Synthesis and Characterization of Ag/SiO2 Nanocomposite Based on Rice Husk Silica Using Sol-Gel Method

被引:0
|
作者
Junaidi [1 ,2 ]
Sulistiani, Wiwin [1 ]
Efridahniar, Yessi [1 ]
Pratiwi, Indah [1 ]
Firdaus, Iqbal [1 ]
Manurung, Posman [1 ]
Karo, Pulung Karo [1 ]
机构
[1] Univ Lampung, Fac Math & Nat Sci, Dept Phys, Bandar Lampung 35145, Indonesia
[2] Univ Lampung, Dept Phys, Intrumentat Res Grp, Bandar Lampung 35145, Indonesia
关键词
silver; silica; rice husk; Uv-Vis; FTIR; XRD; SEM-EDX; SILVER NANOPARTICLES;
D O I
10.4028/p-54swgk
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this study, silver-silica (Ag/SiO2) was synthesized using the sol-gel method by silica from rice husks. Silica derived from rice husk waste was previously synthesized using the sol-gel method. In addition, the Ag material used in this study was also performed into silver nanoparticles (AgNPs). This method was chosen to obtain an Ag/SiO2 composite with nano size and high purity. AgNPs were synthesized using silver nitrate (AgNO3) by reduction method at 90 oC. The reducing agent and stabilizer used is trisodium citrate. UV-Vis, FTIR, XRD, and SEM-EDX were used to analyze Ag/SiO2 composites. Uv-Vis analysis results Ag/SiO2 has an absorption peak at a wavelength of 412 nm with a bandgap energy of 2.25 eV. These peaks indicate that AgNPs have formed in the SiO2 membrane. The FTIR results revealed the Si-O-Si bonds which indicated the presence of silica and the Ag-O functional group, and the presence of AgNPs. The results of XRD analysis showed that the silica structure formed was cristobalite and silver crystals in the face center cubic (fcc) shape. The results of the SEM-EDX morphological analysis showed that the Ag/SiO2 nanocomposite was shaped like sharp stone chips and the presence of small granules (granules) with different particle sizes and shapes, slightly porous and the composition of the compounds in the Ag/SiO2 nanocomposite indicated the presence of various chemical elements in the sample, including carbon, oxygen, sodium, silica, and silver.
引用
收藏
页码:31 / 42
页数:12
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