揭示催化活性 MXene 支持物在提高阴离子交换膜水电解槽钴氧进化反应催化剂的性能和耐用性方面的作用

IF 20.2 1区 化学 Q1 CHEMISTRY, PHYSICAL Applied Catalysis B: Environmental Pub Date : 2024-01-13 DOI:10.1016/j.apcatb.2024.123731
Young Sang Park , Ari Chae , Gwan Hyun Choi , Swetarekha Ram , Seung-Cheol Lee , Satadeep Bhattacharjee , Jiyoon Jung , Hyo Sang Jeon , Cheol-Hee Ahn , Seung Sang Hwang , Dong-Yeun Koh , Insik In , Taegon Oh , Seon Joon Kim , Chong Min Koo , Albert S. Lee
{"title":"揭示催化活性 MXene 支持物在提高阴离子交换膜水电解槽钴氧进化反应催化剂的性能和耐用性方面的作用","authors":"Young Sang Park ,&nbsp;Ari Chae ,&nbsp;Gwan Hyun Choi ,&nbsp;Swetarekha Ram ,&nbsp;Seung-Cheol Lee ,&nbsp;Satadeep Bhattacharjee ,&nbsp;Jiyoon Jung ,&nbsp;Hyo Sang Jeon ,&nbsp;Cheol-Hee Ahn ,&nbsp;Seung Sang Hwang ,&nbsp;Dong-Yeun Koh ,&nbsp;Insik In ,&nbsp;Taegon Oh ,&nbsp;Seon Joon Kim ,&nbsp;Chong Min Koo ,&nbsp;Albert S. Lee","doi":"10.1016/j.apcatb.2024.123731","DOIUrl":null,"url":null,"abstract":"<div><p><span>The role of 2D transition metal carbides, also known as MXenes, as active catalyst supports in Co-based oxygen evolution reaction (OER) catalysts was elucidated through a combination of experimental and computation electrochemistry. Through facile seeding of commericial Co nanoparticles on three different MXene supports (Ti</span><sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub>, Mo<sub>2</sub>Ti<sub>2</sub>C<sub>3</sub>T<sub><em>x</em></sub>, Mo<sub>2</sub>CT<sub><em>x</em></sub>), Co@MXene catalysts were prepared and their electrochemical properties examined for alkaline OER electrocatalysts. The OER activity enhancement of Co was significantly improved for Mo<sub>2</sub>CT<sub><em>x</em></sub> and Mo<sub>2</sub>Ti<sub>2</sub>C<sub>3</sub>T<sub><em>x</em></sub> supports, but marginal on the Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> in rotating disk electrode and membrane electrode assembly tests. The Co@Mo<sub>2</sub>CT<sub><em>x</em></sub> exhibited the highest anion exchange water electrolysis performance of 2.11 A cm<sup>−2</sup> at 1.8 V with over 700 h of stable performance, exceeding previous benchmarks for non-platinum group (non-PGM) metal OER catalysts. The superior performance was attributed to the strong chemical interaction of Co nanoparticle with the Mo<sub>2</sub>CT<sub><em>x</em></sub><span> MXene support. Insights into the electrochemical and chemical oxidation according to MXene type as related to cell durability, as well the effect of electrical conductivity and inherent boosting of electrocatalytic activity of Mo-based MXenes elucidated through density functional theory (DFT) calculations helped explain the performance and durability enhancement of Mo-based MXene supports over Ti</span><sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> supports.</p></div>","PeriodicalId":244,"journal":{"name":"Applied Catalysis B: Environmental","volume":"346 ","pages":"Article 123731"},"PeriodicalIF":20.2000,"publicationDate":"2024-01-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unveiling the role of catalytically active MXene supports in enhancing the performance and durability of cobalt oxygen evolution reaction catalysts for anion exchange membrane water electrolyzers\",\"authors\":\"Young Sang Park ,&nbsp;Ari Chae ,&nbsp;Gwan Hyun Choi ,&nbsp;Swetarekha Ram ,&nbsp;Seung-Cheol Lee ,&nbsp;Satadeep Bhattacharjee ,&nbsp;Jiyoon Jung ,&nbsp;Hyo Sang Jeon ,&nbsp;Cheol-Hee Ahn ,&nbsp;Seung Sang Hwang ,&nbsp;Dong-Yeun Koh ,&nbsp;Insik In ,&nbsp;Taegon Oh ,&nbsp;Seon Joon Kim ,&nbsp;Chong Min Koo ,&nbsp;Albert S. Lee\",\"doi\":\"10.1016/j.apcatb.2024.123731\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p><span>The role of 2D transition metal carbides, also known as MXenes, as active catalyst supports in Co-based oxygen evolution reaction (OER) catalysts was elucidated through a combination of experimental and computation electrochemistry. Through facile seeding of commericial Co nanoparticles on three different MXene supports (Ti</span><sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub>, Mo<sub>2</sub>Ti<sub>2</sub>C<sub>3</sub>T<sub><em>x</em></sub>, Mo<sub>2</sub>CT<sub><em>x</em></sub>), Co@MXene catalysts were prepared and their electrochemical properties examined for alkaline OER electrocatalysts. The OER activity enhancement of Co was significantly improved for Mo<sub>2</sub>CT<sub><em>x</em></sub> and Mo<sub>2</sub>Ti<sub>2</sub>C<sub>3</sub>T<sub><em>x</em></sub> supports, but marginal on the Ti<sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> in rotating disk electrode and membrane electrode assembly tests. The Co@Mo<sub>2</sub>CT<sub><em>x</em></sub> exhibited the highest anion exchange water electrolysis performance of 2.11 A cm<sup>−2</sup> at 1.8 V with over 700 h of stable performance, exceeding previous benchmarks for non-platinum group (non-PGM) metal OER catalysts. The superior performance was attributed to the strong chemical interaction of Co nanoparticle with the Mo<sub>2</sub>CT<sub><em>x</em></sub><span> MXene support. Insights into the electrochemical and chemical oxidation according to MXene type as related to cell durability, as well the effect of electrical conductivity and inherent boosting of electrocatalytic activity of Mo-based MXenes elucidated through density functional theory (DFT) calculations helped explain the performance and durability enhancement of Mo-based MXene supports over Ti</span><sub>3</sub>C<sub>2</sub>T<sub><em>x</em></sub> supports.</p></div>\",\"PeriodicalId\":244,\"journal\":{\"name\":\"Applied Catalysis B: Environmental\",\"volume\":\"346 \",\"pages\":\"Article 123731\"},\"PeriodicalIF\":20.2000,\"publicationDate\":\"2024-01-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Catalysis B: Environmental\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0926337324000420\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Catalysis B: Environmental","FirstCategoryId":"1","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0926337324000420","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

