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NiS modified CdS pyramids with stacking fault structures: Highly efficient and stable photocatalysts for hydrogen production from water

机译:NiS修饰的具有堆叠故障结构的CdS金字塔:用于从水中生产氢气的高效稳定的光催化剂

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NiS modified three-dimensional pyramidic CdS with stacking fault structures were successfully synthesized by using the one-step method and an ammonia aqueous solvent as the hydrothermal solvent. Thus, CdS showed superior photocatalytic activities for hydrogen evolution from water under visible light irradiation (lambda >= 420 nm), which could achieve a hydrogen evolution rate of 49.2 mmol g(-1) h(-1), with an extremely high apparent quantum yield (AQY = 74.6%) at 420 nm. To our knowledge, this value is the highest reported efficiency value for NiSx modified CdS photocatalysts. CdS exhibited a three-dimensional pyramid structure with large specific surface areas, which may provide more active sites for the photocatalytic reaction. Stacking fault structures were observed in CdS by transmission electron microscopy (TEM). P-type NiS nanoparticles were highly dispersed on the surface of n-type CdS pyramids, forming p-n junctions at the interface. The stacking fault structures and junctions strengthened the separation of photo-carriers near the interface, which may greatly enhance the activity of photocatalytic hydrogen production for CdS. The catalyst also showed perfect stability, and the photoactivity showed no significant degradation during continuous hydrogen production over nearly 120 h, which has not been reported in the literature. (C) 2017 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
机译:采用一步法,以氨水溶剂为水热溶剂,成功合成了NiS修饰的具有堆积缺陷结构的三维金字塔CdS。因此,CdS在可见光照射下(λ> = 420 nm)显示出优异的光催化活性,可从水中析氢,可实现49.2 mmol g(-1)h(-1)的析氢速率,具有极高的表观活性。 420 nm时的量子产率(AQY = 74.6%)。据我们所知,该值是NiSx改性CdS光催化剂报道的最高效率值。 CdS的三维金字塔结构具有较大的比表面积,可为光催化反应提供更多的活性位点。通过透射电子显微镜(TEM)在CdS中观察到堆叠断层结构。 P型NiS纳米粒子高度分散在n型CdS金字塔的表面上,在界面处形成p-n结。堆叠的断层结构和结加强了界面附近的光载流子的分离,这可以大大增强CdS的光催化制氢活性。该催化剂还显示出完美的稳定性,并且在连续近120小时的制氢过程中,光活性没有显示出明显的降解,这在文献中还没有报道。 (C)2017氢能出版物有限公司。由Elsevier Ltd.出版。保留所有权利。

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