Department of Polymer Science, The University of Akron , Akron, Ohio 44325-3909, United States.
Solvay Speciality Polymers , 4500 McGinnis Ferry Road, Alpharetta, Georgia 30005, United States.
ACS Nano. 2017 May 23;11(5):4899-4906. doi: 10.1021/acsnano.7b01499. Epub 2017 May 2.
The water/graphene interface has received considerable attention in the past decade due to its relevance in various potential applications including energy storage, sensing, desalination, and catalysis. Most of our knowledge about the interfacial water structure next to graphene stems from simulations, which use experimentally measured water contact angles (WCAs) on graphene (or graphite) to estimate the water-graphene interaction strength. However, the existence of a wide spectrum of reported WCAs on supported graphene and graphitic surfaces makes it difficult to interpret the water-graphene interactions. Here, we have used surface-sensitive infrared-visible sum frequency generation (SFG) spectroscopy to probe the interfacial water structure next to graphene supported on a sapphire substrate. In addition, the ice nucleation properties of graphene have been explored by performing in situ freezing experiments as graphitic surfaces are considered good ice nucleators. For graphene supported on sapphire, we observed a strong SFG peak associated with highly coordinated, ordered water next to graphene. Similar ordering was not detected next to bare sapphire, implying that the observed ordering of water molecules in the former case is a consequence of the presence of graphene. Our analysis indicates that graphene behaves like a hydrophobic (or negatively charged) surface, leading to enhanced ordering of water molecules. Although liquid water orders next to graphene, the ice formed is proton disordered. This research sheds light on water-graphene interactions relevant in optimizing the performance of graphene in various applications.
过去十年,由于水/石墨烯界面在储能、传感、海水淡化和催化等多种潜在应用中具有重要意义,因此受到了广泛关注。我们对石墨烯(或石墨)上界面水结构的大部分了解来自于模拟,这些模拟使用实验测量的石墨烯(或石墨)水接触角(WCA)来估计水-石墨烯相互作用强度。然而,在支撑石墨烯和石墨表面上报道的 WCA 谱具有很宽的范围,这使得难以解释水-石墨烯相互作用。在这里,我们使用表面敏感的红外可见和频光谱(SFG)光谱来探测蓝宝石基底上支撑的石墨烯附近的界面水结构。此外,通过进行原位冷冻实验探索了石墨烯的成冰性质,因为石墨表面被认为是良好的成冰核。对于在蓝宝石上支撑的石墨烯,我们观察到与石墨烯相邻的高度协调、有序的水的强烈 SFG 峰。在裸露的蓝宝石旁边没有检测到类似的有序性,这意味着在前者情况下观察到的水分子有序性是石墨烯存在的结果。我们的分析表明,石墨烯表现为疏水性(或带负电荷)表面,导致水分子的有序性增强。尽管水分子在石墨烯旁边有序排列,但形成的冰是质子无序的。这项研究揭示了在优化石墨烯在各种应用中的性能方面相关的水-石墨烯相互作用。