4.8 Article

Band structure evolution during the ultrafast ferromagnetic-paramagnetic phase transition in cobalt

期刊

SCIENCE ADVANCES
卷 3, 期 3, 页码 -

出版社

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/sciadv.1602094

关键词

-

资金

  1. Deutsche Forschungsgemeinschaft (DFG) [SFB 1073, B07]
  2. International Center for Advanced Studies of Energy Conversion (ICASEC)
  3. DFG [SCHN 353/17-1, AE 19/20-1, SFB/TRR 173]
  4. U.S. Department of Energy Office of Basic Energy Sciences X-Ray Scattering Program [DE-SC0002002]
  5. Gordon and Betty Moore Foundation EPiQS [GBMF4538]
  6. Graduate School of Excellence MAINZ (Excellence Initiative) [DFG/GSC 266]
  7. U.S. Department of Energy (DOE) [DE-SC0002002] Funding Source: U.S. Department of Energy (DOE)

向作者/读者索取更多资源

The evolution of the electronic band structure of the simple ferromagnets Fe, Co, and Ni during their well-known ferromagnetic-paramagnetic phase transition has been under debate for decades, with no clear and even contradicting experimental observations so far. Using time- and spin-resolved photoelectron spectroscopy, we can make a movie on how the electronic properties change in real time after excitation with an ultrashort laser pulse. This allows us to monitor large transient changes in the spin-resolved electronic band structure of cobalt for the first time. We show that the loss of magnetization is not only found around the Fermi level, where the states are affected by the laser excitation, but also reaches much deeper into the electronic bands. We find that the ferromagnetic-paramagnetic phase transition cannot be explained by a loss of the exchange splitting of the spin-polarized bands but instead shows rapid band mirroring after the excitation, which is a clear signature of extremely efficient ultrafast magnon generation. Our result helps to understand band structure formation in these seemingly simple ferromagnetic systems and gives first clear evidence of the transient processes relevant to femtosecond demagnetization.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据