scholarly journals RuSe Electrocatalysts and Single Wall Carbon Nanohorns Supports for the Oxygen Reduction Reaction

2015 ◽  
Vol 12 (2) ◽  
Author(s):  
Katarzyna Morawa Eblagon ◽  
Lúcia Brandão

Selenium modified ruthenium electrocatalysts supported on carbon black were synthesized using NaBH4 reduction of the metal precursor. Prepared Ru/C electrocatalysts showed high dispersion and very small averaged particle size. These Ru/C electrocatalysts were subsequently modified with Se following two procedures: (a) preformed Ru/carbon catalyst was mixed with SeO2 in xylene and reduced in H2 and (b) Ru metal precursor was mixed with SeO2 followed by reduction with NaBH4. The XRD patterns indicate that a pyrite-type structure was obtained at higher annealing temperatures, regardless of the Ru:Se molar ratio used in the preparation step. A pyrite-type structure also emerged in samples that were not calcined; however, in this case, the pyrite-type structure was only prominent for samples with higher Ru:Se ratios. The characterization of the RuSe/C electrocatalysts suggested that the Se in noncalcined samples was present mainly as an amorphous skin. Preliminary study of activity toward oxygen reduction reaction (ORR) using electrocatalysts with a Ru:Se ratio of 1:0.7 indicated that annealing after modification with Se had a detrimental effect on their activity. This result could be related to the increased particle size of crystalline RuSe2 in heat-treated samples. Higher activity of not annealed RuSe/C catalysts could also be a result of the structure containing amorphous Se skin on the Ru crystal. The electrode obtained using not calcined RuSe showed a very promising performance with a slightly lower activity and higher overpotential in comparison with a commercial Pt/C electrode. Single wall carbon nanohorns (SWNH) were considered for application as ORR electrocatalysts' supports. The characterization of SWNH was carried out regarding their tolerance toward strong catalyzed corrosion conditions. Tests indicated that SWNH have a three times higher electrochemical surface area (ESA) loss than carbon black or Pt commercial electrodes.

RSC Advances ◽  
2018 ◽  
Vol 8 (59) ◽  
pp. 33688-33694 ◽  
Author(s):  
Xueyou Tan ◽  
Jinxuan Zhang ◽  
Xiaohui Wu ◽  
Yuanyuan Wang ◽  
Meixian Li ◽  
...  

Palladium nanoparticles with a diameter of 2–4 nm loaded on nitrogen and boron dual-doped single-wall carbon nanohorns (Pd-NBCNHs) are prepared via one-step method and their electrocatalytic activities are studied for the oxygen reduction reaction.


2013 ◽  
Vol 17 (04) ◽  
pp. 252-258 ◽  
Author(s):  
Qinggang He ◽  
Xiao Cheng ◽  
Ying Wang ◽  
Ruimin Qiao ◽  
Wanli Yang ◽  
...  

The dicobalt complex [ Co2(L2) ] of a Schiff-base pyrrole macrocycle adopts a Pacman structure in solution and the solid state and shows much greater catalytic activity and selectivity for the four-electron oxygen reduction reaction (ORR) than the mononuclear cobalt phthalocyanine (CoPc) counterpart. Soft X-ray absorption spectroscopy (XAS) shows that the Co center in Co2(L2) is of the same valence as mononuclear CoPc . However, the former complex shows higher unoccupied Co 3d density which is believed to be beneficial for electron transfers. Furthermore, the XAS data suggests that the crystal fields for Co2(L2) and CoPc are different, and that an interaction remains between two Co atoms in Co2(L2) . DFT calculations imply that the sterically hindered, cofacial structure of the dicobalt complex is critical for the operation of the four-electron reaction pathway during the ORR.


2021 ◽  
Vol MA2021-02 (36) ◽  
pp. 1024-1024
Author(s):  
Hassan Shirzadi Jahromi ◽  
Shivi Saxena ◽  
Sudharsan Sridhar ◽  
Muralidhar K Ghantasala ◽  
Ramakrishna Guda ◽  
...  

2021 ◽  
Vol 104 (8) ◽  
pp. 59-71
Author(s):  
Hassan Shirzadi Jahromi ◽  
Shivi Saxena ◽  
Sudharsan Sridhar ◽  
Muralidhar K Ghantasala ◽  
Ramakrishna Guda ◽  
...  

ChemSusChem ◽  
2013 ◽  
Vol 6 (10) ◽  
pp. 1973-1982 ◽  
Author(s):  
A. Anastasopoulos ◽  
J. C. Davies ◽  
L. Hannah ◽  
B. E. Hayden ◽  
C. E. Lee ◽  
...  

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