scholarly journals Polarization Dependence of Low-Frequency Vibrations from Multiple Faces in an Organic Single Crystal

Crystals ◽  
2019 ◽  
Vol 9 (8) ◽  
pp. 425 ◽  
Author(s):  
Nemtsov ◽  
Aviv ◽  
Mastai ◽  
Tischler
Keyword(s):  
Raman Spectroscopy ◽  
Intermolecular Interactions ◽  
Signal Intensity ◽  
Structural Information ◽  
Low Frequency ◽  
Incident Beam ◽  
Optical Filters ◽  
Polarization Dependence ◽  
Raman Signal ◽  
Shear Modes

Recent developments in optical filters have enabled the facile use of Raman spectroscopy for detection of low frequency (LF) vibrational modes. LF-Raman spectroscopy offers fast and sensitive characterization of LF vibrations, and enables the measurement of single microcrystals and detection of defects. It is useful for probing intermolecular interactions in crystals, which are lower in energy, such as hydrogen bonds, shear modes, and breathing modes. Crystal excitation from multiple faces allows learning the orientation of intermolecular interactions, as polarization dependence varies with the polarizability of the interactions along the planes. Elucidating the orientations of the intermolecular interactions in organic crystals is essential for guiding the reactions or adsorption to a specific crystal face. In this study, we investigated the dependence of the LF-Raman signal intensity on the orientation of an organic single microcrystal of L-alanine. Three incident beam directions provided the orientations of the intermolecular interactions by analyzing the corresponding LF-Raman spectra. The signal intensity correlated well with the proximity between the incident beam’s direction and the orientations of the intermolecular interactions. Excellent compatibility was found between the spectra and simulated orientations based on structural information.

Laser-induced fluorescence (LIF) of lignin and lignin model compounds in Raman spectroscopy

Holzforschung ◽  
2013 ◽  
Vol 67 (5) ◽  
pp. 531-538 ◽  
Author(s):  
Anni Lähdetie ◽  
Paula Nousiainen ◽  
Jussi Sipilä ◽  
Tarja Tamminen ◽  
Anna-Stiina Jääskeläinen
Keyword(s):  
Raman Spectroscopy ◽  
Structural Information ◽  
Laser Induced Fluorescence ◽  
Excitation Wavelength ◽  
Raman Signal ◽  
Model Compounds ◽  
Worst Case ◽  
Lignin Model Compounds ◽  
Key Factor ◽  
Lignin Model

Abstract Raman spectroscopy is a technique that provides structural information on lignin and other components of wood and pulp in situ. However, especially lignin-containing samples may produce laser-induced fluorescence (LIF) that overlaps with Raman bands. In the worst case, this background signal can overwhelm the weaker Raman signal completely. In this study, the LIF of lignin was investigated with the excitation wavelength 532 nm applied in Raman spectroscopy to clarify the correlations between lignin structure and LIF intensity. Raman spectroscopic analyses with lignin model compounds illustrated that the 5-5′ structures induce LIF. It was also shown that the intensity of LIF was significantly less intense when the 5-5′ model compound was structurally rigid (as in dibenzodioxocin) compared with the flexible simple counterpart. The comparison between the free phenolic model compounds with the methylated analogue showed that the presence of the free phenolic structure was not a prerequisite for LIF. It was thus concluded that the conformation of the molecule is the key factor with respect to fluorescence. The role of conformational aspects was further investigated by comparing wood with chemical pulps and isolated lignins.

scholarly journals Barium Titanium Oxynitride from Ammonia-Free Nitridation of Reduced BaTiO3

Inorganics ◽  
2021 ◽  
Vol 9 (8) ◽  
pp. 62
Author(s):  
Hua Guo ◽  
Aleksander Jaworski ◽  
Zheng Chen ◽  
Can Lu ◽  
Adam Slabon ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
Nmr Spectroscopy ◽  
Transition Metal ◽  
Signal Intensity ◽  
Diffuse Reflectance ◽  
Conduction Band Edge ◽  
Vacancy Ordering ◽  
Vis Spectroscopy ◽  
O Vacancy ◽  
Barium Titanium

