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Nobuhiko P. Kobayashi,1 A. Alec Talin,2 Albert V. Davydov,3 M. Saif Islam4
1Univ. of California, Santa Cruz (United States) 2Sandia National Labs. (United States) 3National Institute of Standards and Technology (United States) 4Univ. of California, Davis (United States)
This PDF file contains the front matter associated with SPIE Proceedings Volume 12200, including the Title Page, Copyright information, Table of Contents, and Conference Committee Page.
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Optical, Electronic, and Thermal Properties of Low-Dimensional Materials I
The rapid development of nanophotonic technologies has put forward higher requirements for optoelectronic devices, including ultra-small footprints, high-speed operation, high efficiency, and low power consumption. Optoelectronics based on emerging materials can provide the material framework that can keep pace with future technological demands. Here we will share our latest innovations and device demonstrations of using low-dimensional materials towards discovering high-performance photodetector and electro-optic modulator performances. We will share the concept of strainoptronics enabling to engineer a plurality of material properties (bandgap, workfunction, mobility) and show how a Transition-Metal Dichalcogenides (TMDC)-based efficient photodetector can be realized using MoS2 on a Silicon photonic platform. Furthermore, using scaling-length-theory, we show our roadmap and results of high gain-bandwidth product photodetectors using a metal slot atop a silicon photonic waveguide towards optimizing the carrier-lifetime to transit time ratio. These devices were enabled by a novel 3D-like 2D material transfer system, which also enabled us to demonstrate a 2D material PN junction photodetector operating at zero bias, thus leading to extremely low dark currents and hence very efficient noise-equivalent powers. Finally, we show our latest work on ITO-thin film electro-optic modulators with 40 GHz 3dB roll-off, requiring just 200 meV of the drive voltage. Further development of the modulator platform shows the potential of a 100 GHz fast MZI modulator with a footprint that is 1,000 more compact than standard Silicon photonics and 10,000 more compact compared to Lithium Niobite.
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Two-dimensional (2D) van der Waals solids form a layered structure held together in the solid state through a weak van der Waals interaction out of plane, while the in-plane bonding is through the covalent interaction. In this work, we present our findings on two distinct classes of van der Waals solids, that based on in-organic transition metal dichalcogenides and the other based on a hybrid mixed organic-inorganic composition of 2D perovskites, specifically organo-halides (CH3(CH2)3NH3)2(CH3NH3)n-1PbnI3n+1. In the former case, we will discuss the use of 2D tungsten diselenide (WSe2) and how its light-matter interactions are influenced through the incorporation of organic zerodimensional (0D) on its surface. In the latter case, the optical properties of 2D solution processed Ruddlesden-Popper perovskites are presented towards bendable optoelectronics and the integration of a similar higher dimensional perovskite, methyl ammonium lead iodide (MAPbI3), into solar cell photovoltaics platforms.
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In this invited contribution, we review recent results and report on the phase transitions and de-pinning of the charge-density waves in single-crystal 1T-TaS2 thin-film and 1T-TaS2 / h-BN heterostructure devices. It is known that 1T-TaS2 reveals charge-density-wave phases below and above room temperature. The de-pinning of the charge-density waves in the quasi-2D materials is different from that in “conventional” bulk charge-density-wave materials with quasi-1D motifs in the crystal structure. The de-pinning process in 1T-TaS2 is not accompanied by an observable abrupt increase in electric current – in contrast to de-pinning in the conventional charge-density-wave materials with the quasi-1D crystal structure. The obtained results contribute to the development of the charge-density-wave devices for applications in electronics and optoelectronics.
