P‑Doping Strategy Increasing the Durability of PtCo Nanoparticles for the Oxygen Reduction Reaction
Highly active and durable electrocatalysts for the cathodic oxygen reduction reaction (ORR) are vital for the large-scale commercialization of proton exchange membrane fuel cells. Alloying Pt with transition metals is a promising method to enhance the ORR catalytic activity, but the leaching of tran...
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Veröffentlicht in: | ACS sustainable chemistry & engineering 2023-08, Vol.11 (31), p.11660-11667 |
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creator | Shen, Jun-Fei Hu, Sheng-Nan Tian, Na Li, Meng-Ying Yang, Shuang-Li Tian, Si-Yi Chen, Ming-Shu Zhou, Zhi-You Sun, Shi-Gang |
description | Highly active and durable electrocatalysts for the cathodic oxygen reduction reaction (ORR) are vital for the large-scale commercialization of proton exchange membrane fuel cells. Alloying Pt with transition metals is a promising method to enhance the ORR catalytic activity, but the leaching of transition metals is inevitable, which deteriorates the stability. Here, we report the design of a P-doped PtCo electrocatalyst supported on carbon via a facile one-pot hydrothermal method. On the one hand, the introduction of P into the carbon support by phytic acid can enhance the anchoring ability of the PtCo alloy and inhibit the migration of nanoparticles. On the other hand, the doping of P into the lattice of the PtCo alloy further tunes the electronic effect, which improves activity and stability simultaneously. The mass activity of as-prepared P5-PtCo/C at 0.9 V can reach 0.72 A mgPt –1, which is 4.5 times higher than that of commercial Pt/C. After an accelerated durability test (ADT) of 30,000 potential cycles, the mass activity only decreased by 9.4%. Meanwhile, the average particle size of the catalyst slightly increased from 4.94 to 5.15 nm after the ADT of 70,000 potential cycles. This study provides a facile approach for constructing nonmetal-doped PtM catalysts with improved durability for the ORR. |
doi_str_mv | 10.1021/acssuschemeng.3c02903 |
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Alloying Pt with transition metals is a promising method to enhance the ORR catalytic activity, but the leaching of transition metals is inevitable, which deteriorates the stability. Here, we report the design of a P-doped PtCo electrocatalyst supported on carbon via a facile one-pot hydrothermal method. On the one hand, the introduction of P into the carbon support by phytic acid can enhance the anchoring ability of the PtCo alloy and inhibit the migration of nanoparticles. On the other hand, the doping of P into the lattice of the PtCo alloy further tunes the electronic effect, which improves activity and stability simultaneously. The mass activity of as-prepared P5-PtCo/C at 0.9 V can reach 0.72 A mgPt –1, which is 4.5 times higher than that of commercial Pt/C. After an accelerated durability test (ADT) of 30,000 potential cycles, the mass activity only decreased by 9.4%. Meanwhile, the average particle size of the catalyst slightly increased from 4.94 to 5.15 nm after the ADT of 70,000 potential cycles. This study provides a facile approach for constructing nonmetal-doped PtM catalysts with improved durability for the ORR.</description><identifier>ISSN: 2168-0485</identifier><identifier>EISSN: 2168-0485</identifier><identifier>DOI: 10.1021/acssuschemeng.3c02903</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>ACS sustainable chemistry & engineering, 2023-08, Vol.11 (31), p.11660-11667</ispartof><rights>2023 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a295t-5819a869a879a6ba970de16027136393c051b5cb26c926054603e906ea5923503</citedby><cites>FETCH-LOGICAL-a295t-5819a869a879a6ba970de16027136393c051b5cb26c926054603e906ea5923503</cites><orcidid>0000-0002-8654-6818 ; 0000-0002-4923-9632 ; 0000-0001-5181-0642 ; 