Surface Ba species effective for photoassisted NOx storage over Ba-modified TiO2 photocatalysts

被引:15
作者
Yamamoto, Akira [1 ,2 ]
Mizuno, Yuto [1 ]
Teramura, Kentaro [1 ,2 ,3 ]
Hosokawa, Saburo [1 ,2 ]
Tanaka, Tsunehiro [1 ,2 ]
机构
[1] Kyoto Univ, Grad Sch Engn, Dept Mol Engn, Nishikyo Ku, Kyoto 6158510, Japan
[2] Kyoto Univ, ESICB, Nishikyo Ku, Kyoto 6158520, Japan
[3] Japan Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol PRESTO, Kawaguchi, Saitama 3320012, Japan
基金
日本科学技术振兴机构;
关键词
Photocatalyst; Nitrogen oxides; NOx; Titanium dioxide; NOx storage; SELECTIVE CATALYTIC-REDUCTION; SORPTION/DESORPTION PROCESSES; NITROGEN MONOXIDE; FT-IR; OXIDATION; OXIDE; REMOVAL; UV; NO(X); DEACTIVATION;
D O I
10.1016/j.apcatb.2015.06.036
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
Surface modification of a TiO2 photocatalyst with Ba species was investigated in photoassisted nitrogen oxide (NOx) storage under UV-light irradiation. The NOx storage capacity in the Ba-modified TiO2 photocatalyst was 1.4 times higher than that of the non-modified TiO2 photocatalyst. Structure and role of the surface Ba species on a TiO2 surface were characterized using temperature programmed reaction (TPR), diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, X-ray diffraction (XRD), X-ray photoemission spectroscopy (XPS), and transmission electron microscopy (TEM). The characterization results suggested that Ba-Ti mixed oxides with a two-dimensional layer and amorphous structure on a TiO2 surface were generated via decomposition of Ba(NO3)(2) precursors by O-2 pretreatment at 773 K. Based on the results of the characterizations and the reactions, the generated Ba-Ti mixed oxides on a TiO2 surface stored NOx more densely than the TiO2 surface; therefore, the generation improved the activity in the photoassisted NOx storage under UV-light irradiation. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:283 / 290
页数:8
相关论文
共 47 条
[1]   Fine-Tuning the Dispersion and the Mobility of BaO Domains on NOx Storage Materials via TiO2 Anchoring Sites [J].
Andonova, Stanislava M. ;
Senturk, Goksu S. ;
Ozensoy, Emrah .
JOURNAL OF PHYSICAL CHEMISTRY C, 2010, 114 (40) :17003-17016
[2]   Nature of the Ti-Ba Interactions on the BaO/TiO2/Al2O3 NOx Storage System [J].
Andonova, Stanislava M. ;
Senturk, Goeksu S. ;
Kayhan, Emine ;
Ozensoy, Emrah .
JOURNAL OF PHYSICAL CHEMISTRY C, 2009, 113 (25) :11014-11026
[3]   Chemical and mechanistic aspects of the selective catalytic reduction of NOx by ammonia over oxide catalysts:: A review [J].
Busca, G ;
Lietti, L ;
Ramis, G ;
Berti, F .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1998, 18 (1-2) :1-36
[4]   Nanostructured catalysts for NOx storage-reduction and N2O decomposition [J].
Centi, G ;
Arena, GE ;
Perathoner, S .
JOURNAL OF CATALYSIS, 2003, 216 (1-2) :443-454
[5]   Photocatalytic oxidation of NOx gases using TiO2:: a surface spectroscopic approach [J].
Dalton, JS ;
Janes, PA ;
Jones, NG ;
Nicholson, JA ;
Hallam, KR ;
Allen, GC .
ENVIRONMENTAL POLLUTION, 2002, 120 (02) :415-422
[6]  
Dana L., 2012, URBAN OFF CYCLE NOX
[7]   Light intensity dependence of the kinetics of the photocatalytic oxidation of nitrogen(II) oxide at the surface of TiO2 [J].
Dillert, Ralf ;
Engel, Astrid ;
Grosse, Julia ;
Lindner, Patrick ;
Bahnemann, Detlef W. .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2013, 15 (48) :20876-20886
[8]   Direct Evidence for the Instability and Deactivation of Mixed-Oxide Systems: Influence of Surface Segregation and Subsurface Diffusion [J].
Emmez, Emre ;
Vovk, Evgeny I. ;
Bukhtiyarov, Valerii I. ;
Ozensoy, Emrah .
JOURNAL OF PHYSICAL CHEMISTRY C, 2011, 115 (45) :22438-22443
[9]   Overview of the fundamental reactions and degradation mechanisms of NOx storage/reduction catalysts [J].
Epling, WS ;
Campbell, LE ;
Yezerets, A ;
Currier, NW ;
Parks, JE .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 2004, 46 (02) :163-245
[10]   Role of TiO2 surface hydration on NO oxidation photo-activity [J].
Folli, Andrea ;
Campbell, Steven B. ;
Anderson, James A. ;
Macphee, Donald E. .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2011, 220 (2-3) :85-93