Single-shot ultrafast optical imaging

Single-shot ultrafast optical imaging can capture two-dimensional transient scenes in the optical spectral range at ≥100 million frames per second. This rapidly evolving field surpasses conventional pump-probe methods by possessing real-time imaging capability, which is indispensable for recording nonrepeatable and difficult-to-reproduce events and for understanding physical, chemical, and biological mechanisms. In this mini-review, we survey state-of-the-art single-shot ultrafast optical imaging comprehensively. Based on the illumination requirement, we categorized the field into active-detection and passive-detection domains. Depending on the specific image acquisition and reconstruction strategies, these two categories are further divided into a total of six subcategories. Under each subcategory, we describe operating principles, present representative cutting-edge techniques, with a particular emphasis on their methodology and applications, and discuss their advantages and challenges. Finally, we envision prospects for technical advancement in this field

Single-shot ultrafast imaging attaining 70 trillion frames per second

Real-time imaging of countless femtosecond dynamics requires extreme speeds orders of magnitude beyond the limits of electronic sensors. Existing femtosecond imaging modalities either require event repetition or provide single-shot acquisition with no more than 10¹³ frames per second (fps) and 3 × 10² frames. Here, we report compressed ultrafast spectral photography (CUSP), which attains several new records in single-shot multi-dimensional imaging speeds. In active mode, CUSP achieves both 7 × 10¹³ fps and 10³ frames simultaneously by synergizing spectral encoding, pulse splitting, temporal shearing, and compressed sensing—enabling unprecedented quantitative imaging of rapid nonlinear light-matter interaction. In passive mode, CUSP provides four-dimensional (4D) spectral imaging at 0.5 × 10¹² fps, allowing the first single-shot spectrally resolved fluorescence lifetime imaging microscopy (SR-FLIM). As a real-time multi-dimensional imaging technology with the highest speeds and most frames, CUSP is envisioned to play instrumental roles in numerous pivotal scientific studies without the need for event repetition

Single-shot real-time femtosecond imaging of temporal focusing

While the concept of focusing usually applies to the spatial domain, it is equally applicable to the time domain. Real-time imaging of temporal focusing of single ultrashort laser pulses is of great significance in exploring the physics of the space–time duality and finding diverse applications. The drastic changes in the width and intensity of an ultrashort laser pulse during temporal focusing impose a requirement for femtosecond-level exposure to capture the instantaneous light patterns generated in this exquisite phenomenon. Thus far, established ultrafast imaging techniques either struggle to reach the desired exposure time or require repeatable measurements. We have developed single-shot 10-trillion-frame-per-second compressed ultrafast photography (T-CUP), which passively captures dynamic events with 100-fs frame intervals in a single camera exposure. The synergy between compressed sensing and the Radon transformation empowers T-CUP to significantly reduce the number of projections needed for reconstructing a high-quality three-dimensional spatiotemporal datacube. As the only currently available real-time, passive imaging modality with a femtosecond exposure time, T-CUP was used to record the first-ever movie of non-repeatable temporal focusing of a single ultrashort laser pulse in a dynamic scattering medium. T-CUP’s unprecedented ability to clearly reveal the complex evolution in the shape, intensity, and width of a temporally focused pulse in a single measurement paves the way for single-shot characterization of ultrashort pulses, experimental investigation of nonlinear light-matter interactions, and real-time wavefront engineering for deep-tissue light focusing

Single-shot stereo-polarimetric compressed ultrafast photography for light-speed observation of high-dimensional optical transients with picosecond resolution

Simultaneous and efficient ultrafast recording of multiple photon tags contributes to high-dimensional optical imaging and characterization in numerous fields. Existing high-dimensional optical imaging techniques that record space and polarization cannot detect the photon’s time of arrival owing to the limited speeds of the state-of-the-art electronic sensors. Here, we overcome this long-standing limitation by implementing stereo-polarimetric compressed ultrafast photography (SP-CUP) to record light-speed high-dimensional events in a single exposure. Synergizing compressed sensing and streak imaging with stereoscopy and polarimetry, SP-CUP enables video-recording of five photon tags (x, y, z: space; t: time of arrival; and ψ: angle of linear polarization) at 100 billion frames per second with a picosecond temporal resolution. We applied SP-CUP to the spatiotemporal characterization of linear polarization dynamics in early-stage plasma emission from laser-induced breakdown. This system also allowed three-dimensional ultrafast imaging of the linear polarization properties of a single ultrashort laser pulse propagating in a scattering medium

Amplitude-masked photoacoustic wavefront shaping and application in flowmetry

Optical-resolution photoacoustic flowmetry (PAF) allows noninvasive single-cell flow measurements. However, its operational depth is limited by optical diffusion, which prevents focusing beyond shallow depths in scattering media, as well as reducing the measurement signal-to-noise ratio (SNR). To overcome this limitation, we used binary-amplitude wavefront shaping to enhance light focusing in the presence of scattering. Here, the transmission modes that contributed constructively to the intensity at the optical focus were identified and selectively illuminated, resulting in a 14-fold intensity increase and a corresponding increase in SNR. This technique can potentially extend the operational depth of optical-resolution PAF beyond 1 mm in tissue