{"title":"揭示 Ni3S2 催化剂中的铁对氧进化反应电荷转移的促进作用","authors":"Haoyu Song, Xiaolu Xiong, Jinxiao Gao, Yue Hu, Qun Yang, Dehua Zheng, Jingxuan Hao, Xiao Lin, Linjuan Zhang, Jian-Qiang Wang","doi":"10.1002/smll.202404060","DOIUrl":null,"url":null,"abstract":"<p>In recent years, catalysts based on transition metal sulfides have garnered extensive attention due to their low cost and excellent electrocatalytic activity in the alkaline oxygen evolution reaction. Here, the preparation of Fe-doped Ni<sub>3</sub>S<sub>2</sub> via a one-step hydrothermal approach is reported by utilizing inexpensive transition metals Ni and Fe. In an alkaline medium, Fe–Ni<sub>3</sub>S<sub>2</sub> exhibits outstanding electrocatalytic activity and stability for the OER, and the current density can reach 10 mA cm<sup>−2</sup> with an overpotential of 163 mV. In addition, Pt/C||Fe–Ni<sub>3</sub>S<sub>2</sub> is used as the membrane electrode of the anion exchange membrane water electrolyzer, which is capable of providing a current density of 650 mA cm<sup>−2</sup> at a cell voltage of 2.0 V, outperforming the benchmark Ir/C. The principle is revealed that the doping of Fe enhances the electrocatalytic water decomposition ability of Ni<sub>3</sub>S<sub>2</sub> by in situ Raman and in situ X-ray absorption fine structure. The results indicate that the doping of Fe decreases the charge density near Ni atoms, which renders Fe–Ni<sub>3</sub>S<sub>2</sub> more favorable for the adsorption of OH<sup>−</sup> and the formation of <sup>*</sup>OO<sup>−</sup> intermediates. This work puts forward an effective strategy to significantly improve both the alkaline OER activity and stability of low-cost electrocatalysts.</p>","PeriodicalId":228,"journal":{"name":"Small","volume":"20 48","pages":""},"PeriodicalIF":13.0000,"publicationDate":"2024-09-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Unveiling the Promotion of Fe in Ni3S2 Catalyst on Charge Transfer for the Oxygen Evolution Reaction\",\"authors\":\"Haoyu Song, Xiaolu Xiong, Jinxiao Gao, Yue Hu, Qun Yang, Dehua Zheng, Jingxuan Hao, Xiao Lin, Linjuan Zhang, Jian-Qiang Wang\",\"doi\":\"10.1002/smll.202404060\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>In recent years, catalysts based on transition metal sulfides have garnered extensive attention due to their low cost and excellent electrocatalytic activity in the alkaline oxygen evolution reaction. Here, the preparation of Fe-doped Ni<sub>3</sub>S<sub>2</sub> via a one-step hydrothermal approach is reported by utilizing inexpensive transition metals Ni and Fe. In an alkaline medium, Fe–Ni<sub>3</sub>S<sub>2</sub> exhibits outstanding electrocatalytic activity and stability for the OER, and the current density can reach 10 mA cm<sup>−2</sup> with an overpotential of 163 mV. In addition, Pt/C||Fe–Ni<sub>3</sub>S<sub>2</sub> is used as the membrane electrode of the anion exchange membrane water electrolyzer, which is capable of providing a current density of 650 mA cm<sup>−2</sup> at a cell voltage of 2.0 V, outperforming the benchmark Ir/C. The principle is revealed that the doping of Fe enhances the electrocatalytic water decomposition ability of Ni<sub>3</sub>S<sub>2</sub> by in situ Raman and in situ X-ray absorption fine structure. The results indicate that the doping of Fe decreases the charge density near Ni atoms, which renders Fe–Ni<sub>3</sub>S<sub>2</sub> more favorable for the adsorption of OH<sup>−</sup> and the formation of <sup>*</sup>OO<sup>−</sup> intermediates. This work puts forward an effective strategy to significantly improve both the alkaline OER activity and stability of low-cost electrocatalysts.</p>\",\"PeriodicalId\":228,\"journal\":{\"name\":\"Small\",\"volume\":\"20 48\",\"pages\":\"\"},\"PeriodicalIF\":13.0000,\"publicationDate\":\"2024-09-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Small\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/smll.202404060\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Small","FirstCategoryId":"88","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/smll.202404060","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
近年来,基于过渡金属硫化物的催化剂因其低成本和在碱性氧进化反应中出色的电催化活性而受到广泛关注。本文利用廉价的过渡金属 Ni 和 Fe,通过一步水热法制备了掺杂 Fe 的 Ni3S2。在碱性介质中,Fe-Ni3S2 对氧进化反应具有出色的电催化活性和稳定性,电流密度可达 10 mA cm-2,过电位为 163 mV。此外,Pt/C|||Fe-Ni3S2 被用作阴离子交换膜水电解槽的膜电极,在槽电压为 2.0 V 时可提供 650 mA cm-2 的电流密度,优于基准的 Ir/C。通过原位拉曼和原位 X 射线吸收精细结构揭示了掺杂 Fe 增强 Ni3S2 电催化水分解能力的原理。结果表明,Fe 的掺杂降低了 Ni 原子附近的电荷密度,从而使 Fe-Ni3S2 更有利于 OH- 的吸附和 *OO- 中间产物的形成。这项工作为显著提高低成本电催化剂的碱性 OER 活性和稳定性提出了一种有效的策略。
Unveiling the Promotion of Fe in Ni3S2 Catalyst on Charge Transfer for the Oxygen Evolution Reaction
In recent years, catalysts based on transition metal sulfides have garnered extensive attention due to their low cost and excellent electrocatalytic activity in the alkaline oxygen evolution reaction. Here, the preparation of Fe-doped Ni3S2 via a one-step hydrothermal approach is reported by utilizing inexpensive transition metals Ni and Fe. In an alkaline medium, Fe–Ni3S2 exhibits outstanding electrocatalytic activity and stability for the OER, and the current density can reach 10 mA cm−2 with an overpotential of 163 mV. In addition, Pt/C||Fe–Ni3S2 is used as the membrane electrode of the anion exchange membrane water electrolyzer, which is capable of providing a current density of 650 mA cm−2 at a cell voltage of 2.0 V, outperforming the benchmark Ir/C. The principle is revealed that the doping of Fe enhances the electrocatalytic water decomposition ability of Ni3S2 by in situ Raman and in situ X-ray absorption fine structure. The results indicate that the doping of Fe decreases the charge density near Ni atoms, which renders Fe–Ni3S2 more favorable for the adsorption of OH− and the formation of *OO− intermediates. This work puts forward an effective strategy to significantly improve both the alkaline OER activity and stability of low-cost electrocatalysts.
期刊介绍:
Small serves as an exceptional platform for both experimental and theoretical studies in fundamental and applied interdisciplinary research at the nano- and microscale. The journal offers a compelling mix of peer-reviewed Research Articles, Reviews, Perspectives, and Comments.
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