An organic-inorganic hybrid polyoxoniobate decorated by a Co()-amine complex for electrocatalytic urea splitting
The overall energy efficiency of electrochemical systems is significantly reduced by the conventional anodic oxygen evolution reaction (OER). It is feasible to improve energy efficiency by replacing the OER with the urea oxidation reaction (UOR), which has a lower thermodynamic potential. An organic...
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Veröffentlicht in: | Inorganic chemistry frontiers 2023-08, Vol.1 (16), p.4789-4796 |
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creator | Li, Da-Huan Shi, Nian Wang, Yong-Jiang Cai, Ping-Wei Sun, Yan-Qiong Zheng, Shou-Tian |
description | The overall energy efficiency of electrochemical systems is significantly reduced by the conventional anodic oxygen evolution reaction (OER). It is feasible to improve energy efficiency by replacing the OER with the urea oxidation reaction (UOR), which has a lower thermodynamic potential. An organic-inorganic hybrid polyoxoniobate decorated by a Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O (
Co
2
Nb
6
, en = ethylenediamine) with distinct physicochemical characteristics and well-defined single-crystal structure is reported. The structure of
Co
2
Nb
6
contains Lindqvist {[Co(en)(Nb
6
O
19
)]
2
}
10−
dimer and free [Co(en)
3
]
3+
complexes.
Co
2
Nb
6
exhibits remarkable catalytic activity for the UOR after being firmly attached to the surface of acetylene black by polyethyleneimine (PEI). To the best of our knowledge, this is the first instance of performing the electrocatalytic UOR based on Lindqvist polyoxoniobate clusters, which will pave the path for innovative concepts in the development of POM-based electrocatalysts.
A polyoxoniobate decorated by Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O exhibits remarkable catalytic activity for urea oxidation reaction after being firmly attached to the surface of acetylene black by polyethyleneimine. |
doi_str_mv | 10.1039/d3qi01066j |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2847231585</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2847231585</sourcerecordid><originalsourceid>FETCH-LOGICAL-c281t-423b7c12ad7ecb7c33e5ad258d9b7e8ed26dc76b011977c872fef2df0462a8d43</originalsourceid><addsrcrecordid>eNpNkM1LwzAYxoMoOOYu3oWAFxWq-Wib7jjm12Qggp5LmrydGV3SJSms_73VDfX0_g4_nof3QeickltK-PRO860hlOT5-giNGMlYQrOMH__jUzQJYU0IoTQlNCcj1M4sdn4lrVGJsQfCn33ljcata3q3c9a4SkbAGpTzA2hc9Vjiubu6TuTGWMDKbdoGdrh2HkMDKnqnZJRNH4ewzoPEoW1MjMauztBJLZsAk8Mdo4_Hh_f5c7J8fVrMZ8tEsYLGJGW8EooyqQWogTiHTGqWFXpaCShAs1wrkVfDJ1MhVCFYDTXTNUlzJgud8jG63Oe23m07CLFcu87bobJkRSoYp1mRDdbN3lLeheChLltvNtL3JSXl96jlPX9b_Iz6MsgXe9kH9ev9jc6_AF2BdSo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2847231585</pqid></control><display><type>article</type><title>An organic-inorganic hybrid polyoxoniobate decorated by a Co()-amine complex for electrocatalytic urea splitting</title><source>Royal Society Of Chemistry Journals 2008-</source><creator>Li, Da-Huan ; Shi, Nian ; Wang, Yong-Jiang ; Cai, Ping-Wei ; Sun, Yan-Qiong ; Zheng, Shou-Tian</creator><creatorcontrib>Li, Da-Huan ; Shi, Nian ; Wang, Yong-Jiang ; Cai, Ping-Wei ; Sun, Yan-Qiong ; Zheng, Shou-Tian</creatorcontrib><description>The overall energy efficiency of electrochemical systems is significantly reduced by the conventional anodic oxygen evolution reaction (OER). It is feasible to improve energy efficiency by replacing the OER with the urea oxidation reaction (UOR), which has a lower thermodynamic potential. An organic-inorganic hybrid polyoxoniobate decorated by a Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O (
Co
2
Nb
6
, en = ethylenediamine) with distinct physicochemical characteristics and well-defined single-crystal structure is reported. The structure of
Co
2
Nb
6
contains Lindqvist {[Co(en)(Nb
6
O
19
)]
2
}
10−
dimer and free [Co(en)
3
]
3+
complexes.
Co
2
Nb
6
exhibits remarkable catalytic activity for the UOR after being firmly attached to the surface of acetylene black by polyethyleneimine (PEI). To the best of our knowledge, this is the first instance of performing the electrocatalytic UOR based on Lindqvist polyoxoniobate clusters, which will pave the path for innovative concepts in the development of POM-based electrocatalysts.
