Surface oxygen-mediated ultrathin PtRuM (Ni, Fe, and Co) nanowires boosting methanol oxidation reaction

Improving the electrocatalytic activity and durability of electrocatalysts is of vital importance to the direct methanol fuel cells. PtRu materials are the most effective catalysts for methanol oxidation reaction (MOR) in an acidic medium, but they still exhibits partial defects, such as limited cat...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020, Vol.8 (5), p.2323-233
Hauptverfasser: Li, Hongdong, Pan, Yue, Zhang, Dan, Han, Yi, Wang, Zuochao, Qin, Yingnan, Lin, Shuangyan, Wu, Xueke, Zhao, Huan, Lai, Jianping, Huang, Bolong, Wang, Lei
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container_issue 5
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container_title Journal of materials chemistry. A, Materials for energy and sustainability
container_volume 8
creator Li, Hongdong
Pan, Yue
Zhang, Dan
Han, Yi
Wang, Zuochao
Qin, Yingnan
Lin, Shuangyan
Wu, Xueke
Zhao, Huan
Lai, Jianping
Huang, Bolong
Wang, Lei
description Improving the electrocatalytic activity and durability of electrocatalysts is of vital importance to the direct methanol fuel cells. PtRu materials are the most effective catalysts for methanol oxidation reaction (MOR) in an acidic medium, but they still exhibits partial defects, such as limited catalytic activity. Here, we prepared a series of surface oxygen-mediated ultrathin PtRuM (M = Ni, Fe, and Co) nanowires (NWs) termed PtRuM-O. All these prepared materials showed ultrahigh electrocatalytic activity and excellent durability for MOR in an acidic medium due to their optimal electronic structures induced by the introduction of electroactive O. Until now, in the reported article on Pt-based materials, the optimal Pt 62 Ru 18 Ni 20 -O/C electrocatalyst shows the highest mass activity of 2.72 A mg Pt −1 for MOR in an acidic medium, which is 1.42, 5.14 and 9 times higher than that of Pt 62 Ru 18 Ni 20 /C (1.91 A mg Pt −1 ), Pt 65 Ru 35 /C (0.47 A mg Pt −1 ), and Pt/C (0.30 A mg Pt −1 ) NWs catalysts, respectively. Also, the Pt 62 Ru 18 Ni 20 -O/C catalyst still retains 92% of its initial mass activity after 1000 voltammetry (CV) cycles. The CO stripping experiment results revealed that the peak potential of Pt 62 Ru 18 Ni 20 -O/C shows a negative shift compared with that of Pt 62 Ru 18 Ni 20 /C, Pt 65 Ru 35 /C, and Pt/C NWs catalysts, indicating that the Pt 62 Ru 18 Ni 20 -O/C catalyst has the best CO anti-poisoning. The as-prepared electrocatalysts also showed better MOR performance in an alkaline medium. The density functional theory (DFT) calculations proved that the introduction of O to PtRuNi significantly boosts the MOR performance by strengthening the adsorption of initial CH 3 OH induced by the electroactive O-2p bands. Moreover, a much larger energy barrier for CO generation indicates the much lower probability of the catalyst poisoning of the PtRuNi-O. The surface-oxygen-modified ultrathin Pt 62 Ru 18 Ni 20 -O/C nanowires catalyst exhibits outstanding mass activity, excellent stability, and CO anti-poisoning for methanol oxidation reaction in acidic medium by DFT and electrochemical experiments.
