RESUMEN
The performance of graphene field-effect transistors is limited by the drastically reduced carrier mobility of graphene on silicon dioxide (SiO2) substrates. Here we demonstrate an ultrasensitive ultraviolet (UV) phototransistor featuring an organic self-assembled monolayer (SAM) sandwiched between an inorganic ZnO quantum dots decorated graphene channel and a conventional SiO2/Si substrate. Remarkably, the room-temperature mobility of the chemical-vapor-deposition grown graphene channel on the SAM is an order-of-magnitude higher than on SiO2, thereby drastically reducing electron transit-time in the channel. The resulting recirculation of electrons (in the graphene channel) within the lifetime of the photogenerated holes (in the ZnO) increases the photoresponsivity and gain of the transistor to â¼10(8) A/W and â¼3 × 10(9), respectively with a UV to visible rejection ratio of â¼10(3). Our UV photodetector device manufacturing is also compatible with current semiconductor processing, and suitable for large volume production.
Asunto(s)
Grafito/química , Puntos Cuánticos/química , Dióxido de Silicio/química , Rayos Ultravioleta , Óxido de Zinc/química , SemiconductoresRESUMEN
An environmentally friendly, low-cost, and large-scale method is developed for fabrication of Cl-doped ZnO nanowire arrays (NWAs) on 3D graphene foam (Cl-ZnO NWAs/GF), and investigates its applications as a highly efficient field emitter and photocatalyst. The introduction of Cl-dopant in ZnO increases free electrons in the conduction band of ZnO and also leads to the rough surface of ZnO NWAs, which greatly improves the field emission properties of the Cl-ZnO NWAs/GF. The Cl-ZnO NWAs/GF demonstrates a low turn-on field (≈1.6 V µm(-1)), a high field enhancement factor (≈12844), and excellent field emission stability. Also, the Cl-ZnO NWAs/GF shows high photocatalytic efficiency under UV irradiation, enabling photodegradation of organic dyes such as RhB within ≈75 min, with excellent recyclability. The excellent photocatalytic performance of the Cl-ZnO NWAs/GF originates from the highly efficient charge separation efficiency at the heterointerface of Cl-ZnO and GF, as well as improved electron transport efficiency due to the doping of Cl. These results open up new possibilities of using Cl-ZnO and graphene-based hybrid nanostructures for various functional devices.
RESUMEN
Chemical doping of nitrogen into graphene can significantly enhance the reversible capacity and cyclic stability of the graphene-based lithium ion battery (LIB) anodes, and first principles calculations based on density functional theory suggested that pyridinic-N shows stronger binding with Li with reduced energy barrier for Li diffusion and thus is more effective for Li storage than pyrrolic and graphitic-N. Here, we report a novel and rapid (~30 seconds) process to fabricate nitrogen-doped graphene (NGr) by simultaneous thermal reduction of graphene oxide with ammonium hydroxide. The porous NGr with dominant pyridinic N atoms displays greatly enhanced reversible capacities, rate performance and exceptional cyclic stability as compared with pristine graphene. The reversible discharge capacity of the NGr electrode cycled between 0.01-3 V can reach 453 mA h g(-1) after 550 cycles at a charge rate of 2 A g(-1) (~5.4 C), and 180 mA h g(-1) after 2000 cycles at a high charge rate of 10 A g(-1) (~27 C) without any capacity fading. When charged within 0.01-1.5 V, the NGr anode still exhibits high reversible capacities of 224 mA h g(-1) and 169 mA h g(-1) after 700 cycles and 800 cycles at a charge rate of 1 A g(-1) and 5 A g(-1), respectively. Ex situ X-ray photoelectron spectroscopy (XPS) analysis of the NGr electrode upon lithiation and delithiation indicated that the pyridinic-N dominates the capacity enhancement at 3 V, while the pyrrolic-N contributes primarily to Li ion storage below 1.5 V.
RESUMEN
A high sensitivity, fast ultraviolet (UV) photodetector was fabricated from WO3 nanodiscs (NDs)/reduced graphene oxide (RGO) composite material. The WO3 NDs/reduced GO composite material was synthesized using a facile three-step synthesis procedure. First, the Na2WO4/GO precursor was synthesized by homogeneous precipitation. Second, the Na2WO4/GO precursor was transformed into Na2WO4/GO composites by acidification. Finally, the Na2WO4/GO composites were reduced to WO3 NDs/RGO via a hydrothermal reduction process. The UV photodetector showed a fast transient response and high responsivity, which are attributed to the improved carrier transport and collection efficiency through graphene. The excellent material properties of the WO3 NDs/RGO composite demonstrated in this work may open up new possibilities for using WO3 NDs/RGO for future optoelectronic applications.
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Enhanced near band gap edge (NBE) emissions of PVA-ZnO nanoparticles were achieved by employing SiO(2)-Au core/shell nanostructures whereas the defect-level emission (DLE) is greatly suppressed. A maximum enhancement of nearly 400% was observed using SiO(2)-Au for the emission with optical resonance at 554 nm. SiO(2)-Au core/shell nanostructures also show a superior tunability of resonance energy as compared to that of the pure metal nanoparticles. The enhancement of the NBE emission and suppressed DLE is ascribed to the transfer of the energetic electrons excited by surface plasmon from metal nanoparticles to the conduction band of ZnO nanoparticles.