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Silicon avalanche photodiodes (Si-APD) are widely explored due to their high sensitivity, rapid response time, high quantum efficiency, intrinsic multiplication gain, and low signal-to-noise ratio. We present an experimental demonstration of a wavelength selective APD stack epitaxially grown in two different doping orders:–1) N-on-P and 2) P-on-N.We present a performance comparison between N-on-P and P-on-N based on the quantum external efficiency (EQE), Ion/Ioff ratio, and the reverse biased dark state leakage current. By reversing the doping from P-on-N to N-on-P, we show a 40% increase in the EQE. By introducing the photon-trapping hole array we show a 60% improvement in the EQE. We have utilized a low temperature (450oC) forming gas (5% H2 and 95% N2) annealing process to passivate the surface states and show a dark state leakage current improvement from sub- 10nA to sub-1nA current range. The proposed devices are complementary metal oxide semiconductor process compatible and can enable ‘detectors-on-chip’ technology for numerous applications such as internet-of-things, data communication, biomedical imaging, high-speed cloud computing, remote sensing, as well as single-photon detection.
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Monolayers of transition metal dichalcogenides (TMDCs) have caught the interest of post-silicon electronics and optoelectronics researchers due to their exceptional electronic and optoelectronic properties which stem from their unique two-dimensional (2D) layered structure. In recent years, there has been a focus on exploring van der Waals (vdW) heterojunctions with TMDCs, including with lower dimensionality materials such as zero-dimensional (0D) systems. Integrating 0D-2D assemblies together provides an opportunity to configure a diverse array of material stacks towards optoelectronics and electronics applications. In this study, we synthesized 0D-2D vdW heterostructure by spin coating C60 molecules on halide-assisted-low-pressure chemical-vapor-deposition (HA-LPCVD) produced monolayer WSe2 flakes. Raman and photoluminescence spectroscopy allowed us to assess the charge carrier exchange at the vdW interface. We found that after C60 deposition, the photodetector figures of merit for WSe2 − C60 hybrids improved, and investigations were conducted as a function of illumination power. Our studies reveal that WSe2 − C60 hybrid system is an appealing choice for next generation optical sensing devices.
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Sensing temperature is important for a wide variety of applications such as control systems and instrumentation which are integral to various industrial sectors and in research settings. To date, many prior studies have favored the use of the resistive thermistor approach given its simplicity. However, such devices are less sensitive to temperature changes compared to frequency-dependent approaches which are gaining momentum for detection. The importance of high sensitivity and reliable methods using a frequency-based approach for detecting temperature changes should thus be apparent, particularly if such sensors are also fabricated using low-cost approaches which are amenable toward miniaturized wireless platforms at the same time. In this study, Au rectangular single-arm spiral antennas with varying sizes were fabricated and RF S-parameter measurements were conducted over the frequency range of 300 kHz to 20 GHz. Solution-processed, two-dimensional (2D) hexagonal boron nitride (h-BN) was used with cyclohexanone and terpineol as solvents, and the films were characterized using dc current-voltage and frequency-dependent capacitance measurements. We also characterized our solution-processed h-BN films using Raman spectroscopy. The shift in the resonant frequency through the addition of h-BN over the underlying Au antenna was observed as this dielectric was coated on top of the antennas and the temperature response of the resonance frequency was measured. Alongside the experimental measurements, we also present results from our simulation analysis conducted using High Frequency Structure Simulator (HFSS) from ANSYS.
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We present a multi-quantum well (MQW)-based photodetectors design method for a 1-3 μm wavelength selectivity range using the finite difference time domain (FDTD) Lumerical platform. We demonstrate absorption coefficient and power absorption profile modulation in an III-V-based type-II MQW stack embedded with photon-trapping (PT) surface structures. We present an MQW-based photodetectors design space by varying the MQW stacking period, and the well and the barrier dimensions from 100-200 and 5-10 nm respectively. We show that the power absorption in the MQW increases for a fixed wavelength sensitivity range. However, the well and the barrier dimension variation facilitate the wavelength sensitivity range modulation. The upper bound of 3 μm on the wavelength-selectivity is achieved by tuning the well/barrier widths. We further proposed a modified device structure to cap the lower wavelength optical signal and cap them at 1 μm. We also show a tremendous increase in power absorption by introducing photon-trapping holes into the MQW structure. Finally, we extract the effective absorption coefficient of the MQW using the power absorption profile generated in the FDTD framework to show the desired wavelength selectivity. Finally, we utilize the extracted absorption coefficient to perform a COMSOL-based simulation to show a 31% enhancement in quantum efficiency of the MQW detector with the introduction of photon-trapping holes.
