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Boosted selective catalytic nitrate reduction to ammonia on carbon/bismuth/bismuth oxide photocatalysts
Using solar energy to catalytically convert nitrate into ammonia is attractive for waste recycling and sustainable development. However, the rapid recombination of electron-hole pairs and the poor selectivity are obstructing photocatalytic nitrate reduction to ammonia to be mass applied currently. I...
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Published in: | Journal of cleaner production 2022-01, Vol.331, p.129975, Article 129975 |
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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: | Using solar energy to catalytically convert nitrate into ammonia is attractive for waste recycling and sustainable development. However, the rapid recombination of electron-hole pairs and the poor selectivity are obstructing photocatalytic nitrate reduction to ammonia to be mass applied currently. In this work, we reported a facile synthesis of carbon/bismuth/bismuth oxide photocatalyst via a one-pot hydrothermal reaction without using reducing reagent. Compared with α-bismuth oxide (α-Bi2O3), the photocatalytic ammonia yield of the optimum sample increased 3.65 times. In addition, the ammonia selectivity increased from 65.21% to 95.00%. The highly enhanced photocatalytic performance was attributed to the surface plasmon resonance of metallic bismuth. Meanwhile, the formation of carbon enables to boost the transfer of electrons significantly. Under light irradiation, electrons can be accumulated on metallic bismuth, effectively boosting the reduction of nitrate. The findings of this work will contribute to the recycling of nitrate for ammonia synthesis and sustainable environmental development.
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•A carbon/bismuth/Bi2O3 photocatalyst prepared via a one-pot hydrothermal reaction.•The composites exhibited efficient NO3− reduction to NH3 with high selectivity.•The mechanism for the enhanced photocatalytic activity was studied. |
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ISSN: | 0959-6526 1879-1786 |
DOI: | 10.1016/j.jclepro.2021.129975 |