Boosting the oxygen evolution catalytic performance of perovskites via optimizing calcination temperature
We report a facile and universal strategy with simultaneous modulation of intrinsic activity and active site numbers to optimize the catalytic performance of perovskites via controlling calcination temperature. As a proof-of-concept, the optimized SCF-800 perovskite (SrCo 0.5 Fe 0.5 O 3−δ prepared w...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2020-04, Vol.8 (14), p.6480-6486 |
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container_title | Journal of materials chemistry. A, Materials for energy and sustainability |
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creator | Lin, Qian Zhu, Yinlong Hu, Zhiwei Yin, Yichun Lin, Hong-Ji Chen, Chien-Te Zhang, Xiwang Shao, Zongping Wang, Huanting |
description | We report a facile and universal strategy with simultaneous modulation of intrinsic activity and active site numbers to optimize the catalytic performance of perovskites
via
controlling calcination temperature. As a proof-of-concept, the optimized SCF-800 perovskite (SrCo
0.5
Fe
0.5
O
3−δ
prepared with a calcination temperature of 800 °C) shows prominent OER activity (
e.g.
, 327 mV at 10 mA cm
−2
on a glassy carbon electrode in 0.1 M KOH), outperforming the benchmark noble-metal RuO
2
and ranking the highest among perovskite-based catalysts reported to date. Experimental results reveal that the reduced particle size (increased surface area) due to a lower calcination temperature provides more active sites, and that the favorable electronic structure with high covalency of metal–oxygen bonds, as demonstrated by advanced soft X-ray absorption spectroscopy (sXAS), contributes to the intrinsic activity enhancement. This work provides a new and facile way for improving the catalytic performance
via
only regulating preparation conditions. |
doi_str_mv | 10.1039/C9TA13972A |
format | Article |
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via
controlling calcination temperature. As a proof-of-concept, the optimized SCF-800 perovskite (SrCo
0.5
Fe
0.5
O
3−δ
prepared with a calcination temperature of 800 °C) shows prominent OER activity (
e.g.
, 327 mV at 10 mA cm
−2
on a glassy carbon electrode in 0.1 M KOH), outperforming the benchmark noble-metal RuO
2
and ranking the highest among perovskite-based catalysts reported to date. Experimental results reveal that the reduced particle size (increased surface area) due to a lower calcination temperature provides more active sites, and that the favorable electronic structure with high covalency of metal–oxygen bonds, as demonstrated by advanced soft X-ray absorption spectroscopy (sXAS), contributes to the intrinsic activity enhancement. This work provides a new and facile way for improving the catalytic performance
via
only regulating preparation conditions.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/C9TA13972A</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Absorption spectroscopy ; Catalysts ; Chemical evolution ; Electronic structure ; Glassy carbon ; Noble metals ; Optimization ; Oxygen ; Perovskites ; Roasting ; Soft x rays ; Temperature ; X ray absorption ; X-ray absorption spectroscopy</subject><ispartof>Journal of materials chemistry. A, Materials for energy and sustainability, 2020-04, Vol.8 (14), p.6480-6486</ispartof><rights>Copyright Royal Society of Chemistry 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c296t-59c03f8a4ca1941b47099b3e198fb9753a56d09bb96824e2c29ffbfa7136dec3</citedby><cites>FETCH-LOGICAL-c296t-59c03f8a4ca1941b47099b3e198fb9753a56d09bb96824e2c29ffbfa7136dec3</cites><orcidid>0000-0002-4319-527X ; 0000-0002-4538-4218 ; 0000-0002-9207-2452 ; 0000-0002-9887-5555</orcidid></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></links><search><creatorcontrib>Lin, Qian</creatorcontrib><creatorcontrib>Zhu, Yinlong</creatorcontrib><creatorcontrib>Hu, Zhiwei</creatorcontrib><creatorcontrib>Yin, Yichun</creatorcontrib><creatorcontrib>Lin, Hong-Ji</creatorcontrib><creatorcontrib>Chen, Chien-Te</creatorcontrib><creatorcontrib>Zhang, Xiwang</creatorcontrib><creatorcontrib>Shao, Zongping</creatorcontrib><creatorcontrib>Wang, Huanting</creatorcontrib><title>Boosting the oxygen evolution catalytic performance of perovskites via optimizing calcination temperature</title><title>Journal of materials chemistry. A, Materials for energy and sustainability</title><description>We report a facile and universal strategy with simultaneous modulation of intrinsic activity and active site numbers to optimize the catalytic performance of perovskites
via
controlling calcination temperature. As a proof-of-concept, the optimized SCF-800 perovskite (SrCo
0.5
Fe
0.5
O
3−δ
prepared with a calcination temperature of 800 °C) shows prominent OER activity (
e.g.
