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In recent years, nanolasers based on plasmonic crystal nanocavity structures have attracted significant interest. However, the performance of such lasers is affected significantly by the coupling of the lasing emission to both reflection and transmission sides of the device and to multiple spatial modes in the far field due to higher-order diffraction from plasmonic crystals as well. In this work, we propose a nanolaser design that overcomes the performance degradation of plasmonic crystal based nanolasers and increases the emission intensity significantly. In the proposed nanolaser structure, a nanometer-thick gain medium has a one-dimensional photonic crystal on one side and a metal nanohole array on the other side. An incident pump pulse through the one-dimensional photonic crystal excites optical Tamm states at the metal-gain medium interface that are amplified by the stimulated emission of the gain medium. We find that the intensity of the extraordinary optical transmission through the metal nanohole array increases significantly due to the excitation of optical Tamm states with wavevector perpendicular to the nanohole array surface. We also find that the subwavelength periodicity in the nanohole array confines the lasing emission to the zero-th order mode only, and hence, makes the far-field pattern highly directional. Moreover, the laser emission wavelength can be tuned over a broad range by changing the thicknesses of the photonic crystal layers, gain medium, and in real-time, by changing the angle of incidence of the pump pulse.

Imaging of the cell membrane topography is important for a clear understanding of various biological activities of cells. We propose a technique for imaging the cell membrane topography that uses a metal-photonic crystal structure instead of a glass-water interface used in conventional polarized total internal reflection fluorescence microscopy (pTIRFM) techniques. Through the metal-photonic crystal of the proposed technique, the fluorophore labels on the cell membrane can be excited by both the p- and s-polarized excitation light, and in each case, the p- and s-polarized radiation from the excited fluorophores can be separated to form an image. We calculate the images of the cell membrane topography that is fusing a granule using the proposed technique and pTIRFM. The image obtained by the proposed technique shows a much greater contrast with respect to the background than that of the image obtained by pTIRFM. We also find that the structural similarity index of the image obtained by the proposed technique to a reference image is ~77%, which is only ~16% for the image obtained by pTIRFM. The proposed technique will help to obtain a clearer and more accurate image of the cell membrane topography, and hence, a deeper understanding of different biological activities.

We propose and theoretically demonstrate that two-dimensional materials at the interface between glass and water layers in a total internal reflection fluorescence microscopy (TIRFM) technique can decrease the detection volume of a target sample, and hence improve the resolution of the obtained image. In particular, we calculate the change in fluorescence characteristics of the fluorophore labels on a target sample when monolayer black phosphorus, hexagonal boron nitride, and graphene are added at the glass-water interface of a TIRFM structure. We also calculate the change in the detection volume due to the presence of two-dimensional materials, and when the polarization, wavelength, and angle of the incident light vary. We find $\gtrsim $ 10% and $\gtrsim $ 5% decrease in the detection volume when monolayer black phosphorus and hexagonal boron nitride are used, respectively, and up to ~50% decrease when monolayer graphene is used. The proposed use of the two-dimensional material will significantly improve the resolution of TIRFM technique, and hence facilitate the study of nanoscale biological features.