Abstract

Time-resolved diffraction with femtosecond electron pulses has become a promising technique to directly provide insights into photo induced primary dynamics at the atomic level in molecules and solids. Ultrashort pulse duration as well as extensive spatial coherence are desired, however, space charge effects complicate the bunching of multiple electrons in a single pulse. We experimentally investigate the interplay between spatial and temporal aspects of resolution limits in ultrafast electron diffraction (UED) on our highly compact transmission electron diffractometer. To that end, the initial source size and charge density of electron bunches are systematically manipulated and the resulting bunch properties at the sample position are fully characterized in terms of lateral coherence, temporal width and diffracted intensity. We obtain a so far not reported measured overall temporal resolution of 130 fs (full width at half maximum) corresponding to 60 fs (root mean square) and transversal coherence lengths up to 20 nm. Instrumental impacts on the effective signal yield in diffraction and electron pulse brightness are discussed as well. The performance of our compact UED setup at selected electron pulse conditions is finally demonstrated in a time-resolved study of lattice heating in multilayer graphene after optical excitation.

Highlights

  • The initial steps in chemical reactions or condensed matter transformations are fundamentally characterized by subnanometer atomic motions on a femto- to picosecond timescale [1, 2]

  • We have investigated the transverse coherence length, electron pulse duration, elastic scattered peak intensity and instrumental peak brightness in dependence of the electron pulse charge density

  • The electron pulse emission is below the space charge limited regime and the virtual cathode effect has not been taking into account [59, 60]

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Summary

24 April 2015

Time-resolved diffraction with femtosecond electron pulses has become a promising technique to licence. Ultrashort pulse duration as well as extensive spatial coherence are desired, space attribution to the charge effects complicate the bunching of multiple electrons in a single pulse. We experimentally author(s) and the title of the work, journal citation investigate the interplay between spatial and temporal aspects of resolution limits in ultrafast electron and DOI. The initial source size and charge density of electron bunches are systematically manipulated and the resulting bunch properties at the sample position are fully characterized in terms of lateral coherence, temporal width and diffracted intensity. The performance of our compact UED setup at selected electron pulse conditions is demonstrated in a time-resolved study of lattice heating in multilayer graphene after optical excitation

Introduction
Experimental details
Results and discussion
Summary and conclusions

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