1995
DOI: 10.1016/0022-3093(95)00280-4
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Properties and structure of RONa2OAl2O3P2O5 (R = Mg, Ca, Sr, Ba) glasses

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Cited by 103 publications
(57 citation statements)
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“…[24][25][26][27] The band near 1280 cm À1 is assigned to the asymmetric stretching mode of the two non-bridging oxygen atoms bonded to phosphorus atoms in the Q 2 tetrahedral sites, n as (PO 2 ) À ; the shoulder at 1180 cm À1 is assigned to the symmetric stretch of the same structural unit, n s (PO 2 ) À . The absorption bands near 1100 and 1000 cm À1 are assigned to the asymmetric and symmetric stretching modes of chain-terminating Q 1 groups (n as (PO 3 ) 2À and n s (PO 3 ) 2À ), respectively.…”
Section: Vibrational Spectroscopymentioning
confidence: 99%
See 1 more Smart Citation
“…[24][25][26][27] The band near 1280 cm À1 is assigned to the asymmetric stretching mode of the two non-bridging oxygen atoms bonded to phosphorus atoms in the Q 2 tetrahedral sites, n as (PO 2 ) À ; the shoulder at 1180 cm À1 is assigned to the symmetric stretch of the same structural unit, n s (PO 2 ) À . The absorption bands near 1100 and 1000 cm À1 are assigned to the asymmetric and symmetric stretching modes of chain-terminating Q 1 groups (n as (PO 3 ) 2À and n s (PO 3 ) 2À ), respectively.…”
Section: Vibrational Spectroscopymentioning
confidence: 99%
“…The band close to 1100 cm À1 has a component at 1150 cm À1 assigned to Q 1 end groups associated with Na þ ions. [25] The absorption band near 900 cm À1 is assigned to the asymmetric stretching modes of the P-O-P linkages, n as (P-O-P), and the bands at 770 and 720 cm À1 assigned to the symmetric stretching modes of these linkages, n s (P-O-P). The broad absorption around 540 cm À1 is attributed to O-P-O deformation modes.…”
Section: Vibrational Spectroscopymentioning
confidence: 99%
“…The absorption bands have been assigned according to the literature. [23][24][25][26] assigned to the asymmetric stretching modes of the P-O-P linkages,  as (P-O-P), and the partially split band centred around 750 cm −1 is assigned to the symmetric stretching modes of these linkages,  s (P-O-P). The peak at 540 cm −1 is attributed to OPO deformation modes.…”
Section: Ftir Spectroscopymentioning
confidence: 99%
“…The two bands appeared at 2922 and 2372 cm −1 are related to ethylene glycol which adsorbed on the surface of samples during the smoothing process. The absorption band appeared at 1269 cm −1 corresponding to a P = O vibration band [29], the ‫ע‬ as (PO 2 ) -asymmetric stretching vibrations at 1170 cm −1 [30], the ν as (PO 3 ) asymmetric stretching mode at 1079 cm −1 , the ν s (PO 3 ) symmetric stretching mode at 974 cm −1 [31], the ν as (P-O-P) groups at 906 cm -1 , the ν s (P-O-P) groups at 775 cm −1 and 731 cm −1 [32] and the band at 506 cm −1 due to the deformation mode of (P-O -) groups [33] overlapped with the third longitudinal optical phonon (3LO) of CdTe. There are some differences between the infrared absorption bands for S1 and S2 samples which reflect some important information about the effect of adding ZnO to the glass matrix.…”
Section: Resultsmentioning
confidence: 99%