Amorphous NiFe-layered double hydroxides nanosheets for oxygen evolution reaction

•Amorphous nife-layered double hydroxides nanosheets is controllably prepared.•Amorphous NiFe-LDH has higher catalytic activity than crystalline NiFe-LDH in OER.•The overpotential of amorphous NiFe-LDH for OER is 241 mV at 10 mA cm−2.•Amorphous NiFe-LDH has higher electrocatalytic activity than comm...

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Veröffentlicht in:Electrochimica acta 2020-10, Vol.356, p.136827, Article 136827
Hauptverfasser: Liu, Jiang, Zhou, Jia, Liu, Shuang, Chen, Gui, Wu, Wei, li, Ying, Jin, Pujun, Xu, Chunli
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container_start_page 136827
container_title Electrochimica acta
container_volume 356
creator Liu, Jiang
Zhou, Jia
Liu, Shuang
Chen, Gui
Wu, Wei
li, Ying
Jin, Pujun
Xu, Chunli
description •Amorphous nife-layered double hydroxides nanosheets is controllably prepared.•Amorphous NiFe-LDH has higher catalytic activity than crystalline NiFe-LDH in OER.•The overpotential of amorphous NiFe-LDH for OER is 241 mV at 10 mA cm−2.•Amorphous NiFe-LDH has higher electrocatalytic activity than commercial RuO2. The exposed active sites of NiFe layered double hydroxide (NiFe-LDH) for oxygen evolution reaction (OER) are limited by the compact packing of its two-dimensional lamella. In this work, amorphous NiFe-LDH (A-NiFe-LDH) with abundant active sites are synthesized by using Ni(II) nitrilotriacetate complex anion ([NTANi]−) as morphological control agent, which can expose more active sites of NiFe-LDH by controlling crystalline phase and grain size of NiFe-LDH. Structural characterization demonstrates that [NTANi]− is adsorbed on the surface of A-NiFe-LDH and confirms A-NiFe-LDH is amorphous. The electrocatalytic activity of A-NiFe-LDH for OER is much higher than that of both RuO2 and pristine NiFe-LDH. A-NiFe-LDH has low OER overpotential of 241 mV at 10 mV cm−2 and a small Tafel slope of 55 mV dec−1. The high electrocatalytic activity of A-NiFe-LDH could be attributed to its amorphous structure. [Display omitted]
doi_str_mv 10.1016/j.electacta.2020.136827
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The exposed active sites of NiFe layered double hydroxide (NiFe-LDH) for oxygen evolution reaction (OER) are limited by the compact packing of its two-dimensional lamella. In this work, amorphous NiFe-LDH (A-NiFe-LDH) with abundant active sites are synthesized by using Ni(II) nitrilotriacetate complex anion ([NTANi]−) as morphological control agent, which can expose more active sites of NiFe-LDH by controlling crystalline phase and grain size of NiFe-LDH. Structural characterization demonstrates that [NTANi]− is adsorbed on the surface of A-NiFe-LDH and confirms A-NiFe-LDH is amorphous. The electrocatalytic activity of A-NiFe-LDH for OER is much higher than that of both RuO2 and pristine NiFe-LDH. A-NiFe-LDH has low OER overpotential of 241 mV at 10 mV cm−2 and a small Tafel slope of 55 mV dec−1. The high electrocatalytic activity of A-NiFe-LDH could be attributed to its amorphous structure. [Display omitted]</description><identifier>ISSN: 0013-4686</identifier><identifier>EISSN: 1873-3859</identifier><identifier>DOI: 10.1016/j.electacta.2020.136827</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Amorphous nanosheets ; Amorphous structure ; Grain size ; Hydroxides ; Intermetallic compounds ; Iron compounds ; Lamella ; Layered double hydroxide ; Nanosheets ; Ni(ii) nitrilotriacetate complex anion ; Nickel compounds ; Oxygen evolution reaction ; Oxygen evolution reactions ; Structural