Structure and properties of electrochemical interfaces with grafting polyelectrolyte: A fluid density functional theory study

被引:2
|
作者
Hu, Yuanlong [1 ,2 ]
Cheng, Jin [3 ,4 ]
Yao, Sisheng [1 ,2 ]
Xu, Zheng [3 ,4 ]
Xu, Xujian [1 ,2 ]
Wei, Tianhao [1 ,2 ]
Liu, Honglai [1 ,2 ,3 ,4 ]
Lian, Cheng [1 ,2 ,3 ,4 ]
机构
[1] East China Univ Sci & Technol, Shanghai Engn Res Ctr Hierarch Nanomat, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[2] East China Univ Sci & Technol, Sch Chem Engn, Shanghai 200237, Peoples R China
[3] East China Univ Sci & Technol, Frontiers Sci Ctr Materiobiol & Dynam Chem, Shanghai 200237, Peoples R China
[4] East China Univ Sci & Technol, Sch Chem & Mol Engn, Shanghai 200237, Peoples R China
基金
中国国家自然科学基金;
关键词
Electrochemical interface; Polymerbrush; Electrical double layer; Ionic liquids; Surface modification; ELECTRIC DOUBLE-LAYERS; IONIC LIQUIDS; ENERGY-STORAGE; POLYMER BRUSH; CARBON; BEHAVIOR; MODEL; CAPACITANCE; TRANSITION; ADSORPTION;
D O I
10.1016/j.ces.2024.120321
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The structure of the electrode/electrolyte interface directly determines electrochemical performance. One effective method for controlling this interface structure is by grafting polyelectrolyte onto the electrode surface, which can significantly alter the double layer structure and enhance electrochemical performance. This study focuses on the graft modification of polyelectrolytes at the electrochemical interface and investigates the impact of the length and density of the grafted polyelectrolyte chain on the structure and capacitance of the electrode/ ionic liquid interface using fluid density functional theory (FDFT). The findings indicate that the grafted polymerbrush disrupts the alternating layer of anions and cations at the conventional interface and exerts an additional adsorption effect on counter ions, thereby reducing the density of freely movable co-ions. Consequently, this process increases the effective charge and capacitance of the interface. The results of this investigation contribute to a deeper comprehension of polyelectrolyte solutions at solid-liquid interfaces and guide the regulation of electrochemical interface properties.
引用
收藏
页数:9
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