二硫化钼
材料科学
插层(化学)
催化作用
硫黄
电催化剂
亚稳态
化学计量学
分解水
相(物质)
化学工程
氢
制氢
金属
结晶学
纳米技术
无机化学
物理化学
电化学
化学
有机化学
冶金
工程类
光催化
电极
作者
Joakim Ekspong,Robin Sandström,Lakshmy Pulickal Rajukumar,Mauricio Terrones,Thomas Wågberg,Eduardo Gracia‐Espino
标识
DOI:10.1002/adfm.201802744
摘要
Abstract The metastable 1T′ polymorph of molybdenum disulfide (MoS 2 ) has shown excellent catalytic activity toward the hydrogen evolution reaction (HER) in water‐splitting applications. Its basal plane exhibits high catalytic activity comparable to the edges in 2H MoS 2 and noble metal platinum. However, the production and application of this polymorph are limited by its lower energetic stability compared to the semiconducting 2H MoS 2 phase. Here, the production of stable intercalated 1T′ MoS 2 nanosheets attached on graphitic nanoribbons is reported. The intercalated 1T′ MoS 2 exhibits a stoichiometric S:Mo ratio of 2.3 (±0.1):1 with an expanded interlayer distance of 10 Å caused by a sulfur‐rich intercalation agent and is stable at room temperature for several months even after drying. The composition, structure, and catalytic activity toward HER are investigated both experimentally and theoretically. It is concluded that the 1T′ MoS 2 phase is stabilized by the intercalated agents, which further improves the basal planes′ catalytic activity toward HER.
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