the microstrain decreases from 0.79% to 0.05%, with size–strain scaling consistent with interface-controlled grain growth that follows a normal growth law with exponent $m=2$ and activation energy $Q\approx 155$ kJ ${\mathrm{mol}}^{-1}$. Raman spectroscopy tracks the sharpening of the $F_{2g}$ mode and the fading of defect-related bands, X-ray photoelectron spectroscopy reveals a nonmonotonic evolution of the surface ${\mathrm{Ce}}^{3+}$ fraction and separates lattice from adsorbed oxygen species, and electron paramagnetic resonance detects vacancy-bound ${\mathrm{Ce}}^{3+}$ polarons that weaken at high temperature. Diffuse-reflectance UV–Vis spectra show a modest blue shift of the apparent band gap from $E_g\approx 2.78$ to 2.95 eV as crystallites coarsen, while the Urbach energy $E_u$ follows the ${\mathrm{Ce}}^{3+}$ content and sub-gap tailing. The structural, spectroscopic, and optical results together map out a quantitative connection between grain growth, vacancy populations, and near-edge optical properties in ${\mathrm{CeO}}_{2-\delta }$ nanoparticles. Full article

Thermoelectric (TE) materials represent a critical frontier in sustainable energy conversion technologies, providing direct thermal-to-electrical energy conversion with solid-state reliability. The optimizations of TE performance demand a nuanced comprehension of structure–property relationships across diverse length scales. This review summarizes established and emerging spectroscopic and microscopic techniques used to characterize inorganic and polymer TE materials, specifically poly(3,4-ethylenedioxythiophene): poly(styrenesulfonate) (PEDOT:PSS). For inorganic TE, ultraviolet–visible (UV–Vis) spectroscopy, energy-dispersive X-ray (EDX) spectroscopy, and X-ray photoelectron spectroscopy (XPS) are widely applied for electronic structure characterization. For phase analysis of inorganic TE materials, Raman spectroscopy (RS), electron energy loss spectroscopy (EELS), and nuclear magnetic resonance (NMR) spectroscopy are utilized. For analyzing the surface morphology and crystalline structure, chemical scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD) are commonly used. For polymer TE materials, ultraviolet−visible–near-infrared (UV−Vis−NIR) spectroscopy and ultraviolet photoelectron spectroscopy (UPS) are generally employed for determining electronic structure. For functional group analysis of polymer TE, attenuated total reflectance–Fourier-transform infrared (ATR−FTIR) spectroscopy and RS are broadly utilized. XPS is used for elemental composition analysis of polymer TE. For the surface morphology of polymer TE, atomic force microscopic (AFM) and SEM are applied. Grazing incidence wide-angle X-ray scattering (GIWAXS) and XRD are employed for analyzing the crystalline structures of polymer TE materials. These techniques elucidate electronic, structural, morphological, and chemical properties, aiding in optimizing TE properties like conductivity, thermal stability, and mechanical strength. This review also suggests future research directions, including in situ methods and machine learning-assisted multi-dimensional spectroscopy to enhance TE performance for applications in electronic devices, energy storage, and solar cells. Full article

Nowadays, the development of the food industry and economic recovery have driven escalating consumer demands for high-quality, nutritious, and safe food products, and spectroscopic technologies are increasingly prominent as essential tools for food quality inspection. Concurrently, the rapid rise of artificial intelligence (AI) has created new opportunities for food quality detection. As a critical branch of AI, deep learning synergizes with spectroscopic technologies to enhance spectral data processing accuracy, enable real-time decision making, and address challenges from complex matrices and spectral noise. This review summarizes six cutting-edge nondestructive spectroscopic and imaging technologies, near-infrared/mid-infrared spectroscopy, Raman spectroscopy, fluorescence spectroscopy, hyperspectral imaging (spanning the UV, visible, and NIR regions, to simultaneously capture both spatial distribution and spectral signatures of sample constituents), terahertz spectroscopy, and nuclear magnetic resonance (NMR), along with their transformative applications. We systematically elucidate the fundamental principles and distinctive merits of each technological approach, with a particular focus on their deep learning-based integration with spectral fusion techniques and hybrid spectral-heterogeneous fusion methodologies. Our analysis reveals that the synergy between spectroscopic technologies and deep learning demonstrates unparalleled superiority in speed, precision, and non-invasiveness. Future research should prioritize three directions: multimodal integration of spectroscopic technologies, edge computing in portable devices, and AI-driven applications, ultimately establishing a high-precision and sustainable food quality inspection system spanning from production to consumption. Full article

