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首页> 外文期刊>Catalysis science & technology >Visible light induced efficient hydrogen production through semiconductor-conductor-semiconductor (S-C-S) interfaces formed between g-C3N4 and rGO/Fe2O3 core-shell composites
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Visible light induced efficient hydrogen production through semiconductor-conductor-semiconductor (S-C-S) interfaces formed between g-C3N4 and rGO/Fe2O3 core-shell composites

机译:可见光诱导高效氢生产通过semiconductor-conductor-semiconductor (S-C-S)接口之间形成g-C3N4和rGO / Fe2O3核壳复合材料

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摘要

Herein, we have constructed a type II heterojunction, g-C3N4 supported rGO/Fe2O3 core-shell composite, using a sonochemically assisted hydrothermal method followed by a wet-impregnation method for visible light driven hydrogen production via water splitting. Notably, compared to pristine g-C3N4 (432.4 mu mol g(-1) h(-1)) and g-C3N4/rGO (876 mu mol g(-1) h(-1)), we have achieved similar to 15 and 7.5 fold enhanced photocatalytic H-2 production rates with g-C3N4/rGO/Fe2O3 (6607 mu mol g(-1) h(-1)) composites. The improved photocatalytic H-2 production performance was mainly attributed to the formation of type II heterojunctions between g-C3N4 and Fe2O3 mediated through rGO by forming Fe-O-C and C-N-C bonds as confirmed by XPS analysis. Moreover, the photo-generated carriers are rapidly separated through the electron mediator rGO via the Z-scheme mechanism as is consistent with PL, EIS and photocurrent studies.
机译:在此,我们构造了一个II型异质结,g-C3N4支持rGO / Fe2O3核壳复合材料,使用声化学的紧随其后的是一个辅助水热方法wet-impregnation可见光驱动的方法通过水分解制氢。相对于原始g-C3N4(432.4μ摩尔g (1)h(1))和g-C3N4 / rGO(876亩摩尔g (1) h (1)),我们取得了类似于15和7.5折增强光催化氢生产速度g-C3N4 rGO / Fe2O3(6607亩摩尔g (1) h (1))复合材料。主要是由于生产性能II型之间的垂直的形成g-C3N4 Fe2O3介导通过rGO形成Fe-O-C证实了XPS和C-N-C债券分析。通过电子迅速分离吗中介通过Z-scheme rGO机制与PL一致,EIS和光电流的研究。

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