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Semiconducting two-dimensional transition-metal dichalcogenides (TMDs) have garnered a great deal of interest owing to their large surface-to-volume ratios compared to traditional three-dimensional (3D) semiconductors. One such TMD is tungsten diselenide (WSe2), which at monolayer (1L) exhibits a direct bandgap and tunable charge transport behavior. This, in combination with its large surface-to-volume ratio, has made WSe2 a heavily researched material, including for gas sensing applications. However, the synthesis of monolayer WSe2 has proven to be challenging. In this study, we demonstrate the halide-assisted low-pressure chemical vapor deposition (HA-LPCVD) of high crystalline-quality, monolayer WSe2. The average synthesized WSe2 crystallite possessed an edge length of ~ 30 microns. After synthesis, the properties of the WSe2 membranes were characterized using Raman and photoluminescence spectroscopy. For device fabrication, Cr contacts were deposited atop the WSe2 membranes using photolithography with a dark-field mask and a metal lift-off process with electron-beam evaporation. After device fabrication, we then proceeded to use these devices for gas sensing applications, where two terminal electronic transport measurements allowed us to monitor the modulation in the WSe2 transport characteristics with incoming gas flow. The I-V response to target gases N2 and CO2 were recorded to investigate the effects of surface adsorption mechanisms of extrinsic molecules on our material’s conducting behavior.
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Understanding gas flow behavior is crucial in the ability of materials to sense toxic gasses for environmental, industrial, safety, agriculture, and related applications. Conventional metal oxide-based gas sensors such as SnO2 and TiO2, suffer from poor stability at higher operating temperatures, and can degrade with exposure to higher levels of humidity. Two - dimensional (2D) materials serve as a promising candidate for gas sensing studies because of their large surface area-tovolume ratio, ease of surface functionalization, and the relative simplicity in their integration with microelectronics fabrication approaches within a planar 3D device architecture. In particular, the microstructure of solution-processed graphene appears to be well-suited to surface adsorption processes, as one of the governing mechanisms in devices that are candidates for gas sensing, given its more porous microstructure compared to vapor synthesized materials. In our work we report on here, we measure the electrical transport characteristics of ink jet printed graphene to incoming gas flow, specifically to N2 and CO2. This work serves as a prototypical platform to study the device characteristics of solution processed graphene and other 2D materials for more exotic gases in the future for gas sensing applications.
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Boron-doped diamonds (BDD) are known for their excellent properties such as high thermal conductivity, high mobility, low absorption in visible light, and biocompatibility. In this work, we investigated the electrical, morphological and optical properties of heavily boron-doped diamond thin sheets as a function of methane concentration in the gas phase. Free-standing diamond sheets were fabricated using a microwave plasma-assisted chemical vapor deposition. The methane concentration was controlled by adding CH4 (up to 4%) to the gas phase, while the /[C] ratio was 20,000 ppm. The samples grown with a higher methane concentration show more defects providing additional conduction paths. As a result, the lowest resistance was observed for the sample with a 4% methane concentration in the gas phase. Morphological studies suggest that a strong increase in the standard deviation of grain size and larger thickness of films is correlated with a higher sp2 phase. Moreover, an increase of disordered carbon content is accompanied by a lower transparency of the BDD sheets. This experiment could serve as a stepping stone in the future production of highly conductive large-area boron-doped diamond sheets.
