Co-alloying effect of Co and Cr with Pt for oxygen electro-reduction reaction

The effect of co-alloying of Co and Cr was investigated by synthesizing and analyzing Pt3M and PtM (M=Co and/or Cr) catalysts for the oxygen electro-reduction reaction (ORR) activity. In the Pt3M catalysts, we could not observe significant differences among the alloy catalysts before and after annea...

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Veröffentlicht in:Electrochimica acta 2012-03, Vol.64, p.147-153
Hauptverfasser: Jeon, Min Ku, McGinn, Paul J.
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description The effect of co-alloying of Co and Cr was investigated by synthesizing and analyzing Pt3M and PtM (M=Co and/or Cr) catalysts for the oxygen electro-reduction reaction (ORR) activity. In the Pt3M catalysts, we could not observe significant differences among the alloy catalysts before and after annealing, except for the high specific activity of a Pt3Co/C-900 catalyst (Pt3Co/C catalyst annealed at 900°C under H2/Ar (5.2mol% H2) flow for 5min.). The electrochemical properties of the alloy catalysts were much different in the PtM catalysts. After annealing at 900°C, the specific activities of the PtM catalysts increased in the order of PtCo/C-900 (5000 μA cmpt−2)>PtCo0.5Cr0.5/C-900 (2400 μA cmpt−2)>PtCr/C-900 (1080 μA cmpt−2)>Pt/C (334 μA cmpt−2). On the other hand, ORR mass activity exhibited a different order of PtCo0.5Cr0.5/C-900 (132 mA mgpt−1)>PtCr/C-900 (129 mA mgpt−1)>PtCo/C-900 (37 mA mgpt−1). The low mass activity of the PtCo/C-900 catalyst was explained by small electrochemically active surface area (EAS). The intermediate specific ORR activity and EAS values of the PtCo0.5Cr0.5/C catalyst shows that the two opposite characteristics of PtCo (low mass activity and high specific activity) and PtCr (high mass activity and low specific activity) were combined by co-alloying of Co and Cr with Pt. In addition, this result shows that the electrochemical properties of the ternary catalyst can be tuned by controlling the composition to achieve high mass activity.
doi_str_mv 10.1016/j.electacta.2011.12.124
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In the Pt3M catalysts, we could not observe significant differences among the alloy catalysts before and after annealing, except for the high specific activity of a Pt3Co/C-900 catalyst (Pt3Co/C catalyst annealed at 900°C under H2/Ar (5.2mol% H2) flow for 5min.). The electrochemical properties of the alloy catalysts were much different in the PtM catalysts. After annealing at 900°C, the specific activities of the PtM catalysts increased in the order of PtCo/C-900 (5000 μA cmpt−2)&gt;PtCo0.5Cr0.5/C-900 (2400 μA cmpt−2)&gt;PtCr/C-900 (1080 μA cmpt−2)&gt;Pt/C (334 μA cmpt−2). On the other hand, ORR mass activity exhibited a different order of PtCo0.5Cr0.5/C-900 (132 mA mgpt−1)&gt;PtCr/C-900 (129 mA mgpt−1)&gt;PtCo/C-900 (37 mA mgpt−1). The low mass activity of the PtCo/C-900 catalyst was explained by small electrochemically active surface area (EAS). The intermediate specific ORR activity and EAS values of the PtCo0.5Cr0.5/C catalyst shows that the two opposite characteristics of PtCo (low mass activity and high specific activity) and PtCr (high mass activity and low specific activity) were combined by co-alloying of Co and Cr with Pt. In addition, this result shows that the electrochemical properties of the ternary catalyst can be tuned by controlling the composition to achieve high mass activity.</description><identifier>ISSN: 0013-4686</identifier><identifier>EISSN: 1873-3859</identifier><identifier>DOI: 10.1016/j.electacta.2011.12.124</identifier><identifier>CODEN: ELCAAV</identifier><language>eng</language><publisher>Kidlington: Elsevier Ltd</publisher><subject>Annealing ; Applied sciences ; Catalysis ; Catalysts ; Chromium ; Cobalt ; Cyclic voltammetry ; Electrocatalyst ; Energy ; Energy. 