20 research outputs found
Emerging Artificial Two-Dimensional van der Waals Heterostructures for Optoelectronics
Two-dimensional (2D) materials are attracting explosive attention for their intriguing potential in versatile applications, covering optoelectronics, electronics, sensors, etc. An attractive merit of 2D materials is their viable van der Waals (VdW) stacking in artificial sequence, thus forming different atomic arrangements in vertical direction and enabling unprecedented tailoring of material properties and device application. In this chapter, we summarize the latest progress in assembling VdW heterostructures for optoelectronic applications by beginning with the basic pick-transfer method for assembling 2D materials and then discussing the different combination of 2D materials of semiconductor, conductor, and insulator properties for various optoelectronic devices, e.g., photodiode, phototransistors, optical memories, etc
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Reconfigurable two-dimensional optoelectronic devices enabled by local ferroelectric polarization.
Ferroelectric engineered pn doping in two-dimensional (2D) semiconductors hold essential promise in realizing customized functional devices in a reconfigurable manner. Here, we report the successful pn doping in molybdenum disulfide (MoS2) optoelectronic device by local patterned ferroelectric polarization, and its configuration into lateral diode and npn bipolar phototransistors for photodetection from such a versatile playground. The lateral pn diode formed in this way manifests efficient self-powered detection by separating ~12% photo-generated electrons and holes. When polarized as bipolar phototransistor, the device is customized with a gain ~1000 by its transistor action, reaching the responsivity ~12 A W-1 and detectivity over 1013 Jones while keeping a fast response speed within 20 μs. A promising pathway toward high performance optoelectronics is thus opened up based on local ferroelectric polarization coupled 2D semiconductors
Cellulose nanofiber paper as an ultra flexible nonvolatile memory
On the development of flexible electronics, a highly flexible nonvolatile memory, which is an important circuit component for the portability, is necessary. However, the flexibility of existing nonvolatile memory has been limited, e.g. the smallest radius into which can be bent has been millimeters range, due to the difficulty in maintaining memory properties while bending. Here we propose the ultra flexible resistive nonvolatile memory using Ag-decorated cellulose nanofiber paper (CNP). The Ag-decorated CNP devices showed the stable nonvolatile memory effects with 6 orders of ON/OFF resistance ratio and the small standard deviation of switching voltage distribution. The memory performance of CNP devices can be maintained without any degradation when being bent down to the radius of 350 μm, which is the smallest value compared to those of existing any flexible nonvolatile memories. Thus the present device using abundant and mechanically flexible CNP offers a highly flexible nonvolatile memory for portable flexible electronics.Nagashima, K., Koga, H., Celano, U. et al. Cellulose Nanofiber Paper as an Ultra Flexible Nonvolatile Memory. Sci Rep 4, 5532 (2014). https://doi.org/10.1038/srep05532
Nanoscale Size-Selective Deposition of Nanowires by Micrometer Scale Hydrophilic Patterns
Controlling the post-growth assembly of nanowires is an important challenge in the development of functional bottom-up devices. Although various methods have been developed for the controlled assembly of nanowires, it is still a challenging issue to align selectively heterogeneous nanowires at desired spatial positions on the substrate. Here we report a size selective deposition and sequential alignment of nanowires by utilizing micrometer scale hydrophilic/hydrophobic patterned substrate. Nanowires dispersed within oil were preferentially deposited only at a water/oil interface onto the hydrophilic patterns. The diameter size of deposited nanowires was strongly limited by the width of hydrophilic patterns, exhibiting the nanoscale size selectivity of nanowires deposited onto micrometer scale hydrophilic patterns. Such size selectivity was due to the nanoscale height variation of a water layer formed onto the micrometer scale hydrophilic patterns. We successfully demonstrated the sequential alignment of different sized nanowires on the same substrate by applying this size selective phenomenon. D esigning the post-growth assembly of nanowires on the substrate offers a fascinating way to explore novel functional