1998
DOI: 10.1063/1.368849
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The Raman spectrum of Ti3SiC2

Abstract: In this paper, the Raman spectrum of Ti3SiC2 is reported and compared with that of TiC0.67. All the TiC0.67 first order Raman disorder-induced modes are active, but shifted, in Ti3SiC2. Two additional peaks at 150 and 372 cm−1 are observed in Ti3SiC2. The former is ascribed to a shear mode between the Si and Ti planes; the origin of the latter is unknown. No second order Raman bands are detected. Micro-Raman spectroscopy also reveal the presence of ≈50 Å graphite crystallites in samples hot pressed in graphite… Show more

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Cited by 139 publications
(71 citation statements)
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“…In order to further confirm the phase formation after brazing at variable temperatures, Raman spectrum measured on brazed diamond surface after removing Sn-Ti filler alloy was given in Fig.8. As shown in Fig.8 , TiC peaks at 250, 345, 430 and 609 cm -1 can be clearly observed, which is in a reasonable agreement with previous study using stoichiometric samples [26]. The small shift of TiC peaks is most likely due to varying C contents of TiC in samples brazed at different temperatures, because the Raman peaks is obtained from carbon vacancies in TiC [27].…”
Section: Implications For Integrity Of Brazed Diamond Gritssupporting
confidence: 79%
“…In order to further confirm the phase formation after brazing at variable temperatures, Raman spectrum measured on brazed diamond surface after removing Sn-Ti filler alloy was given in Fig.8. As shown in Fig.8 , TiC peaks at 250, 345, 430 and 609 cm -1 can be clearly observed, which is in a reasonable agreement with previous study using stoichiometric samples [26]. The small shift of TiC peaks is most likely due to varying C contents of TiC in samples brazed at different temperatures, because the Raman peaks is obtained from carbon vacancies in TiC [27].…”
Section: Implications For Integrity Of Brazed Diamond Gritssupporting
confidence: 79%
“…There are also three peaks at approximately 260, 420, and 605 cm −1 . These peaks are comparable to those reported by Klein et al and Amer et al 13,14 However, their work suggests that both the broad peaks at approximately 420 and 605 cm −1 are each the product of two separate overlapping peaks. The spectra for the commercial TiC powder, shown in Fig.…”
Section: Raman Spectroscopy Of As-received Ti C and Ticsupporting
confidence: 74%
“…The literature states that stoichiometric TiC has no Raman-active vibrational modes and that Raman scattering in TiC is due to disorder induced by carbon vacancies. 13,14 Klein et al 13 produced Raman spectra of TiC x , where x = 0.97, 0.90, and 0.80, while Amer et al 14 published a Raman spectrum of TiC 0.67 .…”
Section: Raman Spectroscopymentioning
confidence: 99%
“…Five peaks of TiC were observed at 360, 565, 670, 970 and 1075 cm -1 . The first three values show a fairly good agreement with the Raman spectrum of TiC 0.67 [18]. The differences may arise from the fact that the phase composition might not be the same.…”
Section: Chemical Propertiessupporting
confidence: 67%