Synergetic hydrogen-bond network of functionalized graphene and cations for enhanced atmospheric water capture

Rakesh, Joshi, Xiaojun, Ren, Xiao, Sui, Llewellyn, Owens, Dali, Ji, Xinyue, Wen, Yuta, Nishina, Kamal , Pant, Vanesa, Quintano, Daria , Andreeva, Kostya, Novoselov, Amir, Karton, Tobias, Foller, Daisuke, Asanoma
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Abstract

Water molecules at the solid-liquid interface display intricate behaviours sensitive to small changes. The presence of different interfacial components, such as cations or functional groups, shape the physical and chemical properties of the hydrogen bond network. Understanding such interfacial hydrogen-bond networks is essential for a large range of applications and scientific questions. To probe the interfacial hydrogen-bond network, atmospheric water capture is a powerful tool. Here, we experimentally observe that a calcium ion on a calcium-intercalated graphene oxide aerogel (Ca-GOA) surface captures 3.2 times more water molecules than in its freestanding state. From experimental Van’t Hoff estimation and density functional theory (DFT) calculations, we uncover the synergistically enhanced hydrogen-bond network of the calcium ion-epoxide complex due to significantly larger polarizations and hydrogen bond enthalpies. This study reveals valuable insights into the interfacial water hydrogen-bond network on functionalized carbon-cation complexed surfaces and potential pathways for future atmospheric water generation technologies.
功能化石墨烯与阳离子的协同氢键网络,用于增强大气水捕获能力
固液界面上的水分子对微小变化非常敏感,表现出错综复杂的行为。不同界面成分(如阳离子或官能团)的存在会影响氢键网络的物理和化学性质。了解这种界面氢键网络对于解决大量应用和科学问题至关重要。要探究界面氢键网络,大气水捕获是一个强有力的工具。在这里,我们通过实验观察到,钙离子在钙离子互结氧化石墨烯气凝胶(Ca-GOA)表面捕获的水分子是其独立状态下的 3.2 倍。通过 Van't Hoff 实验估算和密度泛函理论 (DFT) 计算,我们发现钙离子-环氧化物复合物的氢键网络因极化和氢键焓显著增大而协同增强。这项研究揭示了功能化碳阳离子络合物表面的界面水氢键网络以及未来大气制水技术的潜在途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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