| Literature DB >> 27668449 |
Yang Bai1, Liqun Ye1,2, Ting Chen1, Li Wang2, Xian Shi1, Xu Zhang3, Dan Chen4.
Abstract
Bismuth-rich bismuth oxyhalides (Bi-O-X; X = Cl, Br, I) display high photocatalytic reduction activity due to the promoting conduction band potential. In this work, two Bi5O7I nanosheets with different dominant facets were synthesized using either molecular precursor hydrolysis or calcination. Crystal structure characterizations, included X-ray diffraction patterns (XRD), field emission electron microscopy and fast Fourier transformation (FFT) images, showed that hydrolysis and calcination resulted in the dominant exposure of {100} and {001} facets, respectively. Photocatalytic data revealed that Bi5O7I-001 had a higher activity than Bi5O7I-100 for N2 fixation and dye degradation. Photoelectrochemical data revealed that Bi5O7I-001 had higher photoinduced carrier separation efficiency than Bi5O7I-100. The band structure analysis also used to explain the underlying photocatalytic mechanism based on the different conduction band position. This work presents the first report about the facet-dependent photocatalytic performance of bismuth-rich Bi-O-X photocatalysts.Entities:
Keywords: Bi5O7I; N2 fixation; bismuth-rich; facet; photocatalysis
Year: 2016 PMID: 27668449 DOI: 10.1021/acsami.6b08129
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229