2019
DOI: 10.1016/j.vibspec.2019.05.003
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FTIR and Raman spectroscopy studies of ZnO-doped BaO⋅2B2O3 glass matrix

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Cited by 43 publications
(7 citation statements)
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“…In addition, only a weak peak appeared when the BaO concentration was 9 mol%. The bands at 950 and 1200–1500 cm −1 were attributed to the B–O − symmetric stretching vibration of orthoborate groups and the B–O − vibrations of orthoborate anions or pyroborate groups, 20–22 respectively. As shown in Figure 1A, the peak shifts around 950 cm −1 were increased, and the band at 1200–1500 cm −1 center moved toward more energetic vibrations, which can be explained that B–O − vibration enhancement can compensate for the decrease of the characteristic bands at 793 [BO 4 ] and 855 cm −1 [SiO 4 ] 19,20 .…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In addition, only a weak peak appeared when the BaO concentration was 9 mol%. The bands at 950 and 1200–1500 cm −1 were attributed to the B–O − symmetric stretching vibration of orthoborate groups and the B–O − vibrations of orthoborate anions or pyroborate groups, 20–22 respectively. As shown in Figure 1A, the peak shifts around 950 cm −1 were increased, and the band at 1200–1500 cm −1 center moved toward more energetic vibrations, which can be explained that B–O − vibration enhancement can compensate for the decrease of the characteristic bands at 793 [BO 4 ] and 855 cm −1 [SiO 4 ] 19,20 .…”
Section: Resultsmentioning
confidence: 99%
“…At present, the sintering temperature of the copper terminal electrode paste is between 750 and 850 • C. The wetting performance was monitored by a high-temperature microscope with increasing temperature up to 800 • C at 10 • C/min. [16][17][18][19][20][21][22][23][24][25][26][27][28][29][30][31] Figure 4 summarizes the results of the status of the glass powder pile during the 400-800 • C sintering process and the contact angle at 800 • C was recorded, which decreased with increasing BaO content.…”
Section: Effect Of Bao Doping On Sintering Wettabilitymentioning
confidence: 99%
“…The broad bands observed at 1620 and 1384 cm –1 for Co–ZnO–N/C are due to symmetric and antisymmetric stretching vibration modes of C–O, whereas for ZnO–N/C, the peaks are observed at 1616 and 1392 cm –1 . In the higher spectral region, the strong and broad bands at 3423 cm –1 (Co–ZnO–N/C) and 3429 cm –1 (ZnO–N/C) are attributed to the stretching vibrations of the hydroxyl (OH) residues. …”
Section: Resultsmentioning
confidence: 99%
“…The 667 cm -1 wavenumber was caused by the vibrations of TeO3/TeO6 units, whereas the peak was caused by the bending vibrations of the Te-O-Te linkage [11]. The located 1006 cm -1 is the vibration of Ba-O units banding [10], and the band after 2024 cm -1 corresponds to the vibration of the OH group [12], as shown in Table 2 The vibration of Ba-O units banding.…”
Section: Ftirmentioning
confidence: 98%
“…Significant vibrational bands are visible in the spectra at 584, 667, 1006, 2024, 2168, and 2359 cm -1 . The band located about 584 cm -1 is the Zn-O bonds' stretching vibrations and oscillations of the ZnO units bending [10]. The 667 cm -1 wavenumber was caused by the vibrations of TeO3/TeO6 units, whereas the peak was caused by the bending vibrations of the Te-O-Te linkage [11].…”
Section: Ftirmentioning
confidence: 98%