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Atomically thin two-dimensional materials have emerged as a promising system for optoelectronic applications; however, the low quantum yield, mainly caused by nonradiative energy dissipation, has greatly limited practical applications. To reveal the details for nonradiative energy channels, femtosecond pump-probe spectroscopy with a detection wavelength ranging from visible to near-infrared to mid-infrared is performed on few-layer MoS. With this method, the many-body effects, occupation effects, and phonon dynamics are clearly identified. In particular, thermalization of the MoS lattice via electron-phonon scattering is responsible for a redshift of the exciton resonance energy observed within tens to hundreds of picoseconds after photoexcitation, which provides a direct real-time sensor for measuring the change in lattice temperature. We find that the excess energy from the cooling of hot carriers and the formation of bound carriers is efficiently transferred to the internal phonon system within 2 ps, while that from Shockley-Read-Hall recombination (∼9 ps) is mainly dissipated from the MoS surfaces to external phonons.

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An experiment demonstrating single-pixel single-arm complementary compressive microscopic ghost imaging based on a digital micromirror device (DMD) has been performed. To solve the difficulty of projecting speckles or modulated light patterns onto tiny biological objects, we instead focus the microscopic image onto the DMD. With this system, we have successfully obtained a magnified image of micron-sized objects illuminated by the microscope's own incandescent lamp. The image quality of our scheme is more than an order of magnitude better than that obtained by conventional compressed sensing with the same total sampling rate, and moreover, the system is robust against intensity instabilities of the light source and may be used under very weak light conditions. Since only one reflection direction of the DMD is used, the other reflection arm is left open for future infrared light sampling. This represents a big step forward toward the practical application of compressive microscopic ghost imaging in the biological and material science fields. * gjzhai@nssc.ac.cn

By using femtosecond pump-probe spectroscopy with broadband detection from near-infrared to midinfrared, the carrier and phonon dynamics in few-layer 2H–MoTe2 after ultrafast excitation have been investigated in detail. Immediately following the photoexcitation, an ultrafast relaxation of the generated hot carriers by releasing phonons is observed within hundreds of femtoseconds. The subsequent electron-hole recombination with a time constant of ∼1.5 ps is clearly identified and demonstrated to be mediated through a defect-assisted process. Furthermore, we confirm that the observed redshift of the exciton resonance energy on longer time scales arises from the ultrafast thermalization of the 2H–MoTe2 lattice caused by the transfer of electronic excitation to the phonon system. As a result, the thermalization dynamics of the lattice within 2 ps and the following cooling process of the phonon system on the 100 ps time scale are directly monitored.

A fast algorithm with low memory usage is proposed to generate the hologram for full-color 3D display based on a compressed look-up table (C-LUT). The C-LUT is described and built to reduce the memory usage and speed up the calculation of the computer-generated hologram (CGH). Numerical simulations and optical experiments are performed to confirm this method, and several other algorithms are compared. The results show that the memory usage of the C-LUT is kept low when number of depth layers of the 3D object is increased, and the time for building the C-LUT is independent of the number of depth layers of the 3D object. The algorithm based on C-LUT is an efficient method for saving memory usage and calculation time, and it is expected that it could be used for realizing real-time and full-color 3D holographic display in the future.

The transcription factor Bach2 which is predominantly expressed in B and T lymphocytes represses the expression of genes by forming heterodimers with small Maf and Batf proteins and binding to the corresponding sequence on the DNA. In this way, Bach2 serves as a highly conserved repressor which controls the terminal differentiation and maturation of both B and T lymphocytes. It is required for class switch recombination (CSR) and somatic hypermutation (SHM) of immunoglobulin genes in activated B cells, and its function in B cell differentiation has been well-described. Furthermore, emerging data show that Bach2 regulates transcriptional activity in T cells at super enhancers or regions of high transcriptional activity, thus stabilizing immunoregulatory capacity and maintaining T cell homeostasis. Bach2 is also critical for the formation and function of CD4+ T cell lineages (Th1, Th2, Th9, Th17, T follicular helper (Tfh), and regulatory T (Treg) cells). Genetic variations within Bach2 locus are associated with numerous immune-mediated diseases including multiple sclerosis (MS), rheumatoid arthritis (RA), chronic pancreatitis (CP), type 2 chronic airway inflammation, inflammatory bowel disease (IBD), and type 1 diabetes. Here, we reveal a critical role of Bach2 in regulating T cell biology and the correlation with these immune-mediated diseases.

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