Phosphate-Tolerant Oxygen Reduction Catalysts
Increased oxygen reduction reaction (ORR) kinetics, improved CO tolerance, and more efficient water and heat management represent significant advantages that high-temperature polymer electrolyte fuel cells (HT-PEFCs) operating with a phosphoric acid-doped polybenzimidazole (PBI) membrane offer over...
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Veröffentlicht in: | ACS catalysis 2014-09, Vol.4 (9), p.3193-3200 |
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description | Increased oxygen reduction reaction (ORR) kinetics, improved CO tolerance, and more efficient water and heat management represent significant advantages that high-temperature polymer electrolyte fuel cells (HT-PEFCs) operating with a phosphoric acid-doped polybenzimidazole (PBI) membrane offer over traditional Nafion-based, low-temperature PEFCs. However, before such HT-PEFCs become viable, the detrimental effect of phosphate chemisorption on the performance of state-of-the-art Pt-based cathode catalysts needs to be addressed. In this study, we propose a solution to the severe poisoning of Pt-based PEFC cathode catalysts with phosphates (H2PO4 – and HPO4 2–) by replacing standard Pt/C catalysts with phosphate-tolerant, nonprecious metal catalyst (NPMC) formulations. Catalysts with a very high surface area (845 m2 g–1) were synthesized in this work from polyaniline (PANI), iron, and carbon using a high-temperature approach. The effects of metal precursors and metal loading on the morphology, structure, and ORR activity of the NPMCs were systematically studied. Electrochemical measurements indicated that as-prepared Fe-based catalysts (PANI-Fe-C) can tolerate phosphate ions at high concentrations and deliver ORR performance in 5.0 M H3PO4 that is superior to that of Pt/C catalysts. A 30 wt % Fe-derived catalyst was found to have the most porous morphology and the highest surface area among studied Fe-based catalysts, which correlates with the highest ORR activity of that catalyst. These cost-effective and well-performing ORR catalysts can potentially replace Pt/C catalysts in phosphoric acid-based HT-PEFCs. |
doi_str_mv | 10.1021/cs500807v |
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However, before such HT-PEFCs become viable, the detrimental effect of phosphate chemisorption on the performance of state-of-the-art Pt-based cathode catalysts needs to be addressed. In this study, we propose a solution to the severe poisoning of Pt-based PEFC cathode catalysts with phosphates (H2PO4 – and HPO4 2–) by replacing standard Pt/C catalysts with phosphate-tolerant, nonprecious metal catalyst (NPMC) formulations. Catalysts with a very high surface area (845 m2 g–1) were synthesized in this work from polyaniline (PANI), iron, and carbon using a high-temperature approach. The effects of metal precursors and metal loading on the morphology, structure, and ORR activity of the NPMCs were systematically studied. Electrochemical measurements indicated that as-prepared Fe-based catalysts (PANI-Fe-C) can tolerate phosphate ions at high concentrations and deliver ORR performance in 5.0 M H3PO4 that is superior to that of Pt/C catalysts. A 30 wt % Fe-derived catalyst was found to have the most porous morphology and the highest surface area among studied Fe-based catalysts, which correlates with the highest ORR activity of that catalyst. These cost-effective and well-performing ORR catalysts can potentially replace Pt/C catalysts in phosphoric acid-based HT-PEFCs.</description><identifier>ISSN: 2155-5435</identifier><identifier>EISSN: 2155-5435</identifier><identifier>DOI: 10.1021/cs500807v</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><ispartof>ACS catalysis, 2014-09, Vol.4 (9), p.3193-3200</ispartof><rights>Copyright © 2014 American Chemical Society</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a321t-f599ca9f7568dbca6797e93598b21c15612f29b2766c9de134c7d304b7b1ebaf3</citedby><cites>FETCH-LOGICAL-a321t-f599ca9f7568dbca6797e93598b21c15612f29b2766c9de134c7d304b7b1ebaf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/cs500807v$$EPDF$$P50$$Gacs$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/cs500807v$$EHTML$$P50$$Gacs$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,2752,27055,27903,27904,56716,56766</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1150724$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Qing</creatorcontrib><creatorcontrib>Wu, Gang</creatorcontrib><creatorcontrib>Cullen, David A</creatorcontrib><creatorcontrib>More, Karren L</creatorcontrib><creatorcontrib>Mack, Nathan H</creatorcontrib><creatorcontrib>Chung, Hoon T</creatorcontrib><creatorcontrib>Zelenay, Piotr</creatorcontrib><title>Phosphate-Tolerant Oxygen Reduction Catalysts</title><title>ACS catalysis</title><addtitle>ACS Catal</addtitle><description>Increased oxygen reduction reaction (ORR) kinetics, improved CO tolerance, and more efficient water and heat management represent significant advantages that high-temperature polymer electrolyte fuel cells (HT-PEFCs) operating with a phosphoric acid-doped polybenzimidazole (PBI) membrane offer over traditional Nafion-based, low-temperature PEFCs. However, before such HT-PEFCs become viable, the detrimental effect of phosphate chemisorption on the performance of state-of-the-art Pt-based cathode catalysts needs to be addressed. In this study, we propose a solution to the severe poisoning of Pt-based PEFC cathode catalysts with phosphates (H2PO4 – and HPO4 2–) by replacing standard Pt/C catalysts with phosphate-tolerant, nonprecious metal catalyst (NPMC) formulations. Catalysts with a very high surface area (845 m2 g–1) were synthesized in this work from polyaniline (PANI), iron, and carbon using a high-temperature approach. The effects of metal precursors and metal loading on the morphology, structure, and ORR activity of the NPMCs were systematically studied. Electrochemical measurements indicated that as-prepared Fe-based catalysts (PANI-Fe-C) can tolerate phosphate ions at high concentrations and deliver ORR performance in 5.0 M H3PO4 that is superior to that of Pt/C catalysts. A 30 wt % Fe-derived catalyst was found to have the most porous morphology and the highest surface area among studied Fe-based catalysts, which correlates with the highest ORR activity of that catalyst. 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However, before such HT-PEFCs become viable, the detrimental effect of phosphate chemisorption on the performance of state-of-the-art Pt-based cathode catalysts needs to be addressed. In this study, we propose a solution to the severe poisoning of Pt-based PEFC cathode catalysts with phosphates (H2PO4 – and HPO4 2–) by replacing standard Pt/C catalysts with phosphate-tolerant, nonprecious metal catalyst (NPMC) formulations. Catalysts with a very high surface area (845 m2 g–1) were synthesized in this work from polyaniline (PANI), iron, and carbon using a high-temperature approach. The effects of metal precursors and metal loading on the morphology, structure, and ORR activity of the NPMCs were systematically studied. Electrochemical measurements indicated that as-prepared Fe-based catalysts (PANI-Fe-C) can tolerate phosphate ions at high concentrations and deliver ORR performance in 5.0 M H3PO4 that is superior to that of Pt/C catalysts. A 30 wt % Fe-derived catalyst was found to have the most porous morphology and the highest surface area among studied Fe-based catalysts, which correlates with the highest ORR activity of that catalyst. These cost-effective and well-performing ORR catalysts can potentially replace Pt/C catalysts in phosphoric acid-based HT-PEFCs.</abstract><cop>United States</cop><pub>American Chemical Society</pub><doi>10.1021/cs500807v</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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title | Phosphate-Tolerant Oxygen Reduction Catalysts |
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