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The Multiple Promotion Effects of Ammonium Phosphate-Modified Ag3PO4 on Photocatalytic Performance
Phosphate ( PO 4 3 - ) modification of semiconductor photocatalysts such as TiO 2 , C 3 N 4 , BiVO 4 , and etc. has been shown positive effect on the enhancement of photocatalytic performance. In the present study, we demonstrate a novel one-pot surface modification route on Ag 3 PO 4 photocatalyst...
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Published in: | Frontiers in chemistry 2019-12, Vol.7, p.866-866 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Phosphate (
PO
4
3
-
) modification of semiconductor photocatalysts such as TiO
2
, C
3
N
4
, BiVO
4
, and etc. has been shown positive effect on the enhancement of photocatalytic performance. In the present study, we demonstrate a novel one-pot surface modification route on Ag
3
PO
4
photocatalyst by ammonium phosphate [(NH
4
)
3
PO
4
], which combines
PO
4
3
-
modification with ammonium (
NH
4
+
) etching to show multiple effects on the structural variation of Ag
3
PO
4
samples. The modified Ag
3
PO
4
photocatalysts exhibit much higher photocatalytic performance than bare Ag
3
PO
4
for the degradation of organic dye solutions under visible light irradiation. It is indicated that the
NH
4
+
etching favors the surface transition from Ag
3
PO
4
to metallic Ag nanoparticles, resulting in the fast capture of photogenerated electrons and the followed generation of
O
2
·
−
radicals. The strongly adsorbed
PO
4
3
-
on the Ag
3
PO
4
surfaces can further provide more negative electrostatic field, which improves the separation of photogenerated electron-hole pairs by inducing the holes to directly flow to the surface and then enhances the formation of reactive
·
OH radicals. Furthermore, the photocatalytic performance of the modified Ag
3
PO
4
photocatalysts can be optimized by monitoring the concentration of (NH
4
)
3
PO
4
that is 1 mM. |
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ISSN: | 2296-2646 2296-2646 |
DOI: | 10.3389/fchem.2019.00866 |