1968
DOI: 10.1021/j100858a031
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Raman spectroscopy of sulfur, sulfur-selenium, and sulfur-arsenic mixtures

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Cited by 312 publications
(198 citation statements)
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“…The mode at 490 cm -1 corresponds to S S  vibrations possibly in S 8 rings [38][39][40][41][42] or rather in covalent S 2 groups (S -S disulfide bonds) [34,43]. The very weak mode at 205 cm -1 is in accordance with the ab-initio calculated Raman peak at 211 and 212 cm -1 for SGe 3 -S 6/3 cluster in g-GeS 2 [44].…”
supporting
confidence: 68%
“…The mode at 490 cm -1 corresponds to S S  vibrations possibly in S 8 rings [38][39][40][41][42] or rather in covalent S 2 groups (S -S disulfide bonds) [34,43]. The very weak mode at 205 cm -1 is in accordance with the ab-initio calculated Raman peak at 211 and 212 cm -1 for SGe 3 -S 6/3 cluster in g-GeS 2 [44].…”
supporting
confidence: 68%
“…2). The peaks at 193, 232, 330-340 and 493 cm −1 are assigned to various As-S vibrational modes and specifically, the broad peak centered at 340 cm −1 strongly indicates an amorphous arsenic sulfide, or artificial orpiment (g-As 2 S 3 or g-As x S x ) [24][25][26][27][28]. The peak centered at 471 cm −1 is characteristic of free sulfur.…”
Section: Resultsmentioning
confidence: 99%
“…4b. Sulfur shows a series of typical Raman peaks which can be assigned to the S-S bond [32], however, such typical sulfur peaks disappeared in the OMCF-S, indicating that sulfur is successfully embedded into the pores of the OMCF.…”
Section: Resultsmentioning
confidence: 99%