{"title":"用于高活性析氢反应的三元合金纳米粒子。","authors":"Yuto Maruta, Takaaki Toriyama, Tomokazu Yamamoto, Yasukazu Murakami, Shogo Kawaguchi, Yoshiki Kubota, Hiroshi Kitagawa, Kohei Kusada","doi":"10.1002/chem.202503458","DOIUrl":null,"url":null,"abstract":"<p><p>Alloying is effective for enhancing the hydrogen evolution reaction (HER) activity of Pt. Binary PdPt alloys outperform monometallic Pt in terms of HER activity. However, their HER activity can be improved further by incorporating a third element. In this study, we demonstrate that incorporating Au into PdPt alloys alters their electronic structures, enhancing their HER activity. Homogeneous solid-solution Au<sub>20</sub>Pd<sub>40</sub>Pt<sub>40</sub> alloy nanoparticles (NPs) were synthesized using a one-pot polyol method. Elemental mapping using scanning transmission electron microscopy (STEM) combined with energy-dispersive X-ray spectroscopy confirmed the uniform distribution of the three elements within the NPs, demonstrating the formation of a solid-solution alloy. X-ray absorption near-edge structure analysis indicated electron transfer from Au to Pt and Pd, which generated a more reduced electronic state of Pt compared to that in the Pd<sub>50</sub>Pt<sub>50</sub> alloy NPs. Electrochemical measurements in 0.5 M H<sub>2</sub>SO<sub>4</sub> revealed that Au<sub>20</sub>Pd<sub>40</sub>Pt<sub>40</sub> alloy NPs had a lower overpotential (15.4 mV at 10 mA cm<sup>-2</sup>) and a higher intrinsic turnover frequency (TOF) than Pd<sub>50</sub>Pt<sub>50</sub> alloy and monometallic Pt NPs. These findings demonstrate that homogeneously mixing a third element into binary alloy NPs is effective for enhancing the catalytic performance.</p>","PeriodicalId":144,"journal":{"name":"Chemistry - A European Journal","volume":" ","pages":"e03458"},"PeriodicalIF":3.7000,"publicationDate":"2026-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"AuPdPt Ternary Alloy Nanoparticles for Highly Active Hydrogen Evolution Reaction.\",\"authors\":\"Yuto Maruta, Takaaki Toriyama, Tomokazu Yamamoto, Yasukazu Murakami, Shogo Kawaguchi, Yoshiki Kubota, Hiroshi Kitagawa, Kohei Kusada\",\"doi\":\"10.1002/chem.202503458\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Alloying is effective for enhancing the hydrogen evolution reaction (HER) activity of Pt. Binary PdPt alloys outperform monometallic Pt in terms of HER activity. However, their HER activity can be improved further by incorporating a third element. In this study, we demonstrate that incorporating Au into PdPt alloys alters their electronic structures, enhancing their HER activity. Homogeneous solid-solution Au<sub>20</sub>Pd<sub>40</sub>Pt<sub>40</sub> alloy nanoparticles (NPs) were synthesized using a one-pot polyol method. Elemental mapping using scanning transmission electron microscopy (STEM) combined with energy-dispersive X-ray spectroscopy confirmed the uniform distribution of the three elements within the NPs, demonstrating the formation of a solid-solution alloy. X-ray absorption near-edge structure analysis indicated electron transfer from Au to Pt and Pd, which generated a more reduced electronic state of Pt compared to that in the Pd<sub>50</sub>Pt<sub>50</sub> alloy NPs. Electrochemical measurements in 0.5 M H<sub>2</sub>SO<sub>4</sub> revealed that Au<sub>20</sub>Pd<sub>40</sub>Pt<sub>40</sub> alloy NPs had a lower overpotential (15.4 mV at 10 mA cm<sup>-2</sup>) and a higher intrinsic turnover frequency (TOF) than Pd<sub>50</sub>Pt<sub>50</sub> alloy and monometallic Pt NPs. These findings demonstrate that homogeneously mixing a third element into binary alloy NPs is effective for enhancing the catalytic performance.</p>\",\"PeriodicalId\":144,\"journal\":{\"name\":\"Chemistry - A European Journal\",\"volume\":\" \",\"pages\":\"e03458\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2026-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - A European Journal\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1002/chem.202503458\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry - A European Journal","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1002/chem.202503458","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
摘要
合金化能有效提高Pt的析氢反应活性,二元ppt合金的析氢反应活性优于单金属Pt。然而,通过加入第三个元素,它们的HER活性可以进一步提高。在这项研究中,我们证明了在ppt合金中加入Au改变了它们的电子结构,提高了它们的HER活性。采用一锅多元醇法制备了Au20Pd40Pt40合金均相固溶体纳米颗粒。利用扫描透射电子显微镜(STEM)和能量色散x射线能谱相结合的元素映射证实了NPs中三种元素的均匀分布,证明了固溶合金的形成。x射线吸收近边结构分析表明,电子从Au转移到Pt和Pd,产生了比Pd50Pt50合金NPs中更还原的Pt电子态。在0.5 M H2SO4中的电化学测试表明,与Pd50Pt50合金和单金属Pt NPs相比,Au20Pd40Pt40合金NPs具有更低的过电位(10 mA cm-2时15.4 mV)和更高的固有周转率(TOF)。这些结果表明,在二元合金NPs中均匀混合第三种元素可以有效地提高催化性能。
AuPdPt Ternary Alloy Nanoparticles for Highly Active Hydrogen Evolution Reaction.
Alloying is effective for enhancing the hydrogen evolution reaction (HER) activity of Pt. Binary PdPt alloys outperform monometallic Pt in terms of HER activity. However, their HER activity can be improved further by incorporating a third element. In this study, we demonstrate that incorporating Au into PdPt alloys alters their electronic structures, enhancing their HER activity. Homogeneous solid-solution Au20Pd40Pt40 alloy nanoparticles (NPs) were synthesized using a one-pot polyol method. Elemental mapping using scanning transmission electron microscopy (STEM) combined with energy-dispersive X-ray spectroscopy confirmed the uniform distribution of the three elements within the NPs, demonstrating the formation of a solid-solution alloy. X-ray absorption near-edge structure analysis indicated electron transfer from Au to Pt and Pd, which generated a more reduced electronic state of Pt compared to that in the Pd50Pt50 alloy NPs. Electrochemical measurements in 0.5 M H2SO4 revealed that Au20Pd40Pt40 alloy NPs had a lower overpotential (15.4 mV at 10 mA cm-2) and a higher intrinsic turnover frequency (TOF) than Pd50Pt50 alloy and monometallic Pt NPs. These findings demonstrate that homogeneously mixing a third element into binary alloy NPs is effective for enhancing the catalytic performance.
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