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# Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy

## Abstract

Nanosecond temporal resolution enables new methods for wide-field imaging like time-of-flight, gated detection, and fluorescence lifetime. The optical efficiency of existing approaches, however, presents challenges for low-light applications common to fluorescence microscopy and single-molecule imaging. We demonstrate the use of Pockels cells for wide-field image gating with nanosecond temporal resolution and high photon collection efficiency. Two temporal frames are obtained by combining a Pockels cell with a pair of polarizing beam-splitters. We show multi-label fluorescence lifetime imaging microscopy (FLIM), single-molecule lifetime spectroscopy, and fast single-frame FLIM at the camera frame rate with 103–105 times higher throughput than single photon counting. Finally, we demonstrate a space-to-time image multiplexer using a re-imaging optical cavity with a tilted mirror to extend the Pockels cell technique to multiple temporal frames. These methods enable nanosecond imaging with standard optical systems and sensors, opening a new temporal dimension for wide-field low-light microscopy.

## Introduction

Existing sensors for wide-field nanosecond imaging sacrifice performance to gain temporal resolution, failing to compete with scientific CMOS and electron-multiplying CCD sensors in low-signal applications. A variety of detectors currently access the nanosecond regime. Gated optical intensifiers (GOIs) based on microchannel plates (MCPs) allow for sub-nanosecond gating in a single image frame, and segmented GOIs can acquire multiple frames when combined with image splitting1. Gating into n frames in this way limits overall collection efficiency to <1/n, and performance is further limited by photocathode quantum efficiency, MCP pixel density, excess noise, and lateral electron drift1,2,3,4. Streak camera techniques have also been demonstrated for wide-field imaging, but they also require a photocathode conversion step and additional high-loss encoding5,6. Single-photon avalanche detector (SPAD) arrays are an emerging solid-state approach, but they are currently limited to sparse fill factors and high dark currents3,7,8.

The limitations of current nanosecond imaging techniques are particularly manifest in fluorescence lifetime imaging microscopy (FLIM). Fluorescence lifetime is a sensitive probe of local fluorophore environment and can be used to report factors like pH, polarity, ion concentration, Förster resonance energy transfer (FRET), and viscosity. As lifetime imaging is insensitive to excitation intensity noise, labeling density, and sample photobleaching, it is attractive for many applications. FLIM typically relies on confocal scanning combined with time-correlated single photon counting (TC-SPC) detectors9,10. The throughput of TC-SPC is limited by the detector’s maximum count rate (typically 1–100 MHz), and confocal microscopy relies on high excitation intensities that can cause non-linear photodamage to biological samples11,12. Frequency domain wide-field approaches are a promising alternative, but they currently require demodulation with either a GOI or high-noise modulated camera chip13,14,15. Given the disadvantages of existing wide-field and TC-SPC approaches, FLIM especially calls for the development of new, efficient imaging strategies to extend its utility for bio-imaging.

Here, we demonstrate ultrafast imaging techniques—compatible with standard cameras—that have no inherent loss or dead time, allowing access to sub-frame rate sample dynamics at timescales as fast as nanosecond fluorescent lifetimes. First, we show an all-photon wide-field imaging system based simply on polarizing beam-splitters (PBS) and a Pockels cell (PC). This can be used to create two temporal bins or to modulate images on any timescale—from nanoseconds to milliseconds. We use this to demonstrate efficient wide-field FLIM of a multi-labeled sample, single molecules, and a biological benchmark. Second, we demonstrate the use of a re-imaging optical cavity as a time-to-space converter to enable n-frame ultrafast imaging when combined with a Pockels cell gate.

