Jeongyong Kim

High-detectivity multilayer MoS(2) phototransistors with spectral response from ultraviolet to infrared.

Phototransistors based on multilayer MoS(2) crystals are demonstrated with a wider spectral response and higher photoresponsivity than single-layer MoS(2) phototransistors. Multilayer MoS(2) phototransistors further exhibit high room temperature mobilities (>70 cm(2) V(-1) s(-1) ), near-ideal subthreshold swings (~70 mV decade(-1) ), low operating gate biases (<5 V), and negligible shifts in the threshold voltages during illumination.

Lung Function Changes in Sprague-Dawley Rats After Prolonged Inhalation Exposure to Silver Nanoparticles

The antimicrobial activity of silver nanoparticles has resulted in their widespread use in many consumer products. However, despite the continuing increase in the population exposed to silver nanoparticles, the effects of prolonged exposure to silver nanoparticles have not been thoroughly determined. Accordingly, this study attempted to investigate the inflammatory responses and pulmonary function changes in rats during 90 days of inhalation exposure to silver nanoparticles. The rats were exposed to silver nanoparticles (18 nm diameter) at concentrations of 0.7 × 106 particles/cm3 (low dose), 1.4 × 106 particles /cm3 (middle dose), and 2.9 × 106 particles /cm3 (high dose) for 6 h/day in an inhalation chamber for 90 days. The lung function was measured every week after the daily exposure, and the animals sacrificed after the 90-day exposure period. Cellular differential counts and inflammatory measurements, such as albumin, lactate dehydrogenase (LDH), and total protein, were also monitored in the acellular bronchoalveolar lavage (BAL) fluid of the rats exposed to the silver nanoparticles for 90 days. Among the lung function test measurements, the tidal volume and minute volume showed a statistically significant decrease during the 90 days of silver nanoparticle exposure. Although no statistically significant differences were found in the cellular differential counts, the inflammation measurements increased in the high-dose female rats. Meanwhile, histopathological examinations indicated dose-dependent increases in lesions related to silver nanoparticle exposure, such as infiltrate mixed cell and chronic alveolar inflammation, including thickened alveolar walls and small granulomatous lesions. Therefore, when taken together, the decreases in the tidal volume and minute volume and other inflammatory responses after prolonged exposure to silver nanoparticles would seem to indicate that nanosized particle inhalation exposure can induce lung function changes, along with inflammation, at much lower mass dose concentrations when compared to submicrometer particles.

Characterization of InGaAs-GaAs strained-layer lasers with quantum wells near the critical thickness

Data are presented on the efficiency, reliability, and temperature dependence of wavelength and threshold for strained‐layer InxGa1−xAs‐GaAs (x∼0.25, λ>1.06 μm) separate confinement heterostructure lasers for several thicknesses near the critical thickness. Devices with well thicknesses of 100 A exhibit excellent time‐zero characteristics and reliability, while those with 143 A wells have higher initial thresholds and degrade rapidly.

Biexciton Emission from Edges and Grain Boundaries of Triangular WS2 Monolayers

Monolayer tungsten disulfides (WS2) constitute a high quantum yield two-dimensional (2D) system, and can be synthesized on a large area using chemical vapor deposition (CVD), suggesting promising nanophotonics applications. However, spatially nonuniform photoluminescence (PL) intensities and peak wavelengths observed in single WS2 grains have puzzled researchers, with the origins of variation in relative contributions of excitons, trions, and biexcitons to the PL emission not well understood. Here, we present nanoscale PL and Raman spectroscopy images of triangular CVD-grown WS2 monolayers of different sizes, with these images obtained under different temperatures and values of excitation power. Intense PL emissions were observed around the edges of individual WS2 grains and the grain boundaries between partly merged WS2 grains. The predominant origin of the main PL emission from these regions changed from neutral excitons to trions and biexcitons with increasing laser excitation power, with biexcitons completely dominating the PL emission for the high-power condition. The intense PL emission and the preferential formation of biexcitons in the edges and grain boundaries of monolayer WS2 were attributed to larger population of charge carriers caused by the excessive incorporation of growth promoters during the CVD, suggesting positive roles of excessive carriers in the PL efficiency of TMD monolayers. Our comprehensive nanoscale spectroscopic investigation sheds light on the dynamic competition between exciton complexes occurring in monolayer WS2, suggesting a rich variety of ways to engineer new nanophotonic functions using 2D transition metal dichalcogenide monolayers.

Temperature-dependent micro-photoluminescence of individual CdSe self-assembled quantum dots

We use micro- and nano-photoluminescence to study the temperature-dependent excitonic emission from CdSe quantum dots embedded in a ZnSe matrix. By varying the spatial resolution from 200 nm to 1.7 μm, we are able to study the temperature dependence of the ultranarrow (∼200 μeV) emission from excitons confined to single quantum dots, as well as statistical ensembles of up to 200 dots. By measuring the quenching of the photoluminescence (PL) with temperature, we find compelling evidence that the PL emission from these samples results from two different kinds of states. Similar to previous work, we find that a broad PL line persists to 300 K with an activation energy of ∼40 meV. However, we find that the ultranarrow lines are quenched at about 60 K, indicating an effective activation energy of only 4.0 meV.

