纳米孔
二硫化钼
材料科学
钼
密度泛函理论
薄脆饼
化学物理
催化作用
GSM演进的增强数据速率
多孔性
扫描电子显微镜
氢
纳米技术
化学
计算化学
复合材料
电信
有机化学
冶金
生物化学
计算机科学
作者
Xiaoxu Zhao,Deyi Fu,Zijing Ding,Yuyang Zhang,Dongyang Wan,Sherman J. R. Tan,Zhongxin Chen,Kai Leng,Jiadong Dan,Wei Fu,Dechao Geng,Peng Song,Yonghua Du,T. Venkatesan,Sokrates T. Pantelides,Stephen J. Pennycook,Wu Zhou,Kian Ping Loh
出处
期刊:Nano Letters
[American Chemical Society]
日期:2017-12-18
卷期号:18 (1): 482-490
被引量:126
标识
DOI:10.1021/acs.nanolett.7b04426
摘要
The catalytic and magnetic properties of molybdenum disulfide (MoS2) are significantly enhanced by the presence of edge sites. One way to obtain a high density of edge sites in a two-dimensional (2D) film is by introducing porosity. However, the large-scale bottom-up synthesis of a porous 2D MoS2 film remains challenging and the correlation of growth conditions to the atomic structures of the edges is not well understood. Here, using molecular beam epitaxy, we prepare wafer-scale nanoporous MoS2 films under conditions of high Mo flux and study their catalytic and magnetic properties. Atomic-resolution electron microscopy imaging of the pores reveals two new types of reconstructed Mo-terminated edges, namely, a distorted 1T (DT) edge and the Mo-Klein edge. Nanoporous MoS2 films are magnetic up to 400 K, which is attributed to the presence of Mo-terminated edges with unpaired electrons, as confirmed by density functional theory calculation. The small hydrogen adsorption free energy at these Mo-terminated edges leads to excellent activity for the hydrogen evolution reaction.
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