## Results

### Gating with two temporal bins

Light from an imaging system is polarized with a beam-splitter, and the image associated with each polarization is aligned to propagate through different locations in a wide-aperture PC, as shown in Fig. 1. The PC provides an electric field-dependent retardance between the input light’s polarization components, mapping the temporal signature of the applied field onto the polarization state of the imaging beams16. A second PBS after the PC again splits the separated imaging beams, giving four image frames on the camera. The resulting images now encode temporal information, as shown in Fig. 1. To illustrate our method, we consider a step function voltage pulse applied at delay time td with respect to a short (~ns) excitation pulse. The step function with edge at td creates pairs of output images corresponding to integrated signal before and after td. All photons, both before and after the gate, may be collected in a single camera exposure.

In practice, we implement this configuration with either a Gaussian gating pulse at td or a step gate with few nanosecond rise time as described in the following examples. In fact, arbitrary V(t) may be applied to the PC for specific applications (see Discussion). Note that a gating pulse can be applied either as a single shot measurement or over repeated events integrated in one camera frame. Fluorescence lifetime may be recovered by either varying the gate delay td to directly measure the fluorescence decay (see multi-label FLIM below) or by single-frame ratios of gated and ungated channel intensities (see single-molecule FLIM below). In cases where the PC aperture is limited, two separate PC crystals may be used instead of using different areas of the same crystal. Separate gates can be applied to each PC to create four time bins.

### Imaging through Pockels cells

Standard PCs use thick (30–50 mm) potassium dideuterium phosphate (KD*P) crystals with longitudinal field. These give high extinction ratios and are ubiquitous for Q-switching and phase modulation applications. Off-axis rays experience different birefringent phase shifts than those on-axis, limiting the numerical aperture (NA) of the crystal for wide-field imaging. In an image plane, the PC half angular acceptance α limits the NA of collection optics to for small angles, where M is magnification. In a diffraction plane (or infinity corrected space), the field of view (FOV) is instead limited to 2tan(α)fobj where fobj is the imaging objective focal length. For example, a 10 μm FOV may be achieved with a 1.4 NA microscope objective (fobj = 1.8 mm) and 40 mm thick longitudinal KD*P PC crystal in the infinity space (α ~ 4 mrad). FOV can be further improved by magnifying the beam until the PC aperture becomes limiting. Conventional KD*P PCs are limited to long pulse repetition rates in the 10’s of kHz by piezoelectric resonances. We note that ultimate repetition rate depends on high voltage pulse shape and crystal dimensions. Electro-optic pulse pickers can operate to 100 kHz and even into MHz rates with low-piezo materials17,18,19,20. Further, periodic drive avoids exciting piezoelectric resonances and is compatible with frequency domain FLIM at high excitation rates.

To assess gating efficiency, the impact of off-axis birefringence was simulated using Mueller matrices21 to arrive at a conoscopic interference (isogyre) pattern, as viewed through crossed polarizers. Subtracting the transmitted intensity pattern I at zero voltage (V0) from that at the half-wave voltage (Vπ) gives the gating efficiency (Iπ − I0), where the useful NA of the PC is set by the region of high gating efficiency at lower angles (Fig. 1b). The PC is treated as a linear homogeneous retarder with off-axis retardance determined by a coordinate transformation of the crystal axes (Supplementary Note 1)22. Angular acceptance may be improved by making the crystal thinner, with a 3 mm crystal increasing α to ~20 mrad, effectively removing NA and FOV restrictions. Here we show results using a thick 40 mm commercial PC (Figs. 2 and 3) and a custom 3 mm KD*P PC (Fig. 4). Further, complete zero-field cancellation of off-axis birefringence may be obtained by combining the negative uniaxial (ne < no) KD*P crystal with a positive uniaxial (ne > no) static compensating crystal (e.g., MgF2 or YVO4)22,23. Such a crystal fully compensates for off-axis rays at V0 and further improves the NA at Vπ (KDP becomes biaxial with applied field, preventing full high voltage compensation). This strategy is especially promising for thin KD*P crystals. Supplementary Fig. 1 compares the effect of off-axis birefringence for thick, thin, and compensated KDP crystals.

