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观察弱吸附和强吸附聚苯乙烯链在界面上的不同动态行为。

Observing different dynamic behaviors of weakly and strongly adsorbed polystyrene chains at interfaces.

机构信息

State Key Laboratory of Bioelectronics, School of Biological Science & Medical Engineering, Southeast University, Nanjing, 210096, Jiangsu Province, P. R. China.

出版信息

Soft Matter. 2018 Apr 18;14(15):2762-2766. doi: 10.1039/c7sm02503c.

Abstract

Understanding the dynamic behavior of polymer chains adsorbed onto a solid surface is of great importance for elucidating polymer-surface interactions. Here by using sum frequency generation (SFG) vibrational spectroscopy, we probed the conformational changes of weakly adsorbed and strongly adsorbed polystyrene (PS) chains on sapphire surfaces perturbed by a nonsolvent (deuterated water, D2O) and a good solvent (carbon tetrachloride, CCl4). The SFG results indicated that the PS chains in the weakly adsorbed state were flexible and the chain conformation could easily be altered. Differently, the PS chains in the strongly adsorbed state were rigid and the chain conformation could not be changed. The local structural variations of the weakly and strongly adsorbed PS chains at the interfaces were also discussed in detail with respect to the SFG spectral characteristics. These intriguing experimental results shed light on our understanding of molecular behaviors of polymer chains adsorbed onto a solid surface.

摘要

了解吸附在固体表面上的聚合物链的动态行为对于阐明聚合物-表面相互作用非常重要。在这里,我们通过使用和频产生(SFG)振动光谱技术,探测了在非溶剂(氘代水,D2O)和良溶剂(四氯化碳,CCl4)扰动下吸附在蓝宝石表面上的弱吸附和强吸附聚苯乙烯(PS)链的构象变化。SFG 结果表明,弱吸附状态下的 PS 链是柔性的,链构象很容易改变。而在强吸附状态下的 PS 链是刚性的,链构象不能改变。还详细讨论了界面处弱吸附和强吸附 PS 链的局部结构变化,并根据 SFG 光谱特征进行了讨论。这些有趣的实验结果为我们理解吸附在固体表面上的聚合物链的分子行为提供了启示。

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