4.8 Article

Visualizing the non-equilibrium dynamics of photoinduced intramolecular electron transfer with femtosecond X-ray pulses

期刊

NATURE COMMUNICATIONS
卷 6, 期 -, 页码 -

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/ncomms7359

关键词

-

资金

  1. X-ray Free-Electron Laser Priority Strategy Program of MEXT,Japan
  2. Swedish Research Council
  3. Knut and Alice Wallenberg Foundation
  4. Crafoord Foundation
  5. Swedish Energy Administration
  6. Science Faculty at Lund University (MAXIV)
  7. Science Faculty at Lund University (ESS initiative grant)
  8. Danish National Research Foundation Center for Molecular Movies
  9. DANSCATT
  10. Carlsberg Foundation
  11. Lundbeck Foundation
  12. European Research Council [ERC-AdvGVISCHEM-226136, ERC-StG-259709]
  13. European XFEL
  14. German Research Foundation (DFG) [SFB925]
  15. Centre of Ultrafast Imaging (CUI)
  16. Hungarian Academy of Sciences via the Lendulet (Momentum) Program
  17. Bolyai Fellowship
  18. US Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]
  19. Grants-in-Aid for Scientific Research [26102014] Funding Source: KAKEN

向作者/读者索取更多资源

Ultrafast photoinduced electron transfer preceding energy equilibration still poses many experimental and conceptual challenges to the optimization of photoconversion since an atomic-scale description has so far been beyond reach. Here we combine femtosecond transient optical absorption spectroscopy with ultrafast X-ray emission spectroscopy and diffuse X-ray scattering at the SACLA facility to track the non-equilibrated electronic and structural dynamics within a bimetallic donor-acceptor complex that contains an optically dark centre. Exploiting the 100-fold increase in temporal resolution as compared with storage ring facilities, these measurements constitute the first X-ray-based visualization of a non-equilibrated intramolecular electron transfer process over large interatomic distances. Experimental and theoretical results establish that mediation through electronically excited molecular states is a key mechanistic feature. The present study demonstrates the extensive potential of femtosecond X-ray techniques as diagnostics of non-adiabatic electron transfer processes in synthetic and biological systems, and some directions for future studies, are outlined.

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