{"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, Haibin Wang, Feifei Zhang, Siwei Yan, Jingwei Li, Rui Zhang, Jing Yang, Cunku Dong, Pengfei Yin*, Xi-Wen Du and Hui Liu*, ","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, Haibin Wang, Feifei Zhang, Siwei Yan, Jingwei Li, Rui Zhang, Jing Yang, Cunku Dong, Pengfei Yin*, Xi-Wen Du and Hui Liu*, \",\"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。
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.
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).