Hefei National Laboratory for Physical Sciences at Microscale and Department of Chemical Physics, University of Science and Technology of China, Hefei, Anhui, PR China 230026.
Langmuir. 2012 Jan 17;28(2):1374-80. doi: 10.1021/la203690p. Epub 2012 Jan 5.
Interfacial water structure at charged surfaces plays a key role in many physical, chemical, biological, environmental, and industrial processes. Understanding the release of interfacial water from the charged solid surfaces during dehydration process may provide insights into the mechanism of protein folding and the nature of weak molecular interactions. In this work, sum frequency generation vibrational spectroscopy (SFG-VS), supplemented by quartz crystal microbalance (QCM) measurements, has been applied to study the interfacial water structure at polyelectrolyte covered surfaces. Poly[2-(dimethylamino)ethyl methacrylate] (PDMAEMA) chains are grafted on solid surfaces to investigate the change of interfacial water structure with varying surface charge density induced by tuning the solution pH. At pH ≤ 7.1, SFG-VS intensity is linear to the loss of mass of interfacial water caused by the dehydration of PDMAEMA chains, and no reorientation of the strongly bonded water molecules is observed in the light of χ(ppp)/χ(ssp) ratio. χ((3)) contribution to SFG signal is deduced based on the combination of SFG and QCM results. It is the first direct experimental evidence to reveal that the χ((3)) has a negligible contribution to SFG signal of the interfacial water at a charged polymer surface.
在许多物理、化学、生物、环境和工业过程中,带电表面的界面水结构起着关键作用。了解在脱水过程中界面水从带电固体表面的释放,可能为蛋白质折叠的机制和弱分子相互作用的本质提供线索。在这项工作中,和石英晶体微天平(QCM)测量相结合,和频产生振动光谱(SFG-VS)被应用于研究聚电解质覆盖表面的界面水结构。聚[2-(二甲氨基)乙基甲基丙烯酸酯](PDMAEMA)链被接枝到固体表面上,以研究通过调节溶液 pH 值诱导的表面电荷密度变化对界面水结构的改变。在 pH≤7.1 时,SFG-VS 强度与 PDMAEMA 链脱水引起的界面水质量损失成正比,并且根据 χ(ppp)/χ(ssp) 比值,没有观察到强结合水分子的重新取向。根据 SFG 和 QCM 结果的组合,推导出了对 SFG 信号的 χ((3)) 贡献。这是第一个直接的实验证据,表明在带电聚合物表面,χ((3)) 对界面水的 SFG 信号的贡献可以忽略不计。