Ionizing radiations are responsible for bond scission, radical formation, and oxidative degradation of polymer matrices. This study focuses on the effects of gamma irradiation on solid propellant binders, targeting a comprehensive chemical and mechanical characterization of different formulations. Samples were produced either by conventional methods based on hydroxyl-terminated polybutadiene and standard polyaddition reaction using isocyanates, or innovative approaches involving UV-driven radical curing. The samples were irradiated for comparison and to study their evolution as a function of three absorbed doses (25, 45, 130 kGy) for preliminary characterization studies, using a 60-Co gamma source. Samples were irradiated in air at uncontrolled room temperature. The coupling of spectroscopy techniques (Fourier transform infrared—FTIR, Raman and electron paramagnetic resonance—EPR) and dynamic mechanical analysis (DMA) highlighted the key role of antioxidant agents in tailoring mechanical changes in the binder phase. The absence of antioxidants enhances radical formation, oxidation, and cross-linking. These processes lead to progressively increased rigidity and reduced flexibility as a function of the absorbed dose. Complex interactions between photocured components largely influence radical stabilization and material degradation. These findings provide valuable insights for designing novel radiation-resistant binders, enabling the development of solid propellants tailored for reliable, long-term permanence in space, and advancing the knowledge on the applicability of 3D-printed propellants. Full article

TiO₂ mesoporous supports were obtained by the sol–gel method from different precursors (titaniumethoxide, isopropoxide, or butoxide) in the presence of nonionic, cationic, and anionic surfactants. Among these samples, those obtained from Ti isopropoxide, Brij58 w/o activated carbon (AC), were selected as supports. Photocatalysts were obtained by modifying these supports with Ag, Fe, and AgFe (each metal around 1% mass). The characterization results showed a stronger influence of titania precursors, surfactants, and AC on the texture and an insignificant effect on the crystalline structure and morphology of the obtained materials. X-ray photoelectron spectroscopy revealed the effects of AC and Fe on the Ag⁰ concentration and of Ag on Fe-reduced species. Based on this information, the results obtained by H₂-TPR, UV–Vis, Raman, and photoluminescence spectroscopy were explained. The performance of the photocatalysts was evaluated in the degradation of Congo Red (CR) and Crystal Violet (CV) dyes under UV and visible light. The Ag-TiO₂ sample exhibited the best activity in degrading CR at acidic pH and in degrading CV under basic conditions. In visible light, we observed the significant effects of the surface plasmon resonance, AC, Ag, and Fe on the activity in CR photodegradation. The proposed kinetics and mechanisms complete the study of the reactions. Full article

