{"title":"作为双功能电催化剂的掺铁 CoPx 亲水性自支撑纳米棒阵列的电子调节功能可实现卓越的海水整体分离效果","authors":"Bo Sun, Luchen Wang, Chunhu Li, Xiangchao Meng","doi":"10.1021/acssuschemeng.4c09394","DOIUrl":null,"url":null,"abstract":"To address the challenge of designing a highly reactive and stable bifunctional electrocatalyst for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), a hydrophilic Fe-CoP<sub><i>x</i></sub> nanorod array on nickel foam (NF) was designed and prepared in this work. The modulation of a d-band center of Co by adding Fe effectively optimized the adsorption energy of intermediates. The synergistic effect of the bimetallic active sites significantly enhanced the electrocatalytic performance for both reactions. In alkaline seawater, Fe-CoP<sub><i>x</i></sub>/NF exhibited excellent HER (−32 mV at −10 mA cm<sup>–2</sup>) and OER (216 mV at 10 mA cm<sup>–2</sup>) activities, maintaining stability for over 100 h at 100 mA cm<sup>–2</sup>. For overall seawater electrolysis, the catalyst achieved a low cell voltage of 1.54 V at 10 mA cm<sup>–2</sup>, outperforming the conventional RuO<sub>2</sub>∥Pt/C electrode (1.58 V at 10 mA cm<sup>–2</sup>). Additionally, in a simulated industrial flow cell, the catalyst operated stably for over 200 h at 100 mA cm<sup>–2</sup>, indicating its strong potential for practical applications. This study introduced a simple synthesis method for bimetallic phosphides, providing a new avenue for the design of high-performance bifunctional catalysts for seawater electrolysis.","PeriodicalId":25,"journal":{"name":"ACS Sustainable Chemistry & Engineering","volume":"69 1","pages":""},"PeriodicalIF":7.1000,"publicationDate":"2025-01-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electronic Regulation by Fe-Doped CoPx Hydrophilic Self-Supported Nanorod Arrays as Bifunctional Electrocatalysts for Superior Overall Seawater Splitting\",\"authors\":\"Bo Sun, Luchen Wang, Chunhu Li, Xiangchao Meng\",\"doi\":\"10.1021/acssuschemeng.4c09394\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"To address the challenge of designing a highly reactive and stable bifunctional electrocatalyst for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), a hydrophilic Fe-CoP<sub><i>x</i></sub> nanorod array on nickel foam (NF) was designed and prepared in this work. The modulation of a d-band center of Co by adding Fe effectively optimized the adsorption energy of intermediates. The synergistic effect of the bimetallic active sites significantly enhanced the electrocatalytic performance for both reactions. In alkaline seawater, Fe-CoP<sub><i>x</i></sub>/NF exhibited excellent HER (−32 mV at −10 mA cm<sup>–2</sup>) and OER (216 mV at 10 mA cm<sup>–2</sup>) activities, maintaining stability for over 100 h at 100 mA cm<sup>–2</sup>. For overall seawater electrolysis, the catalyst achieved a low cell voltage of 1.54 V at 10 mA cm<sup>–2</sup>, outperforming the conventional RuO<sub>2</sub>∥Pt/C electrode (1.58 V at 10 mA cm<sup>–2</sup>). Additionally, in a simulated industrial flow cell, the catalyst operated stably for over 200 h at 100 mA cm<sup>–2</sup>, indicating its strong potential for practical applications. This study introduced a simple synthesis method for bimetallic phosphides, providing a new avenue for the design of high-performance bifunctional catalysts for seawater electrolysis.\",\"PeriodicalId\":25,\"journal\":{\"name\":\"ACS Sustainable Chemistry & Engineering\",\"volume\":\"69 1\",\"pages\":\"\"},\"PeriodicalIF\":7.1000,\"publicationDate\":\"2025-01-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Sustainable Chemistry & Engineering\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acssuschemeng.4c09394\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Sustainable Chemistry & Engineering","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acssuschemeng.4c09394","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Electronic Regulation by Fe-Doped CoPx Hydrophilic Self-Supported Nanorod Arrays as Bifunctional Electrocatalysts for Superior Overall Seawater Splitting
To address the challenge of designing a highly reactive and stable bifunctional electrocatalyst for both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), a hydrophilic Fe-CoPx nanorod array on nickel foam (NF) was designed and prepared in this work. The modulation of a d-band center of Co by adding Fe effectively optimized the adsorption energy of intermediates. The synergistic effect of the bimetallic active sites significantly enhanced the electrocatalytic performance for both reactions. In alkaline seawater, Fe-CoPx/NF exhibited excellent HER (−32 mV at −10 mA cm–2) and OER (216 mV at 10 mA cm–2) activities, maintaining stability for over 100 h at 100 mA cm–2. For overall seawater electrolysis, the catalyst achieved a low cell voltage of 1.54 V at 10 mA cm–2, outperforming the conventional RuO2∥Pt/C electrode (1.58 V at 10 mA cm–2). Additionally, in a simulated industrial flow cell, the catalyst operated stably for over 200 h at 100 mA cm–2, indicating its strong potential for practical applications. This study introduced a simple synthesis method for bimetallic phosphides, providing a new avenue for the design of high-performance bifunctional catalysts for seawater electrolysis.
期刊介绍:
ACS Sustainable Chemistry & Engineering is a prestigious weekly peer-reviewed scientific journal published by the American Chemical Society. Dedicated to advancing the principles of green chemistry and green engineering, it covers a wide array of research topics including green chemistry, green engineering, biomass, alternative energy, and life cycle assessment.
The journal welcomes submissions in various formats, including Letters, Articles, Features, and Perspectives (Reviews), that address the challenges of sustainability in the chemical enterprise and contribute to the advancement of sustainable practices. Join us in shaping the future of sustainable chemistry and engineering.