Size controlled green synthesis of gold nanoparticles using Coffea arabica seed extract and their catalytic performance in 4-nitrophenol reduction

被引:85
|
作者
Bogireddy, N. K. R. [1 ]
Pal, U. [2 ]
Martinez Gomez, L. [3 ]
Agarwal, V. [1 ]
机构
[1] UAEM, Ctr Invest Ingn & Ciencias Aplicadas, Av Univ 1001, Cuernavaca 62209, Morelos, Mexico
[2] Benemerita Univ Autonoma Puebla, Inst Fis, Apdo Postal J-48, Puebla 72570, Pue, Mexico
[3] Univ Nacl Autonoma Mexico, Inst Ciencias Fis, Ave Univ S-N, Cuernavaca 62210, Morelos, Mexico
关键词
ENHANCED PHOTOCATALYTIC ACTIVITY; SILVER NANOPARTICLES; ELECTRIC-FIELD; DEGRADATION; GROWTH; BLUE;
D O I
10.1039/c8ra04332a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Well crystalline gold nanoparticles (AuNPs) of different sizes were fabricated using sundried Coffea arabica seed (CAS) extract at room temperature by controlling the pH of the green extract. The size, shape and crystallinity of the nanoparticles have been studied using electron microscopy and X-ray diffraction. The presence of phenolic groups (revealed through FT-IR studies) from the CAS extract are responsible both for the reduction of Au ions and stabilization of the formed AuNPs. The efficiency of the CAS extract mediated green synthesis technique for the production of AuNPs has been compared to the conventional chemical Turkevich technique, which not only uses a toxic reductant such as NaBH4, but also operates around the boiling point of water. It has been observed that the CAS extract mediated synthesis process produces relatively bigger AuNPs at similar pH values of the reaction mixture in comparison to the AuNPs produced in the Turkevich process. Although the AuNPs synthesized using CAS extract are relatively larger and polydisperse in nature, their catalytic efficiencies for the degradation of an aromatic nitro compound (4-nitrophenol) are found to be comparable to the chemically fabricated AuNPs. Probable mechanisms associated with the formation of AuNPs and their size control in the CAS extract mediated green synthesis process have been discussed.
引用
收藏
页码:24819 / 24826
页数:8
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