Nanosheet-based Bi2MoxW1- xO6 solid solutions with adjustable band gaps and enhanced visible-light-driven photocatalytic activities

  • Liang Zhou
  • , Minmin Yu
  • , Jie Yang
  • , Yunhua Wang
  • , Chengzhong Yu*
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

90 Scopus citations

Abstract

Bi2MoxW1-xO6 solid solutions with various compositions (x = 0, 0.25, 0.50, 0.75, and 1.00) have been synthesized by a facile hydrothermal crystallization method. All the as-synthesized products are composed of nanosheets with similar orthorhombic Aurivillius layered structures. With decreasing Mo content, the thickness of the nanosheets decreases. The nanosheets begin to intergrow at x = 0.75 and further assemble into hierarchical superstructures through "oriented attachmenta" with even less Mo content. For the Bi2Mo xW1-xO6 solid solutions with x = 0.25, 0.50, and 0.75, the valence band is widened and the conduction band is elevated when compared with the most intensively studied Bi2WO6 photocatalyst. As a result, the Bi2MoxW 1-xO6 solid solutions (x = 0.25, 0.50, and 0.75) show narrowed band gaps of a2.69 eV when compared with Bi2WO6 (2.94 eV) and Bi2MoO6 (2.72 eV). The photocatalytic activities of the as-prepared products have been evaluated using the photodecomposition of methylene blue under visible light irradiation as a model reaction. The sample, Bi2Mo0.25W0.75O 6, exhibits the highest photocatalytic activity. The intrinsic layered structure, nanosheet morphology, manipulated band structure and band gap, and the W content play important roles in the photocatalytic activity. Our approach provides a facile technique to tune both the nanostructure and the band gap of photocatalysts by simply adjusting the composition of the solid solutions, leading to photocatalysts with enhanced visible light photocatalytic activity. This method may be further extended to the designed synthesis of novel and highly efficient visible-light-driven semiconductors for environmental remediation.

Original languageEnglish
Pages (from-to)18812-18818
Number of pages7
JournalJournal of Physical Chemistry C
Volume114
Issue number44
DOIs
StatePublished - 11 Nov 2010
Externally publishedYes

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