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Enhanced stability of PdPtAu alloy catalyst for formic acid oxidation
In this study, the ternary catalyst, PdPtAu, was synthesized for the electrochemical formic acid oxidation reaction. The catalyst was prepared through the co-precipitation using NaBH 4 as a reducing agent. The status of catalyst formation and the extent of average particle size were known by X-ray d...
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Published in: | The Korean journal of chemical engineering 2021, 38(11), 260, pp.2229-2234 |
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container_title | The Korean journal of chemical engineering |
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creator | Jung, Won Suk Han, Jonghee |
description | In this study, the ternary catalyst, PdPtAu, was synthesized for the electrochemical formic acid oxidation reaction. The catalyst was prepared through the co-precipitation using NaBH
4
as a reducing agent. The status of catalyst formation and the extent of average particle size were known by X-ray diffraction (XRD) and transmission electron microscopy (TEM). For this work, we accomplished electrochemical analyses for the PdPtAu, Pd, Pt, and Au, which defines each activity for formic acid oxidation. In durability tests, half cell and single cell tests show even better stability than the Pd and Au catalysts. Stripping tests were carried out after durability tests. Based on results, the ternary PdPtAu catalyst is less deactivated than the Pd, while the catalyst shows higher activity than the Pt. The PdPtAu catalyst represents high resistance for poisoning as compared to the Pd. We demonstrate the stability of the PdPtAu catalyst in the 3-electrode electrochemical system and single cell tests. After 2 h-operation, the deactivation degree of PdPtAu shows 27% loss of the initial current density, while Pd and Pt catalysts lost 39% and 57% of them, respectively. |
doi_str_mv | 10.1007/s11814-021-0909-y |
format | article |
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4
as a reducing agent. The status of catalyst formation and the extent of average particle size were known by X-ray diffraction (XRD) and transmission electron microscopy (TEM). For this work, we accomplished electrochemical analyses for the PdPtAu, Pd, Pt, and Au, which defines each activity for formic acid oxidation. In durability tests, half cell and single cell tests show even better stability than the Pd and Au catalysts. Stripping tests were carried out after durability tests. Based on results, the ternary PdPtAu catalyst is less deactivated than the Pd, while the catalyst shows higher activity than the Pt. The PdPtAu catalyst represents high resistance for poisoning as compared to the Pd. We demonstrate the stability of the PdPtAu catalyst in the 3-electrode electrochemical system and single cell tests. After 2 h-operation, the deactivation degree of PdPtAu shows 27% loss of the initial current density, while Pd and Pt catalysts lost 39% and 57% of them, respectively.</description><identifier>ISSN: 0256-1115</identifier><identifier>EISSN: 1975-7220</identifier><identifier>DOI: 10.1007/s11814-021-0909-y</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Biotechnology ; Catalysis ; Catalysts ; Chemical synthesis ; Chemistry ; Chemistry and Materials Science ; Deactivation ; Durability ; Energy ; Formic acid ; Gold ; High resistance ; Industrial Chemistry/Chemical Engineering ; Materials Science ; Oxidation ; Palladium ; Platinum ; Reducing agents ; Stability ; 화학공학</subject><ispartof>Korean Journal of Chemical Engineering, 2021, 38(11), 260, pp.2229-2234</ispartof><rights>The Korean Institute of Chemical Engineers 2021</rights><rights>The Korean Institute of Chemical Engineers 2021.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c350t-ccf76490c3c8d08d45b6e8e45a230d4b8cb91bb674fa397446fdd6a27e5fa7923</citedby><cites>FETCH-LOGICAL-c350t-ccf76490c3c8d08d45b6e8e45a230d4b8cb91bb674fa397446fdd6a27e5fa7923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002766894$$DAccess content in National Research Foundation of Korea (NRF)$$Hfree_for_read</backlink></links><search><creatorcontrib>Jung, Won Suk</creatorcontrib><creatorcontrib>Han, Jonghee</creatorcontrib><title>Enhanced stability of PdPtAu alloy catalyst for formic acid oxidation</title><title>The Korean journal of chemical engineering</title><addtitle>Korean J. Chem. Eng</addtitle><description>In this study, the ternary catalyst, PdPtAu, was synthesized for the electrochemical formic acid oxidation reaction. The catalyst was prepared through the co-precipitation using NaBH
4