, 327 mV at 10 mA cm
−2
on a glassy carbon electrode in 0.1 M KOH), outperforming the benchmark noble-metal RuO
2
and ranking the highest among perovskite-based catalysts reported to date. Experimental results reveal that the reduced particle size (increased surface area) due to a lower calcination temperature provides more active sites, and that the favorable electronic structure with high covalency of metal–oxygen bonds, as demonstrated by advanced soft X-ray absorption spectroscopy (sXAS), contributes to the intrinsic activity enhancement. This work provides a new and facile way for improving the catalytic performance
via
only regulating preparation conditions.</description><subject>Absorption spectroscopy</subject><subject>Catalysts</subject><subject>Chemical evolution</subject><subject>Electronic structure</subject><subject>Glassy carbon</subject><subject>Noble metals</subject><subject>Optimization</subject><subject>Oxygen</subject><subject>Perovskites</subject><subject>Roasting</subject><subject>Soft x rays</subject><subject>Temperature</subject><subject>X ray absorption</subject><subject>X-ray absorption spectroscopy</subject><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNpFkFFLwzAUhYMoOOZe_AUB34Rq0rRp7mMdOoWBL3svaZbMzLapSTqcv97Wid6Xey985xw4CF1TckcJg_slbErKoEjLMzRLSU6SIgN-_ncLcYkWIezJOIIQDjBD9sG5EG23w_FNY_d53OkO64Nrhmhdh5WMsjlGq3CvvXG-lZ0aMTO97hDebdQBH6zEro-2tV-TkZKNsp380UfdjqSMg9dX6MLIJujF756jzdPjZvmcrF9XL8tynagUeExyUIQZITMlKWS0zgoCUDNNQZgaipzJnG8J1DVwkWY6HVXG1EYWlPGtVmyObk62vXcfgw6x2rvBd2NilTLBgQlGxEjdnijlXQhem6r3tpX-WFFSTWVW_2Wyb0r1aUI</recordid><startdate>20200414</startdate><enddate>20200414</enddate><creator>Lin, Qian</creator><creator>Zhu, Yinlong</creator><creator>Hu, Zhiwei</creator><creator>Yin, Yichun</creator><creator>Lin, Hong-Ji</creator><creator>Chen, Chien-Te</creator><creator>Zhang, Xiwang</creator><creator>Shao, Zongping</creator><creator>Wang, Huanting</creator><general>Royal Society of Chemistry</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><scope>L7M</scope><scope>SOI</scope><orcidid>https://orcid.org/0000-0002-4319-527X</orcidid><orcidid>https://orcid.org/0000-0002-4538-4218</orcidid><orcidid>https://orcid.org/0000-0002-9207-2452</orcidid><orcidid>https://orcid.org/0000-0002-9887-5555</orcidid></search><sort><creationdate>20200414</creationdate><title>Boosting the oxygen evolution catalytic performance of perovskites via optimizing calcination temperature</title><author>Lin, Qian ; Zhu, Yinlong ; Hu, Zhiwei ; Yin, Yichun ; Lin, Hong-Ji ; Chen, Chien-Te ; Zhang, Xiwang ; Shao, Zongping ; Wang, Huanting</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c296t-59c03f8a4ca1941b47099b3e198fb9753a56d09bb96824e2c29ffbfa7136dec3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Absorption spectroscopy</topic><topic>Catalysts</topic><topic>Chemical evolution</topic><topic>Electronic structure</topic><topic>Glassy carbon</topic><topic>Noble metals</topic><topic>Optimization</topic><topic>Oxygen</topic><topic>Perovskites</topic><topic>Roasting</topic><topic>Soft x rays</topic><topic>Temperature</topic><topic>X ray absorption</topic><topic>X-ray absorption spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lin, Qian</creatorcontrib><creatorcontrib>Zhu, Yinlong</creatorcontrib><creatorcontrib>Hu, Zhiwei</creatorcontrib><creatorcontrib>Yin, Yichun</creatorcontrib><creatorcontrib>Lin, Hong-Ji</creatorcontrib><creatorcontrib>Chen, Chien-Te</creatorcontrib><creatorcontrib>Zhang, Xiwang</creatorcontrib><creatorcontrib>Shao, Zongping</creatorcontrib><creatorcontrib>Wang, Huanting</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lin, Qian</au><au>Zhu, Yinlong</au><au>Hu, Zhiwei</au><au>Yin, Yichun</au><au>Lin, Hong-Ji</au><au>Chen, Chien-Te</au><au>Zhang, Xiwang</au><au>Shao, Zongping</au><au>Wang, Huanting</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Boosting the oxygen evolution catalytic performance of perovskites via optimizing calcination temperature</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2020-04-14</date><risdate>2020</risdate><volume>8</volume><issue>14</issue><spage>6480</spage><epage>6486</epage><pages>6480-6486</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>We report a facile and universal strategy with simultaneous modulation of intrinsic activity and active site numbers to optimize the catalytic performance of perovskites
via
controlling calcination temperature. As a proof-of-concept, the optimized SCF-800 perovskite (SrCo
0.5
Fe
0.5
O
3−δ
prepared with a calcination temperature of 800 °C) shows prominent OER activity (
e.g.
, 327 mV at 10 mA cm
−2
on a glassy carbon electrode in 0.1 M KOH), outperforming the benchmark noble-metal RuO
2
and ranking the highest among perovskite-based catalysts reported to date. Experimental results reveal that the reduced particle size (increased surface area) due to a lower calcination temperature provides more active sites, and that the favorable electronic structure with high covalency of metal–oxygen bonds, as demonstrated by advanced soft X-ray absorption spectroscopy (sXAS), contributes to the intrinsic activity enhancement. This work provides a new and facile way for improving the catalytic performance
via
only regulating preparation conditions.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/C9TA13972A</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-4319-527X</orcidid><orcidid>https://orcid.org/0000-0002-4538-4218</orcidid><orcidid>https://orcid.org/0000-0002-9207-2452</orcidid><orcidid>https://orcid.org/0000-0002-9887-5555</orcidid></addata></record> |
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language | eng |
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source | Royal Society Of Chemistry Journals |
subjects | Absorption spectroscopy Catalysts Chemical evolution Electronic structure Glassy carbon Noble metals Optimization Oxygen Perovskites Roasting Soft x rays Temperature X ray absorption X-ray absorption spectroscopy |
title | Boosting the oxygen evolution catalytic performance of perovskites via optimizing calcination temperature |
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