Molybdenum disulfide quantum dots decorated bismuth sulfide as a superior noble-metal-free photocatalyst for hydrogen evolution through harnessing a broad solar spectrum

[Display omitted] •Photoactivity of MoS2QDs doped Bi2S3 extended from visible to NIR range.•Bi-functional roles of MoS2QDs as electron entrapment sites and spectral converters.•The highest H2 evolution of 17.7 mmol/h.g was achieved under stimulated solar light. Molybdenum disulfide quantum dots (MoS...

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Veröffentlicht in:Applied catalysis. B, Environmental Environmental, 2018-09, Vol.232, p.117-123
Hauptverfasser: Lee, W.P. Cathie, Kong, Xin Ying, Tan, Lling-Lling, Gui, Meei Mei, Sumathi, S., Chai, Siang-Piao
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Sprache:eng
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Zusammenfassung:[Display omitted] •Photoactivity of MoS2QDs doped Bi2S3 extended from visible to NIR range.•Bi-functional roles of MoS2QDs as electron entrapment sites and spectral converters.•The highest H2 evolution of 17.7 mmol/h.g was achieved under stimulated solar light. Molybdenum disulfide quantum dots (MoS2QDs) decorated bismuth sulfide (Bi2S3) photocatalyst was synthesized. Photoluminescence characterization showed that the as-developed MoS2QDs possessed intriguing up-conversion and down-conversion properties, indicating their capability to harness energy from the light spectrum ranging from ultraviolet (UV) to near-infrared (NIR). In this study, the highest hydrogen yield of 17.7 mmol/g.h was achieved by 0.14MoS2QD/Bi2S3, which was almost 4.5 folds higher than that of undoped Bi2S3 under stimulated solar light irradiation. Furthermore, examination of the 0.14MoS2QD/Bi2S3 photocatalysts under NIR irradiation showed a significant photocurrent response and an accumulative H2 yield of 53.6 μmol/g after 6 h reaction. This is a major breakthrough as most photocatalysts can only be activated under UV and/or visible light irradiation. This work provides new insights into the design of MoS2QD/Bi2S3 for harnessing energy from a broad solar spectrum to photocatalytically split water to produce hydrogen.
ISSN:0926-3373
1873-3883
DOI:10.1016/j.apcatb.2018.03.019