We investigated the nitridation of reduced BaTiO3, BaTiO2.60H0.08, corresponding to an oxyhydride with a large concentration of O defects (>10%). The material is readily nitrided under flowing N2 gas at temperatures between 400 and 450 °C to yield oxynitrides BaTiO2.6Nx (x = 0.2−0.22) with a slightly tetragonally distorted perovskite structure, a ≈ 4.01 and c ≈ 4.02 Å, and Ti partially remaining in the oxidation state III. The tetragonal structure was confirmed from Raman spectroscopy. 14N MAS NMR spectroscopy shows a single resonance at 270 ppm, which is typical for perovskite transition metal oxynitrides. However, largely different signal intensity for materials with very similar N content suggests N/O/vacancy ordering when prolonging nitridation times to hours. Diffuse reflectance UV-VIS spectroscopy shows a reduction of the intrinsic band gap to 2.4–2.45 eV compared to BaTiO3 (~3.2 eV). Mott-Schottky measurements confirm n-type conductivity and reveal a slight negative shift of the conduction band edge from –0.59 V (BaTiO3) to ~–0.65 eV.

scholarly journals Rapid uropathogen identification using surface enhanced Raman spectroscopy active filters

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Simon D. Dryden ◽  
Salzitsa Anastasova ◽  
Giovanni Satta ◽  
Alex J. Thompson ◽  
Daniel R. Leff ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
Bacterial Infections ◽  
Surface Enhanced Raman Spectroscopy ◽  
Active Filters ◽  
Raman Signal ◽  
Rapid Diagnostics ◽  
Bacterial Classification ◽  
Surface Enhanced ◽  
Surface Enhanced Raman

AbstractUrinary tract infection is one of the most common bacterial infections leading to increased morbidity, mortality and societal costs. Current diagnostics exacerbate this problem due to an inability to provide timely pathogen identification. Surface enhanced Raman spectroscopy (SERS) has the potential to overcome these issues by providing immediate bacterial classification. To date, achieving accurate classification has required technically complicated processes to capture pathogens, which has precluded the integration of SERS into rapid diagnostics. This work demonstrates that gold-coated membrane filters capture and aggregate bacteria, separating them from urine, while also providing Raman signal enhancement. An optimal gold coating thickness of 50 nm was demonstrated, and the diagnostic performance of the SERS-active filters was assessed using phantom urine infection samples at clinically relevant concentrations (105 CFU/ml). Infected and uninfected (control) samples were identified with an accuracy of 91.1%. Amongst infected samples only, classification of three bacteria (Escherichia coli, Enterococcus faecalis, Klebsiella pneumoniae) was achieved at a rate of 91.6%.

Sampling unit for efficient signal detection and application to liquid chromatography-Raman spectroscopy

2021 ◽  
Author(s):  
Yu-Hao Lo ◽  
Shu-Chi Li ◽  
Hirotsugu Hiramatsu
Keyword(s):  
Raman Spectroscopy ◽  
Liquid Chromatography ◽  
Signal Detection ◽  
Signal Intensity ◽  
Sampling Unit ◽  
Raman Spectrometer ◽  
Unit Design

A new sampling unit design enhances the signal intensity and is available to combine Raman spectrometer with liquid chromatography.

scholarly journals Fabrication-friendly polarization-sensitive plasmonic grating for optimal surface-enhanced Raman spectroscopy

2020 ◽  
Vol 16 (1) ◽  
Author(s):  
Arpan Dutta ◽  
Tarmo Nuutinen ◽  
Khairul Alam ◽  
Antti Matikainen ◽  
Peng Li ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
Fill Factor ◽  
Surface Enhanced Raman Spectroscopy ◽  
Transverse Magnetic ◽  
Raman Signal ◽  
Optical Resonance ◽  
Excitation Light ◽  
Surface Enhanced ◽  
Surface Enhanced Raman ◽  
Plasmonic Gratings

