Ethylenediamine-Enhanced Oxidation Resistivity of a Copper Surface during Water-Based Copper Nanowire Synthesis

被引:22
|
作者
Koo, Jahyun [1 ]
Kwon, Soonho [1 ]
Kim, Na Rae [1 ]
Shin, Kihyun [1 ]
Lee, Hyuck Mo [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, 291 Daehak Ro, Daejeon 34141, South Korea
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2016年 / 120卷 / 06期
基金
新加坡国家研究基金会;
关键词
LARGE-SCALE SYNTHESIS; X-RAY PHOTOELECTRON; TRANSPARENT ELECTRODES; GROWTH-MECHANISM; NANOPARTICLES; CUO; ADSORPTION; METALS;
D O I
10.1021/acs.jpcc.5b10733
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Copper nanowires (Cu NWs) are promising materials for transparent electrode applications. However, their growth mechanism during water-based synthesis remains unclear. The steric hindrance of a surfactant, which has been considered in previous studies, is insufficient to explain the suppression of Cu oxide formation during water-based synthesis. In this paper, we suggest that ethylenediamine (EDA, C2H4(NH2)(2)), which is commonly used as a structure-directing agent (SDA), may play an important role as an oxidation inhibitor in water-based synthesis of Cu NWs. High-resolution transmission electron microscopy (HR-TEM) analysis indicated that the Cu NWs grow from icosahedral seeds. Additionally, energy-dispersive X-ray spectroscopy (EDS) and X-ray photoelectron spectroscopy (XPS) suggested that EDA affects the oxidation state of the as-prepared Cu NW surface. Finally, density functional theory (DFT) calculations revealed that the adsorption of EDA effectively hinders the adsorption of oxidizing species and prevents the oxidation of the Cu seeds. This effect is attributed to a filling of the antibonding states and an increase in the electrostatic repulsion between the Cu seeds and the oxidizing species.
引用
收藏
页码:3334 / 3340
页数:7
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