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A comparative study of Stranski-Krastanov (SK), sub-monolayer (SML) and coupled SK on SML InAs quantum dots as active region in InGaAs/GaAs/AlGaAs DDWELL heterostructure was done. Incorporation of additional high band gap confinement enhancing (CE) AlxGa1-xAs barrier helps to create new energy levels, increase the absorption coefficient, reduce dark current and improve crystalline quality of the heterostructure. This is because of the CE barrier which reduces In-adatom out-diffusion. Three different DDWELL heterostructure A, B and C with active regions as SK, SML and SK on SML respectively, had been modelled using the Nextnano simulation tool keeping all other parameters same. Photoluminescence (PL) emission wavelength, biaxial strains and hydrostatic strain profiles of heterostructures A, B and C were compared. Hydrostatic strain with less magnitude leads to better carrier confinement within the conduction band, and biaxial strain with high magnitude increases splitting between heavy-hole and light- hole bands, generating a red-shift in PL emission wavelength. It can be observed from the computed result that biaxial and hydrostatic strain in the SK QD are enhanced in structure C compared to A. Likewise, biaxial strain and hydrostatic strain in the SML QD stacks are enhanced in structure C compared to B. PL emission wavelength of structures A, B, and C were observed to be 1116nm, 864nm and 1170nm respectively. Therefore, structure C exhibits minimum strain among the heterostructures and highest PL emission wavelength for SWIR applications.
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In the current study, Y-doped vertically aligned ZnO nanowires are grown on p-Si substrates by employing cost-effective double-step chemical bath deposition technique. The doping percentages are varied systematically (YxZn1-xO, x= 0.0, 0.01, 0.02, 0.03, 0.04 M) to investigate the impact of rare earth doping on structural, optical and luminescence properties of ZnO nanowires. The crystalline quality, morphology, optical absorbance and defect states of grown nanowires are studied extensively by employing XRD, FESEM, UV-VIS and room-temperature PL. XRD results reveal that Y-doped ZnO nanowires have single phase hexagonal structure without any extra peaks related to the Y-mixed oxides. FESEM analysis indicates that the dopant with higher radius dose not affected the morphology of ZnO nanowires. The optical energy band gaps of such nanowires are calculated by employing UV-VIS spectroscopy and values are estimated to be 3.11 eV to 2.97 eV. The absorption coefficient, reflective index and extinction coefficient are also extracted and analysed for all of such nanowires. PL results showed that the undoped ZnO nanowires exhibit low UV emission (374 nm) and relatively high green emission (552 nm), whereas, after a low amount of Y doping, UV emission peak enhanced along with an additional blue emission peak at 437 nm. Such blue emission peak is associated with the Zn interstitials related defects, which is generally responsible for the enhancement of donor concentrations in ZnO. Significantly, the oxygen vacancy related green emission peak reduces gradually with increasing Y incorporation. The work provides a detailed study on optical properties of Y-doped ZnO nanowires, which is essential for developing the next-generation heterojunction based optoelectronic devices.
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In current study, the variation of sub-capping thickness of InGaAs strain reducing layer (SRL) of InAs quantum dot heterostructure using digital alloy approach is presented. The thickness of 6 nm SRL of conventional structure (sample A) is divided equally with 2 nm thickness (sample B) by using digital alloy approach. Further, using such approach, this thick 6 nm capping is divided in unequal fashion for sample C (1 nm, 2 nm and 3 nm) and sample D (3 nm, 2 nm and 1 nm) from InAs QD towards top GaAs layer. The In-content inside the SRL of the sample A is 15%, whereas, In-content inside the divided-SRL is considered as 45%, 30% and 15% for all other samples. Such composition of SRLs helps in reducing the In-out diffusion, minimizing the lattice mismatch at InAs QD-SRL and SRL-top GaAs layer interfaces, and also reduces the strain inside the overall heterostructures. Two strains, namely hydrostatic and biaxial are calculated by using Nextnano for all the structures and compared simultaneously. The hydrostatic strain inside the QD of sample D is reduced by 4.74%, 1.07% and 2.269% and the biaxial strain inside the QD of sample D is improved by 1.66%, 0.696% and 1.276% as compared to that of samples A, B and C, respectively. The computed PL emission of samples A, B, C and D are observed to be 1305 nm, 1365 nm, 1349 nm and 1375 nm, respectively. Hence, sample D is the optimum choice for fabricating future opto-electronic devices.
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