Jiangfei Wang , Weijia Chen , Yijun Wen , Yuhan Peng , Siqi Liu , Shiwei He
{"title":"在chcl -尿素深共晶溶剂中电化学脱合金:制备多孔FeCoNiAlMo高熵合金的一种增强析氧活性的策略","authors":"Jiangfei Wang , Weijia Chen , Yijun Wen , Yuhan Peng , Siqi Liu , Shiwei He","doi":"10.1016/j.mlblux.2025.100252","DOIUrl":null,"url":null,"abstract":"<div><div>High-entropy alloys (HEAs), as a new type of multi-element alloy, have become widely studied electrocatalytic materials in recent years due to their excellent catalytic performance. The experimental material used FeCoNiAlMo HEA with equal atomic ratio as the precursor, and three-dimensional nanostructures were formed by dealloying in choline chloride-urea (ChCl-Urea). The results indicate that Fe<sub>20</sub>Co<sub>20</sub>Ni<sub>20</sub>Al<sub>20</sub>Mo<sub>20</sub> HEA is mainly composed of body-centered cubic (BCC) phase and face-centered cubic (FCC) phase, with BCC phase accounting for a larger proportion. Due to the different corrosion resistance of elements and the difference in element content distribution between the two phases, the FCC phase is preferentially corroded, resulting in a three-dimensional porous morphology. This unique structure synergistically reduces the energy barrier during the hydrolysis dissociation process, giving the material a significant advantage in the oxygen evolution reaction (OER) process. At a current density of 10 mA cm<sup>−2</sup>, the overpotential of the treated alloy is as low as 312 mV, which is lower than the commercial RuO<sub>2</sub>-IrO<sub>2</sub>, and it has lower resistance and higher charge transfer efficiency.</div></div>","PeriodicalId":18245,"journal":{"name":"Materials Letters: X","volume":"26 ","pages":"Article 100252"},"PeriodicalIF":2.6000,"publicationDate":"2025-07-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemical dealloying in ChCl-Urea Deep eutectic solvent: A strategy to fabricate porous FeCoNiAlMo high-entropy alloy with enhanced oxygen evolution reaction activity\",\"authors\":\"Jiangfei Wang , Weijia Chen , Yijun Wen , Yuhan Peng , Siqi Liu , Shiwei He\",\"doi\":\"10.1016/j.mlblux.2025.100252\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>High-entropy alloys (HEAs), as a new type of multi-element alloy, have become widely studied electrocatalytic materials in recent years due to their excellent catalytic performance. The experimental material used FeCoNiAlMo HEA with equal atomic ratio as the precursor, and three-dimensional nanostructures were formed by dealloying in choline chloride-urea (ChCl-Urea). The results indicate that Fe<sub>20</sub>Co<sub>20</sub>Ni<sub>20</sub>Al<sub>20</sub>Mo<sub>20</sub> HEA is mainly composed of body-centered cubic (BCC) phase and face-centered cubic (FCC) phase, with BCC phase accounting for a larger proportion. Due to the different corrosion resistance of elements and the difference in element content distribution between the two phases, the FCC phase is preferentially corroded, resulting in a three-dimensional porous morphology. This unique structure synergistically reduces the energy barrier during the hydrolysis dissociation process, giving the material a significant advantage in the oxygen evolution reaction (OER) process. At a current density of 10 mA cm<sup>−2</sup>, the overpotential of the treated alloy is as low as 312 mV, which is lower than the commercial RuO<sub>2</sub>-IrO<sub>2</sub>, and it has lower resistance and higher charge transfer efficiency.</div></div>\",\"PeriodicalId\":18245,\"journal\":{\"name\":\"Materials Letters: X\",\"volume\":\"26 \",\"pages\":\"Article 100252\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2025-07-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Materials Letters: X\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2590150825000158\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MATERIALS SCIENCE, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Letters: X","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590150825000158","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
高熵合金(High-entropy alloys, HEAs)作为一种新型的多元素合金,因其优异的催化性能而成为近年来被广泛研究的电催化材料。实验材料以等原子比的FeCoNiAlMo HEA为前驱体,在氯化胆碱-尿素(ChCl-Urea)中进行脱合金处理,形成三维纳米结构。结果表明:Fe20Co20Ni20Al20Mo20 HEA主要由体心立方(BCC)相和面心立方(FCC)相组成,其中BCC相所占比例较大;由于元素的耐蚀性不同以及两相之间元素含量分布的差异,FCC相优先被腐蚀,形成三维多孔形态。这种独特的结构协同降低了水解解离过程中的能垒,使材料在析氧反应(OER)过程中具有显著的优势。在电流密度为10 mA cm−2时,处理后的合金的过电位低至312 mV,低于工业RuO2-IrO2,并且具有更低的电阻和更高的电荷转移效率。
Electrochemical dealloying in ChCl-Urea Deep eutectic solvent: A strategy to fabricate porous FeCoNiAlMo high-entropy alloy with enhanced oxygen evolution reaction activity
High-entropy alloys (HEAs), as a new type of multi-element alloy, have become widely studied electrocatalytic materials in recent years due to their excellent catalytic performance. The experimental material used FeCoNiAlMo HEA with equal atomic ratio as the precursor, and three-dimensional nanostructures were formed by dealloying in choline chloride-urea (ChCl-Urea). The results indicate that Fe20Co20Ni20Al20Mo20 HEA is mainly composed of body-centered cubic (BCC) phase and face-centered cubic (FCC) phase, with BCC phase accounting for a larger proportion. Due to the different corrosion resistance of elements and the difference in element content distribution between the two phases, the FCC phase is preferentially corroded, resulting in a three-dimensional porous morphology. This unique structure synergistically reduces the energy barrier during the hydrolysis dissociation process, giving the material a significant advantage in the oxygen evolution reaction (OER) process. At a current density of 10 mA cm−2, the overpotential of the treated alloy is as low as 312 mV, which is lower than the commercial RuO2-IrO2, and it has lower resistance and higher charge transfer efficiency.