Largely enhanced photocatalytic hydrogen production rate of CdS/(Au-ReS 2 ) nanospheres by the dielectric-plasmon hybrid antenna effect
In this study, we synthesized CdS/(Au-ReS ) nanospheres that have highly efficient photocatalytic hydrogen production activity induced by dielectric-plasmon hybrid antenna resonance. As the diameter (D) of ReS nanospheres consisting of 2D nanosheets increases from 114 ± 11 to 218 ± 25 nm, the resona...
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Published in | Nanoscale Vol. 10; no. 41; pp. 19586 - 19594 |
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Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Royal Society of Chemistry
07.11.2018
|
Subjects | |
Online Access | Get full text |
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Summary: | In this study, we synthesized CdS/(Au-ReS
) nanospheres that have highly efficient photocatalytic hydrogen production activity induced by dielectric-plasmon hybrid antenna resonance. As the diameter (D) of ReS
nanospheres consisting of 2D nanosheets increases from 114 ± 11 to 218 ± 25 nm, the resonance wavelength of the ReS
dielectric antenna is tuned from 380 to 620 nm and the hydrogen production rate for the CdS/(Au-ReS
) nanospheres increases by more than 1.85 times and reaches a value as high as 3060 μmol g
h
, with a 9% weight percentage of Au. Due to the enhancements of the local electromagnetic field and excitation energy transfer by the ReS
-Au dielectric-plasmon hybrid antenna, the hydrogen production rate for the CdS/(Au-ReS
) nanospheres (D = 218 ± 25 nm) is 797, 319, 105 and 12 times larger than that for pure ReS
, Au-ReS
, CdS, and CdS-ReS
, respectively. Additionally, the persistence and reusability measurements indicate a favorable stability of CdS/(Au-ReS
). These results provide a strategy to prepare a new class of dielectric-plasmon hybrid antennas consisting of 2D materials and metal nanoparticles, which have promise in applications ranging from photocatalysis to nonlinear optics. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2040-3364 2040-3372 |
DOI: | 10.1039/c8nr07013j |