### Multi-label FLIM

The two-bin method has no intrinsic gating loss and allows for imaging onto any sensor. Fluorescence lifetime imaging is thus an ideal demonstration for the technique, where the PC gating pulse is applied after delay td from the fluorescence excitation. Lifetime may then be determined by either varying the delay time td over multiple frames (as used here) or by taking the single-frame ratio of pre- and post-gate intensities (following section). In Fig. 2 we image a mixture of three labels having different lifetimes measured individually to be 3.1 ns (2 μm nile red Invitrogen beads), 4.9 ns (0.1 μm orange Invitrogen beads—background), and 2.3 ns (0.1 μm infrared Invitrogen beads—formed into crystals). For this data, the PC was located in the image plane, allowing for wide-field FLIM of bright samples at 0.1 NA and 20× magnification with 100 micron FOV. The sample is excited by laser pulses with duration 1 ns at 532 nm and 5 kHz repetition rate. The fluorescence signal results from the convolution of the decay function with the laser’s Gaussian excitation pulse with FWHM pulse width ~2.4σe. The commercial PC used in Fig. 2 applies a Gaussian gate function g(t − td) in our experiment with a pulse width of 2.6 ns. By sweeping the delay time td, the convolution of the fluorescence with the gating function is measured: f(t, τ, σe) $$\ast$$g(t − td). Temporal information such as fluorescence lifetime may be calculated by directly fitting the measured convolution. Note that the convolution of excitation and gating functions, in this case, gives a Gaussian instrument response function (IRF) with $$\sigma _{{\mathrm{IRF}}} = \sqrt {\sigma _{\mathrm{e}}^2 + \sigma _{\mathrm{g}}^2}$$, measured directly in Fig. 2a. The fitting approach samples the fluorescence decay at more time points and can be advantageous for brightly labeled samples compared to a two-bin measurement. This could be used to more effectively measure multi-exponential decays for instance.

### Wide-field FLIM of single molecules

For signal-limited applications relying on efficient photon collection or requiring fast acquisition rates, fluorescence lifetime is best determined by the ratio of gated and ungated intensity in a single frame. In Fig. 3, we demonstrate wide-field lifetime microscopy of Alexa Fluor 532 molecules on glass in a 10 × 10 μm region. The measured lifetimes are consistent with both the ensemble lifetime of 2.5 ns and the large molecular variation seen in similar studies on glass24,25. The PC is used in the infinity space of the microscope objective to apply the same Gaussian gating function at td = 1.6 ns and 15 kHz repetition rate. The ratio of the gated and ungated intensity is given by

$$R = \frac{{{\int} g (t - t_{\mathrm{d}})f(t,\tau ,\sigma _{\mathrm{e}})dt}}{{{\int} f (t,\tau ,\sigma _{\mathrm{e}})[1 - g(t - t_{\mathrm{d}})]dt}} = \left. {\frac{{g \ast f}}{{(1 - g) \ast f}}} \right|_{t = t_{\mathrm{d}}}.$$
(1)

To calculate lifetime, this ratio is experimentally determined by summing intensity in a region of interest around each molecule. This approach allows single-molecule lifetime spectroscopy while maintaining diffraction-limited resolution and efficient photon collection of ~7 × 103 photons per molecule (15 s exposure time). Figure 3c shows the estimated lifetime and total brightness for each numbered diffraction-limited emitter along with error-bars for the lifetime estimation. Estimation is limited by fluorescence background and dark current here. A low-cost industry CMOS machine vision camera (FLIR) is used for the detector. In this case, the angular acceptance of the PC limits the field of view to 10 μm but still allows photon collection at 1.4 NA. Bleaching dynamics are shown in Supplementary Figs. 4 and 5. Single-molecule lifetime spectroscopy in wide-field remains challenging with confocal approaches24,25,26, whereas here it is readily demonstrated with PC gating and an inexpensive, high-noise camera.

