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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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. |
doi_str_mv | 10.1039/c9ta11745h |
format | Article |
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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. A, Materials for energy and sustainability, 2020, Vol.8 (5), p.2323-233</ispartof><rights>Copyright Royal Society of Chemistry 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c425t-27e2a328c6299ad5d7ce8d9ac771e91f218f44320c6c88421d856814cffab1a03</citedby><cites>FETCH-LOGICAL-c425t-27e2a328c6299ad5d7ce8d9ac771e91f218f44320c6c88421d856814cffab1a03</cites><orcidid>0000-0002-2526-2002 ; 0000-0003-4215-799X ; 0000-0001-7275-4846</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27900,27901,27902</link.rule.ids></links><search><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><title>Surface oxygen-mediated ultrathin PtRuM (Ni, Fe, and Co) nanowires boosting methanol oxidation reaction</title><title>Journal of materials chemistry. 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 & 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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