TY - JOUR
T1 - Oxygen-functionalized few-layer graphene sheets as active catalysts for oxidative dehydrogenation reactions
AU - Schwartz, Viviane
AU - Fu, Wujun
AU - Tsai, Yu Tung
AU - Meyer, Harry M.
AU - Rondinone, Adam J.
AU - Chen, Jihua
AU - Wu, Zili
AU - Overbury, Steven H.
AU - Liang, Chengdu
PY - 2013/5
Y1 - 2013/5
N2 - Nanostructured graphitic forms of carbons have shown intersting potential for catalysis research and are ideal candidates to substitute the conventional metal-oxide catalysts because they can be easily disposed, which enables a greener, more sustainable catalytic process. Few-layer graphene and its functionalized form offer the opportunity to investigate the nature of graphitic active sites for oxidation reactions in well-defined carbon-based catalysts. In this paper, we report the utilization of oxygen-functionalized few-layer graphene sheets containing variable amounts of oxygen in the heterogeneous catalytic oxidative dehydrogenation (ODH) reaction of isobutane at 4008C. Interestingly, there is poor correlation between oxygen content and catalytic performance. Carbonyl groups were found to be highly stable, and graphene that had higher sp2 character, the lowest oxygen content, and fewer edge sites presented the lowest specific rate of isobutane reaction, although the isobutene selectivity remained high. The reoxidation of the graphene surface occurred at the same rate as the ODH reaction suggesting a Mars-van Krevelen type of mechanism, similar to that which takes place on oxide surfaces. These results appear to suggest that a higher fraction of exposed edges where oxygen active sites can be formed and exchanged should lead to more active catalysts for ODH reactions.
AB - Nanostructured graphitic forms of carbons have shown intersting potential for catalysis research and are ideal candidates to substitute the conventional metal-oxide catalysts because they can be easily disposed, which enables a greener, more sustainable catalytic process. Few-layer graphene and its functionalized form offer the opportunity to investigate the nature of graphitic active sites for oxidation reactions in well-defined carbon-based catalysts. In this paper, we report the utilization of oxygen-functionalized few-layer graphene sheets containing variable amounts of oxygen in the heterogeneous catalytic oxidative dehydrogenation (ODH) reaction of isobutane at 4008C. Interestingly, there is poor correlation between oxygen content and catalytic performance. Carbonyl groups were found to be highly stable, and graphene that had higher sp2 character, the lowest oxygen content, and fewer edge sites presented the lowest specific rate of isobutane reaction, although the isobutene selectivity remained high. The reoxidation of the graphene surface occurred at the same rate as the ODH reaction suggesting a Mars-van Krevelen type of mechanism, similar to that which takes place on oxide surfaces. These results appear to suggest that a higher fraction of exposed edges where oxygen active sites can be formed and exchanged should lead to more active catalysts for ODH reactions.
KW - Active centers
KW - Dehydrogenation
KW - Graphene
KW - Heterogeneous catalysis
KW - Oxygen functionalization
UR - http://www.scopus.com/inward/record.url?scp=84878339586&partnerID=8YFLogxK
U2 - 10.1002/cssc.201200756
DO - 10.1002/cssc.201200756
M3 - Article
C2 - 23471876
AN - SCOPUS:84878339586
SN - 1864-5631
VL - 6
SP - 840
EP - 846
JO - ChemSusChem
JF - ChemSusChem
IS - 5
ER -