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PtRu materials are the most effective catalysts for methanol oxidation reaction (MOR) in an acidic medium, but they still exhibits partial defects, such as limited catalytic activity. Here, we prepared a series of surface oxygen-mediated ultrathin PtRuM (M = Ni, Fe, and Co) nanowires (NWs) termed PtRuM-O. All these prepared materials showed ultrahigh electrocatalytic activity and excellent durability for MOR in an acidic medium due to their optimal electronic structures induced by the introduction of electroactive O. Until now, in the reported article on Pt-based materials, the optimal Pt 62 Ru 18 Ni 20 -O/C electrocatalyst shows the highest mass activity of 2.72 A mg Pt −1 for MOR in an acidic medium, which is 1.42, 5.14 and 9 times higher than that of Pt 62 Ru 18 Ni 20 /C (1.91 A mg Pt −1 ), Pt 65 Ru 35 /C (0.47 A mg Pt −1 ), and Pt/C (0.30 A mg Pt −1 ) NWs catalysts, respectively. Also, the Pt 62 Ru 18 Ni 20 -O/C catalyst still retains 92% of its initial mass activity after 1000 voltammetry (CV) cycles. The CO stripping experiment results revealed that the peak potential of Pt 62 Ru 18 Ni 20 -O/C shows a negative shift compared with that of Pt 62 Ru 18 Ni 20 /C, Pt 65 Ru 35 /C, and Pt/C NWs catalysts, indicating that the Pt 62 Ru 18 Ni 20 -O/C catalyst has the best CO anti-poisoning. The as-prepared electrocatalysts also showed better MOR performance in an alkaline medium. The density functional theory (DFT) calculations proved that the introduction of O to PtRuNi significantly boosts the MOR performance by strengthening the adsorption of initial CH 3 OH induced by the electroactive O-2p bands. Moreover, a much larger energy barrier for CO generation indicates the much lower probability of the catalyst poisoning of the PtRuNi-O. The surface-oxygen-modified ultrathin Pt 62 Ru 18 Ni 20 -O/C nanowires catalyst exhibits outstanding mass activity, excellent stability, and CO anti-poisoning for methanol oxidation reaction in acidic medium by DFT and electrochemical experiments.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/c9ta11745h</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Acidic oxides ; Catalysts ; Catalytic activity ; Cobalt ; Density functional theory ; Durability ; Electrocatalysts ; Fuel cells ; Fuel technology ; Iron ; Methanol ; Nanotechnology ; Nanowires ; Nickel ; Oxidation ; Oxygen ; Poisoning</subject><ispartof>Journal of materials chemistry. 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A, Materials for energy and sustainability</title><description>Improving the electrocatalytic activity and durability of electrocatalysts is of vital importance to the direct methanol fuel cells. PtRu materials are the most effective catalysts for methanol oxidation reaction (MOR) in an acidic medium, but they still exhibits partial defects, such as limited catalytic activity. Here, we prepared a series of surface oxygen-mediated ultrathin PtRuM (M = Ni, Fe, and Co) nanowires (NWs) termed PtRuM-O. All these prepared materials showed ultrahigh electrocatalytic activity and excellent durability for MOR in an acidic medium due to their optimal electronic structures induced by the introduction of electroactive O. Until now, in the reported article on Pt-based materials, the optimal Pt 62 Ru 18 Ni 20 -O/C electrocatalyst shows the highest mass activity of 2.72 A mg Pt −1 for MOR in an acidic medium, which is 1.42, 5.14 and 9 times higher than that of Pt 62 Ru 18 Ni 20 /C (1.91 A mg Pt −1 ), Pt 65 Ru 35 /C (0.47 A mg Pt −1 ), and Pt/C (0.30 A mg Pt −1 ) NWs catalysts, respectively. Also, the Pt 62 Ru 18 Ni 20 -O/C catalyst still retains 92% of its initial mass activity after 1000 voltammetry (CV) cycles. The CO stripping experiment results revealed that the peak potential of