Fabrication of Optical Gap Selective Amorphous Carbon Photocatalyst for Hydrogen Production under Irradiation with Visible Light

Si-added amorphous carbon (a-C) nanoparticles with particle diameter of 12.6 nm were synthesized using radio frequency (r.f.) plasma-enhanced chemical vapor deposition method equipped with porous aluminum plate in plasma. The optical gap of Si-added a-C particles with Si/(Si + C) ratio of 0.51 was 1...

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Veröffentlicht in:ECS transactions 2017-01, Vol.75 (50), p.57-74
Hauptverfasser: Okafuji, Keigo, Kobayashi, Ryutaro, Ohtomo, Shinpei, Naragino, Hiroshi, Honda, Kensuke
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Sprache:eng
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Zusammenfassung:Si-added amorphous carbon (a-C) nanoparticles with particle diameter of 12.6 nm were synthesized using radio frequency (r.f.) plasma-enhanced chemical vapor deposition method equipped with porous aluminum plate in plasma. The optical gap of Si-added a-C particles with Si/(Si + C) ratio of 0.51 was 1.92 eV. Band edges of this nanoparticles was estimated to be as follows: i) conduction band edge was located over the standard potential of H+/H2 and ii) valence band edge was located under the standard potential of O2/H2O. From X-ray photoemission spectra, it was clarified that the part of tri-s-triazine structure with higher adsorption property toward water was introduced into nanoparticle with optical gap of 1.92 eV by adding graphitic-carbon nitride (g-C3N4) in a source material. The photo-oxidation measurement of indigo carmine adsorbed on Si-added a-C nanoparticles with tri-s-triazine structure was carried out. As a result, indigo carmine was decomposed at a rate of 0.0197 µmol/h under UV irradiation. This result indicates that Si-added a-C nanoparticle can be applied to photocatalyst for reduction of water (estimated quantum efficiency of 0.049 %). It was experimentally demonstrated that the proposed Si-added a-C nanoparticles are tailor-made photocatalyst material that enables us to adjust band edge and surface functionalities for photo-oxidation (reduction) reactant.
ISSN:1938-5862
1938-6737
1938-6737
1938-5862
DOI:10.1149/07550.0057ecst