Search for: All records

We present a theoretical model describing photoelectron transport dynamics in stepwise-doped GaAs photocathodes. Built-in electric field caused by the doping structure is analyzed, and the time-evolution of electron concentration in the active layer induced by a femtosecond laser pulse is solved. The predictions of the model show excellent agreement with the experimental data measured with pump-probe transient reflectometry, demonstrating the capability of the theoretical model in predicting photoelectron behaviors in real devices. Comparisons are also made between this stepwise doping model and the conventional gradient doping model with a continuous doping profile, thereby providing the first quantitative evaluation of the effectiveness and the limitation of the gradient doping model in describing actual stepwise-doped devices.

We report the discovery of a transient seen in a strongly lensed arc at redshift zs = 1.2567 in Hubble Space Telescope imaging of the Abell 370 galaxy cluster. The transient is detected at 29.51 ± 0.14 AB mag in a WFC3/UVIS F200LP difference image made using observations from two different epochs, obtained in the framework of the Flashlights programme, and is also visible in the F350LP band (mF350LP ≈ 30.53 ± 0.76 AB mag). The transient is observed on the negative-parity side of the critical curve at a distance of ∼0.6 arcsec from it, greater than previous examples of lensed stars. The large distance from the critical curve yields a significantly smaller macromagnification, but our simulations show that bright, O/B-type supergiants can reach sufficiently high magnifications to be seen at the observed position and magnitude. In addition, the observed transient image is a trailing image with an observer-frame time delay of ∼+0.8 d from its expected counterpart, so that any transient lasting for longer than that should have also been seen on the minima side and is thus excluded. This, together with the blue colour we measure for the transient (mF200LP − mF350LP ≈ [−0.3, −1.6] AB), rules out most other transient candidates such as (kilo)novae, for example, and makes a lensed star the prime candidate. Assuming that the transient is indeed a lensed star as suggested, many more such events should be detected in the near future in cluster surveys with the Hubble Space Telescope and JWST.

We report the discovery of an extremely magnified star at redshiftz= 2.65 in the James Webb Space Telescope (JWST) NIRISS pre-imaging of the A2744 galaxy-cluster field. The star’s background host galaxy lies on a fold caustic of the foreground lens, and the cluster creates a pair of images of the region close to the lensed star. We identified the bright transient in one of the merging images at a distance of ∼0.″15 from the critical curve by subtracting the JWST F115W and F150W imaging from coadditions of archival Hubble Space Telescope (HST) F105W and F125W images and F140W and F160W images, respectively. Since the time delay between the two images should be only hours, the transient must be the microlensing event of an individual star, as opposed to a luminous stellar explosion that would persist for days to months. Analysis of individual exposures suggests that the star’s magnification is not changing rapidly during the observations. From photometry of the point source through the F115W, F150W, and F200W filters, we identify a strong Balmer break, and modeling allows us to constrain the star’s temperature to be approximately 7000–12,000 K.

Optical density (OD) is widely used to estimate the density of cells in liquid culture, but cannot be compared between instruments without a standardized calibration protocol and is challenging to relate to actual cell count. We address this with an interlaboratory study comparing three simple, low-cost, and highly accessible OD calibration protocols across 244 laboratories, applied to eight strains of constitutive GFP-expressingE. coli. Based on our results, we recommend calibrating OD to estimated cell count using serial dilution of silica microspheres, which produces highly precise calibration (95.5% of residuals  <1.2-fold), is easily assessed for quality control, also assesses instrument effective linear range, and can be combined with fluorescence calibration to obtain units of Molecules of Equivalent Fluorescein (MEFL) per cell, allowing direct comparison and data fusion with flow cytometry measurements: in our study, fluorescence per cell measurements showed only a 1.07-fold mean difference between plate reader and flow cytometry data.