scholarly journals Alkaline Ethanol Oxidation Reaction on Carbon Supported Ternary PdNiBi Nanocatalyst using Modified Instant Reduction Synthesis Method

2020 ◽  
Vol 11 (2) ◽  
pp. 203-214
Author(s):  
Bernd Cermenek ◽  
Boštjan Genorio ◽  
Thomas Winter ◽  
Sigrid Wolf ◽  
Justin G. Connell ◽  
...  

AbstractDirect ethanol fuel cells (DEFC) still lack active and efficient electrocatalysts for the alkaline ethanol oxidation reaction (EOR). In this work, a new instant reduction synthesis method was developed to prepare carbon supported ternary PdNiBi nanocatalysts with improved EOR activity. Synthesized catalysts were characterized with a variety of structural and compositional analysis techniques in order to correlate their morphology and surface chemistry with electrochemical performance. The modified instant reduction synthesis results in well-dispersed, spherical Pd85Ni10Bi5 nanoparticles on Vulcan XC72R support (Pd85Ni10Bi5/C(II-III)), with sizes ranging from 3.7 ± 0.8 to 4.7 ± 0.7 nm. On the other hand, the common instant reduction synthesis method leads to significantly agglomerated nanoparticles (Pd85Ni10Bi5/C(I)). EOR activity and stability of these three different carbon supported PdNiBi anode catalysts with a nominal atomic ratio of 85:10:5 were probed via cyclic voltammetry and chronoamperometry using the rotating disk electrode method. Pd85Ni10Bi5/C(II) showed the highest electrocatalytic activity (150 mA⋅cm−2; 2678 mA⋅mg−1) with low onset potential (0.207 V) for EOR in alkaline medium, as compared to a commercial Pd/C and to the other synthesized ternary nanocatalysts Pd85Ni10Bi5/C(I) and Pd85Ni10Bi5/C(III). This new synthesis approach provides a new avenue to developing efficient, carbon supported ternary nanocatalysts for future energy conversion devices.

2016 ◽  
Vol 18 (36) ◽  
pp. 25169-25175 ◽  
Author(s):  
Antoine Bach Delpeuch ◽  
Marjorie Jacquot ◽  
Marian Chatenet ◽  
Carsten Cremers

This study aims to provide further understanding of the influence of different parameters that control mass-transport (the revolution rate of the rotating disk electrode and the potential scan rate) on the ethanol oxidation reaction (EOR).


Author(s):  
Si Li ◽  
Anxiang Guan ◽  
Huining Wang ◽  
Yaqin Yan ◽  
Haoliang Huang ◽  
...  

The electrocatalytic ethanol oxidation reaction (EOR) is a critical component for direct ethanol fuel cells, while its reactivity, stability, and selectivity toward C1 products are severely hindered by the poisoning...


Author(s):  
Cong Shen ◽  
Hanming Chen ◽  
Mingye Qiu ◽  
Yuqiang Shi ◽  
Wei Yan ◽  
...  

The sluggish kinetics of ethanol oxidation reaction (EOR), poor C1 selectivity and susceptibility to toxicity of CO intermediates hinder the commercialization of direct ethanol fuel cells (DEFCs). In this paper,...


Author(s):  
Moxuan Liu ◽  
Miao Xie ◽  
Yilan Jiang ◽  
Zhaojun Liu ◽  
Yiming Lu ◽  
...  

The ethanol oxidation reaction (EOR), the anode reaction of direct ethanol fuel cells, suffers from the sluggish oxidation kinetics and its low selectivity toward complete oxidation to CO2. The key...


2020 ◽  
Vol 12 (1) ◽  
pp. 101-102
Author(s):  
Bernd Cermenek ◽  
Boštjan Genorio ◽  
Thomas Winter ◽  
Sigrid Wolf ◽  
Justin G. Connell ◽  
...  

2013 ◽  
Vol 860-863 ◽  
pp. 826-830 ◽  
Author(s):  
Long Long Wang ◽  
Qiao Xia Li ◽  
Tian Yu Zhan ◽  
Qun Jie Xu

Direct ethanol fuel cells are considered a promising power source for future portable electronic and automotive applications. This article reviewed the synthetic methods commonly used to prepare Pd-based catalysts for the ethanol electrooxidation in alkaline media. The progress in the mechanism studies of ethanol oxidation reaction (EOR) on Pd electrode in alkaline medium by cyclic voltammetry and electrochemical in situ FTIR spectroscopy was also reviewed. The recent studies revealed that the EOR is fairly complicated, and it is difficult in CC bond cleavage for the complete oxidation of ethanol to CO2, and ethanol is selectively oxidized to acetate on Pd-based catalysts in alkaline media. Overall, what is most important is to explore new Pd-based alloy catalysts with high ability to break the CC bond to promote complete oxidation of ethanol as well as increase the efficiency of DEFCs.


NANO ◽  
2017 ◽  
Vol 12 (09) ◽  
pp. 1750105 ◽  
Author(s):  
Meiling Peng ◽  
Tao Wang ◽  
Zhenzhen Jiang ◽  
Sheng Wang

In this work, a synthesis method of residue-free PdPt nanodendrites on reduced graphene oxide (rGO) is reported. Using UV light as an energy trigger and methanol as the reducing agent, PdPt nanodendrites are synthesized with clean, residue-free surfaces (e.g., surfactant and polymer). In comparison with commercial Pd/C and Pt/C catalysts, the as-prepared PdPt nanodendrites on rGO have a large electrochemically active surface area, enhanced catalytic activity, high stability, and tolerance toward the ethanol oxidation reaction in alkaline media. Among the nanodendrite composites prepared, those containing a Pd:Pt ratio of 1:2 on rGO exhibit the best stability and durability, and their mass activity is 2.0 and 2.4 times greater than those of commercial Pt/C and Pd/C catalysts, respectively. This strategy presents an environmentally friendly way to fabricate other noble metal catalysts with improved catalytic activity and stability for use in direct alcohol fuel cells.


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