### Fast FLIM with a thin PC

By using a thin PC crystal, these techniques are extended to ultra-wide fields of view. A 3 mm thick KD*P Pockels cell with a 20 mm aperture gates nearly the entire output of a standard inverted microscope with an 0.8 NA objective. A 4.5 ns rising edge pulse (IRF in Supplementary Fig. 2) was used at 5 kHz repetition rate to image a standard FLIM benchmark in Fig. 4. Single frame and trace-fitting analysis demonstrate rapid acquisition of megapixel FLIM images with 300 μm square FOV. Single-frame exposures of 100 ms and 2 ms are demonstrated—the latter may be taken at the maximum camera frame rate. These acquisitions show dramatic throughput advantage for wide-field acquisition. The 100 ms frame in Fig. 4c is formed from single exposure detection of 4.8 × 108 photons by 0.8 megapixels. The inset in Fig. 4c likewise corresponds to a 2 ms exposure of the same frame at higher excitation intensity with 3.1 × 108 detected photons. The number of detected photons is inferred from the known responsivity of the camera. Compared to a 2 MHz TC-SPC photon counting rate (standard to avoid pile-up error), these acquisitions give a 2400× and 78,000× enhancement in photon throughput respectively. Such high throughput and potential for low exposure times will enable future FLIM studies on dynamic samples. The single-frame acquisition method is particularly powerful, as it prevents image motion artifacts (caused by multiple acquisition frames or scanning for example) and allows self-normalization within a single exposure to remove intensity noise. Quantitative lifetimes are easily calculated using the pre-calibrated IRF as described in the prior sections.

### Gated re-imaging cavities for multi-frame imaging

Nanosecond imaging with PCs can be extended beyond two temporal bins through the use of gated re-imaging optical cavities. Larger bin numbers enable increased estimation accuracy for multi-exponential decays, improve lifetime dynamic range, and also allow efficient single-shot ultrafast imaging. We exploit the round-trip optical delay of a re-imaging cavity27 combined with a tilted cavity mirror to provide nanosecond temporal resolution by spatially separating the cavity round trips. While imaging with n-frames using GOIs is limited to <1/n collection efficiency, this re-imaging cavity technique enables efficient photon collection for low-light or single-photon sensitive applications. In related work, cavities have been used for single-channel orbital angular momentum and wavelength to time conversion28,29. Aligned optical cavities have been used for time-folded optical imaging modalities like multi-pass microscopy30,31. Our implementation instead employs a re-imaging cavity as the means to obtain temporal resolution for wide-field imaging.

An image is in-coupled to a 4f cavity at the central focal plane by means of a small mirror M1 as shown in Fig. 5. The 4f configuration re-images the end mirrors (diffraction planes) every round trip. If one end mirror M2 is tilted by angle θ, the image position yi at the central focal plane after n round trips is displaced by yi = fsin(2), where f is the focal length of the 4f cavity. The angle θ is set such that the resulting images are not blocked by the in-coupling mirror. Each sequentially displaced image is delayed in turn by an additional round trip. To extract temporal information, the spatially separated images need to be either gated externally or simultaneously out-coupled from the cavity using a PC. In the externally gated scheme (schematically shown in Fig. 5a), light is passively out-coupled each round trip through a transmissive mirror. The spatially displaced images have a relative time delay Δt = 8fn/c based on their number of round trips n, and an external gate is simultaneously applied to all delayed images to create temporally distinct frames. A step function gate V(t) allows lifetime measurement from the ratios of the time-delayed bins, similar to the two-bin case described above. Using the two-bin PC scheme as the external gate gives four image frames from each round trip output (Fig. 5c). Photon efficiency, the ratio of detected photons to the number input to the cavity, with end-mirror reflectivity r is given by 1 − rn after n round trips, ignoring intracavity loss. This efficiency can be made very high for an appropriate choice of r. For example, 87% efficiency is obtained with r = 0.6 and n = 4. It should be noted that the intensity variation between the different frames is caused by partial transmission after n round trips.