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In the Pt3M catalysts, we could not observe significant differences among the alloy catalysts before and after annealing, except for the high specific activity of a Pt3Co/C-900 catalyst (Pt3Co/C catalyst annealed at 900°C under H2/Ar (5.2mol% H2) flow for 5min.). The electrochemical properties of the alloy catalysts were much different in the PtM catalysts. After annealing at 900°C, the specific activities of the PtM catalysts increased in the order of PtCo/C-900 (5000 μA cmpt−2)&gt;PtCo0.5Cr0.5/C-900 (2400 μA cmpt−2)&gt;PtCr/C-900 (1080 μA cmpt−2)&gt;Pt/C (334 μA cmpt−2). On the other hand, ORR mass activity exhibited a different order of PtCo0.5Cr0.5/C-900 (132 mA mgpt−1)&gt;PtCr/C-900 (129 mA mgpt−1)&gt;PtCo/C-900 (37 mA mgpt−1). The low mass activity of the PtCo/C-900 catalyst was explained by small electrochemically active surface area (EAS). The intermediate specific ORR activity and EAS values of the PtCo0.5Cr0.5/C catalyst shows that the two opposite characteristics of PtCo (low mass activity and high specific activity) and PtCr (high mass activity and low specific activity) were combined by co-alloying of Co and Cr with Pt. In addition, this result shows that the electrochemical properties of the ternary catalyst can be tuned by controlling the composition to achieve high mass activity.</description><subject>Annealing</subject><subject>Applied sciences</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chromium</subject><subject>Cobalt</subject><subject>Cyclic voltammetry</subject><subject>Electrocatalyst</subject><subject>Energy</subject><subject>Energy. 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Thermal use of fuels</topic><topic>Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc</topic><topic>Exact sciences and technology</topic><topic>Fuel cells</topic><topic>Oxygen electro-reduction reaction</topic><topic>Platinum</topic><topic>Polymer electrolyte membrane fuel cell</topic><topic>Rotating disk electrode</topic><topic>Surface area</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jeon, Min Ku</creatorcontrib><creatorcontrib>McGinn, Paul J.</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Electrochimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jeon, Min Ku</au><au>McGinn, Paul J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Co-alloying effect of Co and Cr with Pt for oxygen electro-reduction reaction</atitle><jtitle>Electrochimica acta</jtitle><date>2012-03-01</date><risdate>2012</risdate><volume>64</volume><spage>147</spage><epage>153</epage><pages>147-153</pages><issn>0013-4686</issn><eissn>1873-3859</eissn><coden>ELCAAV</coden><abstract>The effect of co-alloying of Co and Cr was investigated by synthesizing and analyzing Pt3M and PtM (M=Co and/or Cr) catalysts for the oxygen electro-reduction reaction (ORR) activity. In the Pt3M catalysts, we could not observe significant differences among the alloy catalysts before and after annealing, except for the high specific activity of a Pt3Co/C-900 catalyst (Pt3Co/C catalyst annealed at 900°C under H2/Ar (5.2mol% H2) flow for 5min.). The electrochemical properties of the alloy catalysts were much different in the PtM catalysts. After annealing at 900°C, the specific activities of the PtM catalysts increased in the order of PtCo/C-900 (5000 μA cmpt−2)&gt;PtCo0.5Cr0.5/C-900 (2400 μA cmpt−2)&gt;PtCr/C-900 (1080 μA cmpt−2)&gt;Pt/C (334 μA cmpt−2). On the other hand, ORR mass activity exhibited a different order of PtCo0.5Cr0.5/C-900 (132 mA mgpt−1)&gt;PtCr/C-900 (129 mA mgpt−1)&gt;PtCo/C-900 (37 mA mgpt−1). The low mass activity of the PtCo/C-900 catalyst was explained by small electrochemically active surface area (EAS). The intermediate specific ORR activity and EAS values of the PtCo0.5Cr0.5/C catalyst shows that the two opposite characteristics of PtCo (low mass activity and high specific activity) and PtCr (high mass activity and low specific activity) were combined by co-alloying of Co and Cr with Pt. In addition, this result shows that the electrochemical properties of the ternary catalyst can be tuned by controlling the composition to achieve high mass activity.</abstract><cop>Kidlington</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.electacta.2011.12.124</doi><tpages>7</tpages></addata></record>
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source ScienceDirect Journals (5 years ago - present)
subjects Annealing
Applied sciences
Catalysis
Catalysts
Chromium
Cobalt
Cyclic voltammetry
Electrocatalyst
Energy
Energy. Thermal use of fuels
Equipments for energy generation and conversion: thermal, electrical, mechanical energy, etc
Exact sciences and technology
Fuel cells
Oxygen electro-reduction reaction
Platinum
Polymer electrolyte membrane fuel cell
Rotating disk electrode
Surface area
title Co-alloying effect of Co and Cr with Pt for oxygen electro-reduction reaction
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