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2D/2D Heterostructured CdS/WS2 with Efficient Charge Separation Improving H-2 Evolution under Visible Light Irradiation

机译:2D / 2D异质结构CDS / WS2,具有有效电荷分离,改善可见光照射下的H-2演化

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摘要

Efficient Efiicient water splitting for H-2 evolution sender visible light irradiation has attracted more attention for solving the global environmental and energy issues, but it is still a major, challenge to develop an earth-abundant and effluent photocatalyst. Herein, we report two-dimensional (2D))/2D heterostructured CdS/WS2, (CdS/WS2), composed of nano sheet CdS (CdS) and nanosheet WS2 (WS2), as an efficient photocatalyst for H-2 evolution. As a noble metal-free visible light-driven catalyst for H-2, evolution, CdS/WS2 with 10 wt % WS2 exhibited the largest H-2 evolution rate of 14.1 mmol g(-1) h(-1) under visible light,irradiation to be 8 times larger than that if pure Cds. The lifetime and dynamics of photogenerated electrons were evaluated by femtosecond time-resolved diffuse reflectance spectroscopy, indicating that WS2 works as an electron-trapping site and a cocatalyst to cause H-2 evolution under visible light irradiation. This work suggests that Cds/Ws(2) has great potential as a low-cost and highly efficient photocatalyst for water splitting.
机译:H-2演化发件人可见光辐射的高效态度分裂引起了解决全球环境和能源问题的更多关注,但仍然是发展地球丰富和流出的光催化剂的主要,挑战。在此,我们报告由纳米片CDS(CDS)和纳米片WS2(WS2)组成的二维(2D))/ 2D异质结构CDS / WS2,(CDS / WS2),作为H-2进化的有效光催化剂。作为H-2的无贵金属可见光驱动催化剂,进化,具有10wt%WS2的Cds / Ws2,在可见光下表现出14.1mmol G(-1)H(-1)的最大H-2演化速率,辐照比纯CDS的辐照为8倍。通过飞秒时间分辨的漫反射光谱评估光生电子的寿命和动力学,表明WS2作为电子捕获部位和助催化剂,以在可见光照射下引起H-2演变。这项工作表明CDS / WS(2)具有巨大的潜力,作为水分裂的低成本和高效的光催化剂。

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