{"title":"用于坚固海水电解槽的 NiFeOOH 电催化剂的表面非晶化和功能化","authors":"Hao Wang, Nannan Jiang, Bing Huang, Qiangmin Yu and Lunhui Guan","doi":"10.1039/D4EY00106K","DOIUrl":null,"url":null,"abstract":"<p >Hydrogen production of seawater electrolysis has attracted considerable interest due to the abundant seawater resources. However, the chloride ions (Cl<small><sup>−</sup></small>) in seawater not only corrode the electrodes but also cause side reactions, severely impacting the electrode efficiency and stability of the oxygen evolution reaction (OER) in seawater electrolysis. These challenges are the key factors limiting the development of seawater electrolysis technology. Here, we developed a surface-functionalized high-performance catalyst, which not only resists Cl<small><sup>−</sup></small> corrosion using surface-functionalized ions, but also improves the OER activity by surface amorphization. The designed catalyst (Ru<small><sub>0.1</sub></small>-NiFeOOH/PO<small><sub>4</sub></small><small><sup>3−</sup></small>) is composed of Ru<small><sub>0.1</sub></small>-NiFeOOH and surface phosphate. On the one hand, a small amount of Ru doping can increase the surface amorphization of NiFeOOH and thus improve the catalytic activity. On the other hand, the phosphates on Ru<small><sub>0.1</sub></small>-NiFeOOH are resistant to Cl<small><sup>−</sup></small> corrosion, which in turn improves the electrode stability. This catalyst demonstrates robust performance operation over 1000 h in alkaline seawater solutions at an industrial current density of 0.5 A cm<small><sup>−2</sup></small>. The anion exchange membrane seawater electrolyzer assembled with Ru<small><sub>0.1</sub></small>-NiFeOOH/PO<small><sub>4</sub></small><small><sup>3−</sup></small> only needs 1.6 V to achieve 0.5 A cm<small><sup>−2</sup></small> when powered by sustainable solar energy. The electrolyzer efficiency is 75.1% at 0.5 A cm<small><sup>−2</sup></small>, which is superior to the 2030 technical target of 65% set by the U.S. DOE and most reported work. This work offers a new perspective for designing efficient and stable catalysts and is of great significance for advancing seawater electrolysis technology.</p>","PeriodicalId":72877,"journal":{"name":"EES catalysis","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/ey/d4ey00106k?page=search","citationCount":"0","resultStr":"{\"title\":\"Surface amorphization and functionalization of a NiFeOOH electrocatalyst for a robust seawater electrolyzer†\",\"authors\":\"Hao Wang, Nannan Jiang, Bing Huang, Qiangmin Yu and Lunhui Guan\",\"doi\":\"10.1039/D4EY00106K\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Hydrogen production of seawater electrolysis has attracted considerable interest due to the abundant seawater resources. However, the chloride ions (Cl<small><sup>−</sup></small>) in seawater not only corrode the electrodes but also cause side reactions, severely impacting the electrode efficiency and stability of the oxygen evolution reaction (OER) in seawater electrolysis. These challenges are the key factors limiting the development of seawater electrolysis technology. Here, we developed a surface-functionalized high-performance catalyst, which not only resists Cl<small><sup>−</sup></small> corrosion using surface-functionalized ions, but also improves the OER activity by surface amorphization. The designed catalyst (Ru<small><sub>0.1</sub></small>-NiFeOOH/PO<small><sub>4</sub></small><small><sup>3−</sup></small>) is composed of Ru<small><sub>0.1</sub></small>-NiFeOOH and surface phosphate. On the one hand, a small amount of Ru doping can increase the surface amorphization of NiFeOOH and thus improve the catalytic activity. On the other hand, the phosphates on