scholarly journals PdAg/C Electrocatalysts Synthesized by Thermal Decomposition of Polymeric Precursors Improve Catalytic Activity for Ethanol Oxidation Reaction

Catalysts ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 96
Author(s):  
Yonis Fornazier Filho ◽  
Ana Caroliny Carvalho da Cruz ◽  
Rolando Pedicini ◽  
José Ricardo Cezar Salgado ◽  
Rodrigo Vieira Rodrigues ◽  
...  

An efficient ethanol oxidation reaction (EOR) is required to enhance energy production in alcohol-based fuel cells. The use of bimetallic catalysts promises decreasing reliance on platinum group metal (PGM) electrocatalysts by minimizing the use of these expensive materials in the overall electrocatalyst composition. In this article, an alternative method of bimetallic electrocatalyst synthesis based on the use of polymeric precursors is explored. PdAg/C electrocatalysts were synthesized by thermal decomposition of polymeric precursors and used as the anode electrocatalyst for EOR. Different compositions, including pristine Pd/C and Ag/C, as well as bimetallic Pd80Ag20/C, and Pd60Ag40/C electrocatalysts, were evaluated. Synthesized catalysts were characterized, and electrochemical activity evaluated. X-ray diffraction showed a notable change at diffraction peak values for Pd80Ag20/C and Pd60Ag40/C electrocatalysts, suggesting alloying (solid solution) and smaller crystallite sizes for Pd60Ag40/C. In a thermogravimetric analysis, the electrocatalyst Pd60Ag40/C presented changes in the profile of the curves compared to the other electrocatalysts. In the cyclic voltammetry results for EOR in alkaline medium, Pd60Ag40/C presented a more negative onset potential, a higher current density at the oxidation peak, and a larger electrically active area. Chronoamperometry tests indicated a lower poisoning rate for Pd60Ag40/C, a fact also observed in the CO-stripping voltammetry analysis due to its low onset potential. As the best performing electrocatalyst, Pd60Ag40/C has a lower mass of Pd (a noble and expensive metal) in its composition. It can be inferred that this bimetallic composition can contribute to decreasing the amount of Pd required while increasing the fuel cell performance and expected life. PdAg-type electrocatalysts can provide an economically feasible alternative to pure PGM-electrocatalysts for use as the anode in EOR in fuel cells.

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.


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...


2014 ◽  
Vol 50 (89) ◽  
pp. 13732-13734 ◽  
Author(s):  
Jin Zhang ◽  
Yi Cheng ◽  
Shanfu Lu ◽  
Lichao Jia ◽  
Pei Kang Shen ◽  
...  

Inner tubes of CNTs play a significant role in the electrocatalytic activity of supported Pd NPs for the ethanol oxidation reaction.


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