analysis</subject><ispartof>Electrochimica acta, 2020-10, Vol.356, p.136827, Article 136827</ispartof><rights>2020</rights><rights>Copyright Elsevier BV Oct 1, 2020</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c343t-9448d083f0456fec31fc4c003d319209838da66bb6bf7fa782ea893436c48c943</citedby><cites>FETCH-LOGICAL-c343t-9448d083f0456fec31fc4c003d319209838da66bb6bf7fa782ea893436c48c943</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.electacta.2020.136827$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Liu, Jiang</creatorcontrib><creatorcontrib>Zhou, Jia</creatorcontrib><creatorcontrib>Liu, Shuang</creatorcontrib><creatorcontrib>Chen, Gui</creatorcontrib><creatorcontrib>Wu, Wei</creatorcontrib><creatorcontrib>li, Ying</creatorcontrib><creatorcontrib>Jin, Pujun</creatorcontrib><creatorcontrib>Xu, Chunli</creatorcontrib><title>Amorphous NiFe-layered double hydroxides nanosheets for oxygen evolution reaction</title><title>Electrochimica acta</title><description>•Amorphous nife-layered double hydroxides nanosheets is controllably prepared.•Amorphous NiFe-LDH has higher catalytic activity than crystalline NiFe-LDH in OER.•The overpotential of amorphous NiFe-LDH for OER is 241 mV at 10 mA cm−2.•Amorphous NiFe-LDH has higher electrocatalytic activity than commercial RuO2. The exposed active sites of NiFe layered double hydroxide (NiFe-LDH) for oxygen evolution reaction (OER) are limited by the compact packing of its two-dimensional lamella. In this work, amorphous NiFe-LDH (A-NiFe-LDH) with abundant active sites are synthesized by using Ni(II) nitrilotriacetate complex anion ([NTANi]−) as morphological control agent, which can expose more active sites of NiFe-LDH by controlling crystalline phase and grain size of NiFe-LDH. Structural characterization demonstrates that [NTANi]− is adsorbed on the surface of A-NiFe-LDH and confirms A-NiFe-LDH is amorphous. The electrocatalytic activity of A-NiFe-LDH for OER is much higher than that of both RuO2 and pristine NiFe-LDH. A-NiFe-LDH has low OER overpotential of 241 mV at 10 mV cm−2 and a small Tafel slope of 55 mV dec−1. The high electrocatalytic activity of A-NiFe-LDH could be attributed to its amorphous structure. 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The exposed active sites of NiFe layered double hydroxide (NiFe-LDH) for oxygen evolution reaction (OER) are limited by the compact packing of its two-dimensional lamella. In this work, amorphous NiFe-LDH (A-NiFe-LDH) with abundant active sites are synthesized by using Ni(II) nitrilotriacetate complex anion ([NTANi]−) as morphological control agent, which can expose more active sites of NiFe-LDH by controlling crystalline phase and grain size of NiFe-LDH. Structural characterization demonstrates that [NTANi]− is adsorbed on the surface of A-NiFe-LDH and confirms A-NiFe-LDH is amorphous. The electrocatalytic activity of A-NiFe-LDH for OER is much higher than that of both RuO2 and pristine NiFe-LDH. A-NiFe-LDH has low OER overpotential of 241 mV at 10 mV cm−2 and a small Tafel slope of 55 mV dec−1. The high electrocatalytic activity of A-NiFe-LDH could be attributed to its amorphous structure. 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subjects Amorphous nanosheets
Amorphous structure
Grain size
Hydroxides
Intermetallic compounds
Iron compounds
Lamella
Layered double hydroxide
Nanosheets
Ni(ii) nitrilotriacetate complex anion
Nickel compounds
Oxygen evolution reaction
Oxygen evolution reactions
Structural analysis
title Amorphous NiFe-layered double hydroxides nanosheets for oxygen evolution reaction
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