Pt 62 Ru 18 Ni 20 -O/C shows a negative shift compared with that of Pt 62 Ru 18 Ni 20 /C, Pt 65 Ru 35 /C, and Pt/C NWs catalysts, indicating that the Pt 62 Ru 18 Ni 20 -O/C catalyst has the best CO anti-poisoning. The as-prepared electrocatalysts also showed better MOR performance in an alkaline medium. The density functional theory (DFT) calculations proved that the introduction of O to PtRuNi significantly boosts the MOR performance by strengthening the adsorption of initial CH 3 OH induced by the electroactive O-2p bands. Moreover, a much larger energy barrier for CO generation indicates the much lower probability of the catalyst poisoning of the PtRuNi-O. The surface-oxygen-modified ultrathin Pt 62 Ru 18 Ni 20 -O/C nanowires catalyst exhibits outstanding mass activity, excellent stability, and CO anti-poisoning for methanol oxidation reaction in acidic medium by DFT and electrochemical experiments.</description><subject>Acidic oxides</subject><subject>Catalysts</subject><subject>Catalytic activity</subject><subject>Cobalt</subject><subject>Density functional theory</subject><subject>Durability</subject><subject>Electrocatalysts</subject><subject>Fuel cells</subject><subject>Fuel technology</subject><subject>Iron</subject><subject>Methanol</subject><subject>Nanotechnology</subject><subject>Nanowires</subject><subject>Nickel</subject><subject>Oxidation</subject><subject>Oxygen</subject><subject>Poisoning</subject><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpFkE1LAzEURYMoWGo37oWAG5WOJplkJlmWYq1QP9C6HtIk06a0SU0yaP-9Uyv1bd7lcbgPDgDnGN1ilIs7JZLEuKRscQQ6BDGUlVQUx4fM-SnoxbhE7XCECiE6YP7ehFoqA_33dm5ctjbaymQ0bFYpyLSwDr6mt-YJXj3bPhyZPpROw6G_hk46_2WDiXDmfUzWzeHapEV7XbVlVstkvYPBSLULZ-Cklqtoen-7Cz5G99PhOJu8PDwOB5NMUcJSRkpDZE64KogQUjNdKsO1kKossRG4JpjXlOYEqUJxTgnWnBUcU1XXcoYlyrvgct-7Cf6zMTFVS98E176sSM5QzgijO-pmT6ngYwymrjbBrmXYVhhVO5fVUEwHvy7HLXyxh0NUB-7fdf4DOqVwHA</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Li, Hongdong</creator><creator>Pan, Yue</creator><creator>Zhang, Dan</creator><creator>Han, Yi</creator><creator>Wang, Zuochao</creator><creator>Qin, Yingnan</creator><creator>Lin, Shuangyan</creator><creator>Wu, Xueke</creator><creator>Zhao, Huan</creator><creator>Lai, Jianping</creator><creator>Huang, Bolong</creator><creator>Wang, Lei</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><scope>L7M</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0002-2526-2002</orcidid><orcidid>https://orcid.org/0000-0003-4215-799X</orcidid><orcidid>https://orcid.org/0000-0001-7275-4846</orcidid></search><sort><creationdate>2020</creationdate><title>Surface oxygen-mediated ultrathin PtRuM (Ni, Fe, and Co) nanowires boosting methanol oxidation reaction</title><author>Li, Hongdong ; Pan, Yue ; Zhang, Dan ; Han, Yi ; Wang, Zuochao ; Qin, Yingnan ; Lin, Shuangyan ; Wu, Xueke ; Zhao, Huan ; Lai, Jianping ; Huang, Bolong ; Wang, Lei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c425t-27e2a328c6299ad5d7ce8d9ac771e91f218f44320c6c88421d856814cffab1a03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Acidic oxides</topic><topic>Catalysts</topic><topic>Catalytic activity</topic><topic>Cobalt</topic><topic>Density functional theory</topic><topic>Durability</topic><topic>Electrocatalysts</topic><topic>Fuel cells</topic><topic>Fuel