A polyoxoniobate decorated by Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O exhibits remarkable catalytic activity for urea oxidation reaction after being firmly attached to the surface of acetylene black by polyethyleneimine.</description><identifier>ISSN: 2052-1553</identifier><identifier>ISSN: 2052-1545</identifier><identifier>EISSN: 2052-1553</identifier><identifier>DOI: 10.1039/d3qi01066j</identifier><language>eng</language><publisher>London: Royal Society of Chemistry</publisher><subject>Acetylene ; Catalytic activity ; Crystal structure ; Electrocatalysts ; Ethylenediamine ; Inorganic chemistry ; Molecular structure ; Oxidation ; Oxygen evolution reactions ; Polyethyleneimine ; Single crystals ; Ureas</subject><ispartof>Inorganic chemistry frontiers, 2023-08, Vol.1 (16), p.4789-4796</ispartof><rights>Copyright Royal Society of Chemistry 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c281t-423b7c12ad7ecb7c33e5ad258d9b7e8ed26dc76b011977c872fef2df0462a8d43</citedby><cites>FETCH-LOGICAL-c281t-423b7c12ad7ecb7c33e5ad258d9b7e8ed26dc76b011977c872fef2df0462a8d43</cites><orcidid>0000-0001-9480-9721 ; 0000-0001-7958-1781 ; 0000-0002-3365-9747</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Li, Da-Huan</creatorcontrib><creatorcontrib>Shi, Nian</creatorcontrib><creatorcontrib>Wang, Yong-Jiang</creatorcontrib><creatorcontrib>Cai, Ping-Wei</creatorcontrib><creatorcontrib>Sun, Yan-Qiong</creatorcontrib><creatorcontrib>Zheng, Shou-Tian</creatorcontrib><title>An organic-inorganic hybrid polyoxoniobate decorated by a Co()-amine complex for electrocatalytic urea splitting</title><title>Inorganic chemistry frontiers</title><description>The overall energy efficiency of electrochemical systems is significantly reduced by the conventional anodic oxygen evolution reaction (OER). It is feasible to improve energy efficiency by replacing the OER with the urea oxidation reaction (UOR), which has a lower thermodynamic potential. An organic-inorganic hybrid polyoxoniobate decorated by a Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O (
Co
2
Nb
6
, en = ethylenediamine) with distinct physicochemical characteristics and well-defined single-crystal structure is reported. The structure of
Co
2
Nb
6
contains Lindqvist {[Co(en)(Nb
6
O
19
)]
2
}
10−
dimer and free [Co(en)
3
]
3+
complexes.
Co
2
Nb
6
exhibits remarkable catalytic activity for the UOR after being firmly attached to the surface of acetylene black by polyethyleneimine (PEI). To the best of our knowledge, this is the first instance of performing the electrocatalytic UOR based on Lindqvist polyoxoniobate clusters, which will pave the path for innovative concepts in the development of POM-based electrocatalysts.
A polyoxoniobate decorated by Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O exhibits remarkable catalytic activity for urea oxidation reaction after being firmly attached to the surface of acetylene black by polyethyleneimine.</description><subject>Acetylene</subject><subject>Catalytic activity</subject><subject>Crystal structure</subject><subject>Electrocatalysts</subject><subject>Ethylenediamine</subject><subject>Inorganic chemistry</subject><subject>Molecular structure</subject><subject>Oxidation</subject><subject>Oxygen evolution reactions</subject><subject>Polyethyleneimine</subject><subject>Single crystals</subject><subject>Ureas</subject><issn>2052-1553</issn><issn>2052-1545</issn><issn>2052-1553</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNpNkM1LwzAYxoMoOOYu3oWAFxWq-Wib7jjm12Qggp5LmrydGV3SJSms_73VDfX0_g4_nof3QeickltK-PRO860hlOT5-giNGMlYQrOMH__jUzQJYU0IoTQlNCcj1M4sdn4lrVGJsQfCn33ljcata3q3c9a4SkbAGpTzA2hc9Vjiubu6TuTGWMDKbdoGdrh2HkMDKnqnZJRNH4ewzoPEoW1MjMauztBJLZsAk8Mdo4_Hh_f5c7J8fVrMZ8tEsYLGJGW8EooyqQWogTiHTGqWFXpaCShAs1wrkVfDJ1MhVCFYDTXTNUlzJgud8jG63Oe23m07CLFcu87bobJkRSoYp1mRDdbN3lLeheChLltvNtL3JSXl96jlPX9b_Iz6MsgXe9kH9ev9jc6_AF2BdSo</recordid><startdate>20230808</startdate><enddate>20230808</enddate><creator>Li, Da-Huan</creator><creator>Shi, Nian</creator><creator>Wang, Yong-Jiang</creator><creator>Cai, Ping-Wei</creator><creator>Sun, Yan-Qiong</creator><creator>Zheng, Shou-Tian</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0001-9480-9721</orcidid><orcidid>https://orcid.org/0000-0001-7958-1781</orcidid><orcidid>https://orcid.org/0000-0002-3365-9747</orcidid></search><sort><creationdate>20230808</creationdate><title>An