Abstract Plasmonic nanostructures are widely utilized in surface-enhanced Raman spectroscopy (SERS) from ultraviolet to near-infrared applications. Periodic nanoplasmonic systems such as plasmonic gratings are of great interest as SERS-active substrates due to their strong polarization dependence and ease of fabrication. In this work, we modelled a silver grating that manifests a subradiant plasmonic resonance as a dip in its reflectivity with significant near-field enhancement only for transverse-magnetic (TM) polarization of light. We investigated the role of its fill factor, commonly defined as a ratio between the width of the grating groove and the grating period, on the SERS enhancement. We designed multiple gratings having different fill factors using finite-difference time-domain (FDTD) simulations to incorporate different degrees of spectral detunings in their reflection dips from our Raman excitation (488 nm). Our numerical studies suggested that by tuning the spectral position of the optical resonance of the grating, via modifying their fill factor, we could optimize the achievable SERS enhancement. Moreover, by changing the polarization of the excitation light from transverse-magnetic to transverse-electric, we can disable the optical resonance of the gratings resulting in negligible SERS performance. To verify this, we fabricated and optically characterized the modelled gratings and ensured the presence of the desired detunings in their optical responses. Our Raman analysis on riboflavin confirmed that the higher overlap between the grating resonance and the intended Raman excitation yields stronger Raman enhancement only for TM polarized light. Our findings provide insight on the development of fabrication-friendly plasmonic gratings for optimal intensification of the Raman signal with an extra degree of control through the polarization of the excitation light. This feature enables studying Raman signal of exactly the same molecules with and without electromagnetic SERS enhancements, just by changing the polarization of the excitation, and thereby permits detailed studies on the selection rules and the chemical enhancements possibly involved in SERS.

scholarly journals Laser Raman Spectroscopy with Different Excitation Sources and Extension to Surface Enhanced Raman Spectroscopy

2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Md. Wahadoszamen ◽  
Arifur Rahaman ◽  
Nabil Md. Rakinul Hoque ◽  
Aminul I Talukder ◽  
Kazi Monowar Abedin ◽  
...  
Keyword(s):  
Raman Spectroscopy ◽  
Silver Nanoparticles ◽  
Rhodamine 6G ◽  
Detection Efficiency ◽  
Colloidal Suspension ◽  
Surface Enhanced Raman Spectroscopy ◽  
Laser Raman Spectroscopy ◽  
Raman Signal ◽  
Fluorescence Signal ◽  
Present System

A dispersive Raman spectrometer was used with three different excitation sources (Argon-ion, He-Ne, and Diode lasers operating at 514.5 nm, 633 nm, and 782 nm, resp.). The system was employed to a variety of Raman active compounds. Many of the compounds exhibit very strong fluorescence while being excited with a laser emitting at UV-VIS region, hereby imposing severe limitation to the detection efficiency of the particular Raman system. The Raman system with variable excitation laser sources provided us with a desired flexibility toward the suppression of unwanted fluorescence signal. With this Raman system, we could detect and specify the different vibrational modes of various hazardous organic compounds and some typical dyes (both fluorescent and nonfluorescent). We then compared those results with the ones reported in literature and found the deviation within the range of ±2 cm−1, which indicates reasonable accuracy and usability of the Raman system. Then, the surface enhancement technique of Raman spectrum was employed to the present system. To this end, we used chemically prepared colloidal suspension of silver nanoparticles as substrate and Rhodamine 6G as probe. We could observe significant enhancement of Raman signal from Rhodamine 6G using the colloidal solution of silver nanoparticles the average magnitude of which is estimated to be 103.

The Generation of a Carbon Nanotube- Cyclodextrin Complex

2001 ◽  
Vol 703 ◽  
Author(s):  
G.F. Farrell ◽  
G. Chambers ◽  
A.B Dalton ◽  
E. Cummins ◽  
M. McNamara ◽  
...  
Keyword(s):  
Carbon Nanotubes ◽  
Aqueous Solution ◽  
Raman Spectroscopy ◽  
Carbon Nanotube ◽  
Intermolecular Interaction ◽  
Intermolecular Interactions ◽  
Small Diameter ◽  
Cyclodextrin Complex ◽  
Yellow Solution ◽  
Single Wall Nanotubes

