F. F. Bentley

Bio: F. F. Bentley is an academic researcher from Wright-Patterson Air Force Base. The author has contributed to research in topics: Infrared spectroscopy & Far infrared. The author has an hindex of 15, co-authored 29 publications receiving 1946 citations.

Infrared and Raman Selection Rules for Lattice Vibrations: The Correlation Method:

Abstract: With the recent growth in interest in the ir and Raman spectra of crystals, it has become very important to know which vibrational modes are optically active Hornig, Winston and Halford, and Bhagavantam and Venkatarayudu pioneered in developing methods for this However, heretofore the determination has been a laborious procedure fraught with difficulty and with many points of indecision Among the latter is the choice of the primitive cell and the correct site symmetry of each atom What is needed is a short, straightforward, foolproof method We propose here an alternate procedure for obtaining the activity of the vibrations from the correlation tables which comes close to meeting these goals The calculation is reduced to but a few minutes' work The method will be explained in detail by use of numerous examples

Raman spectroscopy of amorphous, nanostructured, diamond-like carbon, and nanodiamond

Abstract: Raman spectroscopy is a standard characterization technique for any carbon system. Here we review the Raman spectra of amorphous, nanostructured, diamond-like carbon and nanodiamond. We show how to use resonant Raman spectroscopy to determine structure and composition of carbon films with and without nitrogen. The measured spectra change with varying excitation energy. By visible and ultraviolet excitation measurements, the G peak dispersion can be derived and correlated with key parameters, such as density, sp(3) content, elastic constants and chemical composition. We then discuss the assignment of the peaks at 1150 and 1480 cm(-1) often observed in nanodiamond. We review the resonant Raman, isotope substitution and annealing experiments, which lead to the assignment of these peaks to trans-polyacetylene.

Raman spectroscopy on amorphous carbon films

Abstract: The origin and interpretation of the Raman features of amorphous (hydrogenated) carbonfilmsdeposited at room temperature in the region of 1000–1700 cm−1 is discussed in this paper. Possible interpretations of the linewidths, positions of the ‘‘G’’ graphite peak and ‘‘D’’ disordered peak, and their intensity ratios are examined using results obtained from magnetron sputtered and magnetic field enhanced plasmadepositedfilms. It is shown that even small ‘‘clusters’’ of condensed benzene rings (cluster size below 20 A) in carbonfilms can explain the observed Raman scattering. Besides the care that should be taken in the correct interpretation of Raman results, the utility of Raman scattering in obtaining an estimate of cluster sizes in amorphous (hydrogenated) carbonfilms is discussed. Carbonfilms prepared by magnetron sputtering show two additional Raman features at 1180 and 1490 cm−1 in addition to the G and D peaks. It is shown that a correlation exists between the 1180 cm−1 peak and the sp 3 content in the films.

Normal mode determination in crystals

Abstract: The group theoretical methods by which the symmetries of normal modes in crystals may be determined are outlined, and a series of tables are presented to facilitate rapid determination of the selection rules for vibrational transitions. Emphasis is placed on the method of nuclear site group analysis in which the number of infrared and Raman active modes of each symmetry may be obtained without detailed analysis of the symmetry elements in the crystallographic unit cell or the construction of tables. By using the tables presented here for most cases identification of the crystallographic space group is sufficient information to allow determination of the vibrational mode selection rules by inspection. Several examples are included in which crystals are analyzed by each of the methods.

Near-infrared Raman spectroscopy for optical diagnosis of lung cancer

Abstract: Raman spectroscopy is a vibrational spectroscopic technique that can be used to optically probe the molecular changes associated with diseased tissues. The objective of our study was to explore near-infrared (NIR) Raman spectroscopy for distinguishing tumor from normal bronchial tissue. Bronchial tissue specimens (12 normal, 10 squamous cell carcinoma (SCC) and 6 adenocarcinoma) were obtained from 10 patients with known or suspected malignancies of the lung. A rapid-acquisition dispersive-type NIR Raman spectroscopy system was used for tissue Raman studies at 785 nm excitation. High-quality Raman spectra in the 700-1,800 cm(-1) range from human bronchial tissues in vitro could be obtained within 5 sec. Raman spectra differed significantly between normal and malignant tumor tissue, with tumors showing higher percentage signals for nucleic acid, tryptophan and phenylalanine and lower percentage signals for phospholipids, proline and valine, compared to normal tissue. Raman spectral shape differences between normal and tumor tissue were also observed particularly in the spectral ranges of 1,000-1,100, 1,200-1,400 and 1,500-1,700 cm(-1), which contain signals related to protein and lipid conformations and nucleic acid's CH stretching modes. The ratio of Raman intensities at 1,445 to 1,655 cm(-1) provided good differentiation between normal and malignant bronchial tissue (p < 0.0001). The results of this exploratory study indicate that NIR Raman spectroscopy provides significant potential for the noninvasive diagnosis of lung cancers in vivo based on the optic evaluation of biomolecules.