Cu-Ag核壳纳米粒子的合成及其电化学表征

Laurencia G. Sutanto, Y. B. Cristian, Jihan N Adzijah, Imanda Widianti, P. K. Jiwanti
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引用次数: 0

摘要

以聚乙烯吡咯烷酮(PVP)为封盖剂,抗坏血酸(C6H8O6)和硼氢化钠(NaBH4)为还原剂,采用化学还原法制备了Cu-Ag核壳纳米粒子(Cu@Ag NPs)。Cu@Ag NPs分别以(Cu:Ag) 1:3、1:4和1:5的比例合成。通过粒度分析仪试验验证了三种变化Cu@Ag NPs样品的均匀性。在270 ~ 280 nm、300 ~ 304 nm和690 ~ 700 nm范围内依次得到Cu@Ag 1:3、1:4和1:5的尺寸。通过Cu@Ag 1:3、1:4和1:5的紫外-可见光谱可以看出Cu@Ag纳米颗粒的成功合成,分别在434 nm、450 nm和428 nm波长处形成AgNP。此外,Cu@Ag纳米颗粒的稳定性在0天、4天、7天、11天和14天内进行了测试。可以观察到,与1:3和1:4的变化相比,1:5的变化趋向于更稳定,因为图表继续经历显著的改进。然后用循环伏安法在0 ~ 1.8 V范围内进行电化学研究。结果表明,铜氧化峰出现在1.2 V电位处,银氧化峰出现在0.9 V电位处。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of Cu-Ag core-shell nanoparticles and its electrochemical characterization
The Cu-Ag core-shell nanoparticles (Cu@Ag NPs) are prepared by chemical reduction method with polyvinyl pyrrolidone (PVP) was used as a capping agent, ascorbic acid (C6H8O6) and sodium borohydride (NaBH4) was used as a reducing agent. Cu@Ag NPs were synthesized with three variations of (Cu:Ag) 1:3, 1:4, and 1:5.. The uniformity of Cu@Ag NPs samples with three variations was verified by the particle size analyzer test. The sizes of Cu@Ag 1:3, 1:4, and 1:5 was obtained sequentially at the range of 270-280 nm, 300-304 nm, and 690-700 nm respectively. Indications of the successful synthesis of Cu@Ag nanoparticles can be seen from UV-Vis spectra of Cu@Ag 1:3, 1:4, and 1:5 respectively forming AgNP at wavelengths of 434 nm, 450 nm, and 428 nm Furthermore, the stability of Cu@Ag NPs was carried out over a period of 0 days, 4 days, 7 days, 11 days, and 14 days. It can be observed that the variation of 1:5 tends to be more stable as the chart continues to experience significant improvements compared to the variation of 1:3 and 1:4. The electrochemical study was then performed by applying cyclic voltammetry from 0 V to 1.8 V. It is clearly shown that the peak of Cu oxidation is appeared at a potential of 1.2 V while the peak value of Ag oxidation is at a potential of 0.9 V.
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