In this study, silver nanoparticles (Ag NPs) were synthesized on the surface of rutile-phase titanium dioxide (R-TiO₂) using a plasma-assisted technique. Comprehensive analyses were conducted to investigate the structural, morphological, optical, and electrical properties of the synthesized nanocomposites. Transmission electron microscopy (TEM) images revealed the uniform decoration of Ag NPs (average size: 29.8 nm) on the R-TiO₂ surface. X-ray diffraction (XRD) confirmed the polycrystalline nature of the samples, with decreased diffraction peak intensity indicating reduced crystallinity due to Ag decoration. The Williamson–Hall analysis showed increased crystallite size and reduced tensile strain, suggesting grain growth and stress relief. Raman spectroscopy revealed quenching and broadening of R-TiO₂ vibrational modes, likely due to increased oxygen vacancies. X-ray photoelectron spectroscopy (XPS) confirmed successful plasma-assisted deposition and the coexistence of Ag⁰ and Ag⁺ states, enhancing surface reactivity. UV-Vis spectroscopy demonstrated enhanced light absorption across the spectral range, attributed to localized surface plasmon resonance (LSPR), and a reduced optical bandgap. Dielectric properties, including dielectric constants, loss factor, and AC conductivity, were evaluated across frequencies (4–8 MHz) and temperatures (20–240 °C). The AC conductivity results indicated correlated barrier hopping (CBH) and overlapping large polaron tunneling (OLPT) as the primary conduction mechanisms. Composition-dependent dielectric behavior was interpreted through the Coulomb blockade effect. These findings suggest the potential of plasma assisted Ag NP-decorated R-TiO₂ nanostructures for photocatalysis, sensor and specific electro electrochemical systems applications. Full article

A graft reaction of polyvinyl chloride (PVC) with furfural was conducted in a tetrahydrofuran solution. The resulting graft structure (FF-g-PVC) was characterized using UV spectroscopy, photoluminescence (PL), Fourier Transform Infrared (FTIR) spectroscopy, Raman spectroscopy, and proton nuclear magnetic resonance (¹H NMR) spectroscopy. The grafting efficiency was determined through ultraviolet spectrophotometry. Thermal stability analysis via thermogravimetric (TG) testing revealed that furfural was successfully grafted onto the PVC chain. In a nitrogen atmosphere, the temperature of the maximum weight loss rate during the first stage of pyrolysis increased from 296.3 °C to 301.7 °C, while the activation energy for the second stage increased from 199.4 kJ/mol to 294.4 kJ/mol, indicating enhanced stability and delayed degradation of the PVC. Additionally, microwave irradiation markedly improved the graft reaction, achieving a grafting rate of 57.76‰ compared to only 1.808‰ with water bath heating. The optimal conditions were found to be a PVC/FF/Zn ratio of 1:1:0.9, with microwave irradiation for 20 min at 40 °C. Full article

Ultraviolet (UV) photodetectors play a crucial role in various applications, ranging from environmental monitoring to biomedical diagnostics. This paper presents the fabrication and characterization of a high-performance UV photodetector using hexagonal boron nitride (hBN) decorated with gold nanoparticles (AuNPs). The hBN flakes were mechanically exfoliated onto SiO₂ substrates, and AuNPs were formed via thermal evaporation, resulting in the creation of a plasmonically active surface that enhanced light absorption and carrier dynamics. Raman spectroscopy, transmission electron microscopy, and electrical measurements were performed to comprehensively analyze the device structure and performance. The photodetector exhibited significantly improved photocurrent and responsivity under UV-B (306 nm) and UV-C (254 nm) illumination, with the responsivity reaching an increase of nearly two orders of magnitude compared to that of the pristine hBN device. These improvements are attributed to the synergistic effects of the wide bandgap of hBN and the localized surface plasmon resonance of the AuNPs. These findings demonstrate the potential of AuNP-decorated hBN for advanced UV photodetection applications and provide a pathway toward more efficient and miniaturized optoelectronic devices. Full article

