ABSTRACT
Beyond-diffraction-limit optical absorption spectroscopy provides in-depth information on the graded band structures of composition-spread and stacked two-dimensional materials, in which direct/indirect bandgap, interlayer coupling, and defects significantly modify their optoelectronic functionalities such as photoluminescence efficiency. We here visualize the spatially varying band structure of monolayer and bilayer transition metal dichalcogenide alloys by using near-field broadband absorption microscopy. The near-field spectral and spatial information manifests the excitonic band shift that results from the interplay of composition spreading and interlayer coupling. These results enable us to identify, notably, the top layer of the bilayer alloy as pure WS2. We also use the aberration-free near-field transmission images to demarcate the exact boundaries of alloyed and pure transition metal dichalcogenides. This technology can offer valuable insights on various layered structures in the era of "stacking science" in the quest of quantum optoelectronic devices.
ABSTRACT
Heterojunctions made by laterally stitching two different transition metal dichalcogenide monolayers create a unique one-dimensional boundary with intriguing local optical properties that can only be characterized by nanoscale-spatial-resolution spectral tools. Here, we use near-field photoluminescence (NF-PL) to reveal the narrowest region (105 nm) ever reported of photoluminescence quenching at the junction of a laterally stitched WS2/MoS2 monolayer. We attribute this quenching to the atomically sharp band offset that generates a strong electric force at the junction to easily dissociate excitons. Besides the sharp heterojunction, a model considering various widths of the alloying interfacial region under low or high optical pumping is presented. With a spatial resolution six times better than that of confocal microscopy, NF-PL provides an unprecedented spectral tool for non-scalable 1D lateral heterojunctions.
ABSTRACT
We report on the generation of a super- and homochiral field where linearly polarized incident light is twisted by plasmonic dimeric nanostructure within the gap. The asymmetry in exciting a molecule's chiral polarizability is enhanced, resulting in discriminatory nanocolorimetry. A chromaticity shift is used to discriminate the handedness of chiral molecules which is sensitive, faster, and self-referenced, and requires only a single scan as compared to existing methods.
Subject(s)
Colorimetry/methods , Light , Metal Nanoparticles/chemistry , Silver/chemistry , Stereoisomerism , Surface Plasmon ResonanceABSTRACT
We develop a front-to-end solution where the shift of chromaticity from scattering of plasmonic nanoparticles is used as the reporter for nano-environmental refractive index variation. By co-projecting possible power combinations of RGB LEDs and digitized color grid density of CCD with various luminance onto the CIE 1931 chromaticity diagram, optimum condition for nanoenvironment sensing can be achieved. The highest resolution for local refractive index change is 0.0021 per distinguishable color, which is higher than that of a typical handheld spectrometer by 4.8 times. This result shows great potential in simplifying nano-environment sensing instruments and is particularly useful for multi-point dynamical process.
ABSTRACT
Comprehensive studies were carried out to understand the origin of the current hysteresis effects in highly efficient C60-CH3NH3PbI3(MAPbI3) heterojunction solar cells, using atomic-force microscopy, transmittance spectra, photoluminescence spectra, X-ray diffraction patterns and a femtosecond time-resolved pump-probe technique. The power conversion efficiency (PCE) of C60-MAPbI3 solar cells can be increased to 18.23% by eliminating the point (lattice) defects in the MAPbI3 thin film which is fabricated by using the one-step spin-coating method with toluene washing treatment. The experimental results show that the point defects and surface defects of the MAPbI3 thin films can be minimized by varying the dropping time of the washing solvent. The point defects (surface defects) can be reduced with an (a) increase (decrease) in the dropping time, resulting in an optimized dropping time for obtaining the defect-minimized MAPbI3 thin film deposited on top of the C60 thin film. Consequently, the formation of the defect-minimized MAPbI3 thin film allows for high-efficiency MAPbI3 solar cells.
ABSTRACT
We demonstrate an as yet unused method to sieve, localize, and steer plasmonic hot spot within metallic nano-interstices close to percolation threshold. Multicolor superlocalization of plasmon mode within 60 nm was constantly achieved by chirp-manipulated superresolved four wave mixing (FWM) images. Since the percolated film is strongly plasmonic active and structurally multiscale invariant, the present method provides orders of magnitude enhanced light localization within single metallic nano-interstice, and can be universally applied to any region of the random film. The result, verified by the maximum likelihood estimation (MLE) and deconvolution stochastic optical reconstruction microscopy (deconSTORM) algorithm, may contribute to label-free multiplex superlocalized spectroscopy of single molecule and sub-cellular activity monitoring combining hot spot steering capability.
