The two-step electrosynthesis of nanocomposites of Ag, Au, and Pd nanoparticles with iron(ii) oxide-hydroxide

2022 ◽  
Author(s):  
Rezeda R. Fazleeva ◽  
Gulnaz R. Nasretdinova ◽  
Aidar T. Gubaidullin ◽  
Vladimir G. Evtyugin ◽  
Vitaliy V. Yanilkin

The two-step electrosynthesis of metal nanoparticle (MNP, M = Ag, Pd, and Au) nanocomposites with iron oxide-hydroxide FeO-xFe(OH)2 was investigated.

2019 ◽  
Author(s):  
Suchanuch Sachdev ◽  
Rhushabh Maugi ◽  
Sam Davis ◽  
Scott Doak ◽  
Zhaoxia Zhou ◽  
...  

<div>The interface between two immiscible liquids represent an ideal substrate for the assembly of nanomaterials. The defect free surface provides a reproducible support for creating densely packed ordered materials. Here a droplet flow reactor is presented for the synthesis and/ or assembly of nanomaterials at the interface of the emulsion. Each droplet acts as microreactor for a reaction between decamethylferrocene (DmFc) within the hexane and metal salts (Ag+/ Pd2+) in the aqueous phase. The hypothesis was that a spontaneous, interfacial reaction would lead to the assembly of nanomaterials creating a Pickering emulsion. The subsequent removal of the solvents showed how the Ag nanoparticles were trapped at the interface and retain the shape of the droplet, however the Pd nanoparticles were dispersed with no tertiary structure. To further exploit this, a one-step process where the particles are synthesised and then assembled into core-shell materials was proposed. The same reactions were performed in the presence of oleic acid stabilise Iron oxide nanoparticles dispersed within the hexane. It was shown that by changing the reaction rate and ratio between palladium and iron oxide a continuous coating of palladium onto iron oxide microspheres can be created. The same reaction with silver, was unsuccessful and resulted in the silver particles being shed into solution, or incorporated within the iron oxide micro particle. These insights offer a new method and chemistry within flow reactors for the creation of palladium and silver nanoparticles. We use the technique to create metal coated iron oxide nanomaterials but the methodology could be easily transferred to the assembly of other materials.</div><div><br></div>


2021 ◽  
Vol 14 (3) ◽  
pp. 174-178 ◽  
Author(s):  
Mingqiang Hou ◽  
Yu He ◽  
Bo Gyu Jang ◽  
Shichuan Sun ◽  
Yukai Zhuang ◽  
...  

2017 ◽  
Vol 8 (1) ◽  
Author(s):  
Kwadwo Asare Owusu ◽  
Longbing Qu ◽  
Jiantao Li ◽  
Zhaoyang Wang ◽  
Kangning Zhao ◽  
...  

2007 ◽  
Vol 47 (4) ◽  
pp. 558-562 ◽  
Author(s):  
Akbar Eskandarpour ◽  
Kensuke Sassa ◽  
Yoshiyuki Bando ◽  
Hiroshi Ikuta ◽  
Kazuhiko Iwai ◽  
...  
Keyword(s):  

2019 ◽  
Vol 4 (17) ◽  
pp. 5019-5032 ◽  
Author(s):  
Astha Shukla ◽  
Rajib K. Singha ◽  
Takehiko Sasaki ◽  
Vemulapalli V. D. N. Prasad ◽  
Rajaram Bal

2016 ◽  
Vol 188 ◽  
pp. 309-321 ◽  
Author(s):  
C. P. O'Brien ◽  
K.-H. Dostert ◽  
M. Hollerer ◽  
C. Stiehler ◽  
F. Calaza ◽  
...  

In order to design catalytic materials, we need to understand the essential causes for material properties resulting from its composite nature. In this paper we discuss two, at first sight, diverse aspects: (a) the effect of the oxide–metal interface on metal nanoparticle properties and (b) the consequences of metal particle modification after activation on the selectivity of hydrogenation reactions. However, these two aspects are intimately linked. The metal nanoparticle’s electronic structure changes at the interface as a catalyst is brought to different reaction temperatures due to morphological modifications in the metal and, as we will discuss, these changes in the chemistry lead to changes in the reaction path. As the morphology of the particle varies, facets of different orientations and sizes are exposed, which may lead to a change in the surface chemistry as well. We use two specific reactions to address these issues in some detail. To the best of our knowledge, the present paper reports the first observations of this kind for well-defined model systems. The changes in the electronic structure of Au nanoparticles due to their size and interaction with a supporting oxide are revealed as a function of temperature using CO2 activation as a probe. The presence of spectator species (oxopropyl), formed during an activation step of acrolein hydrogenation, strongly controls the selectivity of the reaction towards hydrogenation of the unsaturated CO bond vs. the CC bond on Pd(111) when compared with oxide-supported Pd nanoparticles.


2007 ◽  
Vol 47 (4) ◽  
pp. 563-567 ◽  
Author(s):  
Akbar Eskandarpour ◽  
Kensuke Sassa ◽  
Yoshiyuki Bando ◽  
Masazumi Okido ◽  
Kazuhiko Iwai ◽  
...  
Keyword(s):  

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