Abstract:In this work, we present a detailed study concerning the evaluation of the metal-support interaction in high activity gold catalysts for CO oxidation. Using the colloidal deposition method, model catalysts were prepared, which allow the isolation of the effect of the support on the catalytic activity. Prefabricated gold particles were thus deposited on different support materials. Since the deposition process did not change the particle sizes of the gold particles, only the influence of the support could be st… Show more
“…4 nm diameter were deposited on commercial anatase TiO 2 (specific surface area of ~300 m 2 g −1 ; material consists of almost round nanoparticles with a diameter of 10-20 nm; Sachtleben Chemie GmbH, now: Huntsman P&A Germany) and on P25 (specific surface area approximately 50 m 2 g −1 ; rutile/anatase = 20/80; Evonik Industries AG) by the colloidal deposition method as described in Refs. [45][46][47]. One sample was prepared similarly, but not calcined after the colloidal synthesis (Au/anatase uncalc.).…”
transformations might be both thermally or light induced, however, the colloidal deposition synthesis of the Au/TiO 2 catalysts is clearly ruled out as cause for the formation of the reduced phase.
“…4 nm diameter were deposited on commercial anatase TiO 2 (specific surface area of ~300 m 2 g −1 ; material consists of almost round nanoparticles with a diameter of 10-20 nm; Sachtleben Chemie GmbH, now: Huntsman P&A Germany) and on P25 (specific surface area approximately 50 m 2 g −1 ; rutile/anatase = 20/80; Evonik Industries AG) by the colloidal deposition method as described in Refs. [45][46][47]. One sample was prepared similarly, but not calcined after the colloidal synthesis (Au/anatase uncalc.).…”
transformations might be both thermally or light induced, however, the colloidal deposition synthesis of the Au/TiO 2 catalysts is clearly ruled out as cause for the formation of the reduced phase.
“…Gold colloids and nanoparticles have been prepared by different procedures and used as precursors to prepare gold supported on TiO 2 , ZnO, ZrO 2 , Al 2 O 3 , carbon and SiO 2 materials [32,[149][150][151][152][153][154][155][156][157]. The synthesis of gold supported on MSM using gold colloids or presynthesized AuNPs can be achieved by using two different strategies: (i) dispersing the presynthesized gold precursors on the MSM support and (ii) synthesizing the MSM in the presence of presynthesized gold colloids or AuNPs.…”
Section: Synthesis By Dispersion Of Gold Colloids or Presynthesized Amentioning
Mesoporous silica materials (MSM) with ordered and controllable porous structure, high surface area, pore volume and thermal stability are very suitable catalyst supports, because they provide high dispersion of metal nanoparticles and facilitate the access of the substrates to the active sites. Since the conventional wet-impregnation and deposition-precipitation methods are not appropriate for the incorporation of gold nanoparticles (AuNPs) into MSM, considerable efforts have been made to develop suitable methods to synthesize Au/MSM catalysts, because the incorporation of AuNPs into the channel system can prevent their agglomeration and leaching. In this review, we summarize the main methods to synthesize active gold catalysts supported on MSM. Examples and details of the preparative methods, as well as selected applications are provided. We expect this article to be interesting to researchers due to the wide variety of chemical reactions that can be catalyzed by gold supported catalysts.
“…While the particle size of gold nanoparticles is important in optimizing the catalytic activity, the selection of appropriate supports has also been found critical to achieving high catalytic performance and stability of supported gold nanoparticles. In most cases, the size and support effects are likely to operate simultaneously [14], due to the lack of highly reproducible techniques for the controlled preparation of well-defined goldnanoparticle catalysts, separation of size and support effects therefore remains a challenge [15,16]. For example, the importance of the Au TiO 2 interface in CO oxidation over real catalysts has been widely proposed and investigated by comparison of various supported gold nanoparticles or between supported TiO 2 -supported Au nanoparticles and unsupported gold powder [17 20].…”
Au nanoparticles epitaxially grown on Fe 3 O 4 in Au (6.7 nm)-Fe 3 O 4 dumbbell nanoparticles exhibit excellent stability against sintering, but display negligible catalytic activity in CO oxidation. Starting from various supported Au (6.7 nm)-Fe 3 O 4 catalysts prepared by the colloidal deposition method, we have unambiguously identifi ed the signifi cance of the Au-TiO 2 interface in CO oxidation, without any possible size effect of Au. In situ thermal decomposition of TiO 2 precursors on Au-Fe 3 O 4 was found to be an effective way to increase the Au-TiO 2 interface and thereby optimize the catalytic performance of TiO 2 -supported Au-Fe 3 O 4 dumbbell nanoparticles. By reducing the size of Fe 3 O 4 from 15.2 to 4.9 nm, the Au-TiO 2 contact was further increased so that the resulting TiO 2 -supported Au (6.7 nm)-Fe 3 O 4 (4.9 nm) dumbbell particles become highly effi cient catalysts for CO oxidation at room temperature.
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