as a reducing agent. The status of catalyst formation and the extent of average particle size were known by X-ray diffraction (XRD) and transmission electron microscopy (TEM). For this work, we accomplished electrochemical analyses for the PdPtAu, Pd, Pt, and Au, which defines each activity for formic acid oxidation. In durability tests, half cell and single cell tests show even better stability than the Pd and Au catalysts. Stripping tests were carried out after durability tests. Based on results, the ternary PdPtAu catalyst is less deactivated than the Pd, while the catalyst shows higher activity than the Pt. The PdPtAu catalyst represents high resistance for poisoning as compared to the Pd. We demonstrate the stability of the PdPtAu catalyst in the 3-electrode electrochemical system and single cell tests. After 2 h-operation, the deactivation degree of PdPtAu shows 27% loss of the initial current density, while Pd and Pt catalysts lost 39% and 57% of them, respectively.</description><subject>Biotechnology</subject><subject>Catalysis</subject><subject>Catalysts</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Deactivation</subject><subject>Durability</subject><subject>Energy</subject><subject>Formic acid</subject><subject>Gold</subject><subject>High resistance</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Materials Science</subject><subject>Oxidation</subject><subject>Palladium</subject><subject>Platinum</subject><subject>Reducing agents</subject><subject>Stability</subject><subject>화학공학</subject><issn>0256-1115</issn><issn>1975-7220</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kM9LwzAYhoMoOH_8Ad4KnjxUv6RN0hzHmDoYOGSeQ5o0M7NrZpKB_e_trODJw8d7ed6XjwehGwz3GIA_RIwrXOZAcA4CRN6foAkWnOacEDhFEyCU5Rhjeo4uYtwCUMoITNB83r2rTjcmi0nVrnWpz7zNVmaVpodMta3vM62SavuYMuvD8XZOZ0o7k_kvZ1RyvrtCZ1a1sbn-zUv09jhfz57z5cvTYjZd5rqgkHKtLWelAF3oykBlSlqzpmpKqkgBpqwrXQtc14yXVhWClyWzxjBFeEOt4oIUl-hu3O2ClR_aSa_cT268_Ahy-rpeSFFxwqtiYG9Hdh_856GJSW79IXTDe5LQigMTjPOBwiOlg48xNFbug9up0EsM8mhWjmblYFYezcp-6JCxEwe22zThb_n_0jf873si</recordid><startdate>20211101</startdate><enddate>20211101</enddate><creator>Jung, Won Suk</creator><creator>Han, Jonghee</creator><general>Springer US</general><general>Springer Nature B.V</general><general>한국화학공학회</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ACYCR</scope></search><sort><creationdate>20211101</creationdate><title>Enhanced stability of PdPtAu alloy catalyst for formic acid oxidation</title><author>Jung, Won Suk ; Han, Jonghee</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c350t-ccf76490c3c8d08d45b6e8e45a230d4b8cb91bb674fa397446fdd6a27e5fa7923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biotechnology</topic><topic>Catalysis</topic><topic>Catalysts</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Deactivation</topic><topic>Durability</topic><topic>Energy</topic><topic>Formic acid</topic><topic>Gold</topic><topic>High resistance</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Materials Science</topic><topic>Oxidation</topic><topic>Palladium</topic><topic>Platinum</topic><topic>Reducing agents</topic><topic>Stability</topic><topic>화학공학</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jung, Won Suk</creatorcontrib><creatorcontrib>Han, Jonghee</creatorcontrib><collection>CrossRef</collection><collection>Korean Citation Index (Open Access)</collection><jtitle>The Korean journal of chemical engineering</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jung, Won Suk</au><au>Han, Jonghee</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Enhanced stability of PdPtAu alloy catalyst for formic acid oxidation</atitle><jtitle>The Korean journal of chemical engineering</jtitle><stitle>Korean J. Chem. Eng</stitle><date>2021-11-01</date><risdate>2021</risdate><volume>38</volume><issue>11</issue><spage>2229</spage><epage>2234</epage><pages>2229-2234</pages><issn>0256-1115</issn><eissn>1975-7220</eissn><abstract>In this study, the ternary catalyst, PdPtAu, was synthesized for the electrochemical formic acid oxidation reaction. The catalyst was prepared through the co-precipitation using NaBH
4
as a reducing agent. The status of catalyst formation and the extent of average particle size were known by X-ray diffraction (XRD) and transmission electron microscopy (TEM). For this work, we accomplished electrochemical analyses for the PdPtAu, Pd, Pt, and Au, which defines each activity for formic acid oxidation. In durability tests, half cell and single cell tests show even better stability than the Pd and Au catalysts. Stripping tests were carried out after durability tests. Based on results, the ternary PdPtAu catalyst is less deactivated than the Pd, while the catalyst shows higher activity than the Pt. The PdPtAu catalyst represents high resistance for poisoning as compared to the Pd. We demonstrate the stability of the PdPtAu catalyst in the 3-electrode electrochemical system and single cell tests. After 2 h-operation, the deactivation degree of PdPtAu shows 27% loss of the initial current density, while Pd and Pt catalysts lost 39% and 57% of them, respectively.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s11814-021-0909-y</doi><tpages>6</tpages></addata></record> |
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subjects | Biotechnology Catalysis Catalysts Chemical synthesis Chemistry Chemistry and Materials Science Deactivation Durability Energy Formic acid Gold High resistance Industrial Chemistry/Chemical Engineering Materials Science Oxidation Palladium Platinum Reducing agents Stability 화학공학 |
title | Enhanced stability of PdPtAu alloy catalyst for formic acid oxidation |
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