Evidence of Electrochemical Graphene Functionalization by Raman Spectroscopy

2012 ◽  
Vol 717-720 ◽  
pp. 661-664 ◽  
Author(s):  
Kevin M. Daniels ◽  
Biplob K. Daas ◽  
Nishtha Srivastava ◽  
Christopher Williams ◽  
Randall M. Feenstra ◽  
...  

Electrochemical functionalization of treated epitaxial graphene samples on Si-face 6H-SiC are presented in this work. Three semi-insulating 6H-SiC substrates cut from different boules with varying off cut angle (on axis, 0.5° and 1.0° degrees off axis in the [112‾0] direction) were diced into 10mm x 10mm samples and quality EG grown on top. A home-build electrochemical cell was used with current applied though a 10% H2SO4 solution, with a Pt wire and exposed graphene as the anode and cathode respectively. Functionalization was determined using Raman spectroscopy and measured by an increase in D/G ratio, increase in fluorescence background and introduction of C-H bond peak at ~2930 cm-1. Components of the Raman spectra before and after functionalization of all samples used were analyzed to show a substrate dependent effect on functionalization with values such as D/G ratio and normalized fluorescence slope varying between the substrates.

2015 ◽  
Vol 821-823 ◽  
pp. 957-960
Author(s):  
Yan Fei Hu ◽  
Hui Guo ◽  
Yu Ming Zhang ◽  
Yi Men Zhang

Large-area epitaxial graphene formed on C-face SiC has been investigated by Raman Spectroscopy and SEM (scanning electron microscopy). Local Raman spectra showed a large homogeneous area of high quality epitaxial FLG (few layer graphene) has been fabricated on C-face SiC. Our work reveals unexpectedly the shift in Raman peak position across the samples resulting from the inhomogeneity in the strains and impurities of the graphene films, which we exhibit to be correlated with physical topography by combining Raman spectroscopy with scanning electron microscopy (SEM)


2014 ◽  
Vol 778-780 ◽  
pp. 1166-1169
Author(s):  
Felix Fromm ◽  
Martin Hundhausen ◽  
Michl Kaiser ◽  
Thomas Seyller

Raman spectroscopy is commonly applied for studying the properties of epitaxial graphene on silicon carbide (SiC). In principle, the Raman intensity of a single graphene layer is rather low compared to the signal of SiC. In this work we follow an approach to improve the Raman intensity of epitaxial graphene on SiC by recording Raman spectra in a top-down geometry, i.e. a geometry in which the graphene layer is probed with the excitation through the SiC substrate [1]. This technique takes advantage of the fact, that most of the Raman scattered light of the graphene is emitted into the SiC substrate. We analyze in detail the top-down measurement geometry regarding the graphene and SiC Raman intensity, as well as the influence of aberration effects caused by the refraction at the air/SiC interface.


2021 ◽  
Vol 2103 (1) ◽  
pp. 012055
Author(s):  
P E Timchenko ◽  
E V Timchenko ◽  
I V Bazhutova ◽  
O O Frolov ◽  
L T Volova ◽  
...  

Abstract The results of the research of enamel of periodontitis-affected teeth before and after open curettage are presented in the work. The Raman spectroscopy method was used as an evaluation method of curettage influence on tooth enamel. Chemometric analysis of the Raman spectra of tooth enamel before and after curettage was made. Spectral changes of tooth enamel were detected. It was found that after the procedure of open curettage spectral changes occur in tooth enamel related to the changes in mineral composition and organic matrix forming.


Author(s):  
Jay Anderson ◽  
Mustafa Kansiz ◽  
Michael Lo ◽  
Curtis Marcott

Abstract Failure analysis of organics at the microscopic scale is an increasingly important requirement, with traditional analytical tools such as FTIR and Raman microscopy, having significant limitations in either spatial resolution or data quality. We introduce here a new method of obtaining Infrared microspectroscopic information, at the submicron level in reflection (far-field) mode, called Optical-Photothermal Infrared (O-PTIR) spectroscopy, that can also generate simultaneous Raman spectra, from the same spot, at the same time and with the same spatial resolution. This novel combination of these two correlative techniques can be considered to be complimentary and confirmatory, in which the IR confirms the Raman result and vice-versa, to yield more accurate and therefore more confident organic unknowns analysis.


1994 ◽  
Vol 48 (7) ◽  
pp. 875-883 ◽  
Author(s):  
Daniel R. Lombardi ◽  
Chao Wang ◽  
Bin Sun ◽  
Augustus W. Fountain ◽  
Thomas J. Vickers ◽  
...  