Figure 5c, d demonstrates the output from an externally gated tilted mirror cavity. Here a Gaussian gate pulse of width less than the round trip time is used. Lifetime in Fig. 5d is calculated from the ratio R of two frames (Fig. 5b images (row i, column 4) and (row ii, column 4)) in the gated channel delayed by one cavity round trip time trt of 4 ns as $${R=(g^ \ast} f|_{t_d}) / ({g^\ast} f|_{{t_d}+{t_{rt}}} )$$. Alternatively, both gated and ungated frames could be included in the estimation to make use of all photons as in Eq. (1).

In a second gated cavity scheme (proposed in Supplementary Fig. 6), there is instead no transmissive mirror, and all input light is simultaneously out-coupled from the cavity with an intracavity Pockels cell and polarizing beamsplitter. Such a scheme directly gives n images with sequential exposures of trt = 8f/c and leaves no light in the cavity. Either a thin-crystal or compensated PC would be preferable for intracavity gating since the light passes through the PC each round trip. It is interesting to compare n-bin and two-bin lifetime methods in terms of their theoretical estimation accuracy (see Fig. 6). While the overall accuracies may be closely matched for monoexponentials, n-bin methods have the advantage of a wider temporal dynamic range.

These cavity imaging methods have the advantage of zero dead-time between frames and have no inherent limits on collection efficiency beyond intracavity loss. The externally gated cavity is straightforward to implement with thick-crystal PCs, but has the disadvantage of indirect temporal gating. Intracavity gating instead allows for true n-frame ultrafast imaging where each round trip corresponds to one temporally distinct image frame. Round trip times from 1 to 10 ns may be achieved with standard optics. We note that an alternative approach to n-bin imaging could similarly use multiple two-bin gates in series (Fig. 1) with the added complexity of multiple PCs and detectors.

### Theoretical estimation accuracy

Two-bin lifetime estimation can perform surprisingly well when compared to the Cramér-Rao bound for n-bin TC-SPC32. Both two-bin and n-bin estimation accuracy scale with photon counting shot noise. Figure 6 shows that n-bin measurements have a wider dynamic range of lifetime sensitivity, but that a two-bin PC gate can be nearly as accurate for monoexponential decays when tuned to the appropriate gate delay. TC-SPC gains a large number of temporal bins from the bit depth of the ADC, which dominantly affects the dynamic range. With ideal PC gating, estimation within a factor of two of the shot noise limit (SNL) may be obtained over a decade of lifetimes with peak sensitivity ~1.3× SNL. In fact, for a step function gate with 1 ns PC rise time, estimation within 2–3× SNL can be obtained between 1 and 10 ns.

## Discussion

We have presented methods for two and n-bin temporal imaging on nanosecond timescales using Pockels cells. Proof-of-concept experiments with single-molecule lifetime spectroscopy and wide-field FLIM demonstrate the potential to bring nanosecond resolution to signal-limited applications. Our approach is photon efficient and retains the sensitivity and image quality of scientific cameras, making it widely compatible and potentially inexpensive. The ability to perform single-frame FLIM without gating loss is a particularly unique advantage, as it enables dynamic FLIM without the loss, noise, and potential motion and intensity artifacts of other approaches. Replacing point-scanning FLIM with efficient wide-field acquisition may prove especially useful in bio-imaging applications such as lifetime FRET, single-molecule and super-resolution microscopy, multi-modal imaging, and clinical diagnostics. Further applications may be found in ultrafast imaging, time-to-space multiplexing, lock-in detection, and time-of-flight techniques.

