Lobastov Vladimir A, Srinivasan Ramesh, Zewail Ahmed H
Laboratory for Molecular Sciences, Arthur Amos Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena, CA 91125, USA.
Proc Natl Acad Sci U S A. 2005 May 17;102(20):7069-73. doi: 10.1073/pnas.0502607102. Epub 2005 May 9.
Electron microscopy is arguably the most powerful tool for spatial imaging of structures. As such, 2D and 3D microscopies provide static structures with subnanometer and increasingly with angstrom-scale spatial resolution. Here we report the development of 4D ultrafast electron microscopy, whose capability imparts another dimension to imaging in general and to dynamics in particular. We demonstrate its versatility by recording images and diffraction patterns of crystalline and amorphous materials and images of biological cells. The electron packets, which were generated with femtosecond laser pulses, have a de Broglie wavelength of 0.0335 angstroms at 120 keV and have as low as one electron per pulse. With such few particles, doses of few electrons per square ångstrom, and ultrafast temporal duration, the long sought after but hitherto unrealized quest for ultrafast electron microscopy has been realized. Ultrafast electron microscopy should have an impact on all areas of microscopy, including biological imaging.
电子显微镜可以说是用于结构空间成像的最强大工具。因此,二维和三维显微镜能提供具有亚纳米甚至越来越高至埃级空间分辨率的静态结构。在此,我们报告了四维超快电子显微镜的发展,其功能为一般成像,尤其是动力学成像赋予了另一个维度。我们通过记录晶体和非晶材料的图像与衍射图案以及生物细胞的图像来展示其多功能性。由飞秒激光脉冲产生的电子包在120千电子伏特时具有0.0335埃的德布罗意波长,且每个脉冲低至一个电子。由于粒子数量如此之少、每平方埃仅有少量电子的剂量以及超快的持续时间,对超快电子显微镜长期以来梦寐以求但迄今未实现的追求得以实现。超快电子显微镜应会对包括生物成像在内的所有显微镜领域产生影响。