Engineering Partially Oxidized Gold via Oleylamine Modifier as a High-Performance Anode Catalyst in a Direct Borohydride Fuel Cell
Direct borohydride fuel cell (DBFC) is considered a promising energy storage device due to its high theoretical cell voltage and energy density. For DBFC, an Au catalyst has been used as an anode for achieving an ideal eight-electron reaction. However, the poor activity of the Au catalyst for borohy...
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Veröffentlicht in: | ACS applied materials & interfaces 2024-07, Vol.16 (30), p.39295-39304 |
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creator | Xue, Liangyao Liu, Cheng Ye, Jinyu Zhang, Jiaqi Kang, Lin Zhang, Yexuan Shi, Wenjuan Guo, Wen Huang, Xiaoxiong Yang, Xiao Zheng, Lirong Li, Youyong Zhang, Bo |
description | Direct borohydride fuel cell (DBFC) is considered a promising energy storage device due to its high theoretical cell voltage and energy density. For DBFC, an Au catalyst has been used as an anode for achieving an ideal eight-electron reaction. However, the poor activity of the Au catalyst for borohydride oxidation reaction (BOR) limits its large-scale application because of the weak BH4 – adsorption. We found, by density functional theory calculations, that the adsorption of BH4 – on the oxidized Au surface is stronger than that on the metallic Au surface, which can promote the process of the oxidation of BH4 – to *BH3 during the BOR. Here, we reported an oleylamine-modified partially oxidized Au supported on carbon powder (AuC-OLA) with a stable oxidation state. The obtained catalyst delivered a high peak power density of 143 mW/cm2, which is 2 times higher than that of a commercial 40% AuC (Pretemek). The in situ Fourier transform infrared studies showed that the activity of AuC-OLA for BOR is ascribed to the enhanced adsorption for BH4 – on the partially oxidized Au surface. These findings will promote the reasonable design of efficient Au electrocatalysts for DBFCs. |
doi_str_mv | 10.1021/acsami.4c05784 |
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For DBFC, an Au catalyst has been used as an anode for achieving an ideal eight-electron reaction. However, the poor activity of the Au catalyst for borohydride oxidation reaction (BOR) limits its large-scale application because of the weak BH4 – adsorption. We found, by density functional theory calculations, that the adsorption of BH4 – on the oxidized Au surface is stronger than that on the metallic Au surface, which can promote the process of the oxidation of BH4 – to *BH3 during the BOR. Here, we reported an oleylamine-modified partially oxidized Au supported on carbon powder (AuC-OLA) with a stable oxidation state. The obtained catalyst delivered a high peak power density of 143 mW/cm2, which is 2 times higher than that of a commercial 40% AuC (Pretemek). The in situ Fourier transform infrared studies showed that the activity of AuC-OLA for BOR is ascribed to the enhanced adsorption for BH4 – on the partially oxidized Au surface. These findings will promote the reasonable design of efficient Au electrocatalysts for DBFCs.</description><identifier>ISSN: 1944-8244</identifier><identifier>ISSN: 1944-8252</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.4c05784</identifier><identifier>PMID: 39018417</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>adsorption ; anodes ; borohydrides ; carbon ; catalysts ; density functional theory ; electric potential difference ; energy density ; Energy, Environmental, and Catalysis Applications ; Fourier transform infrared spectroscopy ; fuel cells ; oxidation</subject><ispartof>ACS applied materials & interfaces, 2024-07, Vol.16 (30), p.39295-39304</ispartof><rights>2024 