For FLIM applications, nanosecond imaging with PCs enables large improvements in throughput over conventional TC-SPC. Even at low repetition rates, PC FLIM throughput readily surpasses TC-SPC. For example, a PC gated image at a low signal level of 1 photon/pixel/pulse at 15 kHz for a 1-megapixel image would take 7500 times longer to acquire on a 20 MHz confocal TC-SPC system operating at a 10% count rate (standard to avoid pile-up). This throughput advantage grows linearly with signal and pixel number. Note that PCs may gate 1 photon/pixel/pulse without saturation, unlike GOIs or TC-SPC detectors. Wide-field, high throughput lifetime imaging with PCs could enable imaging of biological dynamics at high frame rate. An example of a relevant application would be real-time imaging of cellular signaling, especially in neurons15,33,34,35. FLIM may also be applied as a clinical or in vivo diagnostic and wide-field gating may be readily compatible with endoscopic probes36,37,38.

PC imaging overcomes the limitations of other wide-field technologies. Gated optical intensifiers in particular face technical drawbacks including low photocathode quantum efficiency, reduced resolution, multiplicative noise, and saturation. Further, the loss of ungated photons (collecting 1/n for n temporal bins) necessitates multi-exposure FLIM acquisition. We note that frequency modulated cameras have recently been developed to enable high throughput FLIM, but these suffer from very high dark currents and read noise. PC modulation provides an alternative approach to frequency domain FLIM which can also allow MHz excitation rates.

PC gating may further allow for new microscopy techniques by exploiting the nanosecond temporal dimension. For example, spectral information has been used to enable multi-labeling of biological samples, which proves important in understanding complex intracellular interactions39. Fluorescence lifetime may similarly provide an attractive temporal approach for unmixing multi-labeled signals40. Confocal FLIM has already been applied to this problem41. In studying single molecules, the capability to combine parallel lifetime measurements with spatial and spectral channels could allow for new types of high throughput spectroscopy experiments to study molecular populations and photophysical states42,43,44,45,46. New information from lifetime could also be used to enhance spatial localization in super-resolution microscopy47. Further, temporal gating could be used to suppress background autofluorescence occurring at short lifetimes48.

While we have primarily focused on applications in fluorescence microscopy, we also note that PC nanosecond imaging techniques could be more broadly applied in quantum optics for fast gating, lock-in detection, event selection, or multi-pass microscopy28,30,49. Other useful operation modes may be realized with the two-bin PC scheme by applying different modulations V(t). For example, a linear ramp of V(t) creates a unique mapping of time to output intensity to temporally localize photon bursts (e.g., molecule blinking) by polarization streaking (see Supplementary Fig. 3). Periodic V(t) could also be used to implement wide-field lock-in detection. Traditional fast-imaging applications in plasma physics, laser-induced breakdown spectroscopy, combustion, time-of-flight techniques, and fluid dynamics could also benefit from sensitive single-shot imaging6,31,50,51,52. The n-frame tilted mirror re-imaging cavity is unique in its ability to perform single-shot ultrafast imaging of weak, non-repetitive events with zero deadtime between frames when using an internal PC gate (Supplementary Fig. 6). It could also prove useful for wide dynamic range lifetime imaging. We note that strategies for time-of-flight imaging and LIDAR have also been recently demonstrated using PC modulation for the timing of reflected light pulses53,54,55.

In summary, wide-field PC FLIM was demonstrated in single-frame and time trace modalities. Single-molecule lifetime spectroscopy showed compatibility with signal-limited applications. By using a thin PC crystal, the technique was extended to ultra wide-field FLIM with single-frame acquisition. FLIM images were acquired on a standard biological benchmark with exposure times down to 2 ms and acquisition speeds to the camera frame rate. Finally, a new method using re-imaging cavities to enable ultrafast imaging by time-to-space multiplexing was shown. These techniques promise to open the nanosecond regime to signal-limited applications like wide-field and single-molecule fluorescence microscopy. Further, they are broadly compatible with any imaging system and sensor, giving potential applications in a variety of fields.

