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Immobilization of single argon atoms in nano-cages of two-dimensional zeolite model systems

机译:二维沸石模型系统纳米笼中单个氩原子的固定化

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摘要

The confinement of noble gases on nanostructured surfaces, in contrast to bulk materials, at non-cryogenic temperatures represents a formidable challenge. In this work, individual Ar atoms are trapped at 300 K in nano-cages consisting of (alumino)silicate hexagonal prisms forming a two-dimensional array on a planar surface. The trapping of Ar atoms is detected in situ using synchrotron-based ambient pressure X-ray photoelectron spectroscopy. The atoms remain in the cages upon heating to 400 K. The trapping and release of Ar is studied combining surface science methods and density functional theory calculations. While the frameworks stay intact with the inclusion of Ar atoms, the permeability of gasses (for example, CO) through them is significantly affected, making these structures also interesting candidates for tunable atomic and molecular sieves. These findings enable the study of individually confined noble gas atoms using surface science methods, opening up new opportunities for fundamental research.
机译:与散装材料相比,在非低温条件下将惰性气体限制在纳米结构表面上是一个巨大的挑战。在这项工作中,单个的Ar原子在300 K的范围内被捕获在由(铝)硅酸盐六方柱组成的纳米笼中,该六方柱在平面上形成二维阵列。使用基于同步加速器的环境压力X射线光电子能谱仪原位检测Ar原子的俘获。加热至400 K时原子保留在笼中,结合表面科学方法和密度泛函理论计算研究了Ar的俘获和释放。尽管框架中包含Ar原子保持完好无损,但气体(例如CO)通过它们的渗透性受到显着影响,这使这些结构也成为可调原子和分子筛的有趣候选对象。这些发现使我们能够使用表面科学方法研究单个受限的稀有气体原子,从而为基础研究开辟了新的机遇。

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