对 FeNi-HMT 框架进行配位调节,从而衍生出有效的水氧化混合催化剂。

IF 7.5 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY ChemSusChem Pub Date : 2024-10-27 DOI:10.1002/cssc.202401580
Yunmeng Wang, Luhong Fu, Jiawei Wu, Fulin Yang, Ligang Feng
{"title":"对 FeNi-HMT 框架进行配位调节,从而衍生出有效的水氧化混合催化剂。","authors":"Yunmeng Wang, Luhong Fu, Jiawei Wu, Fulin Yang, Ligang Feng","doi":"10.1002/cssc.202401580","DOIUrl":null,"url":null,"abstract":"<p><p>FeNi-based hybrid materials are promising oxygen evolution reaction (OER) catalysts for water electrolysis in hydrogen generation. In this work, the coordination tuning of FeNi-HMT frameworks was achieved by simply changing the Fe/Ni ratios using hexamethylenetetramine (HMT) as an organic ligand, and the derived hybrid FeNi catalysts with varied compositions were probed for OER. Incorporating varying amounts of Fe<sup>3+</sup> by adjusting the Ni/Fe ratio results in different metal-organic framework (MOF) structures, and higher Fe feed leads to the formation of amorphous structures due to the coordination structure destruction from the weaker coordination capacity of Fe<sup>3+</sup> compared to Ni<sup>2+</sup> combining with the tertiary amine ligand. Among them, the FeNi-HMT (with the Fe/Ni molar ratio of 1/1) derived catalyst, consisting of Fe<sub>0.36</sub>Ni<sub>0.64</sub> alloy/Ni<sub>0.4</sub>Fe<sub>2.6</sub>O<sub>4</sub> spinel oxide heterostructures supported by graphitized carbon matrix, exhibits the highest OER performance. The unique structure facilitates significant electron transfer at the alloy/spinel interface due to the large work function difference between each phase. This strong electronic effect downshifts the d-band center of the catalyst and optimizes the binding energies to the crucial oxygenated intermediates, thereby promoting the OER kinetics. This work highlights the importance of the coordination tuning of FeNi-HMT frameworks for highly efficient catalyst development.</p>","PeriodicalId":149,"journal":{"name":"ChemSusChem","volume":" ","pages":"e202401580"},"PeriodicalIF":7.5000,"publicationDate":"2024-10-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Coordination Tuning of FeNi-HMT Frameworks Derived Effective Hybrid Catalysts for Water Oxidation.\",\"authors\":\"Yunmeng Wang, Luhong Fu, Jiawei Wu, Fulin Yang, Ligang Feng\",\"doi\":\"10.1002/cssc.202401580\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>FeNi-based hybrid materials are promising oxygen evolution reaction (OER) catalysts for water electrolysis in hydrogen generation. In this work, the coordination tuning of FeNi-HMT frameworks was achieved by simply changing the Fe/Ni ratios using hexamethylenetetramine (HMT) as an organic ligand, and the derived hybrid FeNi catalysts with varied compositions were probed for OER. Incorporating varying amounts of Fe<sup>3+</sup> by adjusting the Ni/Fe ratio results in different metal-organic framework (MOF) structures, and higher Fe feed leads to the formation of amorphous structures due to the coordination structure destruction from the weaker coordination capacity of Fe<sup>3+</sup> compared to Ni<sup>2+</sup> combining with the tertiary amine ligand. Among them, the FeNi-HMT (with the Fe/Ni molar ratio of 1/1) derived catalyst, consisting of Fe<sub>0.36</sub>Ni<sub>0.64</sub> alloy/Ni<sub>0.4</sub>Fe<sub>2.6</sub>O<sub>4</sub> spinel oxide heterostructures supported by graphitized carbon matrix, exhibits the highest OER performance. The unique structure facilitates significant electron transfer at the alloy/spinel interface due to the large work function difference between each phase. This strong electronic effect downshifts the d-band center of the catalyst and optimizes the binding energies to the crucial oxygenated intermediates, thereby promoting the OER kinetics. This work highlights the importance of the coordination tuning of FeNi-HMT frameworks for highly efficient catalyst development.</p>\",\"PeriodicalId\":149,\"journal\":{\"name\":\"ChemSusChem\",\"volume\":\" \",\"pages\":\"e202401580\"},\"PeriodicalIF\":7.5000,\"publicationDate\":\"2024-10-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemSusChem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/cssc.202401580\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemSusChem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/cssc.202401580","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