## Methods

### Experimental setup

FLIM was performed with a homemade fluorescence microscope and a thick, commercial PC crystal for Figs. 2, 3, and 5. A Nikon PlanApo 100× VC 1.4 NA oil-immersion objective was used for single-molecule microscopy. All other data were taken with a 20×, 0.8 NA Zeiss PlanApo objective. Excitation pulses (1 ns FWHM) at 532 nm were generated by a Q-switched Nd:YAG at 5 kHz repetition (15 kHz for single-molecule data) (Standa Q10-SH). The detector was a machine vision CMOS camera (FLIR BFS-U3-32S4M-C). A 10 mm aperture, 40 mm thick dual crystal longitudinal KD*P PC embedded in a 50 Ω transmission line was used (Lasermetrics 1072). This PC uses two crystals (rotated 90 degrees and with opposite electric fields), halving the required half-wave voltage. This design gave a comparable acceptance angle to a single-crystal PC of similar thickness (α ~ 4 mrad). We note that in theory, this configuration can achieve some degree of off-axis cancellation with well-matched crystals. High voltage gating pulses were generated into 50 Ω with an amplitude of 1.3 kV, 2.8 ns FWHM (FID GmbH) attaining 85% of Vπ and σIRF = 1.1 ns. Laser and HV pulser were synchronized with a DG 535 delay generator (Stanford Research Systems). Timing jitter was <100 ps. Long transmission lines were used to prevent spurious pulse reflections during fluorescence decay. For single-molecule data, only two of the output frames (one output from first PBS) were used to maximize FOV through the PC, limiting photon efficiency to ~50%. This is not a fundamental limitation of the technique but was used to simplify our implementation with a limited single PC aperture. IRFs were acquired using a frosted glass sample.

The thin PC crystal demonstration in Fig. 4 was performed on an inverted microscope (Zeiss Axiovert) using a 20×, 0.8 NA Zeiss PlanApo objective and Andor Neo5.5 sCMOS. A 3 mm thick, 20 mm aperture KD*P longitudinal PC was home-built along with a high voltage driver capable of supplying nanosecond switching pulses with amplitudes up to 5 kV. A gating efficiency of 0.8 is used with a rise time of 4.5 ns for the data in Fig. 4. Only one polarization channel is demonstrated here. Both channels may be incorporated by adding a second PC or Wollaston prism.

The 4f re-imaging cavity used for the n-bin demonstration used a 3 mm prism mirror (Thorlabs MRA03-G01) for in-coupling and f = 150 mm (trt = 8f/c = 4.0 ns). Passive out-coupling was through a neutral density filter of optical density 1 (R =  0.4 and T = 0.1). Relay lenses were used to create an image plane at the PC and again at the camera (CMOS). Pick-off mirrors combined imaging beams generated by the two PBS with equal path lengths.

### Sample preparation

Alexa 532 (Invitrogen, Thermo Fisher) single-molecule samples were prepared by drop casting dilute solution onto a hydrophobic substrate, then placing and removing a pristine coverslip. A dense field was photobleached to the point that single, diffraction-limited emitters were observed. Step-like photobleaching is shown in Supplementary Figs. 4 and 5 along with blink-on dynamics. While multi-molecule emission within a diffraction-limited spot was certainly also seen, a majority of the emitters were single molecules. Fluorescence bead samples were drop cast onto coverglass from solutions of orange (100 nm), red (1 μm), nile red (2 μm), infrared (100 nm) (Invitrogen, Thermo Fisher) and propidium iodide (10 μm) (Bangs Laboratories, Inc.) beads. The IR bead solution formed crystals as seen in Fig. 2.

