Time Resolved insitu DXAFS Revealing Highly Active Species of PdO Nanoparticle Catalyst for CH4 Oxidation

被引:28
|
作者
Mahara, Yuji [1 ]
Murata, Kazumasa [1 ]
Ueda, Kakuya [1 ]
Ohyama, Junya [1 ,2 ]
Kato, Kazuo [3 ]
Satsuma, Atsushi [1 ,2 ]
机构
[1] Nagoya Univ, Grad Sch Engn, Nagoya, Aichi 4648603, Japan
[2] Kyoto Univ, Unit Elements Strategy Initiat Catalysts Batterie, Kyoto 6158530, Japan
[3] Japan Synchrotron Radiat Res Inst, 1-1 Kouto, Sayo, Hyogo 6795198, Japan
关键词
Dispersive XAFS; In situ XAFS spectroscopy; Methane combustion; Pd redox; Supported Pd catalysts; ENERGY-DISPERSIVE XAFS; METHANE OXIDATION; OXYGEN STORAGE/RELEASE; CONTINUOUS NUCLEATION; ALPHA-ALUMINA; COMBUSTION; MECHANISM; TEMPERATURE; KINETICS; PD/AL2O3;
D O I
10.1002/cctc.201800573
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 highly active species of Pd/Al2O3 catalysts for methane combustion was revealed by insitu time-resolved dispersive X-ray absorption fine structure (DXAFS) spectroscopy. By using CH4 as a reduction agent, PdO in Pd/Al2O3 is reduced in a 2-step model involving Pd-0 nucleation and growth of Pd-0 domain in a PdO particle. Kinetic analysis of the 2-step model reduction of PdO nanoparticles leads to a suggestion that partial formation of Pd-0 in a PdO particle accelerates methane combustion.
引用
收藏
页码:3384 / 3387
页数:4
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