Influence of the precipitation agent in the deposition-precipitation on the formation and properties of Au nanoparticles supported on Al2O3

被引:24
作者
Radnik, J. [1 ]
Wilde, L. [1 ]
Schneider, M. [1 ]
Pohl, M. -M. [1 ]
Herein, D. [1 ]
机构
[1] Univ Rostock, Leibniz Inst Catalysis, D-12489 Berlin, Germany
关键词
D O I
10.1021/jp065514k
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
Au nanoparticles supported on Al2O3 were prepared by deposition-precipitation of HAuCl4 with different precipitation agents NaOH and urea. The samples were investigated by means of different characterization techniques such as X-ray photoelectron spectroscopy (XPS), X-ray absorption spectroscopy (XAS), and transmission electron microscopy (TEM). The results show that depending on the precipitation agent, the Au particles have a different Au-Au coordination number and size after calcination at 523 K. Whereas the use of NaOH leads to the formation of Au nanoparticles with a Au-Au coordination number of 6.7 and a mean diameter below 2 nm, those prepared with urea have a mean size of 3.1 nm. The Au-Au coordination number could be determined as 8.6. At the smaller particles obtained with NaOH, hints for Au-O interactions were found. For these particles TEM results advise a rather flat lenticular morphology. Different deposition mechanisms depending on the precipitation agent are discussed as the reason for the formation of nanoparticles with different shapes, sizes, and valence states.
引用
收藏
页码:23688 / 23693
页数:6
相关论文
共 24 条
[1]   A STRUCTURAL INVESTIGATION ON SMALL GOLD CLUSTERS BY EXAFS [J].
BALERNA, A ;
BERNIERI, E ;
PICOZZI, P ;
REALE, A ;
SANTUCCI, S ;
BURATTINI, E ;
MOBILIO, S .
SURFACE SCIENCE, 1985, 156 (JUN) :206-213
[2]   Partial oxidation of polyvalent oxygen substituted compounds on nano-scale gold catalysts [J].
Berndt, H ;
Martin, A ;
Pitsch, I ;
Prüsse, U ;
Vorlop, KD .
CATALYSIS TODAY, 2004, 91-2 :191-194
[3]   Oxygen adsorption on Au/Al2O3 catalysts and relation to the catalytic oxidation of ethylene glycol to glycolic acid [J].
Berndt, H ;
Pitsch, I ;
Evert, S ;
Struve, K ;
Pohl, MM ;
Radnik, J ;
Martin, A .
APPLIED CATALYSIS A-GENERAL, 2003, 244 (01) :169-179
[4]   FTIR study of the low-temperature water-gas shift reaction on Au/Fe2O3 and Au/TiO2 catalysts [J].
Boccuzzi, F ;
Chiorino, A ;
Manzoli, M ;
Andreeva, D ;
Tabakova, T .
JOURNAL OF CATALYSIS, 1999, 188 (01) :176-185
[5]   Catalysis by gold [J].
Bond, GC ;
Thompson, DT .
CATALYSIS REVIEWS-SCIENCE AND ENGINEERING, 1999, 41 (3-4) :319-388
[6]   Substrate and morphology effects on photoemission from core-levels in gold clusters [J].
Dalacu, D ;
Klernberg-Sapieha, JE ;
Martinu, L .
SURFACE SCIENCE, 2001, 472 (1-2) :33-40
[7]   Surface characterization of Au/HY by Xe-129 NMR and diffuse reflectance IR spectroscopy of adsorbed CO. Formation of electron-deficient gold particles inside HY cavities [J].
Guillemot, D ;
Borovkov, VY ;
Kazansky, VB ;
PolissetThfoin, M ;
Fraissard, J .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS, 1997, 93 (19) :3587-3591
[8]   When gold is not noble: Catalysis by nanoparticles [J].
Haruta, A .
CHEMICAL RECORD, 2003, 3 (02) :75-87
[9]   Size- and support-dependency in the catalysis of gold [J].
Haruta, M .
CATALYSIS TODAY, 1997, 36 (01) :153-166
[10]   GOLD CATALYSTS PREPARED BY COPRECIPITATION FOR LOW-TEMPERATURE OXIDATION OF HYDROGEN AND OF CARBON-MONOXIDE [J].
HARUTA, M ;
YAMADA, N ;
KOBAYASHI, T ;
IIJIMA, S .
JOURNAL OF CATALYSIS, 1989, 115 (02) :301-309