Ultrafine AuPd nanoparticles supported on amine functionalized monochlorotriazinyl β-cyclodextrin as highly active catalysts for hydrogen evolution from formic acid dehydrogenation

2020 ◽  
Vol 10 (15) ◽  
pp. 5281-5287 ◽  
Author(s):  
Xue Liu ◽  
Dawei Gao ◽  
Yue Chi ◽  
Hongli Wang ◽  
Zhili Wang ◽  
...  

Au0.3Pd0.7/A-M-β-CD exhibits remarkable catalytic activity for hydrogen evolution from formic acid, which is attributed to strong metal–support interaction.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Xueke Wu ◽  
Zuochao Wang ◽  
Dan Zhang ◽  
Yingnan Qin ◽  
Minghui Wang ◽  
...  

AbstractExploring a simple, fast, solvent-free synthetic method for large-scale preparation of cheap, highly active electrocatalysts for industrial hydrogen evolution reaction is one of the most promising work today. In this work, a simple, fast and solvent-free microwave pyrolysis method is used to synthesize ultra-small (3.5 nm) Ru-Mo2C@CNT catalyst with heterogeneous structure and strong metal-support interaction in one step. The Ru-Mo2C@CNT catalyst only exhibits an overpotential of 15 mV at a current density of 10 mA cm−2, and exhibits a large turnover frequency value up to 21.9 s−1 under an overpotential of 100 mV in 1.0 M KOH. In addition, this catalyst can reach high current densities of 500 mA cm−2 and 1000 mA cm−2 at low overpotentials of 56 mV and 78 mV respectively, and it displays high stability of 1000 h. This work provides a feasible way for the reasonable design of other large-scale production catalysts.


2018 ◽  
Vol 54 (79) ◽  
pp. 11168-11171 ◽  
Author(s):  
Zhimin Jia ◽  
Fei Huang ◽  
Jiangyong Diao ◽  
Jiayun Zhang ◽  
Jia Wang ◽  
...  

Platinum nanoparticles (Pt NPs) immobilized on a N-doped graphene@Al2O3 hybrid support (Al2O3@CNx) were synthesized and exhibit superior catalytic activity for low temperature CO oxidation, due to a strong metal–support interaction between Pt NPs and the N-doped.


2020 ◽  
Vol 72 (4) ◽  
pp. 99-109
Author(s):  
Xiaofeng Zhu ◽  
Teng Zhao ◽  
Yufan Huang ◽  
Zijun Wang

Layered porous SiO2 (V-SiO2) was designed and prepared from vermiculite by expansion-acidification method, and then used as a catalyst support to prepare Ni/V-SiO2 for dry reforming of methane. It is well known that sintering and carbon deposition of metal particles are two main problems in deactivation of nickel-based catalysts for methane dry reforming. It is reported that strong metal support interaction is a possible solution. Here, a Ni/V-SiO2-H catalyst derived from Ni-phyllosilicate was developed, and compared with the catalyst Ni/V-SiO2-IM by impregnation method. The results showed that the Ni/V-SiO2-H catalyst had high catalytic activity and stability, and the CH4 conversion reached 71.7% at 700 �C. The reason is that on the one hand, the active metal particles in the catalyst are small (8.3 nm) and relatively evenly dispersed; on the other hand, the catalyst has strong metal support interaction, which improves the anti sintering ability of the catalyst and affects the catalytic activity. It is considered that V-SiO2 as a catalyst support for the preparation of Ni-phyllosilicate may have wide application.


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