Suppr超能文献

通过静滴法量化自组装单分子层中的gauche缺陷和相演变。

Quantifying Gauche Defects and Phase Evolution in Self-Assembled Monolayers through Sessile Drops.

作者信息

Chen Jiahao, Chang Boyce, Oyola-Reynoso Stephanie, Wang Zhengjia, Thuo Martin

机构信息

Department of Materials Science and Engineering, Iowa State University, 2220 Hoover Hall, Ames, Iowa 50011, United States.

Division of Materials Science and Engineering, Ames Laboratory, Ames, Iowa 50011, United States.

出版信息

ACS Omega. 2017 May 15;2(5):2072-2084. doi: 10.1021/acsomega.7b00355. eCollection 2017 May 31.

Abstract

Self-assembled monolayers (SAMs) are widely used in surface modifications, specifically in tuning the surface chemistry of materials. The structure and properties of SAMs have been extensively studied often with sophisticated tools, even for the simplest -alkanethiolate SAMs. In SAMs, especially in linear -alkanethiolates, the properties are dependent on the chain length, which is best manifested in the so-called odd-even effect, a simple yet not fully understood phenomenon. One main challenge is fully delineating the origin of length-dependent properties, which can be due to the structure (ideal SAMs), defect evolution, or substrate-molecule effects. This study demonstrates that utilizing the wetting behavior of polar (water) and nonpolar (hexadecane (HD)) solvents on -alkanethiolate SAMs formed on ultraflat gold and silver surfaces, the evolution of chain-length-dependent gauche defects can be revealed and parameterized through a newly defined dimensionless number (χ). The observation of the odd-even effect in hydrophobicity, however, depends on the thiol chain length, and it was only observed on longer-chain (>C) molecules. The trend in this odd-even effect demonstrates that there are three main transitions in the nature of wetting, hence structure, across -alkanethiols. From wetting with HD, the role of dispersive components in wetting reveal that the SAMs are dynamic, which we attribute to rotations associated with previously reported evolution in gauche defects and changes in packing density. Therefore, from re-expression of the Young-Dupre equation, we define a new dimensionless number associated with molecular conformations, whose periodicity mirrors the energetics of Goodman's conformations of -alkanes in unbound states and associated four- or two-twist turns. Therefore, we infer that the evolution in surface energy is largely due to molecular conformations and associated relaxations of the bound thiolates.

摘要

自组装单分子层(SAMs)广泛应用于表面修饰,特别是在调节材料的表面化学性质方面。SAMs的结构和性质已经通过复杂的工具进行了广泛研究,即使是对于最简单的链烷硫醇盐SAMs也是如此。在SAMs中,特别是在线性链烷硫醇盐中,其性质取决于链长,这在所谓的奇偶效应中表现得最为明显,这是一个简单但尚未完全理解的现象。一个主要挑战是全面阐明长度依赖性性质的起源,这可能是由于结构(理想SAMs)、缺陷演化或底物-分子效应。本研究表明,利用极性(水)和非极性(十六烷(HD))溶剂在超平金和银表面形成的链烷硫醇盐SAMs上的润湿性,可以通过新定义的无量纲数(χ)揭示并参数化链长依赖性gauche缺陷的演化。然而,疏水性奇偶效应的观察取决于硫醇链长,并且仅在较长链(>C)分子上观察到。这种奇偶效应的趋势表明,在整个链烷硫醇中,润湿性的本质,即结构,存在三个主要转变。从HD的润湿性来看,润湿性中分散成分的作用表明SAMs是动态的,我们将其归因于与先前报道的gauche缺陷演化和堆积密度变化相关的旋转。因此,通过重新表达杨氏-杜普雷方程,我们定义了一个与分子构象相关的新无量纲数,其周期性反映了未结合状态下链烷的古德曼构象的能量以及相关的四扭或双扭转变。因此,我们推断表面能的演化很大程度上归因于分子构象和结合硫醇盐的相关弛豫。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验