SPECTROSCOPIC CHARACTERIZATION OF THE EVOLUTION OF SELF-ASSEMBLED CDSE QUANTUM DOTS

We have investigated the evolution of molecular beam epitaxy (MBE)-grown, CdSe self-assembled quantum dots on ZnSe surfaces using microphotoluminescence techniques. Bare CdSe dots at room temperature undergo Ostwald ripening over a time scale measured in days. At the elevated temperatures maintained for MBE growth and dot formation, ripening is expected to progress much faster. Capping the dots with a thin ZnSe layer “freezes” the ripening, allowing one to sample different stages of the dot evolution and subsequent characterization. We have grown eleven samples, each with a different time interval, or growth interruption, between dot formation and capping; the growth interruption times ranging from 0 to 300 s, during which the samples were kept at 300 °C. Using microphotoluminescence spectroscopy, we have resolved the sharp emission peaks due to individual dots in each sample and, by analyzing the ensemble characteristics, have identified a new regime in the evolution of CdSe dots.

Light-emitting color barcode nanowires using polymers: nanoscale optical characteristics.

We report on the light-emitting color barcode nanowires (LECB-NWs), which were fabricated by alternating the electrochemical polymerization of light-emitting polymers with various luminescence colors and efficiencies. The nanoscale photoluminescence characteristics of LECB-NWs were investigated using a laser confocal microscope with a high spatial resolution. The alternating light emissions of the LECB-NWs showed orange-yellow, red, and green colors due to the serial combination of poly(3-butylthiophene), poly(3-methylthiophene), and poly(3,4-ethylenedioxythiophene), respectively, with distinct luminescence intensities. The optical detection sensitivity and stability of LECB-NWs have been enhanced through a nanoscale Cu metal coating onto the NWs, based on surface plasmon resonance coupling and protection against oxidation. The flexibility of the LECB-NWs has been investigated through the folding and unfolding of the NWs by an applied nanotip impetus. The flexible LECB-NWs can be used as highly sensitive optical identification nanosystems for nanoscale or microscale products with complex physical shapes.

Spectroscopic Visualization of Grain Boundaries of Monolayer Molybdenum Disulfide by Stacking Bilayers

Polycrystalline growth of molybdenum disulfide (MoS2) using chemical vapor deposition (CVD) methods is subject to the formation of grain boundaries (GBs), which have a large effect on the electrical and optical properties of MoS2-based optoelectronic devices. The identification of grains and GBs of CVD-grown monolayer MoS2 has traditionally required atomic resolution microscopy or nonlinear optical imaging techniques. Here, we present a simple spectroscopic method for visualizing GBs of polycrystalline monolayer MoS2 using stacked bilayers and mapping their indirect photoluminescence (PL) peak positions and Raman peak intensities. We were able to distinguish a GB between two MoS2 grains with tilt angles as small as 6° in their grain orientations and, based on the inspection of several GBs, found a simple empirical rule to predict the location of the GBs. In addition, the large number of twist angle domains traced through our facile spectroscopic mapping technique allowed us to identify a continuous evolution of the coupled structural and optical properties of bilayer MoS2 in the vicinity of the 0° and 60° commensuration angles which were explained by elastic deformation model of the MoS2 membranes.

Spectrally-resolved near-field investigation of proton implanted vertical cavity surface emitting lasers

Emission characteristics of proton implanted vertical cavity surface emitting lasers have been studied by spectrally-resolved near-field scanning optical microscopy (NSOM). Measured spatial intensity distributions of individual transverse modes show a fundamental mode at threshold, and two double-lobed first-order modes excited around aperture edge above 1.3× threshold injection current. The use of high spectral and spatial resolution NSOM enabled the detection of a local resonance wavelength dependence on position across the laser aperture; from these data, a lateral refractive index variation is calculated. As the injection current is increased, these index distributions are found to be consistent with the observed reduction of the spatial width of the intensity distribution and the increase in the spectral mode spacing.

Simultaneous Hosting of Positive and Negative Trions and the Enhanced Direct Band Emission in MoSe2/MoS2 Heterostacked Multilayers

Heterostacking of layered transition-metal dichalcogenide (LTMD) monolayers (1Ls) offers a convenient way of designing two-dimensional exciton systems. Here we demonstrate the simultaneous hosting of positive trions and negative trions in heterobilayers made by vertically stacking 1L MoSe2 and 1L MoS2. The charge transfer occurring between the 1Ls of MoSe2 and MoS2 converted the polarity of trions in 1L MoSe2 from negative to positive, resulting in the presence of positive trions in the 1L MoSe2 and negative trions in the 1L MoS2 of the same heterostacked bilayer. Significantly enhanced MoSe2 photoluminescence (PL) in the heterostacked bilayers compared to the PL of 1L MoSe2 alone suggests that, unlike other previously reported heterostacked bilayers, direct band transition of 1L MoSe2 in heterobilayer was enhanced after the vertical heterostacking. Moreover, by inserting hexagonal BN monolayers between 1L MoSe2 and 1L MoS2, we were able to adjust the charge transfer to maximize the MoSe2 PL of the heteromultilayers and have achieved a 9-fold increase of the PL emission. The enhanced optical properties of our heterostacked LTMDs suggest the exciting possibility of designing LTMD structures that exploit the superior optical properties of 1L LTMDs.