Construction of LSPR-enhanced 0D/2D CdS/MoO3−x S-scheme heterojunctions for visible-light-driven photocatalytic H2 evolution
Plasmonic nonmetal semiconductors with localized surface plasmon resonance (LSPR) effects possess extended light-response ranges and can act as highly efficient H2 generation photocatalysts. Herein, an LSPR-enhanced 0D/2D CdS/MoO3−x heterojunction has been synthesized by the growth of 0D CdS nanopar...
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| Vydáno v: | Chinese journal of catalysis Ročník 42; číslo 1; s. 87 - 96 |
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| Hlavní autoři: | , , , , , |
| Médium: | Journal Article |
| Jazyk: | angličtina |
| Vydáno: |
Elsevier B.V
01.01.2021
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| Témata: | |
| ISSN: | 1872-2067, 1872-2067 |
| On-line přístup: | Získat plný text |
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| Shrnutí: | Plasmonic nonmetal semiconductors with localized surface plasmon resonance (LSPR) effects possess extended light-response ranges and can act as highly efficient H2 generation photocatalysts. Herein, an LSPR-enhanced 0D/2D CdS/MoO3−x heterojunction has been synthesized by the growth of 0D CdS nanoparticles on 2D plasmonic MoO3−x elliptical nanosheets via a simple coprecipitation method. Taking advantage of the LSPR effect of the MoO3−x elliptical nanosheets, the light absorption of the CdS/MoO3−x heterojunction was extended from 600 nm to the near-infrared region (1400 nm). Furthermore, the introduction of 2D plasmonic MoO3−x elliptical nanosheets not only provided a platform for the growth of CdS nanoparticles, but also contributed to the construction of an LSPR-enhanced S-scheme structure due to the interface between the MoO3−x and CdS, accelerating the separation of light-induced electrons and holes. Therefore, the CdS/MoO3−x heterojunction exhibited higher photocatalytic H2 generation activity than pristine CdS under visible light irradiation, including under 420, 450, 550, and 650 nm monochromic light, as well as improved photo-corrosion performance.
The MoO3-x/CdS heterojunctions exhibit improved photocatalytic H2 generation activity, which is accredited to an LSPR-enhanced S-scheme charge transfer mechanism. |
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| ISSN: | 1872-2067 1872-2067 |
| DOI: | 10.1016/S1872-2067(20)63595-1 |