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Mapping Atomic Motions with Ultrabright Electrons: Fundamental Space-Time Limits to Imaging Chemistry and Biology
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主讲人: Prof. Dr. Dwayne Miller, University of Toronto, Canada
地点: 物理楼 中215 Rm.215, Physics Bldg.,Zoom链接: 880 5364 1017 Passcode: 2021
时间: 2021/11/25 (星期四 Thursday) 8:30-9:30 (Beijing Time)
主持 联系人: 李铮 (Email: zheng.li@pku.edu.cn)
主讲人简介: R. J. Dwayne Miller 教授是加拿大多伦多大学学院教授(University Professor),2010年-2019年任德国马克斯普朗克物质结构与动力学研究所所长(Max Planck Director),在超快光物理和分子物理领域享有盛誉。Miller教授是超快电子衍射技术的开创者之一,曾获得欧洲物理学会激光科学奖,皇家化学会百年纪念奖(Centenary Prize),皇家化学会卢瑟福奖章(Rutherford Medal),在超快分子动力学领域发表论文300余篇,其中包括Nature和Science正刊10篇。

One of the long sought objectives in science has been to watch atomic motions on the primary timescales governing structural transitions. From a chemistry perspective, this capability would give a direct observation of reaction forces and probe the central unifying concept of transition states that links chemistry to biology. To achieve this objective, there are not only extraordinary requirements for simultaneous spatial-temporal resolution but equally important, due to sample limitations, also one on source brightness. With the development of ultrabright electrons capable of literally lighting up atomic motions, this experiment has been realized (Siwicket al Science 2003) and efforts accelerated with the onset of XFELs (Miller, Science 2014). A number of different chemical reactions will be discussed from electrocyclization with conserved stereochemistry, intermolecular electron transfer for organic systems, metal to metal electron transfer, to the direct observation of a bimolecular collision and bond formation in condensed phase for the classic I3- system, in a process analogous to a molecular Newton’s cradle. These studies have discovered that these high dimensional problems, order 3N (N number of atoms in the reaction volume) representing the number of degrees of freedom in the system, distilled down to atomic projections along a few principle reaction coordinates. The specific details depend on the spatial resolution to these motions, for which <.01 Å changes in atomic position (less than the background thermal motion) has now been achieved on the 100 fs timescale. Without any detailed analysis, the key large-amplitude modes can be identified by eye from the molecular movies. This reduction in dimensionality appears to be general, arising from the very strong anharmonicity of the many body potential in the barrier crossing region. We now are beginning to see the underlying physics for the generalized reaction mechanisms that have been empirically discovered over time. The “magic of chemistry” is this enormous reduction in dimensionality in the barrier crossing region that ultimately makes chemical concepts transferrable. How far can this reductionist view be extended with respect to complexity? The spatial-temporal correlationsdiscoverdin this work provide new insight into how chemistry scaled up to biological systems – led to living systems. New challenges in making connection will be discussed in the context of the prospect of imaging single molecule trajectories. As a final challenge, the possibility of quantum tomography to go beyond the classical picture of structural dynamics to retrieve nuclear probability distributions will be discussed.