Role of the carbon defects in the catalytic oxygen reduction by graphite nanoparticles: a spectromagnetic, electrochemical and computational integrated approach

2019 ◽  
Vol 21 (11) ◽  
pp. 6021-6032 ◽  
Author(s):  
Claudio Greco ◽  
Ugo Cosentino ◽  
Demetrio Pitea ◽  
Giorgio Moro ◽  
Saveria Santangelo ◽  
...  

The surface defects of graphite play a key role in its catalytic activity towards the oxygen reduction reaction.

RSC Advances ◽  
2020 ◽  
Vol 10 (15) ◽  
pp. 8709-8716
Author(s):  
Lin Gu ◽  
Yunyun Dong ◽  
Yan Zhang ◽  
Bo Wang ◽  
Qing Yuan ◽  
...  

The PPYTZ–Fe/C catalyst containing Fe–N active sites exhibited high ORR catalytic activity and stability in alkaline media with a four-electron pathway progress.


2015 ◽  
Vol 17 (23) ◽  
pp. 15146-15155 ◽  
Author(s):  
R. Rahul ◽  
R. K. Singh ◽  
B. Bera ◽  
R. Devivaraprasad ◽  
M. Neergat

Surface adsorbed species can significantly alter the catalytic activity and product selectivity.


2017 ◽  
Vol 200 ◽  
pp. 99-106 ◽  
Author(s):  
K. Sudarshan ◽  
S.K. Sharma ◽  
Ruma Gupta ◽  
Santosh K. Gupta ◽  
F.N. Sayed ◽  
...  

2017 ◽  
Vol 2 (31) ◽  
pp. 10300-10303 ◽  
Author(s):  
Liang Zhang ◽  
Xianchun Liu ◽  
Yuanhong Wang ◽  
Gang Chen ◽  
Shuangxi Xing

2018 ◽  
Vol 2018 ◽  
pp. 1-13
Author(s):  
Aleksey M. Trunov

Analysis of the role of oxygen-containing nanoclusters in oxygen reduction reaction (ORR) on Pt-electrodes in alkaline media is provided on the basis of the concept of electrochemical processes with slowed stage of consecutive heterogeneous chemical reaction (ConHCR). Under the ConHCR concept, the main factor determining the ORR characteristics is energetic inhomogeneity of electrode surface (EIES) according to Temkin. A new concept, according to which EIES is determined by the Gibbs energy of formation of oxygen-containing surface structures with inclusions of surface defects of the platinum crystal structure, Pts,d, is formulated. A correlation between the level of EIES of Pt-electrodes and packing density of Pts,d atoms on the surface of Pt(hkl) monocrystals is determined. The concept, according to which the stationary potential of ORR process is considered as a “mixed potential” of two reactions (electrochemical reduction of surface atom PtIIs,d and consecutive oxidation of PtIs,d by molecular oxygen), is substantiated. It is proposed that the formation of surface nanocluster transition state [⁎(OO)PtIIs,d(OH)] defines the rate of the entire ORR process on Pt-electrodes in alkaline media.


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