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Title: | Highly efficient visible-light-driven photocatalytic hydrogen evolution by all-solid-state Z-scheme CdS/QDs/ZnIn2S4 architectures with MoS2 quantum dots as solid-state electron mediator | Authors: | Chen, Wei Yan, Rui-Qiang Zhu, Jian-Qun Huang, Guo-Bo Chen, Zhong |
Keywords: | Engineering::Materials | Issue Date: | 2019 | Source: | Chen, W., Yan, R., Zhu, J., Huang, G. & Chen, Z. (2019). Highly efficient visible-light-driven photocatalytic hydrogen evolution by all-solid-state Z-scheme CdS/QDs/ZnIn2S4 architectures with MoS2 quantum dots as solid-state electron mediator. Applied Surface Science, 504, 144406-. https://dx.doi.org/10.1016/j.apsusc.2019.144406 | Journal: | Applied Surface Science | Abstract: | All-solid-state Z-scheme CdS/QDs/ZnIn2S4 architectures with MoS2 quantum dots as solid-state electron mediator were successfully designed and constructed by optimally combining one-dimensional CdS nanorods, zero-dimensional MoS2 quantum dots (QDs) and two-dimensional ZnIn2S4 nanosheets. The photocatalytic water splitting for hydrogen evolution demonstrated that such structural design can synergistically trigger remarkably improved visible-light-driven photocatalytic activity. Photocatalytic H2-evolution at 2107.5 μmol g−1 h−1 was achieved on this CdS/QDs/ZnIn2S4 architectures under visible light irradiation, exceeding those of bare CdS nanorods and pure ZnIn2S4 nanosheets by a factor of 26 and 62, respectively. This highly efficient photocatalytic activity arises from the effective charge separation and favourable electron mediator of MoS2 QDs. The Z-scheme charge separation mechanism was verified by the ESR, PL-TA and organic electron acceptor test. | URI: | https://hdl.handle.net/10356/150386 | ISSN: | 0169-4332 | DOI: | 10.1016/j.apsusc.2019.144406 | Rights: | © 2019 Elsevier B.V. All rights reserved. This paper was published in Applied Surface Science and is made available with permission of Elsevier B.V. | Fulltext Permission: | open | Fulltext Availability: | With Fulltext |
Appears in Collections: | MSE Journal Articles |
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