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阳离子表面活性剂在金金属-液体界面吸附形态的直接观察

Direct Observation of Adsorption Morphologies of Cationic Surfactants at the Gold Metal-Liquid Interface.

作者信息

Khan Md Rubel, Singh Himanshu, Sharma Sumit, Asetre Cimatu Katherine Leslee

机构信息

Department of Chemistry and Biochemistry, Ohio University, 100 University Terrace, 136 Clippinger Laboratories, Athens, Ohio 45701-2979, United States.

Department of Chemical and Biomolecular Engineering, Ohio University, Athens, Ohio 45701, United States.

出版信息

J Phys Chem Lett. 2020 Nov 19;11(22):9901-9906. doi: 10.1021/acs.jpclett.0c02517. Epub 2020 Nov 10.

Abstract

Understanding interfacial phenomena is important in processes like corrosion, catalysis, and electrochemical reactions. Specifically, in corrosion inhibition, the assembly of adsorbed surfactants at metal-water interfaces in well-packed, ordered layers is desired. We provide direct evidence of the role of alkyl tails of surfactants in the formation of ordered adsorbed layers at metal-water interfaces. We have employed surface-specific sum frequency generation (SFG) spectroscopy to probe the adsorption and self-assembly of cationic surfactants, alkyldimethylbenzyl ammonium bromides of tail lengths = 4 (C4) and 12 (C12), without any applied potential or stimulus, at the gold-water interface. Our SFG measurements show that C12 Quat adsorbs as an ordered monolayer, whereas C4 Quat adsorbs in a disordered monolayer. All-atom molecular dynamics (MD) simulations of these surfactants corroborate with SFG results. These findings provide new insights on how hydrophobic interactions between alkyl tails of surfactants affect their self-assembly at metal-water interfaces.

摘要

了解界面现象在腐蚀、催化和电化学反应等过程中很重要。具体而言,在缓蚀方面,希望吸附的表面活性剂在金属 - 水界面以排列紧密、有序的层状形式组装。我们提供了直接证据,证明表面活性剂的烷基链在金属 - 水界面有序吸附层形成过程中的作用。我们采用了表面特异性和频振动光谱(SFG)来探测阳离子表面活性剂(碳链长度分别为4(C4)和12(C12)的烷基二甲基苄基溴化铵)在无任何外加电势或刺激的情况下于金 - 水界面的吸附和自组装情况。我们的SFG测量结果表明,C12季铵盐以有序单层形式吸附,而C4季铵盐以无序单层形式吸附。这些表面活性剂的全原子分子动力学(MD)模拟结果与SFG结果相符。这些发现为表面活性剂的烷基链之间的疏水相互作用如何影响其在金属 - 水界面的自组装提供了新的见解。

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