### Data analysis

Lifetimes were computed by both ratiometric calculation from image intensities and by time-trace fitting. In ratiometric calculation, a numerically generated lookup table is used to convert between the measured ratio and estimated lifetime according to the equations in the text and the pre-characterized IRF. Due to our specific td and Gaussian gate pulse in Fig. 3, lifetimes below 1.1 ns are redundant with those above 1.1 ns in the numerical conversion. We report the larger lifetime value. In timing trace calculation, fitting by least squares was used to estimate lifetime. The PC applies a time-varying retardance to linearly polarized input as $$\delta = 2\pi r_{63}Vn_{\mathrm{o}}^3/\lambda$$, where the birefringent phase shift δ is determined by the applied voltage V, ordinary index of refraction no, and the longitudinal electro-optic coefficient r63. Transmission in the parallel and perpendicular beamsplitter channels is T = sin2(δ/2) and T = cos2(δ/2). Lifetime calculations account for the imperfect gating efficiency of the Pockels cell as captured in the IRF. In Figs. 2, 3, and 5, a constant IRF is assumed across a conservative FOV. This may cause position-dependent lifetime errors. In Fig. 4, spatial variation is more apparent due to large FOV and is included in lifetime calculations. A beamsplitter in the microscope filter slider allows rapid switching between fluorescence and frosted glass IRF calibration. IRF calibration may also be performed with a short lifetime dye.

Single-molecule gated and ungated intensities were determined by summing Np pixels corresponding to each molecule region of interest after background subtraction. Error bars in Fig. 3c account for shot noise in the gated (G) and ungated (U) frames and for the background standard deviations σG and σU in the ratio SE σR as

$$\sigma _R = \frac{G}{U}\sqrt {\frac{1}{G} + \frac{1}{U} + N_p\left( {\frac{{\sigma _{\mathrm{G}}^2}}{{G^2}} + \frac{{\sigma _{\mathrm{U}}^2}}{{U^2}}} \right)} .$$

Background is the dominant error term here combining background signal with a high camera dark current.

Lifetime estimation accuracy for an ideal two-bin PC gate is given by $$\sqrt N \sigma _\tau /\tau = \frac{\tau }{{t_{\mathrm{d}}}}\sqrt {e^{t_{\mathrm{d}}/\tau } - 1}$$. The Cramér-Rao bound for n-bin lifetime estimation in a fixed time window of width T may be directly calculated from a multinomial probability distribution32. Fixed window bounds in Fig. 6 were found by setting T = n × trt for n round trips. In the large n limit, these bounds demonstrate the performance of TC-SPC. The photon normalized Cramér-Rao bound for n bins is

$$\frac{{\sqrt N \sigma _\tau }}{\tau } = \frac{{n\tau }}{T}\sqrt {(1 - e^{ - T/\tau })} \left[ {\frac{{e^{\frac{T}{{n\tau }}}(1 - e^{ - T/\tau })}}{{(e^{\frac{T}{{n\tau }}} - 1)^2}} \, - \, \frac{{n^2}}{{e^{T/\tau } - 1}}} \right]^{ - 1/2}.$$

### Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

## Data availability

Source data for Fig. 3 are provided with the paper. The rest of the data that support the findings of this study are available from the corresponding author upon reasonable request.

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## Acknowledgements

We thank Yonatan Israel and Rachel Gruenke. This research was funded by the Gordon and Betty Moore Foundation. A.B. and B.K. acknowledge support from the Stanford Graduate Fellowship. A.B. acknowledges support from the National Science Foundation Graduate Research Fellowship Program under grant 1656518.

## Author information

Authors

### Contributions

A.B. conceived the idea and performed the experiments. B.K. and T.J. performed initial work on P.C. gating. A.B. and M.K. prepared the manuscript.

## Ethics declarations

### Competing interests

The authors declare no competing interests.

Peer review information Nature Communications thanks Scott Howard and other anonymous reviewer(s) for their contribution to the peer review of this work.

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Bowman, A.J., Klopfer, B.B., Juffmann, T. et al. Electro-optic imaging enables efficient wide-field fluorescence lifetime microscopy. Nat Commun 10, 4561 (2019). https://doi.org/10.1038/s41467-019-12535-5

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