Edge Epitaxy of Two-Dimensional MoSe<sub>2</sub> and MoS<sub>2</sub> Nanosheets on One-Dimensional Nanowires
Article 2017 en
Authors
JC
Junze Chen
XW
Xue‐Jun Wu
YG
Yue Gong
Abstract
1 min read
Rational design and synthesis of heterostructures based on transition metal dichalcogenides (TMDs) have attracted increasing interests because of their promising applications in electronics, catalysis, etc. However, the construction of epitaxial heterostructures with an interface at the edges of TMD nanosheets (NSs) still remains a great challenge. Here, we report a strategy for controlled synthesis of a new type of heterostructure in which TMD NSs, including MoS<sub>2</sub> and MoSe<sub>2</sub>, vertically grow along the longitudinal direction of one-dimensional (1D) Cu<sub>2-x</sub>S nanowires (NWs) in an epitaxial manner. The obtained Cu<sub>2-x</sub>S-TMD heterostructures with tunable loading amount and lateral size of TMD NSs are achieved by the consecutive growth of TMD NSs on Cu<sub>2-x</sub>S NWs through gradual injection of chalcogen precursors. After cation exchange of Cu in Cu<sub>2-x</sub>S-TMD heterostructures with Cd, the obtained CdS-MoS<sub>2</sub> heterostructures retained their original architectures. Compared to the pure CdS NWs, the CdS-MoS<sub>2</sub> heterostructures with 7.7 wt % loading of MoS<sub>2</sub> NSs exhibit the best performance in the photocatalytic hydrogen evolution reaction with a H<sub>2</sub> production rate up to 4647 μmol·h<sup>-1</sup>·g<sup>-1</sup>, about 58 times that catalyzed with pure CdS NWs. Our synthetic strategy opens up a new way for the controlled synthesis of TMD-based heterostructures, which could have various promising applications.
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