Abstract
Shape-engineered atomically thin transition metal dichalcogenide (TMD) crystals are highly intriguing systems with regard to both fundamental and applied science. Herein, a chemical vapor deposition-assisted generalized synthesis strategy for the triangular- and dendritic-shaped TMDs and their ternary alloys is proposed, and the TMD structures' potential for electrocatalytic hydrogen evolution reaction (HER) applications is demonstrated. The alloy formation is confirmed via micro-Raman and photoluminescence studies and further verified using transmission electron microscopy and X-ray photoelectron spectroscopy. The HER activities of MoS 2 and MoSe 2 triangles are compared with those of their dendritic structures, and an enormous improvement in terms of overpotential and current density is observed for the dendritic structures. A further enhancement of the HER activity is observed in MoS 2(1−x)Se 2x triangular and dendritic structures, with dendritic MoS 2(1−x)Se 2x providing the best activity. The demonstrated nonequilibrium growth technique opens new avenues for the synthesis of morphology-controlled, large area, complex, and atomically thin TMD structures, which can have unprecedented properties, such as the enormous catalytic activity, tunable luminescence, etc., as presented in this article.
Original language | English |
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Article number | 1900257 |
Pages (from-to) | 1-10 |
Number of pages | 10 |
Journal | Physica Status Solidi - Rapid Research Letters |
Volume | 13 |
Issue number | 12 |
Early online date | 25 Jun 2019 |
DOIs | |
Publication status | Published - Dec 2019 |
Keywords
- atomically thin alloys
- chemical vapor deposition
- dendritic structures
- hydrogen evolution
- transition metal dichalcogenides
ASJC Scopus subject areas
- General Materials Science
- Condensed Matter Physics
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