Laurencia G. Sutanto, Y. B. Cristian, Jihan N Adzijah, Imanda Widianti, P. K. Jiwanti
{"title":"Cu-Ag核壳纳米粒子的合成及其电化学表征","authors":"Laurencia G. Sutanto, Y. B. Cristian, Jihan N Adzijah, Imanda Widianti, P. K. Jiwanti","doi":"10.20473/jatm.v2i1.43717","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":384259,"journal":{"name":"Journal of Advanced Technology and Multidiscipline","volume":"20 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of Cu-Ag core-shell nanoparticles and its electrochemical characterization\",\"authors\":\"Laurencia G. Sutanto, Y. B. Cristian, Jihan N Adzijah, Imanda Widianti, P. K. Jiwanti\",\"doi\":\"10.20473/jatm.v2i1.43717\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":384259,\"journal\":{\"name\":\"Journal of Advanced Technology and Multidiscipline\",\"volume\":\"20 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-05-31\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Advanced Technology and Multidiscipline\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.20473/jatm.v2i1.43717\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Advanced Technology and Multidiscipline","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.20473/jatm.v2i1.43717","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.