nanoscale devices. In general, such assembling processes of nanowires can be performed at relatively low temperatures , which are much lower than typical nanowire growth temperatures This study proposes a size selective deposition technique and sequential alignment of nanowires by utilizing micrometer scale hydrophilic/hydrophobic patterned substrate. We utilized nanowires dispersed within oil, which were preferentially deposited only at a water/oil interface onto the hydrophilic patterns. We found the nanoscale size selectivity of nanowires deposited onto micrometer scale hydrophilic patterns. This nanoscale size selectivity by micrometer scale patterns can be extended to the sequential alignment of different sized nanowires on the same substrate. Result
Effect of defect content on the unipolar resistive switching characteristics of ZnO thin film memory devices
In this study, unipolar resistive switching (URS) characteristics in ZnO thin film memory devices were systematically investigated with variable defect content. ZnO films displayed typically URS behavior while oxygen-deficient ZnO 1-x films did not show resistive switching effects. The devices with two intentional Ohmic interfaces still show URS. These results show that appearance of URS behavior can be dominated by initial oxygen vacancy content in ZnO thin films. Modest increase in oxygen vacancy content in ZnO films will lead to forming-free and narrower distributions of switching parameters (set and reset voltage, high and low resistance states). It indicates that controlling the initial oxygen vacancy content was an effective method to enhance the URS performance
Simultaneously ultrafast and robust two-dimensional flash memory devices based on phase-engineered edge contacts
Abstract As the prevailing non-volatile memory (NVM), flash memory offers mass data storage at high integration density and low cost. However, due to the ‘speed-retention-endurance’ dilemma, their typical speed is limited to ~microseconds to milliseconds for program and erase operations, restricting their application in scenarios with high-speed data throughput. Here, by adopting metallic 1T-LixMoS2 as edge contact, we show that ultrafast (10–100 ns) and robust (endurance>106 cycles, retention>10 years) memory operation can be simultaneously achieved in a two-dimensional van der Waals heterostructure flash memory with 2H-MoS2 as semiconductor channel. We attribute the superior performance to the gate tunable Schottky barrier at the edge contact, which can facilitate hot carrier injection to the semiconductor channel and subsequent tunneling when compared to a conventional top contact with high density of defects at the metal interface. Our results suggest that contact engineering can become a strategy to further improve the performance of 2D flash memory devices and meet the increasing demands of high speed and reliable data storage
All-nanocellulose nonvolatile resistive memory
Celano, U., Nagashima, K., Koga, H. et al. All-nanocellulose nonvolatile resistive memory. NPG Asia Mater 8, e310 (2016). https://doi.org/10.1038/am.2016.144
Van der Waals Coupled Organic Molecules with Monolayer MoS<sub>2</sub> for Fast Response Photodetectors with Gate-Tunable Responsivity
As a direct-band-gap
transition metal dichalcogenide (TMD), atomic
thin MoS<sub>2</sub> has attracted extensive attention in photodetection,
whereas the hitherto unsolved persistent photoconductance (PPC) from
the ungoverned charge trapping in devices has severely hindered their
employment. Herein, we demonstrate the realization of ultrafast photoresponse
dynamics in monolayer MoS<sub>2</sub> by exploiting a charge transfer
interface based on surface-assembled zinc phthalocyanine (ZnPc) molecules.
The formed MoS<sub>2</sub>/ZnPc van der Waals interface is found to
favorably suppress the PPC phenomenon in MoS<sub>2</sub> by instantly
separating photogenerated holes toward the ZnPc molecules, away from
the traps in MoS<sub>2</sub> and the dielectric interface. The derived
MoS<sub>2</sub> detector then exhibits significantly improved photoresponse
speed by more than 3 orders (from over 20 s to less than 8 ms for
the decay) and a high responsivity of 430 A/W after Al<sub>2</sub>O<sub>3</sub> passivation. It is also demonstrated that the device
could be further tailored to be 2–10-fold more sensitive without
severely sacrificing the ultrafast response dynamics using gate modulation.
The strategy presented here based on surface-assembled organic molecules
may thus pave the way for realizing high-performance TMD-based photodetection
with ultrafast speed and high sensitivity