铁镍基杂化材料是一种很有前途的氧进化反应(OER)催化剂,可用于电解水制氢。在这项工作中,使用六亚甲基四胺(HMT)作为有机配体,通过简单地改变铁/镍比实现了铁镍-HMT 框架的配位调节,并对不同组成的铁镍杂化催化剂进行了 OER 试验。通过调整镍/铁比例加入不同量的 Fe3+ 会产生不同的金属有机框架(MOF)结构,与 Ni2+ 相比,Fe3+ 的配位能力较弱,与叔胺配体结合会导致配位结构破坏,因此加入更多的 Fe 会形成无定形结构。其中,FeNi-HMT(Fe/Ni 摩尔比为 1/1)衍生催化剂由石墨化碳基体支撑的 Fe0.36Ni0.64 合金/Ni0.4Fe2.6O4 尖晶石氧化物异质结构组成,具有最高的 OER 性能。由于各相之间存在较大的功函数差,这种独特的结构有利于在合金/尖晶石界面上实现显著的电子转移。这种强烈的电子效应使催化剂的 d 波段中心下移,优化了与关键含氧中间体的结合能,从而促进了 OER 动力学。这项工作强调了铁镍-HMT 框架配位调整对于高效催化剂开发的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Coordination Tuning of FeNi-HMT Frameworks Derived Effective Hybrid Catalysts for Water Oxidation.

FeNi-based hybrid materials are promising oxygen evolution reaction (OER) catalysts for water electrolysis in hydrogen generation. In this work, the coordination tuning of FeNi-HMT frameworks was achieved by simply changing the Fe/Ni ratios using hexamethylenetetramine (HMT) as an organic ligand, and the derived hybrid FeNi catalysts with varied compositions were probed for OER. Incorporating varying amounts of Fe3+ by adjusting the Ni/Fe ratio results in different metal-organic framework (MOF) structures, and higher Fe feed leads to the formation of amorphous structures due to the coordination structure destruction from the weaker coordination capacity of Fe3+ compared to Ni2+ combining with the tertiary amine ligand. Among them, the FeNi-HMT (with the Fe/Ni molar ratio of 1/1) derived catalyst, consisting of Fe0.36Ni0.64 alloy/Ni0.4Fe2.6O4 spinel oxide heterostructures supported by graphitized carbon matrix, exhibits the highest OER performance. The unique structure facilitates significant electron transfer at the alloy/spinel interface due to the large work function difference between each phase. This strong electronic effect downshifts the d-band center of the catalyst and optimizes the binding energies to the crucial oxygenated intermediates, thereby promoting the OER kinetics. This work highlights the importance of the coordination tuning of FeNi-HMT frameworks for highly efficient catalyst development.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
期刊最新文献
Covalent Organic Frameworks with Regulated Water Adsorption Sites for Efficient Cooling of Electronics. A TEMPO-N3 Complex Enables the Electrochemical C-H Azidation of N-Heterocycles through the Cleavage of Alkoxyamines. PEI-templated ZIF-8 nanoparticles impart the NF membrane with high Mg2+/Li+ separation performance. Green Electrochemical Point-of-Care Devices: Transient Materials and Sustainable Fabrication Methods. Metal-free N, P-Codoped Carbon for Syngas Production with Tunable Composition via CO2 Electrolysis: Addressing the Competition Between CO2 Reduction and H2 Evolution.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1