Raman spectra have been measured for a number of nitrates, nitrites, sulfates, ferrocyanides, and ferricyanides, both in the solid phase and in aqueous solution. Accurate locations of peak maxima are given. Limits of detection for some of the compounds are given for solutions and for solid mixtures in NaNO3. Preliminary measurements have been made on core material recovered from the storage tanks on the Hanford site in Richland, Washington. Representative spectra are presented, showing that it is possible to observe responses of individual components from measurements made directly on untreated cores, with the use of a fiberoptic sampling probe.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Siti Norbaini Sabtu ◽  
S. F. Abdul Sani ◽  
L. M. Looi ◽  
S. F. Chiew ◽  
Dharini Pathmanathan ◽  
...  

AbstractThe epithelial-mesenchymal transition (EMT) is a crucial process in cancer progression and metastasis. Study of metabolic changes during the EMT process is important in seeking to understand the biochemical changes associated with cancer progression, not least in scoping for therapeutic strategies aimed at targeting EMT. Due to the potential for high sensitivity and specificity, Raman spectroscopy was used here to study the metabolic changes associated with EMT in human breast cancer tissue. For Raman spectroscopy measurements, tissue from 23 patients were collected, comprising non-lesional, EMT and non-EMT formalin-fixed and paraffin embedded breast cancer samples. Analysis was made in the fingerprint Raman spectra region (600–1800 cm−1) best associated with cancer progression biochemical changes in lipid, protein and nucleic acids. The ANOVA test followed by the Tukey’s multiple comparisons test were conducted to see if there existed differences between non-lesional, EMT and non-EMT breast tissue for Raman spectroscopy measurements. Results revealed that significant differences were evident in terms of intensity between the non-lesional and EMT samples, as well as the EMT and non-EMT samples. Multivariate analysis involving independent component analysis, Principal component analysis and non-negative least square were used to analyse the Raman spectra data. The results show significant differences between EMT and non-EMT cancers in lipid, protein, and nucleic acids. This study demonstrated the capability of Raman spectroscopy supported by multivariate analysis in analysing metabolic changes in EMT breast cancer tissue.


1982 ◽  
Vol 36 (4) ◽  
pp. 471-473 ◽  
Author(s):  
Klaus Witke

A sample cell for investigating suspensions or emulsions by Raman spectroscopy in the optically favorable 90° scattering arrangement is described. The Raman spectra of pyridine in a suspension of Aerosil 200 in carbon tetrachloride are recorded. The adsorption isotherm of pyridine is determined from the intensities of the Raman lines at 1008 and 990 cm−1. Over a long range of coverage a linear relationship exists between reciprocal concentrations of chemisorbed and dissolved molecules. The minimal surface area that is occupied by a chemisorbed molecule is determined to be approximately 0.75 nm2.


1981 ◽  
Vol 7 ◽  
Author(s):  
B.S. Elman ◽  
H. Mazurek ◽  
M.S. Dresselhaus ◽  
G. Dresselhaus

ABSTRACTRaman spectroscopy is used in a variety of ways to monitor different aspects of the lattice damage caused by ion implantation into graphite. Particular attention is given to the use of Raman spectroscopy to monitor the restoration of lattice order by the annealing process, which depends critically on the annealing temperature and on the extent of the original lattice damage. At low fluences the highly disordered region is localized in the implanted region and relatively low annealing temperatures are required, compared with the implantation at high fluences where the highly disordered region extends all the way to the surface. At high fluences, annealing temperatures comparable to those required for the graphitization of carbons are necessary to fully restore lattice order.


1954 ◽  
Vol 32 (5) ◽  
pp. 330-338 ◽  
Author(s):  
B. P. Stoicheff

An apparatus for obtaining intense Raman spectra of gases excited by the Hg 4358 line is described. It consists of a mirror-type Raman tube irradiated by two high-current mercury lamps, completely enclosed in a reflector of magnesium oxide. The lamps are externally water-cooled along their entire length and emit sharp lines of high intensity.Rotational Raman spectra of gases at a pressure of 1 atm. have been photographed in the second order of a 21 ft. grating in exposure times of 6 to 24 hr. The Raman lines are sharp and a resolving power of about 100,000 has been achieved. It will be possible to resolve the rotational Raman spectra, and hence to evaluate the rotational constants of molecules having moments of inertia of up to 300 × 10−10 gm. cm.2 Such investigations will be especially useful for non-polar molecules.


1999 ◽  
Vol 19 (1-4) ◽  
pp. 71-74 ◽  
Author(s):  
Xuming Zheng ◽  
David Lee Phillips

We have obtained A-band absorption resonance Raman spectra of 1-chloro-2- iodoethane in cyclohexane solution. We have done preliminary time-dependent wavepacket calculations to simulate the resonance Raman intensities and absorption spectrum in order to learn more about the short-time photodissociation dynamics. We compare our preliminary results for 1-chloro-2-iodoethane with previous resonance Raman results for iodoethane and find that there appears to be more motion along non- C—I stretch modes for 1-chloro-2-iodoethane than for iodoethane. This is consistent with results of TOF photofragment spectroscopy experiments which indicate much more internal excitation of the photoproducts from 1-chloro-2-iodoethane photodissociation than the photoproducts from iodoethane photodissociation.


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