Physical Biology Center for Ultrafast Science and Technology, Arthur Amos Noyes Laboratory of Chemical Physics, California Institute of Technology, Pasadena, CA 91125, USA.
Science. 2012 Jan 6;335(6064):59-64. doi: 10.1126/science.1213504.
Single-particle imaging of structures has become a powerful methodology in nanoscience and molecular and cell biology. We report the development of subparticle imaging with space, time, and energy resolutions of nanometers, femtoseconds, and millielectron volts, respectively. By using scanning electron probes across optically excited nanoparticles and interfaces, we simultaneously constructed energy-time and space-time maps. Spectrum images were then obtained for the nanoscale dielectric fields, with the energy resolution set by the photon rather than the electron, as demonstrated here with two examples (silver nanoparticles and the metallic copper-vacuum interface). This development thus combines the high spatial resolution of electron microscopy with the high energy resolution of optical techniques and ultrafast temporal response, opening the door to various applications in elemental analysis as well as mapping of interfaces and plasmonics.
单颗粒成像已经成为纳米科学、分子和细胞生物学领域一种强大的方法。我们报告了亚颗粒成像的发展,其空间、时间和能量分辨率分别为纳米、飞秒和毫电子伏特。通过在光学激发的纳米颗粒和界面上使用扫描电子探针,我们同时构建了能量-时间和空间-时间图谱。然后,通过两个示例(银纳米颗粒和金属铜-真空界面),获得了纳米级介电场的光谱图像,其能量分辨率由光子而非电子确定。这样的发展结合了电子显微镜的高空间分辨率和光学技术的高能量分辨率以及超快的时间响应,为元素分析以及界面和等离子体学的映射等各种应用开辟了道路。