Reaction of Formic Acid over Amorphous Manganese Oxide Catalytic Systems: An In Situ Study

被引:50
作者
Durand, Jason P. [1 ]
Senanayake, Sanjaya D. [2 ]
Suib, Steven L. [1 ,3 ]
Mullins, David R. [2 ]
机构
[1] Univ Connecticut, Dept Chem, Storrs, CT 06269 USA
[2] Oak Ridge Natl Lab, Oak Ridge, TN 37830 USA
[3] Univ Connecticut, Inst Mat Sci, Storrs, CT 06269 USA
关键词
OCTAHEDRAL MOLECULAR-SIEVES; VIBRATIONAL-SPECTRA; PARTICLE-SIZE; OXIDATION; ALCOHOLS; FORMATE; DECOMPOSITION; SPECTROSCOPY; ADSORPTION; CHEMISTRY;
D O I
10.1021/jp104629j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The interaction of formic acid with amorphous manganese oxide (AMO) is investigated using in situ photoelectron and infrared spectroscopy techniques. Soft X-ray photoelectron spectroscopy (sXPS) and in situ FTIR illustrate two possible modes of formate bound species at the AMO surface. Two peaks in the IR region from 1340-1390 cm(-1) are indicative of formate species bound to the surface in a bidentate configuration. However, a 224 cm(-1) band gap between v(s)OCO and v(as)OCO suggests formate is bound in a bridging configuration. Temperature-programmed desorption studies confirm the formate bound species desorbs as carbon dioxide from the surface at multiple binding sites. At temperatures above 700 K, the presence of K+center dot center dot center dot OC complex suggests the bound species interacts at vacant sites related to framework oxygen and cation mobility.
引用
收藏
页码:20000 / 20006
页数:7
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