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| dc.contributor.author | 
Nouicer, Z. | 
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| dc.contributor.author | 
Hioul, M.L. | 
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| dc.date.accessioned | 
2022-12-25T16:38:20Z | 
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| dc.date.available | 
2022-12-25T16:38:20Z | 
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| dc.date.issued | 
2016-12-15 | 
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| dc.identifier.uri | 
http://depot.umc.edu.dz/handle/123456789/13849 | 
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| dc.description.abstract | 
In this work, Ag/SiO2 composites were studied for various silver contents (2.5, 5, 7.5 and10% wt). In a first step, Ag+ ions were adsorbed on silica by ionic exchange. In a secondstep, the samples were annealedin air at several temperatures (100-700° C). Several experimentaltechniques (SEM, XRD, FTIR, UV-Visible) were used to characterizethe samples. 
After ionic exchange, XRD revealed the presence of several silicate phases (Ag2Si2O5; Ag2SiO3 andAg3Si). After heat treatment, for a 5% wt Ag content, silver silicates (Ag4SiO4; Ag6Si2O7; Ag10Si4O13) and Ag phase were identified by XRD. All of the observed phases were nanosized. 
FTIR spectraof Ag/SiO2presentfivebandsin the region400 to 2000cm-1assigned to thevibration of Si-O-Si, Ag-O, Ag-SO4, Si-O andSi-OH groups.The increaseofthesilvercontentcausesan overlap ofSi-O andSi-OH peaks. A shift of the FTIRspectrumtoward the lowwave numberswas observedafter annealing at200° C.For highertemperatures(300-700° C), thespectrumwas moved inthe opposite direction.This correlates withthe formation of silver nanoparticles. 
TheUV-visibleabsorptionspectrumof Ag/SiO2nanocomposites presentes awideband situated between 300 to370 nm. This absorptionwas attributed to thesurface plasmonresonance of Agn clusters. After heat treatment, a shiftof this bandtotheblueisobserved, which correlates with the formation of larger silver nanoparticles. | 
fr_FR | 
| dc.language.iso | 
en | 
fr_FR | 
| dc.publisher | 
Université Frères Mentouri - Constantine 1 | 
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| dc.subject | 
Nanocomposites | 
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| dc.subject | 
Silver | 
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| dc.subject | 
Silica | 
fr_FR | 
| dc.subject | 
SiO2 | 
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| dc.subject | 
Ag/SiO2 | 
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| dc.title | 
Structural and optical properties of Ag/Si02 nanocomposites | 
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| dc.type | 
Article | 
fr_FR | 
             
        
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