Marennine is the specific bluish pigment produced by the marine diatom Haslea ostrearia Gaillon (Simonsen), responsible for the greening of oysters in France’s Atlantic coast. For decades, H. ostrearia was considered the only blue diatom and described as such. However, new blue Haslea species have been described recently, among which Haslea karadagensis Davidovich, Gastineau, and Mouget (Black Sea, Crimea, Ukraine); Haslea provincialis Gastineau, Hansen, and Mouget (Mediterranean Sea, southern France); Haslea silbo Gastineau, Hansen, and Mouget (West Atlantic Ocean, USA); and one not characterized yet, Haslea sp. nov., isolated in Tenerife (Spain). These species produce marennine-like pigments, for which little information is available yet. The present work aims at studying spectral characteristics of these pigments by UV–visible spectrometry, Raman spectrometry, infrared spectrometry, nuclear magnetic resonance, energy-dispersive X-ray spectroscopy, and cyclic voltammetry, and comparing them to those of marennine produced by H. ostrearia strains originating from the north Atlantic Ocean (western France and Macaronesia), and north Pacific Ocean (southwestern USA). Results show that marennine produced by H. ostrearia strains and marennine-like pigments produced by H. provincialis, H. silbo, and Haslea sp. nov. are quite similar regarding their polysaccharide skeleton, and absorption in the UV–visible, infrared, and Raman regions. The most different marennine-like pigment is produced by H. karadagensis, but all Haslea blue pigments studied so far belong to the same family of organic molecules. Full article

A novel and efficient method for synthesizing Au-decorated ZnO nanoparticles (NPs) with enhanced photocatalytic activity is presented. The synthesis involves a two-step process: hydrothermal preparation of ZnO NPs followed by nonthermal plasma-assisted deposition of Au nanoparticles on their surface. Comprehensive characterization of the ZnO and ZnO–Au NPs was carried out using X-ray diffraction (XRD), transmission electron microscopy (TEM), scanning electron microscopy (SEM), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). Optical properties were evaluated via UV-Vis absorption and fluorescence measurements. The synthesized ZnO NPs displayed a hexagonal wurtzite structure, and the successful deposition of Au NPs was confirmed by TEM and XPS analysis, along with Raman and fluorescence data showing the quenching effect caused by Au. The incorporation of Au nanoparticles led to the appearance of localized surface plasmon resonance (LSPR) at 540 nm, enhancing visible light absorption and improving photocatalytic performance. Notably, the methylene blue (MB) degradation efficiency increased from 78% with pure ZnO NPs to 91.6% with ZnO–Au NPs under UV-Vis irradiation, demonstrating superior photocatalytic activity. This study introduces a simple and scalable method for synthesizing plasmonic ZnO-Au hybrid nanomaterials using plasma technology and highlights the critical role of Au NPs in enhancing photocatalytic performance by reducing electron–hole recombination. Full article

Bacterial infections and their increasing resistance to antibiotics pose a significant challenge in medical treatment. This study presents the synthesis and characterization of novel carbon dots (CDs) using levofloxacin (Lf), curcumin (Cur), and tea polyphenols (TP) through a facile hydrothermal method. The synthesized curcumin-tea polyphenol@carbon dots (Cur-TP@CDs) and levofloxacin-tea polyphenol@carbon dots (Lf-TP@CDs) were characterized using transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy, confirming their unique structural and chemical properties. Cur-TP@CDs exhibited an average particle size of 1.32 nanometers (nm), while Lf-TP@CDs averaged 1.58 nm. Both types demonstrated significant antibacterial activity, with Lf-TP@CDs showing superior effectiveness against Staphylococcus aureus (S. aureus) and Escherichia coli (E. coli) in broth dilution and disc diffusion assays. Biofilm inhibition assays revealed a significant reduction in biofilm formation at higher concentrations. The ultraviolet-visible (UV-vis) and photoluminescence (PL) spectral analyses indicated efficient photon emission, and electron paramagnetic resonance (EPR) analysis showed increased singlet oxygen generation, enhancing bactericidal effects. Live and dead bacterial staining followed by scanning electron microscopy (SEM) analysis confirmed dose-dependent bacterial cell damage and morphological deformities. These findings suggest that Cur-TP@CDs and Lf-TP@CDs are promising antibacterial agents, potentially offering a novel approach to combat antibiotic-resistant bacterial infections. Full article

