The Electrocatalytic Oxidation of Methane-Derived Liquid Fuel in a Direct Oxidation Fuel Cell

Author(s):  
M. Williams ◽  
T. Horita ◽  
K. Yamagi ◽  
N. Sakai ◽  
H. Yokokawa

There are at least four basic fuel cell thermodynamic features: maximum intrinsic thermal efficiency (electrical efficiency), reversible potential, and two new ones—intrinsic cooling requirement and intrinsic exergetic efficiency. A basic electrochemical thermodynamic analysis of fuel cells using MALT reveals that it is probably for thermodynamic reasons that cooling strategies other than excess oxidant, such as water cooling, have generally been adopted for lower temperature fuel cells such as polymer electrolyte fuel cell (PEFC) and phosphoric acid fuel cell (PAFC). One can mathematically demonstrate that for a simple hybrid system, any fuel cell, any operating temperature, and any pressure, the maximum reversible work is equal to the free energy of reaction at the standard state. This study gives information of new opportunity fuels having increasing importance is all future energy scenarios. The results of this analysis show that ammonia and direct methanol give greater maximum intrinsic thermal efficiency than hydrogen oxidation. From these simple studies alone, one would conclude that the great payoff in terms of theoretical efficiency potential for research is direct carbon fuel cell (DCFT), PEFC, and direct oxidation of methane, intermediate temperature solid oxide fuel cell (SOFC), and simple fuel cell turbine hybrids.


Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 17
Author(s):  
Unni Engedahl ◽  
Adam A. Arvidsson ◽  
Henrik Grönbeck ◽  
Anders Hellman

As transportation continues to increase world-wide, there is a need for more efficient utilization of fossil fuel. One possibility is direct conversion of the solution gas bi-product CH4 into an energy-rich, easily usable liquid fuel such as CH3OH. However, new catalytic materials to facilitate the methane-to-methanol reaction are needed. Using density functional calculations, the partial oxidation of methane is investigated over the small-pore copper-exchanged zeolite SSZ-13. The reaction pathway is identified and the energy landscape elucidated over the proposed motifs Z2[Cu2O] and Z2[Cu2OH]. It is shown that the Z2[Cu2O] motif has an exergonic reaction path, provided water is added as a solvent for the desorption step. However, a micro-kinetic model shows that neither Z2[Cu2O] nor Z2[Cu2OH] has any notable activity under the reaction conditions. These findings highlight the importance of the detailed structure of the active site and that the most stable motif is not necessarily the most active.


2021 ◽  
Author(s):  
Kinga Mlekodaj ◽  
Mariia Lemishka ◽  
Stepan Sklenak ◽  
Jiri Dedecek ◽  
Edyta Tabor

Here we demonstrate for the first time the splitting of dioxygen at RT over distant binuclear transition metal (M = Ni, Mn, and Co) centers stabilized in ferrierite zeolite. Cleaved...


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