High Activity Carbide Supported Catalysts for Water Gas Shift
被引:273
作者:
Schweitzer, Neil M.
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Univ Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USAUniv Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Schweitzer, Neil M.
[1
,2
]
Schaidle, Joshua A.
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机构:
Univ Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USAUniv Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Schaidle, Joshua A.
[1
,2
]
Ezekoye, Obiefune K.
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机构:
Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USAUniv Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Ezekoye, Obiefune K.
[3
]
Pan, Xiaoqing
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Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USAUniv Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Pan, Xiaoqing
[3
]
Linic, Suljo
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Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USAUniv Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Linic, Suljo
[2
]
Thompson, Levi T.
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Univ Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USAUniv Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
Thompson, Levi T.
[1
,2
]
机构:
[1] Univ Michigan, Hydrogen Energy Technol Lab, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Chem Engn, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Dept Mat Sci & Engn, Ann Arbor, MI 48109 USA
Nanostructured carbides are refractory materials with high surface areas that could be used as alternatives to the oxide materials that are widely used as support materials for heterogeneous catalysts. Carbides are also catalytically active for a variety of reactions, offering additional opportunities to tune the overall performance of the catalyst. In this paper we describe the synthesis of molybdenum carbide supported platinum (Pt/Mo2C) catalysts and their rates for the water gas shift reaction. The synthesis method allowed interaction of the metal precursor with the native, unpassivated support. The resulting materials possessed very high WGS rates and atypical Pt particle morphologies. Under differential conditions, rates for these catalysts were higher than those for the most active oxide-supported Pt catalysts and a commercial Cu-Zn-Al catalyst. Experimental and computational results suggested that active sites on the Pt/Mo2C catalysts were located on the perimeter of the Pt particles and that strong interactions between Pt and the Mo2C surface gave rise to raft-like particles.
机构:
Kogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, JapanKogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, Japan
Iida, H
;
Igarashi, A
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Kogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, JapanKogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, Japan
机构:
Kogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, JapanKogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, Japan
Iida, H
;
Igarashi, A
论文数: 0引用数: 0
h-index: 0
机构:
Kogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, JapanKogakuin Univ, Fac Engn, Dept Environm Chem Engn, Hachioji, Tokyo 1920015, Japan