Photocatalytic Hydrogen Evolution from Silica-Templated Polymeric Graphitic Carbon Nitride-Is the Surface Area Important?

Low‐surface‐area, mesoporous silica‐templated polymeric graphitic carbon nitride (SBA–g‐C3N4), when irradiated with visible light, exhibits a greatly improved photocatalytic hydrogen evolution rate as compared to that of conventional bulk g‐C3N4 synthesized directly from the condensation of dicyandi...

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Vydáno v:ChemCatChem Ročník 7; číslo 1; s. 121 - 126
Hlavní autoři: Li, Xiaobo, Masters, Anthony F., Maschmeyer, Thomas
Médium: Journal Article
Jazyk:angličtina
Vydáno: Weinheim WILEY-VCH Verlag 01.01.2015
WILEY‐VCH Verlag
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ISSN:1867-3880, 1867-3899
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Shrnutí:Low‐surface‐area, mesoporous silica‐templated polymeric graphitic carbon nitride (SBA–g‐C3N4), when irradiated with visible light, exhibits a greatly improved photocatalytic hydrogen evolution rate as compared to that of conventional bulk g‐C3N4 synthesized directly from the condensation of dicyandiamide. It also performs very similarly to high‐surface‐area mesoporous g‐C3N4 on a per‐unit mass basis. However, on the per‐unit area basis it greatly outperforms the other materials. The intrinsically high surface activity of SBA–g‐C3N4 was confirmed by using two different co‐catalysts, in situ photodeposited Pt and a structurally well‐defined molecular cobaloxime. Instead of the magnitude of the surface area as the dominant feature that determines activity, it was established that the high activity of SBA–g‐C3N4 results from a much higher number of delocalized electrons present and a suppressed recombination probability of photogenerated electron–hole pairs. More H2 through silica templating: Mesoporous‐silica‐templated, low‐surface‐area, polymeric graphitic carbon nitride (SBA–g‐C3N4) exhibits a greatly improved photocatalytic hydrogen evolution rate on a per‐surface area basis compared to that of conventional bulk graphitic carbon nitrides. The intrinsically high surface activity of SBA–g‐C3N4 was confirmed for both homo‐ (cobaloxime) and heterogeneous (Pt) co‐catalyst systems (TEOA=triethanolamine).
Bibliografie:istex:8ED49F2BF35AADF4935FAC8A70406AC7F38B8FF9
ark:/67375/WNG-G2K39L93-7
Wellcome Trust
Australian Research Council
ArticleID:CCTC201402567
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
ISSN:1867-3880
1867-3899
DOI:10.1002/cctc.201402567