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首页> 外文期刊>Applied Surface Science >DFT investigation on two-dimensional GeS/WS2 van der Waals heterostructure for direct Z-scheme photocatalytic overall water solittins
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DFT investigation on two-dimensional GeS/WS2 van der Waals heterostructure for direct Z-scheme photocatalytic overall water solittins

机译:DFT研究直接Z方案光催化整体水溶性固体的二维GeS / WS2 van der Waals异质结构

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摘要

Graphical abstractDisplay OmittedHighlightsThe GeS/WS2heterojunction is a candidate for the direct Z-scheme photocatalysts.The interface Z-scheme electron transfer is investigated through DFT.The internal electric field can promote the separation of charge carriers.Reducing the interfacial distance could improve the catalytic activity.AbstractRecently, extensive attention has been paid to the direct Z-scheme systems for photocatalytic water splitting where carriers migrate directly between the two semiconductors without a redox mediator. In the present work, the electronic structure and related properties of two-dimensional (2D) van de Waals (vdW) GeS/WX2(X=O, S, Se, Te) heterojunction are systematically investigated by first-principles calculations. Our results demonstrate that, the GeS/WS2heterojunction could form a direct Z-scheme system for photocatalytic water splitting, whereas the GeS/WX2(X=O, Se, Te) can’t, because of their respective unsuitable electronic structures. For the GeS/WS2heterojunction, the GeS and WS2monolayers serve as photocatalysts for the hydrogen evolution reactionand oxygen evolution reaction, respectively. The internal electric field induced by the electron transfer at the interface can promote the separation of photo-generated charge carriers and formation of the interface Z-scheme electron transfer. Remarkably, the designed GeS/WS2heterojunction not only enhances the hydrogen production activity of GeS and the oxygen production ability of WS2but also improves the light absorption of the two monolayers by reducing the band gaps. Moreover, it is found that narrowing the interlayer distance could enhance the internal electric field, improving the photocatalytic ability of the vdW heterojunction. This work provides fundamental insights for further design and preparation of emergent metal dichalcogenide catalysts, beneficial for the development in clean energy.
机译: 图形摘要 < ce:simple-para>省略显示 突出显示 GeS / WS 2 异质结是直接使用Z方案光催化剂的候选对象。 界面Z方案电子转移通过DFT进行调查。 内部电场可以促进电荷载流子的分离。 减小界面距离可以提高催化活性。 摘要 最近,直接广告已引起广泛关注用于光催化水分解的Z方案系统,其中载流子直接在两个半导体之间迁移而没有氧化还原介体。在本工作中,二维(2D)van de Waals(vdW)GeS / WX 2 (X = O,S ,Se,Te)异质结通过第一性原理计算得到系统地研究。我们的结果表明,GeS / WS 2 异质结可以形成用于光催化水分解的直接Z方案系统,而GeS / WX 2 (X = O,Se,Te)不能,因为它们各自的电子结构不合适。对于GeS / WS 2 异质结,GeS和WS 2 单分子层可作为以下物质的光催化剂分别是氢气析出反应和氧气析出反应。由界面处的电子转移感应的内部电场可促进光生电荷载流子的分离和界面Z方案电子转移的形成。值得注意的是,设计的GeS / WS 2 异质结不仅增强了GeS的产氢活性,而且增强了WS 2 ,但还可以通过减小带隙来改善两个单层的光吸收。此外,发现缩小层间距离可以增强内部电场,提高vdW异质结的光催化能力。这项工作为进一步设计和制备新兴的金属二硫化氢催化剂提供了基础见解,有利于清洁能源的发展。

著录项

  • 来源
    《Applied Surface Science》 |2018年第15期|365-374|共10页
  • 作者单位

    School of Physics, State Key Laboratory of Crystal Materials, Shandong University,School of Physics and Electric Engineering, Anyang Normal University;

    School of Physics, State Key Laboratory of Crystal Materials, Shandong University;

    School of Physics, State Key Laboratory of Crystal Materials, Shandong University;

    School of Physics, State Key Laboratory of Crystal Materials, Shandong University;

    School of Physics, State Key Laboratory of Crystal Materials, Shandong University;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Direct Z-scheme; Heterojunction; GeS/WS2; Water splitting;

    机译:直接Z方案;异质结;GeS / WS2;水分解;

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