Chemical Bond Activation Observed with an X-ray Laser

被引:24
作者
Beye, Martin [1 ,2 ,3 ]
Oberg, Henrik [4 ]
Xin, Hongliang [5 ]
Dakovski, Georgi L. [6 ]
Dell'Angela, Martina [7 ,8 ]
Foehlisch, Alexander [1 ,9 ]
Gladh, Jorgen [4 ]
Hantschmann, Markus [1 ]
Hieke, Florian [7 ,8 ]
Kaya, Sarp [5 ]
Kuehn, Danilo [1 ]
LaRue, Jerry [5 ,10 ]
Mercurio, Giuseppe [7 ,8 ]
Minitti, Michael P. [6 ]
Mitra, Ankush [4 ,6 ]
Moeller, Stefan P. [6 ]
Ng, May Ling [5 ]
Nilsson, Anders [2 ,5 ]
Nordlund, Dennis [2 ]
Norskov, Jens [5 ]
Ostrom, Henrik [4 ]
Ogasawara, Hirohito [2 ]
Persson, Mats [11 ,12 ]
Schlotter, William F. [6 ]
Sellberg, Jonas A. [2 ,4 ,13 ]
Wolf, Martin [14 ]
Abild-Pedersen, Frank [5 ]
Pettersson, Lars G. M. [4 ]
Wurth, Wilfried [3 ,7 ,8 ]
机构
[1] Helmholtz Zentrum Berlin Mat & Energie GmbH, Inst Methods & Instrumentat Synchrotron Radiat Re, D-12489 Berlin, Germany
[2] SLAC Natl Accelerator Lab, SSRL, Menlo Pk, CA 94025 USA
[3] DESY Photon Sci, D-22607 Hamburg, Germany
[4] Stockholm Univ, Dept Phys, S-10691 Stockholm, Sweden
[5] SLAC Natl Accelerator Lab, SUNCAT, Menlo Pk, CA 94025 USA
[6] SLAC Natl Accelerator Lab, LCLS, Menlo Pk, CA 94025 USA
[7] Univ Hamburg, Phys Dept, D-22761 Hamburg, Germany
[8] Ctr Free Electron Laser Sci, D-22761 Hamburg, Germany
[9] Univ Potsdam, Inst Phys & Astron, D-14476 Potsdam, Germany
[10] Chapman Univ, Orange, CA 92866 USA
[11] Univ Liverpool, Surface Sci Res Ctr, Liverpool L69 3BX, Merseyside, England
[12] Univ Liverpool, Dept Chem, Liverpool L69 3BX, Merseyside, England
[13] KTH Royal Inst Technol, Dept Appl Phys, S-10691 Stockholm, Sweden
[14] Fritz Haber Inst Max Planck Gesell, D-14195 Berlin, Germany
来源
JOURNAL OF PHYSICAL CHEMISTRY LETTERS | 2016年 / 7卷 / 18期
基金
瑞典研究理事会;
关键词
DENSITY-FUNCTIONAL THEORY; CATALYTIC CO OXIDATION; EMISSION-SPECTROSCOPY; SURFACE ADSORBATES; DYNAMICS; DESORPTION; MOLECULES; SPECTRA;
D O I
10.1021/acs.jpclett.6b01543
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The concept of bonding and antibonding orbitals is fundamental in chemistry. The population of those orbitals and the energetic difference between the two reflect the strength of the bonding interaction. Weakening the bond is expected to reduce this energetic splitting, but the transient character of bond-activation has so far prohibited direct experimental access. Here we apply time-resolved soft X-ray spectroscopy at a free electron laser to directly observe the decreased bonding antibonding splitting following bond-activation using an ultrashort optical laser pulse.
引用
收藏
页码:3647 / 3651
页数:5
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