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In relation to this article, we declare that there is no conflict of interest.
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Received March 29, 2018
Accepted July 18, 2018
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Photo-synthesized copper phenylacetylide nanobelts with preferential photocatalytic active facet exposure

Key Lab of Synthetic and Natural Functional Molecule Chemistry of Ministry of Education, College of Chemistry & Materials Science, Northwest University, Xi’an 710127, P. R. China
Korean Journal of Chemical Engineering, October 2018, 35(10), 2127-2132(6), 10.1007/s11814-018-0121-x
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Abstract

We recently reported that PhC2Cu nanobelt exhibits excellent photocatalytic degradation of organic pollutants and activation of molecular O2. However, there has been no further research about the relationship between its crystal structure and photocatalytic activity. Herein, a new safe and energy-save method, photo-synthesis, to prepare PhC2Cu nanobelts with preferential active exposure facet was developed. It was used to study the relationship between its crystal structure and photocatalytic activity, compared to the PhC2Cu nanobelts prepared by thermal-synthesis method. The prepared samples were characterized by X-ray powder diffractometer (XRD), field-emission scanning electron microscopy (FE-SEM), ultraviolet-visible (UV-vis) absorbance spectra and diffuse reflectance spectra (UV-vis Abs and DRS), N2 adsorption-desorption isotherms, FT-IR and Raman spectra. The degradation of MB experiments under visible light irradiation shows that the photocatalytic activity of PhC2Cu prepared by photo-synthesis method is much higher than that by traditional thermal-synthesis method. Moreover, the photocatalytic mechanism of PhC2Cu nanobelts was further studied by the photocatalytic generation of O2 - · and .OH.

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