Collaborative Mechanistic Effects between Vanadia and Titania during the Oxidative Dehydrogenation of Propane Investigated by Operando and Transient Spectroscopies

被引:12
作者
Schumacher, Leon [1 ]
Pfeiffer, Johannes [1 ]
Shen, Jun [1 ]
Gutmann, Torsten [1 ]
Breitzke, Hergen [1 ]
Buntkowsky, Gerd [1 ]
Hofmann, Kathrin [1 ]
Hess, Christian [1 ]
机构
[1] Tech Univ Darmstadt, Eduard Zintl Inst Anorgan & Phys Chem, Dept Chem, D-64287 Darmstadt, Germany
关键词
propane ODH; vanadia; titania; transientIR spectroscopy; operando spectroscopy; nuclearitydependence; support interaction; SELECTIVE CATALYTIC-REDUCTION; OXIDE CATALYSTS; PHOTOCATALYTIC ACTIVITY; RAMAN-SPECTROSCOPY; SURFACE-PROPERTIES; OPTICAL-PROPERTIES; TIO2; SUPPORT; ANATASE; RUTILE;
D O I
10.1021/acscatal.3c01404
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 oxidative dehydrogenation (ODH) of propane is of great technical importance, and supported VOx catalysts have shown promising properties for the reaction. One of the most prominent and active supports is titania, which exhibits a high activity but many questions regarding the catalyst system are still in debate. In this study, we elucidate the mechanism of the propane ODH reaction over VOx/TiO2, using P25 and ALD (atomic layer deposition) synthesized TiO2/SBA-15 as a support, with X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), V-51 solid-state (ss)NMR, operando multiwavelength Raman, operando UV-vis, and transient IR spectroscopies. Bare titania shows a small conversion, leading to carbon formation, and the reaction occurs at the interface between anatase and rutile. In comparison, in VOx/TiO2 catalysts, the activity shifts from titania to vanadia sites. UV-Raman spectroscopy and structural characterization data revealed the reaction to involve preferentially the V=O bonds of dimeric species rather than doubly bridged V-O-V bonds, which leads to higher propene selectivities. The active vanadium site shows a nuclearity-dependent behavior; that is, at higher loadings, when oligomeric vanadia is present, it shifts from V=O bonds to linear V-O-V bonds in oligomers, leading to less selective oxidation due to the better reducibility. Our operando/transient spectroscopic results demonstrate the direct participation of the titania support in the reaction by influencing the degree of vanadia oligomerization and enabling rapid hydrogen transfer from propane to vanadia via Ti-OH groups on anatase, accelerating the rate-determining step of the initial C-H bond breakage. The broader applicability of the results is confirmed by the behavior of the ALD-synthesized sample, which resembles that of P25. Our results highlight the detailed level of mechanistic understanding accessible from multiple spectroscopic approaches, which can be readily transferred to other materials and/or reactions.
引用
收藏
页码:8139 / 8160
页数:22
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