通过实验和计算电化学相结合的方法,阐明了二维过渡金属碳化物(又称 MXene)作为活性催化剂载体在 Co 基氧进化反应(OER)催化剂中的作用。通过在三种不同的 MXene 支撑物(Ti3C2Tx、Mo2Ti2C3Tx、Mo2CTx)上简便地播种普通 Co 纳米颗粒,制备了 Co@MXene 催化剂,并考察了它们在碱性 OER 电催化剂中的电化学特性。在旋转盘电极和膜电极组装测试中,Mo2CTx 和 Mo2Ti2C3Tx 支持物对 Co 的 OER 活性有显著提高,但在 Ti3C2Tx 支持物上则微不足道。Co@Mo2CTx 的阴离子交换水电解性能最高,在 1.8 V 电压下达到 2.11 A cm-2,性能稳定超过 700 小时,超过了以往非铂族(非PGM)金属 OER 催化剂的基准。优异的性能归功于钴纳米粒子与 Mo2CTx MXene 支承的强烈化学作用。通过密度泛函理论(DFT)计算阐明了与电池耐久性相关的 MXene 类型的电化学和化学氧化作用,以及导电性的影响和 Mo 基 MXene 电催化活性的固有增强,这有助于解释 Mo 基 MXene 支持物相对于 Ti3C2Tx 支持物的性能和耐久性增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

