通过铁合金提高铜基电催化剂在电催化甲醛氧化中的稳定性并延长其使用寿命

IF 5.1 Q1 POLYMER SCIENCE ACS Macro Letters Pub Date : 2024-11-13 DOI:10.1002/adfm.202417545
Xiafei Gao, Yuping Pan, Janghui Qiu, Juan Peng, Shuangyin Wang, Yuqin Zou
{"title":"通过铁合金提高铜基电催化剂在电催化甲醛氧化中的稳定性并延长其使用寿命","authors":"Xiafei Gao, Yuping Pan, Janghui Qiu, Juan Peng, Shuangyin Wang, Yuqin Zou","doi":"10.1002/adfm.202417545","DOIUrl":null,"url":null,"abstract":"Electrocatalytic formaldehyde oxidation with metal Cu electrocatalyst has attracted significant interest since it can produce H<sub>2</sub> at the anode and make it possible to construct a bipolar hydrogen production cell with low voltage. However, the activity of the Cu electrocatalyst will be greatly weakened after oxidizing it to Cu<sup>+</sup> or Cu<sup>2+</sup>. Here, a CuFe bimetallic catalyst is developed to efficiently catalyze the electro-oxidation process of HCHO to produce H<sub>2</sub> at a potential of 0.10 V<sub>RHE</sub> with a current density of 100 mA cm<sup>−2</sup>. It is confirmed that introducing Fe in a CuFe catalyst can regulate the electron configuration to prevent Cu<sup>0</sup> oxidation and improve the stability of the catalysts. The introduction of Fe can reduce the energy barrier of the reaction process, and make the C─H bond more easily split on CuFe. A bipolar hydrogen production device is constructed by combining the anodic oxidation of HCHO with the cathodic hydrogen evolution. The current density of 500 mA cm<sup>−2</sup> is achieved at a cell voltage of 0.6 V. The faradaic efficiency is ≈100% and the device is stable for ≈50 h. The research provides a promising path toward the secure, effective, and expandable generation of high-purity H<sub>2</sub> at both anodic and cathodic electrodes.","PeriodicalId":18,"journal":{"name":"ACS Macro Letters","volume":"12 1","pages":""},"PeriodicalIF":5.1000,"publicationDate":"2024-11-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Enhancing the Stability of Cu-Based Electrocatalyst via Fe Alloy in Electrocatalytic Formaldehyde Oxidation with Long Durability\",\"authors\":\"Xiafei Gao, Yuping Pan, Janghui Qiu, Juan Peng, Shuangyin Wang, Yuqin Zou\",\"doi\":\"10.1002/adfm.202417545\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Electrocatalytic formaldehyde oxidation with metal Cu electrocatalyst has attracted significant interest since it can produce H<sub>2</sub> at the anode and make it possible to construct a bipolar hydrogen production cell with low voltage. However, the activity of the Cu electrocatalyst will be greatly weakened after oxidizing it to Cu<sup>+</sup> or Cu<sup>2+</sup>. Here, a CuFe bimetallic catalyst is developed to efficiently catalyze the electro-oxidation process of HCHO to produce H<sub>2</sub> at a potential of 0.10 V<sub>RHE</sub> with a current density of 100 mA cm<sup>−2</sup>. It is confirmed that introducing Fe in a CuFe catalyst can regulate the electron configuration to prevent Cu<sup>0</sup> oxidation and improve the stability of the catalysts. The introduction of Fe can reduce the energy barrier of the reaction process, and make the C─H bond more easily split on CuFe. A bipolar hydrogen production device is constructed by combining the anodic oxidation of HCHO with the cathodic hydrogen evolution. The current density of 500 mA cm<sup>−2</sup> is achieved at a cell voltage of 0.6 V. The faradaic efficiency is ≈100% and the device is stable for ≈50 h. The research provides a promising path toward the secure, effective, and expandable generation of high-purity H<sub>2</sub> at both anodic and cathodic electrodes.\",\"PeriodicalId\":18,\"journal\":{\"name\":\"ACS Macro Letters\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":5.1000,\"publicationDate\":\"2024-11-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Macro Letters\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://doi.org/10.1002/adfm.202417545\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Macro Letters","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202417545","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

摘要

使用金属 Cu 电催化剂进行电催化甲醛氧化引起了人们的极大兴趣,因为它可以在阳极产生 H2,并使低电压双极制氢电池的构建成为可能。然而,Cu 电催化剂在氧化成 Cu+ 或 Cu2+ 后,其活性会大大减弱。本文开发了一种 CuFe 双金属催化剂,可在 0.10 VRHE 的电位和 100 mA cm-2 的电流密度下高效催化 HCHO 的电氧化过程以产生 H2。研究证实,在 CuFe 催化剂中引入 Fe 可以调节电子构型,防止 Cu0 氧化,提高催化剂的稳定性。铁的引入可以降低反应过程的能障,使 C─H 键更容易在 CuFe 上分裂。通过将 HCHO 的阳极氧化与阴极氢气进化相结合,构建了一种双极制氢装置。该研究为在阳极和阴极安全、有效和可扩展地生成高纯度 H2 提供了一条可行之路。
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
Enhancing the Stability of Cu-Based Electrocatalyst via Fe Alloy in Electrocatalytic Formaldehyde Oxidation with Long Durability
Electrocatalytic formaldehyde oxidation with metal Cu electrocatalyst has attracted significant interest since it can produce H2 at the anode and make it possible to construct a bipolar hydrogen production cell with low voltage. However, the activity of the Cu electrocatalyst will be greatly weakened after oxidizing it to Cu+ or Cu2+. Here, a CuFe bimetallic catalyst is developed to efficiently catalyze the electro-oxidation process of HCHO to produce H2 at a potential of 0.10 VRHE with a current density of 100 mA cm−2. It is confirmed that introducing Fe in a CuFe catalyst can regulate the electron configuration to prevent Cu0 oxidation and improve the stability of the catalysts. The introduction of Fe can reduce the energy barrier of the reaction process, and make the C─H bond more easily split on CuFe. A bipolar hydrogen production device is constructed by combining the anodic oxidation of HCHO with the cathodic hydrogen evolution. The current density of 500 mA cm−2 is achieved at a cell voltage of 0.6 V. The faradaic efficiency is ≈100% and the device is stable for ≈50 h. The research provides a promising path toward the secure, effective, and expandable generation of high-purity H2 at both anodic and cathodic electrodes.
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
CiteScore
10.40
自引率
3.40%
发文量
209
审稿时长
1 months
期刊介绍: ACS Macro Letters publishes research in all areas of contemporary soft matter science in which macromolecules play a key role, including nanotechnology, self-assembly, supramolecular chemistry, biomaterials, energy generation and storage, and renewable/sustainable materials. Submissions to ACS Macro Letters should justify clearly the rapid disclosure of the key elements of the study. The scope of the journal includes high-impact research of broad interest in all areas of polymer science and engineering, including cross-disciplinary research that interfaces with polymer science. With the launch of ACS Macro Letters, all Communications that were formerly published in Macromolecules and Biomacromolecules will be published as Letters in ACS Macro Letters.
期刊最新文献
Issue Editorial Masthead Highly Alternating Copolymer of [1.1.1]Propellane and Perfluoro Vinyl Ether: Forming a Hydrophobic and Oleophobic Surface with <50% Fluorine Monomer Content. Semiaromatic Polyester-Ethers with Tunable Degradation Profiles. Eutectic Strategy for the Solvent-Free Synthesis of Hydrophobic Cellulosic Cross-Linked Networks with Broad Multifunctional Applications. Poly(arylene ether)s via Cu(II)-Catalysis.
×
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