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-a248t-886368af1d7d8749c59bb881e65d094462f40c0aae64f24198a264333b7327073</cites><orcidid>0000-0002-7853-979X ; 0000-0002-5248-2756</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/acsami.4c05784$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.4c05784$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,778,782,2754,27059,27907,27908,56721,56771</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39018417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xue, Liangyao</creatorcontrib><creatorcontrib>Liu, Cheng</creatorcontrib><creatorcontrib>Ye, Jinyu</creatorcontrib><creatorcontrib>Zhang, Jiaqi</creatorcontrib><creatorcontrib>Kang, Lin</creatorcontrib><creatorcontrib>Zhang, Yexuan</creatorcontrib><creatorcontrib>Shi, Wenjuan</creatorcontrib><creatorcontrib>Guo, Wen</creatorcontrib><creatorcontrib>Huang, Xiaoxiong</creatorcontrib><creatorcontrib>Yang, Xiao</creatorcontrib><creatorcontrib>Zheng, Lirong</creatorcontrib><creatorcontrib>Li, Youyong</creatorcontrib><creatorcontrib>Zhang, Bo</creatorcontrib><title>Engineering Partially Oxidized Gold via Oleylamine Modifier as a High-Performance Anode Catalyst in a Direct Borohydride Fuel Cell</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>Direct borohydride fuel cell (DBFC) is considered a promising energy storage device due to its high theoretical cell voltage and energy density. For DBFC, an Au catalyst has been used as an anode for achieving an ideal eight-electron reaction. However, the poor activity of the Au catalyst for borohydride oxidation reaction (BOR) limits its large-scale application because of the weak BH4 – adsorption. We found, by density functional theory calculations, that the adsorption of BH4 – on the oxidized Au surface is stronger than that on the metallic Au surface, which can promote the process of the oxidation of BH4 – to *BH3 during the BOR. Here, we reported an oleylamine-modified partially oxidized Au supported on carbon powder (AuC-OLA) with a stable oxidation state. The obtained catalyst delivered a high peak power density of 143 mW/cm2, which is 2 times higher than that of a commercial 40% AuC (Pretemek). The in situ Fourier transform infrared studies showed that the activity of AuC-OLA for BOR is ascribed to the enhanced adsorption for BH4 – on the partially oxidized Au surface. These findings will promote the reasonable design of efficient Au electrocatalysts for DBFCs.</description><subject>adsorption</subject><subject>anodes</subject><subject>borohydrides</subject><subject>carbon</subject><subject>catalysts</subject><subject>density functional theory</subject><subject>electric potential difference</subject><subject>energy density</subject><subject>Energy, Environmental, and Catalysis Applications</subject><subject>Fourier transform infrared spectroscopy</subject><subject>fuel cells</subject><subject>oxidation</subject><issn>1944-8244</issn><issn>1944-8252</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkUtP3DAUhS1UVCjttsvKywopg19JnCUMT4lqWLTr6E58Mxg5NthJ1XTZX16jGdghVvcuvnPu4xDylbMFZ4KfQJdgsAvVsbLWao8c8kapQotSfHjtlTogn1J6YKySgpUfyYFsGNeK14fk34XfWI8Yrd_QO4ijBedmuvpjjf2Lhl4FZ-hvC3TlcHZ5lEf6IxjbW4wUEgV6bTf3xR3GPsQBfIf01AeDdAkjuDmN1PoMnduI3UjPQgz3s4k2A5cTOrpE5z6T_R5cwi-7ekR-XV78XF4Xt6urm-XpbQFC6bHQupKVhp6b2uhaNV3ZrNdac6xKw_KhlegV6xgAVqoXijcaRKWklOtaiprV8oh83_o-xvA0YRrbwaYuLwAew5RayUtZcy4b_T7KtJAsu6uMLrZoF0NKEfv2MdoB4txy1j5H1G4jancRZcG3nfe0HtC84i-ZZOB4C2Rh-xCm6PNX3nL7D8timog</recordid><startdate>20240731</startdate><enddate>20240731</enddate><creator>Xue, Liangyao</creator><creator>Liu, Cheng</creator><creator>Ye, Jinyu</creator><creator>Zhang, Jiaqi</creator><creator>Kang, Lin</creator><creator>Zhang, Yexuan</creator><creator>Shi, Wenjuan</creator><creator>Guo, Wen</creator><creator>Huang, Xiaoxiong</creator><creator>Yang, Xiao</creator><creator>Zheng, Lirong</creator><creator>Li, Youyong</creator><creator>Zhang, Bo</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><orcidid>https://orcid.org/0000-0002-7853-979X</orcidid><orcidid>https://orcid.org/0000-0002-5248-2756</orcidid></search><sort><creationdate>20240731</creationdate><title>Engineering