technology</topic><topic>Iron</topic><topic>Methanol</topic><topic>Nanotechnology</topic><topic>Nanowires</topic><topic>Nickel</topic><topic>Oxidation</topic><topic>Oxygen</topic><topic>Poisoning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Hongdong</creatorcontrib><creatorcontrib>Pan, Yue</creatorcontrib><creatorcontrib>Zhang, Dan</creatorcontrib><creatorcontrib>Han, Yi</creatorcontrib><creatorcontrib>Wang, Zuochao</creatorcontrib><creatorcontrib>Qin, Yingnan</creatorcontrib><creatorcontrib>Lin, Shuangyan</creatorcontrib><creatorcontrib>Wu, Xueke</creatorcontrib><creatorcontrib>Zhao, Huan</creatorcontrib><creatorcontrib>Lai, Jianping</creatorcontrib><creatorcontrib>Huang, Bolong</creatorcontrib><creatorcontrib>Wang, Lei</creatorcontrib><collection>CrossRef</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Hongdong</au><au>Pan, Yue</au><au>Zhang, Dan</au><au>Han, Yi</au><au>Wang, Zuochao</au><au>Qin, Yingnan</au><au>Lin, Shuangyan</au><au>Wu, Xueke</au><au>Zhao, Huan</au><au>Lai, Jianping</au><au>Huang, Bolong</au><au>Wang, Lei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Surface oxygen-mediated ultrathin PtRuM (Ni, Fe, and Co) nanowires boosting methanol oxidation reaction</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2020</date><risdate>2020</risdate><volume>8</volume><issue>5</issue><spage>2323</spage><epage>233</epage><pages>2323-233</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>Improving the electrocatalytic activity and durability of electrocatalysts is of vital importance to the direct methanol fuel cells. PtRu materials are the most effective catalysts for methanol oxidation reaction (MOR) in an acidic medium, but they still exhibits partial defects, such as limited catalytic activity. Here, we prepared a series of surface oxygen-mediated ultrathin PtRuM (M = Ni, Fe, and Co) nanowires (NWs) termed PtRuM-O. All these prepared materials showed ultrahigh electrocatalytic activity and excellent durability for MOR in an acidic medium due to their optimal electronic structures induced by the introduction of electroactive O. Until now, in the reported article on Pt-based materials, the optimal Pt 62 Ru 18 Ni 20 -O/C electrocatalyst shows the highest mass activity of 2.72 A mg Pt −1 for MOR in an acidic medium, which is 1.42, 5.14 and 9 times higher than that of Pt 62 Ru 18 Ni 20 /C (1.91 A mg Pt −1 ), Pt 65 Ru 35 /C (0.47 A mg Pt −1 ), and Pt/C (0.30 A mg Pt −1 ) NWs catalysts, respectively. Also, the Pt 62 Ru 18 Ni 20 -O/C catalyst still retains 92% of its initial mass activity after 1000 voltammetry (CV) cycles. The CO stripping experiment results revealed that the peak potential of Pt 62 Ru 18 Ni 20 -O/C shows a negative shift compared with that of Pt 62 Ru 18 Ni 20 /C, Pt 65 Ru 35 /C, and Pt/C NWs catalysts, indicating that the Pt 62 Ru 18 Ni 20 -O/C catalyst has the best CO anti-poisoning. The as-prepared electrocatalysts also showed better MOR performance in an alkaline medium. The density functional theory (DFT) calculations proved that the introduction of O to PtRuNi significantly boosts the MOR performance by strengthening the adsorption of initial CH 3 OH induced by the electroactive O-2p bands. Moreover, a much larger energy barrier for CO generation indicates the much lower probability of the catalyst poisoning of the PtRuNi-O. The surface-oxygen-modified ultrathin Pt 62 Ru 18 Ni 20 -O/C nanowires catalyst exhibits outstanding mass activity, excellent stability, and CO anti-poisoning for methanol oxidation reaction in acidic medium by DFT and electrochemical experiments.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/c9ta11745h</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-2526-2002</orcidid><orcidid>https://orcid.org/0000-0003-4215-799X</orcidid><orcidid>https://orcid.org/0000-0001-7275-4846</orcidid></addata></record>
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source Royal Society Of Chemistry Journals 2008-
subjects Acidic oxides
Catalysts
Catalytic activity
Cobalt
Density functional theory
Durability
Electrocatalysts
Fuel cells
Fuel technology
Iron
Methanol
Nanotechnology
Nanowires
Nickel
Oxidation
Oxygen
Poisoning
title Surface oxygen-mediated ultrathin PtRuM (Ni, Fe, and Co) nanowires boosting methanol oxidation reaction
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