organic-inorganic hybrid polyoxoniobate decorated by a Co()-amine complex for electrocatalytic urea splitting</title><author>Li, Da-Huan ; Shi, Nian ; Wang, Yong-Jiang ; Cai, Ping-Wei ; Sun, Yan-Qiong ; Zheng, Shou-Tian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c281t-423b7c12ad7ecb7c33e5ad258d9b7e8ed26dc76b011977c872fef2df0462a8d43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acetylene</topic><topic>Catalytic activity</topic><topic>Crystal structure</topic><topic>Electrocatalysts</topic><topic>Ethylenediamine</topic><topic>Inorganic chemistry</topic><topic>Molecular structure</topic><topic>Oxidation</topic><topic>Oxygen evolution reactions</topic><topic>Polyethyleneimine</topic><topic>Single crystals</topic><topic>Ureas</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Da-Huan</creatorcontrib><creatorcontrib>Shi, Nian</creatorcontrib><creatorcontrib>Wang, Yong-Jiang</creatorcontrib><creatorcontrib>Cai, Ping-Wei</creatorcontrib><creatorcontrib>Sun, Yan-Qiong</creatorcontrib><creatorcontrib>Zheng, Shou-Tian</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Inorganic chemistry frontiers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Da-Huan</au><au>Shi, Nian</au><au>Wang, Yong-Jiang</au><au>Cai, Ping-Wei</au><au>Sun, Yan-Qiong</au><au>Zheng, Shou-Tian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An organic-inorganic hybrid polyoxoniobate decorated by a Co()-amine complex for electrocatalytic urea splitting</atitle><jtitle>Inorganic chemistry frontiers</jtitle><date>2023-08-08</date><risdate>2023</risdate><volume>1</volume><issue>16</issue><spage>4789</spage><epage>4796</epage><pages>4789-4796</pages><issn>2052-1553</issn><issn>2052-1545</issn><eissn>2052-1553</eissn><abstract>The overall energy efficiency of electrochemical systems is significantly reduced by the conventional anodic oxygen evolution reaction (OER). It is feasible to improve energy efficiency by replacing the OER with the urea oxidation reaction (UOR), which has a lower thermodynamic potential. An organic-inorganic hybrid polyoxoniobate decorated by a Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O (
Co
2
Nb
6
, en = ethylenediamine) with distinct physicochemical characteristics and well-defined single-crystal structure is reported. The structure of
Co
2
Nb
6
contains Lindqvist {[Co(en)(Nb
6
O
19
)]
2
}
10−
dimer and free [Co(en)
3
]
3+
complexes.
Co
2
Nb
6
exhibits remarkable catalytic activity for the UOR after being firmly attached to the surface of acetylene black by polyethyleneimine (PEI). To the best of our knowledge, this is the first instance of performing the electrocatalytic UOR based on Lindqvist polyoxoniobate clusters, which will pave the path for innovative concepts in the development of POM-based electrocatalysts.
A polyoxoniobate decorated by Co(
iii
)-amine complex, Na
4
(H
2
O)
15
[Co(en)
3
]
2
{[Co(en)(Nb
6
O
19
)]
2
}·34H
2
O exhibits remarkable catalytic activity for urea oxidation reaction after being firmly attached to the surface of acetylene black by polyethyleneimine.</abstract><cop>London</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d3qi01066j</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-9480-9721</orcidid><orcidid>https://orcid.org/0000-0001-7958-1781</orcidid><orcidid>https://orcid.org/0000-0002-3365-9747</orcidid></addata></record> |
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issn | 2052-1553 2052-1545 2052-1553 |
language | eng |
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source | Royal Society Of Chemistry Journals 2008- |
subjects | Acetylene Catalytic activity Crystal structure Electrocatalysts Ethylenediamine Inorganic chemistry Molecular structure Oxidation Oxygen evolution reactions Polyethyleneimine Single crystals Ureas |
title | An organic-inorganic hybrid polyoxoniobate decorated by a Co()-amine complex for electrocatalytic urea splitting |
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