0000-0003-2327-4090</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acssuschemeng.3c02903$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acssuschemeng.3c02903$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids></links><search><creatorcontrib>Shen, Jun-Fei</creatorcontrib><creatorcontrib>Hu, Sheng-Nan</creatorcontrib><creatorcontrib>Tian, Na</creatorcontrib><creatorcontrib>Li, Meng-Ying</creatorcontrib><creatorcontrib>Yang, Shuang-Li</creatorcontrib><creatorcontrib>Tian, Si-Yi</creatorcontrib><creatorcontrib>Chen, Ming-Shu</creatorcontrib><creatorcontrib>Zhou, Zhi-You</creatorcontrib><creatorcontrib>Sun, Shi-Gang</creatorcontrib><title>P‑Doping Strategy Increasing the Durability of PtCo Nanoparticles for the Oxygen Reduction Reaction</title><title>ACS sustainable chemistry & engineering</title><addtitle>ACS Sustainable Chem. Eng</addtitle><description>Highly active and durable electrocatalysts for the cathodic oxygen reduction reaction (ORR) are vital for the large-scale commercialization of proton exchange membrane fuel cells. Alloying Pt with transition metals is a promising method to enhance the ORR catalytic activity, but the leaching of transition metals is inevitable, which deteriorates the stability. Here, we report the design of a P-doped PtCo electrocatalyst supported on carbon via a facile one-pot hydrothermal method. On the one hand, the introduction of P into the carbon support by phytic acid can enhance the anchoring ability of the PtCo alloy and inhibit the migration of nanoparticles. On the other hand, the doping of P into the lattice of the PtCo alloy further tunes the electronic effect, which improves activity and stability simultaneously. The mass activity of as-prepared P5-PtCo/C at 0.9 V can reach 0.72 A mgPt –1, which is 4.5 times higher than that of commercial Pt/C. After an accelerated durability test (ADT) of 30,000 potential cycles, the mass activity only decreased by 9.4%. Meanwhile, the average particle size of the catalyst slightly increased from 4.94 to 5.15 nm after the ADT of 70,000 potential cycles. 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Eng</addtitle><date>2023-08-07</date><risdate>2023</risdate><volume>11</volume><issue>31</issue><spage>11660</spage><epage>11667</epage><pages>11660-11667</pages><issn>2168-0485</issn><eissn>2168-0485</eissn><abstract>Highly active and durable electrocatalysts for the cathodic oxygen reduction reaction (ORR) are vital for the large-scale commercialization of proton exchange membrane fuel cells. Alloying Pt with transition metals is a promising method to enhance the ORR catalytic activity, but the leaching of transition metals is inevitable, which deteriorates the stability. Here, we report the design of a P-doped PtCo electrocatalyst supported on carbon via a facile one-pot hydrothermal method. On the one hand, the introduction of P into the carbon support by phytic acid can enhance the anchoring ability of the PtCo alloy and inhibit the migration of nanoparticles. On the other hand, the doping of P into the lattice of the PtCo alloy further tunes the electronic effect, which improves activity and stability simultaneously. The mass activity of as-prepared P5-PtCo/C at 0.9 V can reach 0.72 A mgPt –1, which is 4.5 times higher than that of commercial Pt/C. After an accelerated durability test (ADT) of 30,000 potential cycles, the mass activity only decreased by 9.4%. Meanwhile, the average particle size of the catalyst slightly increased from 4.94 to 5.15 nm after the ADT of 70,000 potential cycles. This study provides a facile approach for constructing nonmetal-doped PtM catalysts with improved durability for the ORR.</abstract><pub>American Chemical Society</pub><doi>10.1021/acssuschemeng.3c02903</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-8654-6818</orcidid><orcidid>https://orcid.org/0000-0002-4923-9632</orcidid><orcidid>https://orcid.org/0000-0001-5181-0642</orcidid><orcidid>https://orcid.org/0000-0003-2327-4090</orcidid></addata></record> |
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title | P‑Doping Strategy Increasing the Durability of PtCo Nanoparticles for the Oxygen Reduction Reaction |
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