Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> Photocatalysts
Two series of new photocatalysts were synthesized based on modification with Pd of the commercial P25 photocatalyst (EVONIK<sup>®</sup>). Two techniques were employed to incorporate Pd nanoparticles on the P25 surface: photodeposition (series Pd-P) and impregnation (series Pd-I). Both se...
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| Format: | Article |
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MDPI AG
2020-11-01
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| Series: | Nanomaterials |
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| Online Access: | https://www.mdpi.com/2079-4991/10/12/2354 |
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| author | M. J. Hernández Rodríguez E. Pulido Melián J. Araña J. A. Navío O. M. González Díaz Dunia E. Santiago J. M. Doña Rodríguez |
| author_facet | M. J. Hernández Rodríguez E. Pulido Melián J. Araña J. A. Navío O. M. González Díaz Dunia E. Santiago J. M. Doña Rodríguez |
| author_sort | M. J. Hernández Rodríguez |
| collection | DOAJ |
| description | Two series of new photocatalysts were synthesized based on modification with Pd of the commercial P25 photocatalyst (EVONIK<sup>®</sup>). Two techniques were employed to incorporate Pd nanoparticles on the P25 surface: photodeposition (series Pd-P) and impregnation (series Pd-I). Both series were characterized in depth using a variety of instrumental techniques: BET, DRS, XRD, XPS, TEM, FTIR and FESEM. The modified series exhibited a significant change in pore size distribution, but no differences compared to the original P25 with respect to crystalline phase ratio or particle size were observed. The Pd<sup>0</sup> oxidation state was predominant in the Pd-P series, while the presence of the Pd<sup>2+</sup> oxidation state was additionally observed in the Pd-I series. The photoactivity tests were performed in a continuous photoreactor with the photocatalysts deposited, by dip-coating, on borosilicate glass plates. A total of 500 ppb of NO was used as input flow at a volumetric flow rate of 1.2 L·min<sup>−1</sup>, and different relative humidities from 0 to 65% were tested. The results obtained show that under UV-vis or Vis radiation, the presence of Pd nanoparticles favors NO removal independently of the Pd incorporation method employed and independently of the tested relative humidity conditions. This improvement seems to be related to the different interaction of the water with the surface of the photocatalysts in the presence or absence of Pd. It was found in the catalyst without Pd that disproportionation of NO<sub>2</sub> is favored through its reaction with water, with faster surface saturation. In contrast, in the catalysts with Pd, disproportionation took place through nitro-chelates and adsorbed NO<sub>2</sub> formed from the photocatalytic oxidation of the NO. This different mechanism explains the greater efficiency in NO<sub>x</sub> removal in the catalysts with Pd. Comparing the two series of catalysts with Pd, Pd-P and Pd-I, greater activity of the Pd-P series was observed under both UV-vis and Vis radiation. It was shown that the Pd<sup>0</sup> oxidation state is responsible for this greater activity as the Pd-I series improves its activity in successive cycles due to a reduction in Pd<sup>2+</sup> species during the photoactivity tests. |
| first_indexed | 2024-03-10T14:31:07Z |
| format | Article |
| id | doaj.art-78c49e7054e342e1acf892d10b026f43 |
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| language | English |
| last_indexed | 2024-03-10T14:31:07Z |
| publishDate | 2020-11-01 |
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| series | Nanomaterials |
| spelling | doaj.art-78c49e7054e342e1acf892d10b026f432023-11-20T22:33:39ZengMDPI AGNanomaterials2079-49912020-11-011012235410.3390/nano10122354Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> PhotocatalystsM. J. Hernández Rodríguez0E. Pulido Melián1J. Araña2J. A. Navío3O. M. González Díaz4Dunia E. Santiago5J. M. Doña Rodríguez6Grupo de Fotocatálisis y Espectroscopia para Aplicaciones Medioambientales (FEAM. Unidad Asociada al CSIC por el Instituto de Ciencias de Materiales de Sevilla), Departamento de Química, Instituto de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas, SpainGrupo de Fotocatálisis y Espectroscopia para Aplicaciones Medioambientales (FEAM. Unidad Asociada al CSIC por el Instituto de Ciencias de Materiales de Sevilla), Departamento de Química, Instituto de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas, SpainGrupo de Fotocatálisis y Espectroscopia para