Minimization of Pt-electrocatalyst deactivation in CO 2 reduction using a polymer electrolyte cell
Diluted CO 2 feeding was recently reported to efficiently generate CH 4 at the theoretical Pt electrode potential, however, the reaction was easily deactivated. To solve this problem, we investigated the reaction/deactivation mechanism to produce CH 4 from CO 2 electroreduction. Using a polymer elec...
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Veröffentlicht in: | Reaction chemistry & engineering 2020-06, Vol.5 (6), p.1064-1070 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Diluted CO
2
feeding was recently reported to efficiently generate CH
4
at the theoretical Pt electrode potential, however, the reaction was easily deactivated. To solve this problem, we investigated the reaction/deactivation mechanism to produce CH
4
from CO
2
electroreduction. Using a polymer electrolyte single cell containing a Pt/C catalyst, CO
2
was reduced to CH
4
without overpotential by simply controlling the CO
2
feed concentration. The CH
4
synthesis proceeded if the Pt–CO/Pt–H ratio formed on the Pt-catalyst surface was 1 : 11 or higher. The deactivation of the CH
4
generating reaction also depends on the Pt–CO/Pt–H ratio (the ratio does not satisfy 1 : 11 or higher). The optimum Pt–CO/Pt–H ratio to produce CH
4
was 1 : 18. Furthermore, we achieved 86% recovery of CH
4
activity by sweeping the deactivated Pt surface on the cathode up to 0.3 V where the CO
2
/Pt–CO redox reaction occurred simultaneously. As a result, an efficient less energy-intensive reactivation reaction that we defined as a poisoning-elimination method was established. Overall, this work demonstrated that the application of a polymer electrolyte cell together with a low concentration of CO
2
is effective to minimize Pt-electrocatalyst deactivation. |
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ISSN: | 2058-9883 2058-9883 |
DOI: | 10.1039/D0RE00083C |