Water structure at the multilayers of palladium deposited at nanostructured Au electrodes

被引:4
|
作者
Zhang, Yue-Jiao [1 ]
Su, Zhang-Fei [2 ]
Li, Jian-Feng [1 ]
Lipkowski, Jacek [2 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Coll Chem & Chem Engn, iChEM,Coll Energy, Xiamen 361005, Peoples R China
[2] Univ Guelph, Dept Chem, Guelph, ON N1G 2W1, Canada
基金
加拿大自然科学与工程研究理事会; 中国国家自然科学基金;
关键词
ATR-SEIRA; Water structure; Palladium multilayers; THIN PD OVERLAYERS; ZERO CHARGE; PART I; HYDROGEN; AU(111); SURFACE; ABSORPTION; ADSORPTION; MONOLAYER; COADSORPTION;
D O I
10.1016/j.jelechem.2021.115243
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
In situ ATR-SEIRAS experiments were carried out to describe water structure at the surface of multilayers of Pd modified nanopatterned gold film electrodes in contact with aqueous 0.1 M HClO4 solution. The results show that the surface water becomes more ordered when the thickness of the Pd film increases. The "ice-like water" band becomes stronger and for the electrode with 5 ML Pd@Au, the ratio of "ice-like water" to "liquid-like water" becomes larger than that in bulk water. Concomitantly, the population of "monomers" or small water clusters diminishes. All surface water bands increase when hydrogen adsorption takes place. The bending band corresponding to "monomers" or "multimers" water is observed chiefly at the potentials of hydrogen adsorption.
引用
收藏
页数:7
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