One-step CVD fabrication and optoelectronic properties of SnS2/SnS vertical heterostructures
Heterostructures constructed by two-dimensional (2D) material layers, which are usually prepared via a transfer/stacking method or van der Waals epitaxy, have achieved significant success in various optoelectronic devices including solar cells, light-emitting diodes and photodetectors. However, to d...
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Veröffentlicht in: | Inorganic chemistry frontiers 2018-08, Vol.5 (8), p.1828-1835 |
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Sprache: | eng |
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Zusammenfassung: | Heterostructures constructed by two-dimensional (2D) material layers, which are usually prepared via a transfer/stacking method or van der Waals epitaxy, have achieved significant success in various optoelectronic devices including solar cells, light-emitting diodes and photodetectors. However, to date, most of these heterostructures comprise 2D materials with a similar crystal structure. Thus, preparation of heterostructures with different crystal structures is desirable but still a great challenge. Herein, we report a one-step CVD strategy to successfully grow SnS2/SnS vertical heterostructures on a mica substrate. Raman spectroscopy, atomic force microscopy (AFM) and transmission electron microscopy (TEM) characterizations reveal that the heterostructure is formed by stacking of pyramid-shaped SnS2 of the hexagonal structure onto the rhombus SnS flake of the orthorhombic structure. The photodetector based on the SnS2/SnS heterostructure demonstrates high optoelectronic performance: a 27.7 A W−1 photoresponsivity, 2.2 × 103 on/off ratio, less than 10 ms response time and 2.1 × 1010 jones specific detectivity. The superior performance originates from the high crystal quality of the as-grown heterostructure and its vertical device architecture. This study can expand our capability to fabricate a variety of two-dimensional heterostructures and make these heterostructures highly desirable as novel building blocks for potential applications in electronic and optoelectronic devices. |
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ISSN: | 2052-1545 2052-1553 |
DOI: | 10.1039/c8qi00251g |