کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4907780 | 1426576 | 2017 | 10 صفحه PDF | دانلود رایگان |
عنوان انگلیسی مقاله ISI
Differentiated interactions in phosphate solutions: Comparing Ag(111) and Ag(100) surfaces
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کلمات کلیدی
موضوعات مرتبط
مهندسی و علوم پایه
مهندسی شیمی
مهندسی شیمی (عمومی)
پیش نمایش صفحه اول مقاله
![عکس صفحه اول مقاله: Differentiated interactions in phosphate solutions: Comparing Ag(111) and Ag(100) surfaces Differentiated interactions in phosphate solutions: Comparing Ag(111) and Ag(100) surfaces](/preview/png/4907780.png)
چکیده انگلیسی
The electrochemical behavior of phosphate species on Ag(111) and Ag(100) single crystal surfaces was studied by experimental techniques and theoretical calculations. Characteristic cathodic/anodic potential peaks (Vp) appear in the current density-potential curves (j-V) for H2PO4â, H3PO4, and in the case of PO43â for concentrations lower than 0.1Â M, where the interaction is stronger for the Ag(100) electrode. This demonstrate that the adsorption is sensitive to the surface structure. The adsorption energy (Eads) of the different species on both surfaces was studied by means of DFT-vdW calculations. All phosphate species have tri-dentate binding. The |Eads| increased for the H3PO4; H2PO4â; HPO42â and PO43â sequence, and the tetrahedral structures are compressed. Although the same trend was observed on both crystalline surfaces, the films have the symmetry of the substrate, C3v and C4v. The influence of hydroxide co-adsorption was studied for different [HPO42â]/[PO43â] ratios in solution. The strength of adsorption obtained from experimental and theoretical calculations show an excellent qualitative correlation.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Electroanalytical Chemistry - Volume 799, 15 August 2017, Pages 487-496
Journal: Journal of Electroanalytical Chemistry - Volume 799, 15 August 2017, Pages 487-496
نویسندگان
Claudia B. Salim Rosales, Mariana I. Rojas, LucÃa B. Avalle,