TY - JOUR
T1 - Tungsten carbide as supports for Pt electrocatalysts with improved CO tolerance in methanol oxidation
AU - Cui, Guofeng
AU - Shen, Pei Kang
AU - Meng, Hui
AU - Zhao, Jie
AU - Wu, Gang
PY - 2011/8/1
Y1 - 2011/8/1
N2 - One anti-CO-poisoning Pt-WC/C catalyst for methanol electro-oxidation is prepared in this work, through depositing platinum on tungsten carbide support using an intermittent microwave heating (IMH) method. The catalyst presents an improved methanol oxidation performance evidenced by a negative shift in onset potential, and increase of peak current density, compared with a commercial Pt/C one. CO stripping experiments indicate that the adsorbed CO is able to be oxidized and removed from the Pt-WC/C catalyst more easily, attesting the enhanced capability of anti-poisoning to CO-like species. Theoretical calculation further provides evidence that the surface electronic structure in Pt-WC/C and Pt/C catalysts is likely different. WC supports could lead to much stronger negative electronic property, which is beneficial for avoiding CO adsorption on the Pt-WC/C catalyst. In the mean time, the electron donating effect generated by WC supports also promotes the ability to oxidize the adsorbed CO-like species on catalysts. In good agreement with experimental results, the theoretical calculation proves the anti-CO-poisoning nature of the Pt-WC/C catalyst, and well explains the origin of the improvement in the electrochemical catalytic performance for effectively accelerating the oxidation of CO to CO2 in methanol oxidation.
AB - One anti-CO-poisoning Pt-WC/C catalyst for methanol electro-oxidation is prepared in this work, through depositing platinum on tungsten carbide support using an intermittent microwave heating (IMH) method. The catalyst presents an improved methanol oxidation performance evidenced by a negative shift in onset potential, and increase of peak current density, compared with a commercial Pt/C one. CO stripping experiments indicate that the adsorbed CO is able to be oxidized and removed from the Pt-WC/C catalyst more easily, attesting the enhanced capability of anti-poisoning to CO-like species. Theoretical calculation further provides evidence that the surface electronic structure in Pt-WC/C and Pt/C catalysts is likely different. WC supports could lead to much stronger negative electronic property, which is beneficial for avoiding CO adsorption on the Pt-WC/C catalyst. In the mean time, the electron donating effect generated by WC supports also promotes the ability to oxidize the adsorbed CO-like species on catalysts. In good agreement with experimental results, the theoretical calculation proves the anti-CO-poisoning nature of the Pt-WC/C catalyst, and well explains the origin of the improvement in the electrochemical catalytic performance for effectively accelerating the oxidation of CO to CO2 in methanol oxidation.
KW - CO poisoning
KW - Fuel cells
KW - Methanol oxidation
KW - Theoretical calculation
KW - Tungsten carbide
UR - https://www.scopus.com/pages/publications/79956354123
U2 - 10.1016/j.jpowsour.2011.03.042
DO - 10.1016/j.jpowsour.2011.03.042
M3 - Article
AN - SCOPUS:79956354123
SN - 0378-7753
VL - 196
SP - 6125
EP - 6130
JO - Journal of Power Sources
JF - Journal of Power Sources
IS - 15
ER -