Partially Oxidized Gold via Oleylamine Modifier as a High-Performance Anode Catalyst in a Direct Borohydride Fuel Cell</title><author>Xue, Liangyao ; Liu, Cheng ; Ye, Jinyu ; Zhang, Jiaqi ; Kang, Lin ; Zhang, Yexuan ; Shi, Wenjuan ; Guo, Wen ; Huang, Xiaoxiong ; Yang, Xiao ; Zheng, Lirong ; Li, Youyong ; Zhang, Bo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a248t-886368af1d7d8749c59bb881e65d094462f40c0aae64f24198a264333b7327073</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>adsorption</topic><topic>anodes</topic><topic>borohydrides</topic><topic>carbon</topic><topic>catalysts</topic><topic>density functional theory</topic><topic>electric potential difference</topic><topic>energy density</topic><topic>Energy, Environmental, and Catalysis Applications</topic><topic>Fourier transform infrared spectroscopy</topic><topic>fuel cells</topic><topic>oxidation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xue, Liangyao</creatorcontrib><creatorcontrib>Liu, Cheng</creatorcontrib><creatorcontrib>Ye, Jinyu</creatorcontrib><creatorcontrib>Zhang, Jiaqi</creatorcontrib><creatorcontrib>Kang, Lin</creatorcontrib><creatorcontrib>Zhang, Yexuan</creatorcontrib><creatorcontrib>Shi, Wenjuan</creatorcontrib><creatorcontrib>Guo, Wen</creatorcontrib><creatorcontrib>Huang, Xiaoxiong</creatorcontrib><creatorcontrib>Yang, Xiao</creatorcontrib><creatorcontrib>Zheng, Lirong</creatorcontrib><creatorcontrib>Li, Youyong</creatorcontrib><creatorcontrib>Zhang, Bo</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xue, Liangyao</au><au>Liu, Cheng</au><au>Ye, Jinyu</au><au>Zhang, Jiaqi</au><au>Kang, Lin</au><au>Zhang, Yexuan</au><au>Shi, Wenjuan</au><au>Guo, Wen</au><au>Huang, Xiaoxiong</au><au>Yang, Xiao</au><au>Zheng, Lirong</au><au>Li, Youyong</au><au>Zhang, Bo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Engineering Partially Oxidized Gold via Oleylamine Modifier as a High-Performance Anode Catalyst in a Direct Borohydride Fuel Cell</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. 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Here, we reported an oleylamine-modified partially oxidized Au supported on carbon powder (AuC-OLA) with a stable oxidation state. The obtained catalyst delivered a high peak power density of 143 mW/cm2, which is 2 times higher than that of a commercial 40% AuC (Pretemek). The in situ Fourier transform infrared studies showed that the activity of AuC-OLA for BOR is ascribed to the enhanced adsorption for BH4 – on the partially oxidized Au surface. These findings will promote the reasonable design of efficient Au electrocatalysts for DBFCs.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>39018417</pmid><doi>10.1021/acsami.4c05784</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-7853-979X</orcidid><orcidid>https://orcid.org/0000-0002-5248-2756</orcidid></addata></record> |
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subjects | adsorption anodes borohydrides carbon catalysts density functional theory electric potential difference energy density Energy, Environmental, and Catalysis Applications Fourier transform infrared spectroscopy fuel cells oxidation |
title | Engineering Partially Oxidized Gold via Oleylamine Modifier as a High-Performance Anode Catalyst in a Direct Borohydride Fuel Cell |
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