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Exploring the Hydration Water Character on Atomically Dislocated Surfaces by Surface Enhanced Raman Spectroscopy

机译:表面增强拉曼光谱法在原子脱位表面上探索水合水性

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Hydration is ubiquitous in any kind of water–substance interaction such as in various interfacial and biological processes. Despite substantial progress made to date, however, still less explored is the hydration behavior on complex heterogeneous surfaces, such as the water surrounding the protein, which requires a platform that enables systematic investigation at the atomic scale. Here, we realized a heterogeneous self-assembled monolayer system that allows both controllable mixing with hydrophobic or hydrophilic groups and precise distance control of the functional carboxyl groups from the surface by methylene spacer groups. Using surface-enhanced Raman spectroscopy (SERS), we first demonstrated the hydrophobic (or hydrophilic) mixing ratio-dependent pKsuba/sub variation of the carboxyl group. Interestingly, we observed a counterintuitive, non-monotonic behavior that a fractionally mixed hydrophobic group can induce significant enhancement of dielectric strength of the interfacial water. In particular, such a fractional mixing substantially decreases the amide coupling efficiency at the surface, as manifested by the corresponding pKsuba/sub decrease. The SERS-based platform we demonstrated can be widely applied for atomically precise control and molecular-level characterization of hydration water on various heterogeneous surfaces of biological and industrial importance.
机译:在任何种类的水质相互作用如各种界面和生物过程中,水合是普遍的。然而,尽管迄今为止取得了实质性进展,但仍然尚不依赖于复杂的异质表面上的水化行为,例如蛋白质周围的水,这需要一个能够在原子尺度上进行系统调查的平台。这里,我们实现了一种异质的自组装单层系统,其允许与疏水或亲水基团的可控混合,并通过亚甲基间隔基团的功能羧基的精确距离控制。使用表面增强拉曼光谱(SERS),首先证明了羧基的疏水性(或亲水性)混合比依赖性PK A 变异。有趣的是,我们观察到违反直觉,非单调的行为,即部分混合的疏水基团可以诱导界面水的介电强度的显着提高。特别地,这种分数混合显着降低了表面的酰胺耦合效率,如相应的PK A 减少。我们证明的基于SERS的平台可广泛应用于在生物和工业重要性的各种异质表面上的原子精确控制和分子水平表征。

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