Shun Kashiwaya, Yuchen Shi, Jun Lu, Davide G. Sangiovanni, Grzegorz Greczynski, Martin Magnuson, Mike Andersson, Johanna Rosen, Lars Hultman
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引用次数: 0
摘要
迄今为止,单层金的合成仅限于独立的几个原子厚的金层,或局限在模板上或模板内的单层金。在这里,我们报告了通过湿化学蚀刻从纳米层状 Ti3AuC2 中剥离出单原子厚金的过程,这种纳米层状 Ti3AuC2 最初是通过用金取代 Ti3SiC2 中的硅而形成的。Ti3SiC2 是一种著名的 MAX 相,其中 M 是过渡金属,A 是 A 族元素,X 是 C 或 N。这种二维层被称为金烯层。通过电子显微镜观察到,金烯层的晶格收缩率约为块金的 9%。虽然 ab initio 分子动力学模拟显示二维烯金本质上是稳定的,但实验显示存在一些卷曲和团聚现象,表面活性剂可以减轻这些现象。X 射线光电子能谱显示,金 4f 结合能增加了 0.88 eV。此外,还介绍了从其他非范德华金互层相制备金烯的前景,包括开发蚀刻方案。
Synthesis of goldene comprising single-atom layer gold
The synthesis of monolayer gold has so far been limited to free-standing several-atoms-thick layers, or monolayers confined on or inside templates. Here we report the exfoliation of single-atom-thick gold achieved through wet-chemically etching away Ti3C2 from nanolaminated Ti3AuC2, initially formed by substituting Si in Ti3SiC2 with Au. Ti3SiC2 is a renown MAX phase, where M is a transition metal, A is a group A element, and X is C or N. Our developed synthetic route is by a facile, scalable and hydrofluoric acid-free method. The two-dimensional layers are termed goldene. Goldene layers with roughly 9% lattice contraction compared to bulk gold are observed by electron microscopy. While ab initio molecular dynamics simulations show that two-dimensional goldene is inherently stable, experiments show some curling and agglomeration, which can be mitigated by surfactants. X-ray photoelectron spectroscopy reveals an Au 4f binding energy increase of 0.88 eV. Prospects for preparing goldene from other non-van der Waals Au-intercalated phases, including developing etching schemes, are presented. Atomically thin gold nanosheets are predicted to have interesting properties but their synthesis is challenging. Here the exfoliation of two-dimensional single-atom-thick gold, termed goldene, is achieved through wet-chemically etching Ti3C2 from Ti3AuC2. The synthesized goldene has promising properties as a heterocatalyst.