Enhanced Catalytic Activity of Cobalt Porphyrin in CO2 Electroreduction upon Immobilization on Carbon Materials

2017 ◽  
Vol 56 (23) ◽  
pp. 6468-6472 ◽  
Author(s):  
Xin-Ming Hu ◽  
Magnus H. Rønne ◽  
Steen U. Pedersen ◽  
Troels Skrydstrup ◽  
Kim Daasbjerg
2017 ◽  
Vol 129 (23) ◽  
pp. 6568-6572 ◽  
Author(s):  
Xin-Ming Hu ◽  
Magnus H. Rønne ◽  
Steen U. Pedersen ◽  
Troels Skrydstrup ◽  
Kim Daasbjerg

2021 ◽  
Vol 298 ◽  
pp. 117196
Author(s):  
Xue Zhang ◽  
Fanghua Li ◽  
Jiahong Wang ◽  
Haitao Zhao ◽  
Xue-Feng Yu

2008 ◽  
Vol 139 ◽  
pp. 41-46 ◽  
Author(s):  
K. Okazaki-Maeda ◽  
Y. Morikawa ◽  
Shingo Tanaka ◽  
Masanori Kohyama

Pt nano-particles are supported on carbon materials at the electrode catalysts of protonexchange menbrane fuel cells. Pt nano-particles are desirable to be strongly adsorbed on carbon materials for high dispersion, although strong Pt-C interactions may affect the catalytic activity of small clusters. Thus we have examined H-atom absorption on Pt clusters supported or unsupported on graphene sheets, using first-principles calculations. For Pt-atom/graphene systems, a H atom is more weakly adsorbed than for a free Pt atom, and the H-Pt interaction becomes weaker if the interaction between a Pt atom and graphene becomes stronger. For the Ptn-cluster/graphene systems (n=2-4), the H-Pt interactions are also substantially changed from those for free Pt clusters. In the Pt clusters on graphene, the Pt-Pt distances are substantially changed associated with the electronicstructure changes by the Pt-C interactions. These structural and electronic changes in the Pt clusters as well as the presence of graphene itself seem to cause the changes in the absorption energies and preferential sites of H-atom absorption.


1996 ◽  
Vol 454 ◽  
Author(s):  
Zakiyyah Smith ◽  
Michael Palmieri ◽  
Nancy Buecheler ◽  
Susan A. Jansen

AbstractHeteropoly acids, HPA are well known solid acid and oxidation catalysts that find application in hetergeneous and homogeneous reactions. In the former, surface area and stability problems are diminshed by supporting the HPA. Typical supports include oxide substrates and porous carbon materials. The HPA's show some instability on these supports however. In this work, we demonstrate that HPA encapsulated in sol-gel silica matrices show enhanced catalytic performance without compromising the catalytic activity of the HPA. In addition, the specific role of the support in the catalytic process is described as well.


2019 ◽  
Vol 3 (7) ◽  
pp. 1833-1840 ◽  
Author(s):  
Dilan Karapinar ◽  
Ngoc-Huan Tran ◽  
Domitille Giaume ◽  
Nastaran Ranjbar ◽  
Frédéric Jaouen ◽  
...  

Iron- and nitrogen-doped carbon materials (FeNC) are excellent catalysts for CO2 electroreduction to CO. Current density and selectivity can be significantly improved by mixing FeNC with carbon materials such as carbon nanofibers.


2017 ◽  
Vol 5 (21) ◽  
pp. 10574-10583 ◽  
Author(s):  
Dmitri A. Bulushev ◽  
Andrey L. Chuvilin ◽  
Vladimir I. Sobolev ◽  
Svetlana G. Stolyarova ◽  
Yury V. Shubin ◽  
...  

N-doping of carbon support prevents sintering of Cu and provides its high catalytic activity in H2 formation from formic acid.


2007 ◽  
Vol 85 (2) ◽  
pp. 118-123 ◽  
Author(s):  
T Tsoncheva ◽  
S Vankova ◽  
O Bozhkov ◽  
D Mehandjiev

Bicomponent manganese and rhenium modified activated carbon materials, prepared by different methods, are studied and compared with the corresponding monocomponent materials as catalysts in methanol decomposition to CO and hydrogen. The best catalytic activity and stability is observed for the sample obtained by simultaneous deposition of Mn and Re precursors. The complex character of the catalytic active centre, including manganese and rhenium irons in various oxidative states, is discussed. The determining role of the Mn(II) ions in the improvement of the catalytic properties is assumed.Key words: rhenium, manganese, activated carbon, methanol decomposition.


2012 ◽  
Vol 573-574 ◽  
pp. 27-30
Author(s):  
Huan Bao Fa ◽  
Li Ping Zhang ◽  
Wei Yin ◽  
Jing Ting Zhou ◽  
Nan Nan Xu ◽  
...  

The monocarboxyphenyl cobalt porphyrin (CoMCPP) was synthesized and incorporated into carbon carrier acetylene black (ACET) for proton exchange membrane fuel cell cathode oxygen reduction. The influence of different thermal treatment temperature on the catalytic performance of the composite catalysts was discussed. The synthetic compound catalyst was analyzed by XRD、IR. The electrochemical catalytic performance of catalyst, which was heat-treated under different temperature, for oxygen reduction was tested by linear sweep voltammetry (LSV). The result shows that the best thermal treatment temperature is 6000C, and its catalytic activity also shows the best, the catalytic activity site changes from CoN4 to C-N-Co.


2017 ◽  
Vol 53 (10) ◽  
pp. 1194-1203 ◽  
Author(s):  
A. Wadas ◽  
I. A. Rutkowska ◽  
M. Bartel ◽  
S. Zoladek ◽  
K. Rajeshwar ◽  
...  

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