Aplicaciones Medioambientales (FEAM. Unidad Asociada al CSIC por el Instituto de Ciencias de Materiales de Sevilla), Departamento de Química, Instituto de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas, SpainCentro Mixto CSIC-Universidad de Sevilla, Departamento de Química Inorgánica, Instituto de Ciencia de Materiales de Sevilla, Universidad de Sevilla, Avenida Américo Vespucio s/n, 41092 Sevilla, SpainGrupo de Fotocatálisis y Espectroscopia para Aplicaciones Medioambientales (FEAM. Unidad Asociada al CSIC por el Instituto de Ciencias de Materiales de Sevilla), Departamento de Química, Instituto de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas, SpainGrupo de Fotocatálisis y Espectroscopia para Aplicaciones Medioambientales (FEAM. Unidad Asociada al CSIC por el Instituto de Ciencias de Materiales de Sevilla), Departamento de Química, Instituto de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas, SpainGrupo de Fotocatálisis y Espectroscopia para Aplicaciones Medioambientales (FEAM. Unidad Asociada al CSIC por el Instituto de Ciencias de Materiales de Sevilla), Departamento de Química, Instituto de Estudios Ambientales y Recursos Naturales (i-UNAT), Universidad de Las Palmas de Gran Canaria, 35017 Las Palmas, SpainTwo series of new photocatalysts were synthesized based on modification with Pd of the commercial P25 photocatalyst (EVONIK<sup>®</sup>). Two techniques were employed to incorporate Pd nanoparticles on the P25 surface: photodeposition (series Pd-P) and impregnation (series Pd-I). Both series were characterized in depth using a variety of instrumental techniques: BET, DRS, XRD, XPS, TEM, FTIR and FESEM. The modified series exhibited a significant change in pore size distribution, but no differences compared to the original P25 with respect to crystalline phase ratio or particle size were observed. The Pd<sup>0</sup> oxidation state was predominant in the Pd-P series, while the presence of the Pd<sup>2+</sup> oxidation state was additionally observed in the Pd-I series. The photoactivity tests were performed in a continuous photoreactor with the photocatalysts deposited, by dip-coating, on borosilicate glass plates. A total of 500 ppb of NO was used as input flow at a volumetric flow rate of 1.2 L·min<sup>−1</sup>, and different relative humidities from 0 to 65% were tested. The results obtained show that under UV-vis or Vis radiation, the presence of Pd nanoparticles favors NO removal independently of the Pd incorporation method employed and independently of the tested relative humidity conditions. This improvement seems to be related to the different interaction of the water with the surface of the photocatalysts in the presence or absence of Pd. It was found in the catalyst without Pd that disproportionation of NO<sub>2</sub> is favored through its reaction with water, with faster surface saturation. In contrast, in the catalysts with Pd, disproportionation took place through nitro-chelates and adsorbed NO<sub>2</sub> formed from the photocatalytic oxidation of the NO. This different mechanism explains the greater efficiency in NO<sub>x</sub> removal in the catalysts with Pd. Comparing the two series of catalysts with Pd, Pd-P and Pd-I, greater activity of the Pd-P series was observed under both UV-vis and Vis radiation. It was shown that the Pd<sup>0</sup> oxidation state is responsible for this greater activity as the Pd-I series improves its activity in successive cycles due to a reduction in Pd<sup>2+</sup> species during the photoactivity tests.https://www.mdpi.com/2079-4991/10/12/2354photocatalysisNO<sub>x</sub>TiO<sub>2</sub>PdwaterFTIR |
| spellingShingle | M. J. Hernández Rodríguez E. Pulido Melián J. Araña J. A. Navío O. M. González Díaz Dunia E. Santiago J. M. Doña Rodríguez Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> Photocatalysts Nanomaterials photocatalysis NO<sub>x</sub> TiO<sub>2</sub> Pd water FTIR |
| title | Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> Photocatalysts |
| title_full | Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> Photocatalysts |
| title_fullStr | Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> Photocatalysts |
| title_full_unstemmed | Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> Photocatalysts |
| title_short | Influence of Water on the Oxidation of NO on Pd/TiO<sub>2</sub> Photocatalysts |
| title_sort | influence of water on the oxidation of no on pd tio sub 2 sub photocatalysts |
| topic | photocatalysis NO<sub>x</sub> TiO<sub>2</sub> Pd water FTIR |
| url | https://www.mdpi.com/2079-4991/10/12/2354 |
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