首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Enhanced photoexcited carrier separation in CdS-SnS2 heteronanostructures: a new 1D-0D visible-light photocatalytic system for the hydrogen evolution reaction
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Enhanced photoexcited carrier separation in CdS-SnS2 heteronanostructures: a new 1D-0D visible-light photocatalytic system for the hydrogen evolution reaction

机译:Cds-SNS2异系结构中增强的光透镜载体分离:用于氢进化反应的新的1D-0D可见光光催化系统

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摘要

Photocatalytic water splitting to produce hydrogen is a significant reaction for renewable energy storage and needs highly efficient and stable catalysts. Considering the attractive properties such as a suitable bandgap, high specific surface area and appropriate band structure one-dimensional CdS is a promising visible-light photocatalyst; however, its severe recombination rate and photocorrosion impede its widespread application. Fabrication of heterostructures composed of heterojunctions is a very effective approach to design highly stable and active photocatalytic systems. Here, we report for the first time the fabrication of one-dimensional (1D)/zero-dimensional (0D) core-shell heteronanostructures (CSHNSs), where 0D SnS2 quantum dots are grown on the surface of 1D CdS nanorods to realize efficient H-2 evolution reaction under sunlight. The proposed CdS-SnS2 CSHNS system significantly improved the electron-hole separation efficiency between CdS and SnS2 components. Meanwhile in the core-shell structure, the deposited SnS2 quantum dots not only act as a shielding layer to restrain CdS photocorrosion but also have a large contact interface which can further improve the electron-hole separation efficiency. As a result, the optimized CdS-SnS2 CSHNS photocatalyst exhibits excellent visible light absorption and shows a superior hydrogen evolution rate of 35.65 mmol g(-1) h(-1) under the illumination of simulated sunlight with very good stability.
机译:光催化水分分裂以产生氢是可再生能量储存的重要反应,需要高效且稳定的催化剂。考虑到诸如合适的带隙,高比表面积和适当的带结构一维CD的有吸引性的性质是一个有希望的可见光光催化剂;然而,其严重的重组率和光腐蚀阻碍了其广泛的应用。由异质结组成的异质结构的制备是设计高稳态和活性光催化系统的非常有效的方法。在这里,我们第一次报告一维(1D)/零维(0d)核 - 壳杂壳属性(CSHNS)的制造,其中0D SNS2量子点在1D CD纳米棒的表面上生长以实现有效的H. -2阳光下的进化反应。所提出的CDS-SNS2 CSHNS系统显着改善了CD和SNS2组分之间的电子空穴分离效率。同时在核心壳结构中,沉积的SNS2量子点不仅用作屏蔽层以抑制CDS光腐蚀,而且还具有大的接触界面,其可以进一步提高电子 - 空穴分离效率。结果,优化的CDS-SNS2 CSHNS光催化剂表现出优异的可见光吸收,并且在模拟阳光照射下显示出35.65mmol G(-1)H(-1)的优异氢进化速率,其稳定性非常好。

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