In this work, Surface-Enhanced Raman Spectroscopy (SERS) was employed as an effective detection technique for folpet, characterized by its notable specificity and sensitivity. The investigation involved the use of UV–Vis, Raman, and SERS spectroscopy of folpet at different concentrations for a comprehensive study of plasmon-driven effects such as plasmon resonance, plasmon hybridization, and electric field enhancement resulting in the SERS’ intensification. Specifically, SERS detection of folpet solutions at concentrations below 100 µM is presented in detail by using Ag nanoparticles prepared with hydroxylamine reduction. The experimentation encompassed diverse conditions to optimize the detection process, with Raman spectra acquired for both folpet powder and aqueous solution of folpet at the natural pH. SERS analyses were conducted across a concentration range of 9.5 × 10⁻⁸ to 1.61 × 10⁻⁴ M, employing 532 nm excitation. The differences in the spectral profiles observed for folpet Raman powder and SERS are ascribed to N–S cleavage; these changes are attributed to plasmon catalysis induced by the used Ag nanoparticles. Transmission electron microscopy (TEM) was also important in the present analysis to better understand which mechanism of nanoparticles aggregation is more favorable for the SERS detection regarding the formation of hot spots in the suspension. Complementing the experimental data, the molecular structure and theoretical Raman spectra of the folpet molecule were calculated through density functional theory (DFT) methods. The outcomes of these calculations were crucial in the elucidation of folpet’s vibrational modes. The culmination of this research resulted in the successful detection of folpet, achieving a notable limit of detection at 4.78 × 10⁻⁸ M. This comprehensive approach amalgamates experimental and theoretical methodologies, offering significant insights into the detection capabilities and molecular characteristics of folpet via SERS analysis. Full article

Surface-enhanced Raman spectroscopy (SERS) is a promising and highly sensitive molecular fingerprint detection technology. However, the development of SERS nanocomposites that are label-free, highly sensitive, selective, stable, and reusable for gaseous volatile organic compounds (VOCs) detection remains a challenge. Here, we report a novel TiO₂NTs/AuNPs@ZIF−8 nanocomposite for the ultrasensitive SERS detection of VOCs. The three-dimensional TiO₂ nanotube structure with a large specific surface area provides abundant sites for the loading of Au NPs, which possess excellent local surface plasmon resonance (LSPR) effects, further leading to the formation of a large number of SERS active hotspots. The externally wrapped porous MOF structure adsorbs more gaseous VOC molecules onto the noble metal surface. Under the synergistic mechanism of physical and chemical enhancement, a better SERS enhancement effect can be achieved. By optimizing experimental conditions, the SERS detection limit for acetophenone, a common exhaled VOC, is as low as 10⁻¹¹ M. And the relative standard deviation of SERS signal intensity from different points on the same nanocomposite surface is 4.7%. The acetophenone gas achieves a 1 min response and the signal reaches stability in 4 min. Under UV irradiation, the surface-adsorbed acetophenone can be completely degraded within 40 min. The experimental results demonstrate that this nanocomposite has good detection sensitivity, repeatability, selectivity, response speed, and reusability, making it a promising sensor for gaseous VOCs. Full article

The identification and quantification of caffeine is a common need in the food and pharmaceutical industries and lately also in the field of environmental science. For that purpose, Raman spectroscopy has been used as an analytical technique, but the interpretation of the spectra requires reliable and accurate computational protocols, especially as regards the Resonance Raman (RR) variant. Herein, caffeine solutions are sampled using Molecular Dynamics simulations. Upon quantification of the strength of the non-covalent intermolecular interactions such as hydrogen bonding between caffeine and water, UV-Vis, Raman, and RR spectra are computed. The results provide general insights into the hydrogen bonding role in mediating the Raman spectral signals of caffeine in aqueous solution. Also, by analyzing the dependence of RR enhancement on the absorption spectrum of caffeine, it is proposed that the sensitivity of the RR technique could be exploited at excitation wavelengths moderately far from 266 nm, yet achieving very low detection limits in the quantification caffeine content. Full article