{"title":"核壳CoPt@C通过ch4沉积策略组装分级催化剂，实现高效的整体水分解","authors":"Zi-Ya Li, De-Ling Wang, Chao Zhang, Hai-Peng Wang, De-Lu Zhang, Gao-Qiang Zhao, Zhi-Guo Lv, Fu-Jin Sun","doi":"10.1007/s12598-025-03345-4","DOIUrl":null,"url":null,"abstract":"<div><p>This study, a core–shell CoPt@C assembled hierarchical catalyst (named CoPt@C) was prepared using a unique CH<sub>4</sub> deposition strategy for highly efficient overall water splitting. CoPt@C is composed of dense CoPt@C core–shell nanoparticles (NPs) and a minor proportion of curled CoPt@nanotubes (CoPt@CNTs). Moreover, by adjusting the CH<sub>4</sub> deposition time, the carbon shell thickness can be effectively regulated. Benefiting from the synergistic interaction between CoPt alloy and carbon shell, coupled with the high conductivity of the carbon shell, the overpotential of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) for CoPt@C is 15 and 120 mV at 10 mA cm<sup>−2</sup>. In addition, CoPt@C requires only 1.58 V to achieve 10 mA cm<sup>−2</sup> for overall water splitting and maintains excellent stability over 80 h of continuous electrolysis. Density functional theory (DFT) calculations suggest that electrons transfer from the CoPt alloy NPs to the carbon shell, rendering the carbon shell electron-rich. Additionally, the hydrogen adsorption energy (Δ<i>G</i><sub>*H</sub>) and the rate-determining step (Δ<i>G</i><sub>*OOH</sub>) on CoPt@C are only −0.22 and 1.9 eV, respectively.</p><h3>Graphical abstract</h3>\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>","PeriodicalId":749,"journal":{"name":"Rare Metals","volume":"44 9","pages":"6232 - 6245"},"PeriodicalIF":11.0000,"publicationDate":"2025-05-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Core–shell CoPt@C assembled hierarchical catalysts via CH4-deposition strategy for efficient overall water splitting\",\"authors\":\"Zi-Ya Li, De-Ling Wang, Chao Zhang, Hai-Peng Wang, De-Lu Zhang, Gao-Qiang Zhao, Zhi-Guo Lv, Fu-Jin Sun\",\"doi\":\"10.1007/s12598-025-03345-4\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>This study, a core–shell CoPt@C assembled hierarchical catalyst (named CoPt@C) was prepared using a unique CH<sub>4</sub> deposition strategy for highly efficient overall water splitting. CoPt@C is composed of dense CoPt@C core–shell nanoparticles (NPs) and a minor proportion of curled CoPt@nanotubes (CoPt@CNTs). Moreover, by adjusting the CH<sub>4</sub> deposition time, the carbon shell thickness can be effectively regulated. Benefiting from the synergistic interaction between CoPt alloy and carbon shell, coupled with the high conductivity of the carbon shell, the overpotential of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) for CoPt@C is 15 and 120 mV at 10 mA cm<sup>−2</sup>. In addition, CoPt@C requires only 1.58 V to achieve 10 mA cm<sup>−2</sup> for overall water splitting and maintains excellent stability over 80 h of continuous electrolysis. Density functional theory (DFT) calculations suggest that electrons transfer from the CoPt alloy NPs to the carbon shell, rendering the carbon shell electron-rich. Additionally, the hydrogen adsorption energy (Δ<i>G</i><sub>*H</sub>) and the rate-determining step (Δ<i>G</i><sub>*OOH</sub>) on CoPt@C are only −0.22 and 1.9 eV, respectively.</p><h3>Graphical abstract</h3>\\n<div><figure><div><div><picture><source><img></source></picture></div></div></figure></div></div>\",\"PeriodicalId\":749,\"journal\":{\"name\":\"Rare Metals\",\"volume\":\"44 9\",\"pages\":\"6232 - 6245\"},\"PeriodicalIF\":11.0000,\"publicationDate\":\"2025-05-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Rare Metals\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s12598-025-03345-4\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Rare Metals","FirstCategoryId":"88","ListUrlMain":"https://link.springer.com/article/10.1007/s12598-025-03345-4","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
本研究采用独特的CH4沉积策略制备了一种核壳CoPt@C组装级联催化剂（命名为CoPt@C），用于高效的整体水分解。CoPt@C由致密的CoPt@C核壳纳米粒子（NPs）和少量卷曲的CoPt@nanotubes （CoPt@CNTs）组成。此外，通过调整CH4沉积时间，可以有效调节碳壳厚度。得益于CoPt合金与碳壳的协同作用，再加上碳壳的高导电性，CoPt@C在10 mA cm−2下析氢反应（HER）和析氧反应（OER）的过电位分别为15和120 mV。此外，CoPt@C只需要1.58 V就可以实现10 mA cm−2的整体水分解，并在80小时的连续电解中保持出色的稳定性。密度泛函理论（DFT）计算表明，电子从CoPt合金NPs转移到碳壳层，使碳壳层富含电子。此外，在CoPt@C上的氢吸附能（ΔG*H）和速率决定步长（ΔG*OOH）分别仅为−0.22和1.9 eV。图形抽象
Core–shell CoPt@C assembled hierarchical catalysts via CH4-deposition strategy for efficient overall water splitting
This study, a core–shell CoPt@C assembled hierarchical catalyst (named CoPt@C) was prepared using a unique CH4 deposition strategy for highly efficient overall water splitting. CoPt@C is composed of dense CoPt@C core–shell nanoparticles (NPs) and a minor proportion of curled CoPt@nanotubes (CoPt@CNTs). Moreover, by adjusting the CH4 deposition time, the carbon shell thickness can be effectively regulated. Benefiting from the synergistic interaction between CoPt alloy and carbon shell, coupled with the high conductivity of the carbon shell, the overpotential of hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) for CoPt@C is 15 and 120 mV at 10 mA cm−2. In addition, CoPt@C requires only 1.58 V to achieve 10 mA cm−2 for overall water splitting and maintains excellent stability over 80 h of continuous electrolysis. Density functional theory (DFT) calculations suggest that electrons transfer from the CoPt alloy NPs to the carbon shell, rendering the carbon shell electron-rich. Additionally, the hydrogen adsorption energy (ΔG*H) and the rate-determining step (ΔG*OOH) on CoPt@C are only −0.22 and 1.9 eV, respectively.
期刊介绍：
Rare Metals is a monthly peer-reviewed journal published by the Nonferrous Metals Society of China. It serves as a platform for engineers and scientists to communicate and disseminate original research articles in the field of rare metals. The journal focuses on a wide range of topics including metallurgy, processing, and determination of rare metals. Additionally, it showcases the application of rare metals in advanced materials such as superconductors, semiconductors, composites, and ceramics.
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