Use of chemical descriptors approach and DFT to analyze the C C bond cleavage on Pt 3 Re 1 alloy in the ethanol oxidation reaction for fuel cells

2017 ◽  
Vol 791 ◽  
pp. 185-195 ◽  
Author(s):  
Alejandro E. Pérez ◽  
Rafael Ribadeneira
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...


2017 ◽  
Vol 19 (38) ◽  
pp. 26210-26220 ◽  
Author(s):  
Han Xu ◽  
Bei Miao ◽  
Minhua Zhang ◽  
Yifei Chen ◽  
Lichang Wang

The C–C and C–H cleavage of hydrocarbons in EOR on Cu2O(111) and the specific effects of +U were investigated by DFT+U.


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.


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.


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