Effectively Synchronizing 4D-STEM Detectors with Probe Movement

  • Bammes B
  • Zhang C
  • Bilhorn R
  • et al.
N/ACitations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Abstract

Use of a pixelated detector in scanning transmission electron microscopy (STEM) enables 4D-STEM, which is the simultaneous acquisition of both the dark-field (DF) and bright-field (BF) diffraction patterns at every STEM probe position on the specimen. By detecting the scattering angle of nearly all the primary electrons that interact with the specimen, this technique promises to provide much more information about the specimen than conventional STEM using only conventional integrating detectors [1]. One experimental challenge to using pixelated STEM detectors is their dramatically limited speed compared to conventional BF, annular dark-field (ADF), and high-angle annular dark-field (HAADF) detectors. Since the pixelated detector must record an image at each STEM probe position on the specimen, the relatively slow speed of these detectors severely limits the specimen field-of-view and resolution that can be captured in a reasonable amount of time and without deleterious effects of specimen or beam instability over long acquisition times. Newer complementary metal-oxide semiconductor (CMOS) based detectors promise the higher frame rates (together with single-electron sensitivity) that are necessary for practical 4D-STEM data collection. However, optimizing 4D-STEM data quality requires that the detector's frame rate be carefully synchronized with the movement of the STEM probe across the specimen, so that each frame from the detector records the diffraction from one and only one STEM probe position on the specimen. One potential obstacle to achieving synchronization is the common use by CMOS sensors of a rolling shutter [2]. In rolling shutter mode, each row from the sensor is read out sequentially from top to bottom throughout each acquisition. For simple CMOS pixel designs, this pipelined readout enables high-speed data acquisition. However, with rolling shutter readout, the timestamp of each row varies across each frame, ultimately making it impossible to synchronize the readout of the entire sensor (all rows) with any single external event. Most CCD cameras, in contrast, utilize a global shutter in which every pixel in an image corresponds to the same timestamp. To evaluate the influence of shutter mode on the synchronization between the camera frame rate and the STEM probe movement, we performed a simple experiment where the scan generator moved STEM probe alternately between an empty specimen area and a copper grid bar. The camera's trigger delay was adjusted to maximize the difference in the average intensity of the bright-field disk for frames when the STEM probe was over an empty specimen area (where the intensity should be maximized) and when the STEM probe was over the copper grid bar (where the intensity should be minimized). We repeated experiment for a DE-16 camera operated in rolling shutter mode and in global shutter mode. Figure 1 shows that rolling shutter acquisition mixes information from the two probe positions in every acquisition and that global shutter acquisition does not. In rolling shutter, the intensity difference between bright and dark frames is lower, and there is intensity gradient across the bright-field disk (Fig. 1a, top). These artifacts were always visible in rolling shutter data, regardless of the camera's trigger delay setting. 68

Cite

CITATION STYLE

APA

Bammes, B., Zhang, C., Bilhorn, R., & Voyles, P. M. (2019). Effectively Synchronizing 4D-STEM Detectors with Probe Movement. Microscopy and Microanalysis, 25(S2), 68–69. https://doi.org/10.1017/s1431927619001077

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free