Chemical Reaction and Bonding Mechanism at the Polymer–Metal Interface

材料科学 X射线光电子能谱 化学键 微尺度化学 聚合物 二次离子质谱法 扫描电子显微镜 阳极连接 化学工程 共价键 能量色散X射线光谱学 纳米技术 复合材料 离子 有机化学 图层(电子) 化学 数学教育 工程类 数学
作者
Xin Zou,Ke Chen,Haining Yao,Cong Chen,Xueping Lu,Ping Ding,Min Wang,Xueming Hua,Aidang Shan
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:14 (23): 27383-27396 被引量:73
标识
DOI:10.1021/acsami.2c04971
摘要

Polymer-metal hybrid structures have attracted significant attention recently due to their advantage of great weight reduction and excellent integrated physical/chemical properties. However, due to great physicochemical differences between polymers and metals, obtaining an interface with high bonding strength is a challenge, which makes it critically important to clarify the underlying bonding mechanisms. In the present research, we focused on revealing the underlying bonding mechanisms of a laminated Cr-coated steel-ethylene acrylic acid (EAA) strip prepared by hot roll bonding from the microscale to the molecular scale with experimental evidence. The microscale mechanical interlocking was analyzed and proven by scanning white light interferometry and scanning electron microscopy (SEM) by means of observing the surface and cross-sectional morphologies. Additionally, interfacial phases and chemical compositions were analyzed by transmission electron microscopy (TEM) and energy-dispersive X-ray spectroscopy (EDX). More directly and effectively, the interface was successfully exposed for X-ray photoelectron spectroscopy (XPS) analysis. Combined with time-of-flight secondary ion mass spectroscopy (ToF-SIMS) and depth profiling analysis, the formation of -(O═)C-O-Cr and -C-(O-Cr)2 covalent bonds through chemical reactions at the interface between -COOH and Cr2O3 was verified. Based on these characterization results, interfacial bonding mechanisms for the laminated Cr-coated steel-EAA strip were clearly identified to be chemical bonding and micromechanical interlocking, along with hydrogen bonding, which were all demonstrated with solid experimental evidence. In addition, 3D-render view and cross-section images of typical ion fragments at the interface were used to reveal the interfacial structure more comprehensively. The contributions of hydrogen bonds and covalent bonds to the interface were evaluated and compared for the first time. This study provides both methodological and theoretical guidance for investigating and understanding interfacial bonding formation in polymer-metal hybrid structures.
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