Role of the Metal-Oxide Support in the Catalytic Activity of Pd Nanoparticles for Ethanol Electrooxidation in Alkaline Media

2015 ◽  
Vol 3 (2) ◽  
pp. 218-227 ◽  
Author(s):  
Evans Angwenyi Monyoncho ◽  
Spyridon Ntais ◽  
Nicolas Brazeau ◽  
Jhing-Jhou Wu ◽  
Chia-Liang Sun ◽  
...  
2016 ◽  
Vol 3 (2) ◽  
pp. 175-175
Author(s):  
Evans Angwenyi Monyoncho ◽  
Spyridon Ntais ◽  
Nicolas Brazeau ◽  
Jhing-Jhou Wu ◽  
Chia-Liang Sun ◽  
...  

Catalysts ◽  
2019 ◽  
Vol 9 (11) ◽  
pp. 933
Author(s):  
Ji Sun Yoon ◽  
Min Bum Park ◽  
Youngmin Kim ◽  
Dong Won Hwang ◽  
Ho-Jeong Chae

We investigated the interactions between nickel oxide and silica–alumina supports, which were applied to the catalytic oligomerization of ethylene by powder X-ray diffraction, UV diffuse reflectance spectroscopy, H2 temperature-programmed reduction, and X-ray photoelectron spectroscopy. The catalytic activity was also correlated with the acidity of catalysts determined by NH3 temperature-programmed desorption and pyridine FT-IR spectroscopy. Although all the catalysts had similar Ni contents, their catalytic performances were strongly influenced by the strength of the metal oxide–support interaction. Strong interaction promoted the formation of nickel aluminate on the catalyst surface, and resulted in low catalytic activity due to reducing the amount of nickel oxide active sites. However, weak interaction favored the aggregation of nickel oxide species into larger particles, and thus resulted in low ethylene conversion and selectivity to oligomers. Eventually, the optimal activity was realized at the medium interaction strength, preserving a high amount of both active nickel oxides and acid sites.


2020 ◽  
Author(s):  
Shaine Raseale ◽  
Wijnand Marquart ◽  
Kai Jeske ◽  
Gonzalo Prieto ◽  
Michael Claeys ◽  
...  

The effect of both the Fe:Ni ratio (5 to 1:1) and the relative Lewis acidity of a metal oxide support on catalytic activity, selectivity and stability was investigated in the...


2014 ◽  
Vol 486 ◽  
pp. 19-31 ◽  
Author(s):  
Tarek T. Ali ◽  
Katabathini Narasimharao ◽  
Nesreen S. Ahmed ◽  
Sulaiman Basahel ◽  
Shaeel Al-Thabaiti ◽  
...  

Author(s):  
Yoyo Hinuma ◽  
Shinya Mine ◽  
Takashi Toyao ◽  
Zen Maeno ◽  
Ken-ichi Shimizu

Metal/oxide support perimeter sites are known to provide unique properties because the nearby metal changes the local environment on the support surface. In particular, the electron scavenger effect reduces the...


2019 ◽  
Vol 20 ◽  
pp. 188-195 ◽  
Author(s):  
Feili Lai ◽  
Jianrui Feng ◽  
Tobias Heil ◽  
Gui-Chang Wang ◽  
Peter Adler ◽  
...  

2020 ◽  
Vol 234 (5) ◽  
pp. 787-812 ◽  
Author(s):  
Hong Nhan Nong ◽  
Hoang Phi Tran ◽  
Camillo Spöri ◽  
Malte Klingenhof ◽  
Lorenz Frevel ◽  
...  

AbstractThe usage of iridium as an oxygen-evolution-reaction (OER) electrocatalyst requires very high atom efficiencies paired with high activity and stability. Our efforts during the past 6 years in the Priority Program 1613 funded by the Deutsche Forschungsgemeinschaft (DFG) were focused to mitigate the molecular origin of kinetic overpotentials of Ir-based OER catalysts and to design new materials to achieve that Ir-based catalysts are more atom and energy efficient, as well as stable. Approaches involved are: (1) use of bimetallic mixed metal oxide materials where Ir is combined with cheaper transition metals as starting materials, (2) use of dealloying concepts of nanometer sized core-shell particle with a thin noble metal oxide shell combined with a hollow or cheap transition metal-rich alloy core, and (3) use of corrosion-resistant high-surface-area oxide support materials. In this mini review, we have highlighted selected advances in our understanding of Ir–Ni bimetallic oxide electrocatalysts for the OER in acidic environments.


Sign in / Sign up

Export Citation Format

Share Document