{"title":"W(110)上超薄铀膜的外延生长机理及电子性能","authors":"Xiangfei Yang , Jian Wu , Ying Jiang , Qin Liu, Qiuyun Chen, Qiang Zhang, Yun Zhang, Xiaobo Fan, Xiegang Zhu, Shiyong Tan, Qunqing Hao, Wei Feng, Xinchun Lai","doi":"10.1016/j.apsusc.2025.163030","DOIUrl":null,"url":null,"abstract":"<div><div>Epitaxial growth of uranium films is essential for exploring the exotic properties of U 5f electrons. However, the growth mechanism during the initial stages of U film formation remains unclear. In this study, the adsorption behavior of uranium (U) atoms on a tungsten (W)(110) substrate was investigated using scanning tunneling microscopy (STM) and first-principles calculations. It was found that an isolated U atom is more stable on the hollow site of the W(110) surface compared to the top and bridge sites. Additionally, two U atoms tend to adsorb on neighboring edge-sharing rhomboid hollow sites of W(110). As the concentration of U atoms increases, a directional two-dimensional (2D) growth trend along two high-symmetry directions of 0° and approximately 105° is observed. When the film thickness reaches 4 monolayers (ML), the close-packed U atoms exhibit a pseudo-hexagonal arrangement, accompanied by an enhanced tunneling signal near the Fermi level. Furthermore, thickness-dependent <em>dI/dV</em> spectra were obtained, showing strong consistency with the calculated results. These findings provide a clearer understanding of the initial growth mechanism of ultra-thin U films on the W(110) surface and open new scientific avenues for exploring the remarkable properties of uranium.</div></div>","PeriodicalId":247,"journal":{"name":"Applied Surface Science","volume":"697 ","pages":"Article 163030"},"PeriodicalIF":6.9000,"publicationDate":"2025-03-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Epitaxial growth mechanism and electronic properties of ultra-thin uranium films on W(110)\",\"authors\":\"Xiangfei Yang , Jian Wu , Ying Jiang , Qin Liu, Qiuyun Chen, Qiang Zhang, Yun Zhang, Xiaobo Fan, Xiegang Zhu, Shiyong Tan, Qunqing Hao, Wei Feng, Xinchun Lai\",\"doi\":\"10.1016/j.apsusc.2025.163030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Epitaxial growth of uranium films is essential for exploring the exotic properties of U 5f electrons. However, the growth mechanism during the initial stages of U film formation remains unclear. In this study, the adsorption behavior of uranium (U) atoms on a tungsten (W)(110) substrate was investigated using scanning tunneling microscopy (STM) and first-principles calculations. It was found that an isolated U atom is more stable on the hollow site of the W(110) surface compared to the top and bridge sites. Additionally, two U atoms tend to adsorb on neighboring edge-sharing rhomboid hollow sites of W(110). As the concentration of U atoms increases, a directional two-dimensional (2D) growth trend along two high-symmetry directions of 0° and approximately 105° is observed. When the film thickness reaches 4 monolayers (ML), the close-packed U atoms exhibit a pseudo-hexagonal arrangement, accompanied by an enhanced tunneling signal near the Fermi level. Furthermore, thickness-dependent <em>dI/dV</em> spectra were obtained, showing strong consistency with the calculated results. These findings provide a clearer understanding of the initial growth mechanism of ultra-thin U films on the W(110) surface and open new scientific avenues for exploring the remarkable properties of uranium.</div></div>\",\"PeriodicalId\":247,\"journal\":{\"name\":\"Applied Surface Science\",\"volume\":\"697 \",\"pages\":\"Article 163030\"},\"PeriodicalIF\":6.9000,\"publicationDate\":\"2025-03-22\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied Surface Science\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0169433225007445\",\"RegionNum\":2,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied Surface Science","FirstCategoryId":"88","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0169433225007445","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Epitaxial growth mechanism and electronic properties of ultra-thin uranium films on W(110)
Epitaxial growth of uranium films is essential for exploring the exotic properties of U 5f electrons. However, the growth mechanism during the initial stages of U film formation remains unclear. In this study, the adsorption behavior of uranium (U) atoms on a tungsten (W)(110) substrate was investigated using scanning tunneling microscopy (STM) and first-principles calculations. It was found that an isolated U atom is more stable on the hollow site of the W(110) surface compared to the top and bridge sites. Additionally, two U atoms tend to adsorb on neighboring edge-sharing rhomboid hollow sites of W(110). As the concentration of U atoms increases, a directional two-dimensional (2D) growth trend along two high-symmetry directions of 0° and approximately 105° is observed. When the film thickness reaches 4 monolayers (ML), the close-packed U atoms exhibit a pseudo-hexagonal arrangement, accompanied by an enhanced tunneling signal near the Fermi level. Furthermore, thickness-dependent dI/dV spectra were obtained, showing strong consistency with the calculated results. These findings provide a clearer understanding of the initial growth mechanism of ultra-thin U films on the W(110) surface and open new scientific avenues for exploring the remarkable properties of uranium.
期刊介绍:
Applied Surface Science covers topics contributing to a better understanding of surfaces, interfaces, nanostructures and their applications. The journal is concerned with scientific research on the atomic and molecular level of material properties determined with specific surface analytical techniques and/or computational methods, as well as the processing of such structures.