Ru<small><sub>0.1</sub></small>-NiFeOOH are resistant to Cl<small><sup>−</sup></small> corrosion, which in turn improves the electrode stability. This catalyst demonstrates robust performance operation over 1000 h in alkaline seawater solutions at an industrial current density of 0.5 A cm<small><sup>−2</sup></small>. The anion exchange membrane seawater electrolyzer assembled with Ru<small><sub>0.1</sub></small>-NiFeOOH/PO<small><sub>4</sub></small><small><sup>3−</sup></small> only needs 1.6 V to achieve 0.5 A cm<small><sup>−2</sup></small> when powered by sustainable solar energy. The electrolyzer efficiency is 75.1% at 0.5 A cm<small><sup>−2</sup></small>, which is superior to the 2030 technical target of 65% set by the U.S. DOE and most reported work. This work offers a new perspective for designing efficient and stable catalysts and is of great significance for advancing seawater electrolysis technology.</p>\",\"PeriodicalId\":72877,\"journal\":{\"name\":\"EES catalysis\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-06-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2024/ey/d4ey00106k?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"EES catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/ey/d4ey00106k\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"EES catalysis","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/ey/d4ey00106k","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
由于海水资源丰富,海水电解制氢引起了广泛关注。然而,海水中的氯离子(Cl-)不仅会腐蚀电极,还会引起副反应,严重影响电极效率和海水电解中氧进化反应(OER)的稳定性。这些挑战是制约海水电解技术发展的关键因素。在此,我们开发了一种表面功能化的高性能催化剂,它不仅能利用表面功能化离子抵抗 Cl- 腐蚀,还能通过表面非晶化提高 OER 活性。设计的催化剂(Ru0.1-NiFeOOH/PO43-)由 Ru0.1-NiFeOOH 和表面磷酸盐组成。一方面,少量的 Ru 掺杂可以增加 NiFeOOH 的表面非晶化,从而提高催化活性。另一方面,Ru0.1-NiFeOOH 上的磷酸盐具有抗 Cl- 腐蚀性,从而提高了电极的稳定性。在 0.5 A cm-2 的工业电流密度下,这种催化剂在碱性海水溶液中运行 1000 小时以上,表现出强劲的性能。使用 Ru0.1-NiFeOOH/PO43- 装配的阴离子交换膜海水电解槽在使用可持续太阳能供电时,只需 1.6 V 电压即可达到 0.5 A cm-2。在 0.5 A cm-2 的条件下,电解槽的效率为 75.1%,优于美国能源部设定的 2030 年 65% 的技术目标,也优于大多数相关报道。这项研究为设计高效、稳定的催化剂提供了新的视角,对推动海水电解技术的发展具有重要意义。
Surface amorphization and functionalization of a NiFeOOH electrocatalyst for a robust seawater electrolyzer†
Hydrogen production of seawater electrolysis has attracted considerable interest due to the abundant seawater resources. However, the chloride ions (Cl−) in seawater not only corrode the electrodes but also cause side reactions, severely impacting the electrode efficiency and stability of the oxygen evolution reaction (OER) in seawater electrolysis. These challenges are the key factors limiting the development of seawater electrolysis technology. Here, we developed a surface-functionalized high-performance catalyst, which not only resists Cl− corrosion using surface-functionalized ions, but also improves the OER activity by surface amorphization. The designed catalyst (Ru0.1-NiFeOOH/PO43−) is composed of Ru0.1-NiFeOOH and surface phosphate. On the one hand, a small amount of Ru doping can increase the surface amorphization of NiFeOOH and thus improve the catalytic activity. On the other hand, the phosphates on Ru0.1-NiFeOOH are resistant to Cl− corrosion, which in turn improves the electrode stability. This catalyst demonstrates robust performance operation over 1000 h in alkaline seawater solutions at an industrial current density of 0.5 A cm−2. The anion exchange membrane seawater electrolyzer assembled with Ru0.1-NiFeOOH/PO43− only needs 1.6 V to achieve 0.5 A cm−2 when powered by sustainable solar energy. The electrolyzer efficiency is 75.1% at 0.5 A cm−2, which is superior to the 2030 technical target of 65% set by the U.S. DOE and most reported work. This work offers a new perspective for designing efficient and stable catalysts and is of great significance for advancing seawater electrolysis technology.