MnOx-CeOx Nanoparticles Supported on Graphene Aerogel for Selective Catalytic Reduction of Nitric Oxides
Removal of nitric oxides (NOx) from stationary and transportation sources has been desired for environmental benefits. Selective catalytic reduction (SCR) of NOx by NH3 is attractive for its cost effectiveness and high efficiency but still technically challenging in consideration of operable tempera...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
Hindawi Limited
2019-01-01
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Series: | Journal of Nanomaterials |
Online Access: | http://dx.doi.org/10.1155/2019/4239764 |
Summary: | Removal of nitric oxides (NOx) from stationary and transportation sources has been desired for environmental benefits. Selective catalytic reduction (SCR) of NOx by NH3 is attractive for its cost effectiveness and high efficiency but still technically challenging in consideration of operable temperatures. In this research, MnOx-CeOx hybrid nanoparticles supported on graphene aerogel (MnOx-CeOx/GA) are fabricated as the monolithic catalysts for potential applications to low-temperature SCR. The impacts of the particle size along with the amount and valency of catalytic elements in the nanocomposite on the catalytic activities are studied with the help of scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The catalyst crystallites are a few tens of nanometers and uniformly disperse on the surface of three-dimensional (3D) directionally aligned hierarchical porous graphene aerogel (GA) networks. The novel nanocomposite catalysts exhibit over 90% NOx conversion rate in a broad temperature range (200–300°C). Addition of CeOx into the MnOx-GA catalysts significantly reduces the operational temperature at the same conversion rate. In addition to Mn4+ ions in the catalysts, the adsorbed oxygen species which can be increased by the presence of low-valence cerium contribute to high catalytic activities in the MnOx-CeOx/GA catalysts. |
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ISSN: | 1687-4110 1687-4129 |