ABSTRACTIn this study the intermolecular interactions of small diameter (∼0.7nm) carbon nanotubes and γ-cyclodextrin were examined. Four samples of γ cyclodextrin and HiPco carbon nanotubes were prepared. The first, by grinding the tubes and the cyclodextrin (1:30 ratio) together in a dry mixture, the second was prepared in a similar fashion but was ground in the presence of water (1ml). Finally an aqueous solution of γ-cyclodextrin (0.3M) and HiPco carbon nanotubes (5mg) was prepared by refluxing for ∼100 hours, forming a pale yellow solution from which a number of crystals were produced, both the solution and the recrystallised material were analysed. The samples were analysed using UV-Vis-NIR and Raman spectroscopy. The results presented are the first spectroscopic evidence of an intermolecular interaction between γ-cyclodextrin and single wall nanotubes.

Raman Spectroscopy for the Study of XVI-XVII Centuries Colonial Paintings

2014 ◽  
Vol 1618 ◽  
pp. 141-151 ◽  
Author(s):  
Ma. A. García-Bucio ◽  
E. Casanova-González ◽  
J. L. Ruvalcaba-Sil
Keyword(s):  
Raman Spectroscopy ◽  
San Francisco ◽  
Reference Materials ◽  
Analytical Techniques ◽  
Surface Enhanced Raman Spectroscopy ◽  
Raman Signal ◽  
Invasive Approach ◽  
Full Characterization ◽  
Surface Enhanced Raman ◽  
Historical Objects

ABSTRACTOutstanding information about the material composition and pictorial techniques of the New Spain Colonial painting can be obtained via a full characterization using a set of analytical techniques. Given the cultural importance of this painting, a non-invasive approach is preferred. Moreover, the preparation and use of reference materials using original recipes is necessary for a correct interpretation of the spectroscopic data from historical objects. Here, we present the results obtained via an in-situ Raman spectroscopic analysis of a set of pictorial reference materials, created according to XVI and XVII centuries’ recipes. Several difficulties were encountered, such as the low Raman detection signal, an intrinsic fluorescence of the material, and in some cases even laser-induced degradation. For this reason, the usual molecular Raman analysis was extended to Surface Enhanced Raman Spectroscopy (SERS), which enhances the Raman signal and quenches the fluorescence. It was then applied to the analysis of two wood paintings from the ex-convent San Francisco Tepeyanco, in Tlaxcala.

scholarly journals Current and Future Advancements of Raman Spectroscopy Techniques in Cancer Nanomedicine

2021 ◽  
Vol 22 (23) ◽  
pp. 13141
Author(s):  
Elisabetta Canetta
Keyword(s):  
Raman Spectroscopy ◽  
Imaging Techniques ◽  
Rapid Development ◽  
Surface Enhanced Raman Spectroscopy ◽  
Cancer Diagnostics ◽  
Raman Signal ◽  
Therapeutic Effects ◽  
Cancer Nanomedicine

Raman scattering is one of the most used spectroscopy and imaging techniques in cancer nanomedicine due to its high spatial resolution, high chemical specificity, and multiplexity modalities. The flexibility of Raman techniques has led, in the past few years, to the rapid development of Raman spectroscopy and imaging for nanodiagnostics, nanotherapy, and nanotheranostics. This review focuses on the applications of spontaneous Raman spectroscopy and bioimaging to cancer nanotheranostics and their coupling to a variety of diagnostic/therapy methods to create nanoparticle-free theranostic systems for cancer diagnostics and therapy. Recent implementations of confocal Raman spectroscopy that led to the development of platforms for monitoring the therapeutic effects of anticancer drugs in vitro and in vivo are also reviewed. Another Raman technique that is largely employed in cancer nanomedicine, due to its ability to enhance the Raman signal, is surface-enhanced Raman spectroscopy (SERS). This review also explores the applications of the different types of SERS, such as SERRS and SORS, to cancer diagnosis through SERS nanoprobes and the detection of small-size biomarkers, such as exosomes. SERS cancer immunotherapy and immuno-SERS (iSERS) microscopy are reviewed.

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