首页> 外文期刊>Advanced Functional Materials >N-Doped CsTaWO_6 as a New Photocatalyst for Hydrogen Production from Water Splitting Under Solar Irradiation
【24h】

N-Doped CsTaWO_6 as a New Photocatalyst for Hydrogen Production from Water Splitting Under Solar Irradiation

机译:N掺杂的CsTaWO_6作为新型光催化剂,用于在太阳辐射下分解水制氢

获取原文
获取原文并翻译 | 示例
           

摘要

Photocatalysts for efficient solar hydrogen production are highly sought after. Here a new type of nitrogen-doped tantalum tungstenate (CsTaWO_6) material, which demonstrates excellent visible light absorption and improved photocatalytic activity, is demonstrated. X-ray diffraction (XRD) patterns reveal that the defect pyrochlore-type structure of CsTaWO_6 remained intact upon nitrogen doping. UV-vis spectra indicate that nitrogen doping in the compound results in a red-shift of the absorption edge from 358 nm to 580 nm, thus offering significantly increased visible light absorption. X-ray photoelectron spectroscopy (XPS) further indicates that [Ta/W]-N bonds were formed by inducing nitrogen to replace a small amount of oxygen in the material, resulting in a compound of CsTaWO6_xN_x. The explanation of the experimental results is supported by density functional theory calculations. The density of states (DOS) and the projected DOS after substitutional doping of nitrogen in CsTaWO_6 indicated that N-doping reduces the bandgap significantly from 3.8 to 2.3 eV due to N 2p and O 2p orbital mixing. The role of the new N 2p states is also investigated by studying the production of theOH radicals in the visible light region (>420 nm). In CsTaWO_(6-x)N_x, the N 2p orbitals are the main contributors to the top of the valence band, causing bandgap narrowing while the bottom of conduction band, due to Ta 4d orbitals, remains almost unchanged. Compared with its undoped counterpart, nitrogen-doped CsTaWO_(6_x)N_x exhibits a nearly 100% increase in solar hydrogen production efficiency.
机译:高效生产太阳能氢的光催化剂备受追捧。在这里,展示了一种新型的氮掺杂钨酸钽(CsTaWO_6)材料,该材料具有出色的可见光吸收能力和改善的光催化活性。 X射线衍射(XRD)图谱表明,氮掺杂后CsTaWO_6的缺陷烧绿石型结构保持完整。紫外可见光谱表明,化合物中的氮掺杂会导致吸收边从358 nm到580 nm发生红移,从而提供了明显增加的可见光吸收。 X射线光电子能谱(XPS)进一步表明,[Ta / W] -N键是通过诱导氮替代材料中的少量氧而形成的,从而形成CsTaWO6_xN_x的化合物。实验结果的解释得到密度泛函理论计算的支持。 CsTaWO_6中氮的置换掺杂后的状态密度(DOS)和预计的DOS表明,由于N 2p和O 2p的轨道混合,N掺杂将带隙从3.8 eV显着降低。还通过研究可见光区域(> 420 nm)中OH自由基的产生来研究新的N 2p态的作用。在CsTaWO_(6-x)N_x中,N 2p轨道是价带顶部的主要贡献者,导致带隙变窄,而由于Ta 4d轨道,导带的底部几乎保持不变。与未掺杂的同类产品相比,掺氮的CsTaWO_(6_x)N_x的太阳能制氢效率提高了近100%。

著录项

  • 来源
    《Advanced Functional Materials》 |2011年第1期|p.126-132|共7页
  • 作者单位

    ARC Centre of Excellence for Functional Nanomaterials School of Chemical Engineering, and Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia, Brisbane, QLD 4072, Australia;

    ARC Centre of Excellence for Functional Nanomaterials School of Chemical Engineering, and Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia, Brisbane, QLD 4072, Australia;

    ARC Centre of Excellence for Functional Nanomaterials School of Chemical Engineering, and Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia, Brisbane, QLD 4072, Australia;

    Centre for Computational Molecular Science Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia, Brisbane, QLD 4072, Australia;

    Centre for Computational Molecular Science Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia, Brisbane, QLD 4072, Australia;

    ARC Centre of Excellence for Functional Nanomaterials School of Chemical Engineering, and Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia, Brisbane, QLD 4072, Australia;

    ARC Centre of Excellence for Functional Nanomaterials School of Chemical Engineering, and Australian Institute for Bioengineering and Nanotechnology The University of Queensland St Lucia, Brisbane, QLD 4072, Australia;

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

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号