2023Unpublished venueRequires access

High frame rate, phase and amplitude resolved imaging of single events using beam-sampling single-shot ptychography

Jonathan Barolak, David Goldberger, Claudia Schrama, Charles G. Durfee, Daniel E. Adams

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Abstract

High frame rate (HFR) phase-and-amplitude contrast imaging is imperative for a better understanding of the underlying physics in dynamically evolving phenomena. Here we present, to our knowledge, the first experimental HFR ptychographic reconstructions using a novel Time-Resolved Imaging via Multiplexed Ptychography (TIMP) system. Our TIMP system is composed of a time-encoding device, which creates a train of temporally separated pulses of different phase profiles, and a novel beam-sampling single-shot ptychography microscope. HFR imaging is achieved by reconstructing the complex object from each pulse independently and time ordering the reconstructed objects based on the phase structure of the reconstructed probes.

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What this paper is about

High frame rate (HFR) phase-and-amplitude contrast imaging is imperative for a better understanding of the underlying physics in dynamically evolving phenomena. Here we present, to our knowledge, the first experimental HFR ptychographic reconstructions using a novel Time-Resolved Imaging via Multiplexed Ptychography (TIMP) system. Our TIMP system is composed of a time-encoding device, which creates a train of temporally separated pulses of different phase profiles, and a novel beam-sampling single-shot ptychography microscope. HFR imaging is achieved by reconstructing the complex object from each pulse independently and time ordering the reconstructed objects based on the phase structure of the reconstructed probes.

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Available abstract

High frame rate (HFR) phase-and-amplitude contrast imaging is imperative for a better understanding of the underlying physics in dynamically evolving phenomena. Here we present, to our knowledge, the first experimental HFR ptychographic reconstructions using a novel Time-Resolved Imaging via Multiplexed Ptychography (TIMP) system. Our TIMP system is composed of a time-encoding device, which creates a train of temporally separated pulses of different phase profiles, and a novel beam-sampling single-shot ptychography microscope. HFR imaging is achieved by reconstructing the complex object from each pulse independently and time ordering the reconstructed objects based on the phase structure of the reconstructed probes.

Key concepts: Ptychography, Optics, Phase-contrast imaging, Single shot, Phase (matter), Frame rate, Sampling (signal processing), Phase retrieval

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