One-pot synthesis of S-scheme MoS 2 /g-C 3 N 4 heterojunction as effective visible light photocatalyst
Despite pioneering as the holy grail in photocatalysts, abundant reports have demonstrated that g-C N performs poor photocatalytic activity due to its high recombination rate of photo-induced charge carriers. Many efforts have been conducted to overcome this limitation in which the semiconductor-sem...
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Veröffentlicht in: | Scientific reports 2021-07, Vol.11 (1), p.14787 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
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Zusammenfassung: | Despite pioneering as the holy grail in photocatalysts, abundant reports have demonstrated that g-C
N
performs poor photocatalytic activity due to its high recombination rate of photo-induced charge carriers. Many efforts have been conducted to overcome this limitation in which the semiconductor-semiconductor coupling strategies toward heterojunction formation were considered as the easiest but the most effective method. Herein, a one-pot solid-state reaction of thiourea and sodium molybdate as precursors at different temperatures under N
gas was applied for preparing composites of MoS
/g-C
N
. The physicochemical characterization of the final products determines the variation in contents of components (MoS
and g-C
N
) via the increase of synthesis temperature. The enhanced photocatalytic activity of the MoS
/g-C
N
composites was evaluated by the degradation of Rhodamine B in an aqueous solution under visible light. Therein, composites synthesized at 500 °C showed the best photocatalytic performance with a degradation efficiency of 90%, much higher than that of single g-C
N
. The significant improvement in photocatalytic performance is attributed to the enhancement in light-harvesting and extension in photo-induced charge carriers' lifetime of composites which are originated from the synergic effect between the components. Besides, the photocatalytic mechanism is demonstrated to well-fit into the S-scheme pathway with apparent evidences. |
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ISSN: | 2045-2322 |