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通过整合紫色氧化钨纳米线和硫化镉纳米球构建三维S型异质结用于高效光催化产氢

Three-dimensional S-scheme heterojunction by integration of purple tungsten oxide nanowires and cadmium sulfide nanospheres for effective photocatalytic hydrogen generation.

作者信息

Liu Teng, Li Yuezheng, Lv Yinghao, Qiu Pengyuan, Xiong Ya, Tian Jian

机构信息

School of Materials Science and Engineering, Shandong University of Science and Technology, Qingdao 266590, China.

School of Materials Science and Engineering, Shandong University of Science and Technology, Qingdao 266590, China.

出版信息

J Colloid Interface Sci. 2023 Jun 15;640:568-577. doi: 10.1016/j.jcis.2023.02.150. Epub 2023 Mar 3.

Abstract

The practical photocatalytic application of cadmium sulfide (CdS) has been significantly constrained by fast carrier recombination and significant photocorrosion. Therefore, we developed a three-dimensional (3D) step-by-step (S-scheme) heterojunction using the coupling interface between purple tungsten oxide (WO) nanowires and CdS nanospheres. The photocatalytic hydrogen evolution rate of optimized WO/CdS 3D S-scheme heterojunction can reach 9.7 mmol·h·g, 7.5 and 16.2 times greater than pure CdS (1.3 mmol·h·g) and 10 wt%-WO/CdS (mechanical mixing, 0.6 mmol·h·g), proving that the tight S-scheme heterojunction constructed by the hydrothermal method can efficiently enhance the carrier separation. Notably, the apparent quantum efficiency (AQE) of WO/CdS 3D S-scheme heterojunction approaches 7.5% and 3.5% at 370 nm and 456 nm, respectively, which is 7.5 and 8.8 times than pure CdS (1.0% and 0.4%). The produced WO/CdS catalyst also has relative stability of structure and hydrogen production. Additionally, the H evolution rate of WO/CdS 3D S-scheme heterojunction is 1.2 times greater than 1 wt%-platinum (Pt)/CdS (8.2 mmol·h·g), which indicates that the WO can effectively replace the precious metal for boosting the hydrogen production rate.

摘要

硫化镉(CdS)的实际光催化应用受到快速的载流子复合和显著的光腐蚀的严重限制。因此,我们利用紫色氧化钨(WO)纳米线与CdS纳米球之间的耦合界面,开发了一种三维(3D)分步(S型)异质结。优化后的WO/CdS 3D S型异质结的光催化析氢速率可达9.7 mmol·h·g,分别是纯CdS(1.3 mmol·h·g)和10 wt%-WO/CdS(机械混合,0.6 mmol·h·g)的7.5倍和16.2倍,证明通过水热法构建的紧密S型异质结能够有效地提高载流子分离效率。值得注意的是,WO/CdS 3D S型异质结在370 nm和456 nm处的表观量子效率(AQE)分别接近7.5%和3.5%,分别是纯CdS(1.0%和0.4%)的7.5倍和8.8倍。所制备的WO/CdS催化剂还具有相对稳定的结构和产氢性能。此外,WO/CdS 3D S型异质结的析氢速率比1 wt%-铂(Pt)/CdS(8.2 mmol·h·g)高1.2倍,这表明WO可以有效地替代贵金属来提高产氢速率。

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