Mingda Liu, Zhichao Zhang, Chenyu Li, Sen Jin, Kunlei Zhu, Shoushan Fan, Jia Li, Kai Liu
{"title":"High-entropy alloyed single-atom Pt for methanol oxidation electrocatalysis","authors":"Mingda Liu, Zhichao Zhang, Chenyu Li, Sen Jin, Kunlei Zhu, Shoushan Fan, Jia Li, Kai Liu","doi":"10.1038/s41467-025-61376-y","DOIUrl":null,"url":null,"abstract":"<p>The methanol oxidation reaction is the bottleneck for direct methanol fuel cells. Unfortunately, the state-of-the-art Pt-based catalysts suffer heavily from the CO poisoning problem. Isolating Pt atoms in a material can avoid CO poisoning. However, single-atom Pt catalysts alone are inert towards methanol oxidation reaction. Here, we report high-entropy alloyed single-atom Pt catalysts, in which single-atom Pt sites are alloyed with non-noble elements in a high-entropy structure. This catalyst not only possesses active Pt sites but also inherits the ability of single-atom Pt to resist CO poisoning. Consequently, the catalyst shows a notable mass activity of 35.3 A mg<sup>−1</sup> at only 2.3 at% Pt and maintains high activity even after operation for 180,000 s. Both experimental and theoretical results reveal that the high-entropy structure induces a synergistic effect, wherein the elements coordinated around single-atom Pt sites effectively remove adsorbed CO from Pt. This mechanism facilitates the key reaction steps of methanol oxidation reaction and avoids CO poisoning. This work presents a high-entropy alloyed single-atom strategy to realize efficient and durable methanol oxidation reaction catalysis with low costs.</p>","PeriodicalId":19066,"journal":{"name":"Nature Communications","volume":"43 1","pages":""},"PeriodicalIF":14.7000,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Nature Communications","FirstCategoryId":"103","ListUrlMain":"https://doi.org/10.1038/s41467-025-61376-y","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
The methanol oxidation reaction is the bottleneck for direct methanol fuel cells. Unfortunately, the state-of-the-art Pt-based catalysts suffer heavily from the CO poisoning problem. Isolating Pt atoms in a material can avoid CO poisoning. However, single-atom Pt catalysts alone are inert towards methanol oxidation reaction. Here, we report high-entropy alloyed single-atom Pt catalysts, in which single-atom Pt sites are alloyed with non-noble elements in a high-entropy structure. This catalyst not only possesses active Pt sites but also inherits the ability of single-atom Pt to resist CO poisoning. Consequently, the catalyst shows a notable mass activity of 35.3 A mg−1 at only 2.3 at% Pt and maintains high activity even after operation for 180,000 s. Both experimental and theoretical results reveal that the high-entropy structure induces a synergistic effect, wherein the elements coordinated around single-atom Pt sites effectively remove adsorbed CO from Pt. This mechanism facilitates the key reaction steps of methanol oxidation reaction and avoids CO poisoning. This work presents a high-entropy alloyed single-atom strategy to realize efficient and durable methanol oxidation reaction catalysis with low costs.
甲醇氧化反应是直接甲醇燃料电池的瓶颈。不幸的是,最先进的基于pt的催化剂受到CO中毒问题的严重影响。隔离材料中的铂原子可以避免CO中毒。然而,单原子Pt催化剂本身对甲醇氧化反应是惰性的。在这里,我们报道了高熵合金单原子Pt催化剂,其中单原子Pt位点以高熵结构与非贵金属元素合金。该催化剂不仅具有活性Pt位点,而且继承了单原子Pt抗CO中毒的能力。结果表明,在% Pt条件下,该催化剂的质量活性为35.3 a mg−1,且在运行180,000 s后仍保持较高的活性。实验和理论结果均表明,高熵结构诱导了协同效应,在单原子Pt位周围配位的元素可以有效地去除Pt上吸附的CO,这一机制促进了甲醇氧化反应的关键反应步骤,避免了CO中毒。本文提出了一种高熵合金单原子策略,以低成本实现高效、持久的甲醇氧化反应催化。
期刊介绍:
Nature Communications, an open-access journal, publishes high-quality research spanning all areas of the natural sciences. Papers featured in the journal showcase significant advances relevant to specialists in each respective field. With a 2-year impact factor of 16.6 (2022) and a median time of 8 days from submission to the first editorial decision, Nature Communications is committed to rapid dissemination of research findings. As a multidisciplinary journal, it welcomes contributions from biological, health, physical, chemical, Earth, social, mathematical, applied, and engineering sciences, aiming to highlight important breakthroughs within each domain.