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
Unveiling the role of catalytically active MXene supports in enhancing the performance and durability of cobalt oxygen evolution reaction catalysts for anion exchange membrane water electrolyzers

The role of 2D transition metal carbides, also known as MXenes, as active catalyst supports in Co-based oxygen evolution reaction (OER) catalysts was elucidated through a combination of experimental and computation electrochemistry. Through facile seeding of commericial Co nanoparticles on three different MXene supports (Ti3C2Tx, Mo2Ti2C3Tx, Mo2CTx), Co@MXene catalysts were prepared and their electrochemical properties examined for alkaline OER electrocatalysts. The OER activity enhancement of Co was significantly improved for Mo2CTx and Mo2Ti2C3Tx supports, but marginal on the Ti3C2Tx in rotating disk electrode and membrane electrode assembly tests. The Co@Mo2CTx exhibited the highest anion exchange water electrolysis performance of 2.11 A cm−2 at 1.8 V with over 700 h of stable performance, exceeding previous benchmarks for non-platinum group (non-PGM) metal OER catalysts. The superior performance was attributed to the strong chemical interaction of Co nanoparticle with the Mo2CTx MXene support. Insights into the electrochemical and chemical oxidation according to MXene type as related to cell durability, as well the effect of electrical conductivity and inherent boosting of electrocatalytic activity of Mo-based MXenes elucidated through density functional theory (DFT) calculations helped explain the performance and durability enhancement of Mo-based MXene supports over Ti3C2Tx supports.

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
Applied Catalysis B: Environmental
Applied Catalysis B: Environmental 环境科学-工程:化工
CiteScore
38.60
自引率
6.30%
发文量
1117
审稿时长
24 days
期刊介绍: Applied Catalysis B: Environment and Energy (formerly Applied Catalysis B: Environmental) is a journal that focuses on the transition towards cleaner and more sustainable energy sources. The journal's publications cover a wide range of topics, including: 1.Catalytic elimination of environmental pollutants such as nitrogen oxides, carbon monoxide, sulfur compounds, chlorinated and other organic compounds, and soot emitted from stationary or mobile sources. 2.Basic understanding of catalysts used in environmental pollution abatement, particularly in industrial processes. 3.All aspects of preparation, characterization, activation, deactivation, and regeneration of novel and commercially applicable environmental catalysts. 4.New catalytic routes and processes for the production of clean energy, such as hydrogen generation via catalytic fuel processing, and new catalysts and electrocatalysts for fuel cells. 5.Catalytic reactions that convert wastes into useful products. 6.Clean manufacturing techniques that replace toxic chemicals with environmentally friendly catalysts. 7.Scientific aspects of photocatalytic processes and a basic understanding of photocatalysts as applied to environmental problems. 8.New catalytic combustion technologies and catalysts. 9.New catalytic non-enzymatic transformations of biomass components. The journal is abstracted and indexed in API Abstracts, Research Alert, Chemical Abstracts, Web of Science, Theoretical Chemical Engineering Abstracts, Engineering, Technology & Applied Sciences, and others.
期刊最新文献
Conversion of CO2 to higher alcohols on K-CuZnAl/Zr-CuFe composite Effects of the chemical states of N sites and mesoporosity of N-doped carbon supports on single-atom Ru catalysts during CO2-to-formate conversion Visible-light responsive TiO2 for the complete photocatalytic decomposition of volatile organic compounds (VOCs) and its efficient acceleration by thermal energy Controlled doping of ultralow amounts Ru on Ni cathode for PEMWE: Experimental and theoretical elucidation of enhanced performance Mesoporous zeolite ZSM-5 confined Cu nanoclusters for efficient selective catalytic reduction of NOx by NH3
×
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