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集成在硫化镉纳米棒上的异质结构 WS - 硫化钼超薄纳米片,用于促进电荷分离和迁移并改善太阳能驱动的光催化析氢性能。

Heterostructured WS -MoS Ultrathin Nanosheets Integrated on CdS Nanorods to Promote Charge Separation and Migration and Improve Solar-Driven Photocatalytic Hydrogen Evolution.

作者信息

Reddy D Amaranatha, Park Hanbit, Ma Rory, Kumar D Praveen, Lim Manho, Kim Tae Kyu

机构信息

Department of Chemistry and Chemical Institute for Functional Materials, Pusan National University, Busan, 46241, Republic of Korea.

出版信息

ChemSusChem. 2017 Apr 10;10(7):1563-1570. doi: 10.1002/cssc.201601799. Epub 2017 Mar 2.

DOI:10.1002/cssc.201601799
PMID:28121391
Abstract

Solar-driven photocatalytic hydrogen evolution is important to bring solar-energy-to-fuel energy-conversion processes to reality. However, there is a lack of highly efficient, stable, and non-precious photocatalysts, and catalysts not designed completely with expensive noble metals have remained elusive, which hampers their large-scale industrial application. Herein, for the first time, a highly efficient and stable noble-metal-free CdS/WS -MoS nanocomposite was designed through a facile hydrothermal approach. When assessed as a photocatalyst for water splitting, the CdS/WS -MoS nanostructures exhibited remarkable photocatalytic hydrogen-evolution performance and impressive durability. An excellent hydrogen evolution rate of 209.79 mmol g  h was achieved under simulated sunlight irradiation, which is higher than the values for CdS/MoS (123.31 mmol g  h ) and CdS/WS nanostructures (169.82 mmol g  h ) and the expensive CdS/Pt benchmark catalyst (34.98 mmol g  h ). The apparent quantum yield reached 51.4 % at λ=425 nm in 5 h. Furthermore, the obtained hydrogen evolution rate was better than those of several noble-metal-free catalysts reported previously. The observed high rate of hydrogen evolution and remarkable stability may be a result of the ultrafast separation of photogenerated charge carriers and transport between the CdS nanorods and the WS -MoS nanosheets, which thus increases the number of electrons involved in hydrogen production. The proposed designed strategy is believed to potentially open a door to the design of advanced noble-metal-free photocatalytic materials for efficient solar-driven hydrogen production.

摘要

太阳能驱动的光催化析氢对于将太阳能转化为燃料的能量转换过程成为现实至关重要。然而,缺乏高效、稳定且非贵金属的光催化剂,完全不使用昂贵贵金属设计的催化剂仍然难以实现,这阻碍了它们的大规模工业应用。在此,首次通过简便的水热法设计了一种高效且稳定的无贵金属CdS/WS -MoS纳米复合材料。当作为光解水的光催化剂进行评估时,CdS/WS -MoS纳米结构表现出卓越的光催化析氢性能和令人印象深刻的耐久性。在模拟太阳光照射下,实现了209.79 mmol g  h的优异析氢速率,高于CdS/MoS(123.31 mmol g  h )和CdS/WS纳米结构(169.82 mmol g  h )以及昂贵的CdS/Pt基准催化剂(34.98 mmol g  h )的值。在5小时内于λ=425 nm处表观量子产率达到51.4%。此外,获得的析氢速率优于先前报道的几种无贵金属催化剂。观察到的高析氢速率和显著稳定性可能是光生电荷载流子超快分离以及在CdS纳米棒和WS -MoS纳米片之间传输的结果,从而增加了参与产氢的电子数量。所提出的设计策略有望为设计用于高效太阳能驱动产氢的先进无贵金属光催化材料打开一扇门。

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