edta介导的Ag-Ni双原子电沉积在Cu衬底上促进碱性析氢

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Linjie Zhang, Haibin Wang, Feifei Zhang, Siwei Yan, Jingwei Li, Rui Zhang, Jing Yang, Cunku Dong, Pengfei Yin*, Xi-Wen Du and Hui Liu*, 
{"title":"edta介导的Ag-Ni双原子电沉积在Cu衬底上促进碱性析氢","authors":"Linjie Zhang,&nbsp;Haibin Wang,&nbsp;Feifei Zhang,&nbsp;Siwei Yan,&nbsp;Jingwei Li,&nbsp;Rui Zhang,&nbsp;Jing Yang,&nbsp;Cunku Dong,&nbsp;Pengfei Yin*,&nbsp;Xi-Wen Du and Hui Liu*,&nbsp;","doi":"10.1021/acs.langmuir.5c01158","DOIUrl":null,"url":null,"abstract":"<p >Dual-atom catalysts (DACs) are designed to enhance catalytic activity through synergy among adjacent heteroatoms. Herein, we report the synthesis of an CuAg<sub>1</sub>Ni<sub>1</sub>–DAC, where AgNi dual atoms are complexed with ethylenediaminetetraacetic acid and electrodeposited onto a copper nanoparticles deposited on copper substrates. The presence of AgNi dual atoms was confirmed by electron energy loss spectrometer and high-angle annular dark field–scanning transmission electron microscopy. CuAg<sub>1</sub>Ni<sub>1</sub>-DAC showed outstanding catalytic activity for the hydrogen evolution reaction (HER) in alkaline electrolytes, needing merely 69 mV overpotential to reach a current density of 10 mA cm<sup>–2</sup>. Notably, its performance outperformed that of commercial Pt/C at a current density of 200 mA cm<sup>–2</sup>, and it demonstrated excellent stability over a period of 120 h. This work uncovers a new method for producing DACs, demonstrating their potential applications in electrocatalytic HER.</p>","PeriodicalId":50,"journal":{"name":"Langmuir","volume":"41 25","pages":"16033–16039"},"PeriodicalIF":3.9000,"publicationDate":"2025-06-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"EDTA-Mediated Electrodeposition of Ag–Ni Dual-Atom on the Cu Substrate for Enhanced Alkaline Hydrogen Evolution\",\"authors\":\"Linjie Zhang,&nbsp;Haibin Wang,&nbsp;Feifei Zhang,&nbsp;Siwei Yan,&nbsp;Jingwei Li,&nbsp;Rui Zhang,&nbsp;Jing Yang,&nbsp;Cunku Dong,&nbsp;Pengfei Yin*,&nbsp;Xi-Wen Du and Hui Liu*,&nbsp;\",\"doi\":\"10.1021/acs.langmuir.5c01158\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Dual-atom catalysts (DACs) are designed to enhance catalytic activity through synergy among adjacent heteroatoms. Herein, we report the synthesis of an CuAg<sub>1</sub>Ni<sub>1</sub>–DAC, where AgNi dual atoms are complexed with ethylenediaminetetraacetic acid and electrodeposited onto a copper nanoparticles deposited on copper substrates. The presence of AgNi dual atoms was confirmed by electron energy loss spectrometer and high-angle annular dark field–scanning transmission electron microscopy. CuAg<sub>1</sub>Ni<sub>1</sub>-DAC showed outstanding catalytic activity for the hydrogen evolution reaction (HER) in alkaline electrolytes, needing merely 69 mV overpotential to reach a current density of 10 mA cm<sup>–2</sup>. Notably, its performance outperformed that of commercial Pt/C at a current density of 200 mA cm<sup>–2</sup>, and it demonstrated excellent stability over a period of 120 h. This work uncovers a new method for producing DACs, demonstrating their potential applications in electrocatalytic HER.</p>\",\"PeriodicalId\":50,\"journal\":{\"name\":\"Langmuir\",\"volume\":\"41 25\",\"pages\":\"16033–16039\"},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2025-06-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Langmuir\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.langmuir.5c01158\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Langmuir","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.langmuir.5c01158","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

双原子催化剂是通过相邻杂原子间的协同作用来提高催化活性的催化剂。在此,我们报道了CuAg1Ni1-DAC的合成,其中AgNi双原子与乙二胺四乙酸络合并电沉积在沉积在铜衬底上的铜纳米颗粒上。利用电子能量损失谱仪和高角环形暗场扫描透射电镜证实了银双原子的存在。CuAg1Ni1-DAC在碱性电解质中表现出优异的析氢反应(HER)催化活性,只需69 mV过电位即可达到10 mA cm-2的电流密度。值得注意的是,在电流密度为200 mA cm-2时,其性能优于商用Pt/C,并且在120小时内表现出出色的稳定性。这项工作揭示了一种生产dac的新方法,展示了它们在电催化HER中的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

EDTA-Mediated Electrodeposition of Ag–Ni Dual-Atom on the Cu Substrate for Enhanced Alkaline Hydrogen Evolution

EDTA-Mediated Electrodeposition of Ag–Ni Dual-Atom on the Cu Substrate for Enhanced Alkaline Hydrogen Evolution

Dual-atom catalysts (DACs) are designed to enhance catalytic activity through synergy among adjacent heteroatoms. Herein, we report the synthesis of an CuAg1Ni1–DAC, where AgNi dual atoms are complexed with ethylenediaminetetraacetic acid and electrodeposited onto a copper nanoparticles deposited on copper substrates. The presence of AgNi dual atoms was confirmed by electron energy loss spectrometer and high-angle annular dark field–scanning transmission electron microscopy. CuAg1Ni1-DAC showed outstanding catalytic activity for the hydrogen evolution reaction (HER) in alkaline electrolytes, needing merely 69 mV overpotential to reach a current density of 10 mA cm–2. Notably, its performance outperformed that of commercial Pt/C at a current density of 200 mA cm–2, and it demonstrated excellent stability over a period of 120 h. This work uncovers a new method for producing DACs, demonstrating their potential applications in electrocatalytic HER.

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
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信