(40d) Core-Shell Type Magnetically Active Fe3O4@Au Nanoparticles As Supported Nanocatalysts for CO Oxidation
AIChE Annual Meeting
2011
2011 Annual Meeting
Catalysis and Reaction Engineering Division
Nanoscale Materials as Catalysts I
Monday, October 17, 2011 - 8:30am to 8:50am
Size-defined
and thiol-ligated Au clusters vcan be used to prepare nanoparticles (NPs) with
less than 2 nm in diameter. These materials exhibit distinct quantum
confinement effects that differ significantly from bulk Au, for example
exhibitingdiscrete electronic electronic structure and molecular properties
such as HOMO-LUMO transitions and intrinsic magnetism. These properties may
have an interesting effect on catalysis by these clusters.
Recently,
dumbbell shaped Au-Fe3O4 nanoparticles prepared by colloidal
deposition and supported on TiO2 have been successfully tested as
catalysts for CO oxidation[1]. The particle size of Au in that study was 2.5-3.5
nm and that of Fe3O4 was about 15-16 nm, and the dumbbell
shape ensured a strong interaction between the metals. In such NPs, a strong
interaction exists between Au and Fe3O4 due to the
epitaxial growth of Fe3O4 on Au[1].
Here, we
report the catalytic activity of core-shell type SPIONs@Au supported on TiO2
for CO oxidation. The NPs were synthesized as described earlier[2, 3] by modifying a reported method
for the synthesis of these particles[4]. The Au/Fe3O4 particles were
impregnated on TiO2 (P25, Degussa) to give Au/Fe3O4/TiO2
catalysts. These catalysts were treated in an oxidative environment at 300°C,
400°C, and 500°C, respectively before CO oxidation to remove the sulfur ligands.
Fresh and treated catalysts were characterized by HRTEM, XPS, XRD, and by CO
oxidation. Results show that Au/Fe3O4/TiO2 is
an active catalyst for CO oxidation, only if calcined at 300°C. Other treatment
methods sintered the catalysts, which results in no catalytic activity.
References:
[1] H. Yin,
C. Wang, H. Zhu, S.H. Overbury, S. Sun, S. Dai, Chemical Communications (2008)
4357-4359.
[2] F.
Mohammad, G. Balaji, A. Weber, R.M. Uppu, C.S.S.R. Kumar, The Journal of
Physical
Chemistry
C. 114 (2010) 19194-19201.
[3] C.S.S.R.
Kumar, F. Mohammad, The Journal of Physical Chemistry Letters. 1 (2010)
3141-3146.
[4] WangWang,
J. Luo, Q. Fan, M. Suzuki, I.S. Suzuki, M.H. Engelhard, Y. Lin, N. Kim, J.Q.
Wang,
C.-J.
Zhong, The Journal of Physical Chemistry B. 109 (2005) 21593-21601.