dc.contributor.author | Tasbihi, Minoo | |
dc.contributor.author | Acharjya, Amitava | |
dc.contributor.author | Thomas, Arne | |
dc.contributor.author | Reli, Martin | |
dc.contributor.author | Ambrožová, Nela | |
dc.contributor.author | Kočí, Kamila | |
dc.contributor.author | Schomäcker, Reinhard | |
dc.date.accessioned | 2018-03-15T13:19:06Z | |
dc.date.available | 2018-03-15T13:19:06Z | |
dc.date.issued | 2018 | |
dc.identifier.citation | Journal of Nanoscience and Nanotechnology. 2018, vol. 18, no. 8, p. 5636-5644. | cs |
dc.identifier.issn | 1533-4880 | |
dc.identifier.issn | 1533-4899 | |
dc.identifier.uri | http://hdl.handle.net/10084/124944 | |
dc.description.abstract | In this paper, a sol-gel derived mesoporous polymeric carbon nitride has been investigated as a photocatalyst for CO2 photocatalytic reduction. Noble-metal Pt nanoparticles were deposited on carbon nitride (sg-CN) in order to investigate the performance of both Pt-sg-CN and sg-CN for photocatalytic CO2 reduction. Physicochemical properties of prepared nanocomposites were comprehensively characterized by using powder XRD, N-2 physisorption, UV-Vis DRS, ICP-AES, FTIR, solid-state NMR, SEM, TEM and photoelectrochemical measurements. Compared with pure sg-CN, the resulting Pt-loaded sg-CN (Pt-sg-CN) exhibited significant improvement on the CO2 photocatalytic reduction to CH4 in the presence of water vapor at ambient condition under UV irradiation. 1.5 wt.% Pt-loaded sg-CN (Pt-sg-CN) photocatalyst formed the highest methane yield of 13.9 mu mol/g(cat). after 18 h of light irradiation, which was almost 2 times and 32 times improvement in comparison to pure sg-CN and commercial TiO2 Evonik P25, respectively. The substantial photocatalytic activity of Pt-sg-CN photocatalyst for the yield product of the CO2 photocatalytic reduction was attributed to the efficient interfacial transfer of photogenerated electrons from sg-CN to Pt due to the lower Fermi level of Pt in the Pt-sg-CN hybrid heterojunctions as also evidenced by photoelectrochemical measurements. This resulted in the reduction of electron-hole pairs recombination for effective spatial charge separation, consequently increasing the photocatalytic efficiency. | cs |
dc.language.iso | en | cs |
dc.publisher | American Scientific Publishers | cs |
dc.relation.ispartofseries | Journal of Nanoscience and Nanotechnology | cs |
dc.relation.uri | https://doi.org/10.1166/jnn.2018.15445 | cs |
dc.subject | photocatalysis | cs |
dc.subject | g-C3N4 | cs |
dc.subject | CO2 reduction | cs |
dc.subject | CH4 | cs |
dc.title | Photocatalytic CO2 reduction by mesoporous polymeric carbon nitride photocatalysts | cs |
dc.type | article | cs |
dc.identifier.doi | 10.1166/jnn.2018.15445 | |
dc.type.status | Peer-reviewed | cs |
dc.description.source | Web of Science | cs |
dc.description.volume | 18 | cs |
dc.description.issue | 8 | cs |
dc.description.lastpage | 5644 | cs |
dc.description.firstpage | 5636 | cs |
dc.identifier.wos | 000426059800053 | |