Karuppaiah Selvakumar , Muthuraj Arunpandian , Abdellatif M. Sadeq , Abdalrahman Alajmi , Tae Hwan Oh , Asma A. Alothman , Saikh Mohammad , Meenakshisundaram Swaminathan
{"title":"锚定在双金属氧化物上的三元单金属原子氧化物在碱性介质中增强电催化析氧反应","authors":"Karuppaiah Selvakumar , Muthuraj Arunpandian , Abdellatif M. Sadeq , Abdalrahman Alajmi , Tae Hwan Oh , Asma A. Alothman , Saikh Mohammad , Meenakshisundaram Swaminathan","doi":"10.1016/j.jelechem.2025.118963","DOIUrl":null,"url":null,"abstract":"<div><div>A stronger electrocatalytic oxygen evolution reaction (OER) may be achieved by anchoring W, Cu, and Co single metal atom oxides (SMAO) nanocomposite catalysts with Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub> coupled rGO (R-Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-WCC-3). The as-obtained catalyst materials are subjected to studies employing powder XRD, XPS, FESEM, HRTEM, and STEM-HAADF to assess the material’s structural purity, oxidation state of components, surface morphology, and presence of SMAO. The SMAO anchoring by a highly scalable one-step sonication synthesis significantly enhanced the catalysts’ mass, charge transfer, and active site density. Excellent catalytic activity for OER under alkaline circumstances was accordingly shown by the R-Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-WCC electrocatalysts. Particularly, the optimal R-Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-WCC-3 catalyst had a relatively small Tafel slope of 52 mV dec<sup>–1</sup> and low overpotentials of 282 and 353 mV for current densities of 10 and 100 mA cm<sup>−2</sup> respectively. Additionally, we used the DFT calculation to examine the OER activity of a single W atom anchoring on the CO<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub> materials. All of these results suggest that Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-rGO could be used as an anchor for transition single metal atom catalysts to make new, interesting, and useful electrocatalysts.</div></div>","PeriodicalId":355,"journal":{"name":"Journal of Electroanalytical Chemistry","volume":"981 ","pages":"Article 118963"},"PeriodicalIF":4.1000,"publicationDate":"2025-03-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ternary single metal atom oxides anchored on bimetal oxides for enhanced electrocatalytic oxygen evolution reaction in alkaline medium\",\"authors\":\"Karuppaiah Selvakumar , Muthuraj Arunpandian , Abdellatif M. Sadeq , Abdalrahman Alajmi , Tae Hwan Oh , Asma A. Alothman , Saikh Mohammad , Meenakshisundaram Swaminathan\",\"doi\":\"10.1016/j.jelechem.2025.118963\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>A stronger electrocatalytic oxygen evolution reaction (OER) may be achieved by anchoring W, Cu, and Co single metal atom oxides (SMAO) nanocomposite catalysts with Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub> coupled rGO (R-Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-WCC-3). The as-obtained catalyst materials are subjected to studies employing powder XRD, XPS, FESEM, HRTEM, and STEM-HAADF to assess the material’s structural purity, oxidation state of components, surface morphology, and presence of SMAO. The SMAO anchoring by a highly scalable one-step sonication synthesis significantly enhanced the catalysts’ mass, charge transfer, and active site density. Excellent catalytic activity for OER under alkaline circumstances was accordingly shown by the R-Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-WCC electrocatalysts. Particularly, the optimal R-Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-WCC-3 catalyst had a relatively small Tafel slope of 52 mV dec<sup>–1</sup> and low overpotentials of 282 and 353 mV for current densities of 10 and 100 mA cm<sup>−2</sup> respectively. Additionally, we used the DFT calculation to examine the OER activity of a single W atom anchoring on the CO<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub> materials. All of these results suggest that Co<sub>3</sub>O<sub>4</sub>-CeO<sub>2</sub>-rGO could be used as an anchor for transition single metal atom catalysts to make new, interesting, and useful electrocatalysts.</div></div>\",\"PeriodicalId\":355,\"journal\":{\"name\":\"Journal of Electroanalytical Chemistry\",\"volume\":\"981 \",\"pages\":\"Article 118963\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-03-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Electroanalytical Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1572665725000360\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/1/28 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Electroanalytical Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1572665725000360","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
摘要
Co3O4-CeO2偶联rGO (R-Co3O4-CeO2-WCC-3)锚定W、Cu和Co单金属原子氧化物(SMAO)纳米复合催化剂可以实现更强的电催化析氧反应(OER)。采用粉末XRD, XPS, FESEM, HRTEM和STEM-HAADF对所得催化剂材料进行研究,以评估材料的结构纯度,组分的氧化状态,表面形貌和SMAO的存在。通过高度可扩展的一步超声合成,smo锚定显著提高了催化剂的质量、电荷转移和活性位点密度。R-Co3O4-CeO2-WCC电催化剂在碱性条件下对OER具有良好的催化活性。特别是,最佳的R-Co3O4-CeO2-WCC-3催化剂在电流密度分别为10和100 mA cm−2时,Tafel斜率相对较小,为52 mV dec1,过电位较低,分别为282和353 mV。此外,我们使用DFT计算来检查固定在CO3O4-CeO2材料上的单个W原子的OER活性。这些结果表明,Co3O4-CeO2-rGO可以作为过渡单金属原子催化剂的锚点,制备出新颖、有趣、有用的电催化剂。
Ternary single metal atom oxides anchored on bimetal oxides for enhanced electrocatalytic oxygen evolution reaction in alkaline medium
A stronger electrocatalytic oxygen evolution reaction (OER) may be achieved by anchoring W, Cu, and Co single metal atom oxides (SMAO) nanocomposite catalysts with Co3O4-CeO2 coupled rGO (R-Co3O4-CeO2-WCC-3). The as-obtained catalyst materials are subjected to studies employing powder XRD, XPS, FESEM, HRTEM, and STEM-HAADF to assess the material’s structural purity, oxidation state of components, surface morphology, and presence of SMAO. The SMAO anchoring by a highly scalable one-step sonication synthesis significantly enhanced the catalysts’ mass, charge transfer, and active site density. Excellent catalytic activity for OER under alkaline circumstances was accordingly shown by the R-Co3O4-CeO2-WCC electrocatalysts. Particularly, the optimal R-Co3O4-CeO2-WCC-3 catalyst had a relatively small Tafel slope of 52 mV dec–1 and low overpotentials of 282 and 353 mV for current densities of 10 and 100 mA cm−2 respectively. Additionally, we used the DFT calculation to examine the OER activity of a single W atom anchoring on the CO3O4-CeO2 materials. All of these results suggest that Co3O4-CeO2-rGO could be used as an anchor for transition single metal atom catalysts to make new, interesting, and useful electrocatalysts.
期刊介绍:
The Journal of Electroanalytical Chemistry is the foremost international journal devoted to the interdisciplinary subject of electrochemistry in all its aspects, theoretical as well as applied.
Electrochemistry is a wide ranging area that is in a state of continuous evolution. Rather than compiling a long list of topics covered by the Journal, the editors would like to draw particular attention to the key issues of novelty, topicality and quality. Papers should present new and interesting electrochemical science in a way that is accessible to the reader. The presentation and discussion should be at a level that is consistent with the international status of the Journal. Reports describing the application of well-established techniques to problems that are essentially technical will not be accepted. Similarly, papers that report observations but fail to provide adequate interpretation will be rejected by the Editors. Papers dealing with technical electrochemistry should be submitted to other specialist journals unless the authors can show that their work provides substantially new insights into electrochemical processes.