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Normal incident photodetection at mid infrared spectral region is achieved using the intersublevel transitions from strain-free GaAs quantum dot pairs in Al(0.3)Ga(0.7)As matrix. The GaAs quantum dot pairs are fabricated by high temperature droplet epitaxy, through which zero strain quantum dot pairs are obtained from lattice matched materials. Photoluminescence, photoluminescence excitation optical spectroscopy, and visible-near-infrared photoconductivity measurement are carried out to study the electronic structure of the photodetector. Due to the intersublevel transitions from GaAs quantum dot pairs, a broadband photoresponse spectrum is observed from 3 to 8 microm with a full width at half-maximum of approximately 2.0 microm.
Asunto(s)
Arsenicales/química , Galio/química , Nanotecnología/métodos , Fotometría/métodos , Puntos Cuánticos , Temperatura , Luminiscencia , Nanotecnología/instrumentación , Fotometría/instrumentación , Análisis EspectralRESUMEN
In this work, we demonstrate an ultrasensitive, visible-blind ultraviolet (UV) photodetector based on perovskite-polymer hybrid structure. A novel wide-band-gap vacancy-ordered lead-free inorganic perovskite Cs2SnCl6 with Nd3+ doping is employed in the active layer of this hybrid photodetector. Remarkably, with interfacial charge-controlled hole-injection operating mechanism, our device achieves a maximum detectivity of 6.3 × 1015 Jones at 372 nm, fast photoresponse speed with rise time and fall time in the order of milliseconds, and a large linear dynamic range of 118 dB. The performance is significantly better than most of the existing organic and inorganic semiconductor UV photodetectors reported so far, and its detectivity is close to 1 order of magnitude higher than that of the photomultiplication tube (PMT) in the UV region. In addition, the photodetector demonstrated excellent environmental stability, which is critical for commercial deployment of perovskite-based optoelectronic devices. The results presented in this work open a new route toward development of high-performance optoelectronic devices using perovskite-based hybrid nanomaterial systems.
RESUMEN
Graphene, a single layer of carbon atoms bonded in a hexagonal lattice, is the thinnest, strongest, and stiffest known material and an excellent conductor of heat and electricity. However, these superior properties have yet to be realized for graphene-derived macroscopic structures such as graphene fibers. We report the fabrication of graphene fibers with high thermal and electrical conductivity and enhanced mechanical strength. The inner fiber structure consists of large-sized graphene sheets forming a highly ordered arrangement intercalated with small-sized graphene sheets filling the space and microvoids. The graphene fibers exhibit a submicrometer crystallite domain size through high-temperature treatment, achieving an enhanced thermal conductivity up to 1290 watts per meter per kelvin. The tensile strength of the graphene fiber reaches 1080 megapascals.
RESUMEN
An ultraviolet (UV) photodetector is fabricated by sandwiching a nanocomposite active layer between charge-selective semiconducting polymers. The nanocomposite active layer composed of TiO2 nanoparticles (NPs) blended with 1,3-bis(N-carbazolyl)benzene (mCP), which acts as a "valve" controller that enables hole injection into the device upon UV illumination. The UV photodetector demonstrated a high photocurrent to dark current ratio (â¼10(4)), a large linear dynamic range of 60 dB, and a remarkable external quantum efficiency (â¼8.5 × 10(4)%) for the UV light at 351 nm. In addition to discussing the performance of the UV photodetector, a general strategy for design and fabrication of high-performance UV photodetectors with hole injection operation mode is suggested.
RESUMEN
Mechanical and chemical degradations of high-capacity anodes, resulting from lithiation-induced stress accumulation, volume expansion and pulverization, and unstable solid-electrolyte interface formation, represent major mechanisms of capacity fading, limiting the lifetime of electrodes for lithium-ion batteries. Here we report that the mechanical degradation on cycling can be deliberately controlled to finely tune mesoporous structure of the metal oxide sphere and optimize stable solid-electrolyte interface by high-rate lithiation-induced reactivation. The reactivated Co3O4 hollow sphere exhibits a reversible capacity above its theoretical value (924 mAh g(-1) at 1.12 C), enhanced rate performance and a cycling stability without capacity fading after 7,000 cycles at a high rate of 5.62 C. In contrast to the conventional approach of mitigating mechanical degradation and capacity fading of anodes using nanostructured materials, high-rate lithiation-induced reactivation offers a new perspective in designing high-performance electrodes for long-lived lithium-ion batteries.
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We report fabrication of a flexible, thorn-like ZnO-multiwalled carbon nanotube (MWCNT) hybrid paper with high aspect ratio for efficient ultraviolet (UV) sensing and photocatalyst applications. The thorn-like ZnO-MWCNT hybrid paper was synthesized via atomic layer deposition (ALD) of a uniform ZnO thin film on the outside surface of the MWCNT followed by hydrothermal growth of ZnO branches. The hybrid paper achieved very high surface to volume ratio, which is favorable for photodetector and photocatalyst applications. A photodetector fabricated from the hybrid paper demonstrates a high sensitivity to UV light with a maximum photoresponsivity of 45.1 A W(-1) at 375 nm, corresponding to an external quantum efficiency as high as 14927%. The rise time and fall time of the UV photodetector are 29 ms and 33 ms, respectively, indicating fast transient response characteristics for the device. The high photoresponsivity and fast transient response are attributed to efficient carrier transport and collection efficiency of the hybrid paper. Besides, the thorn-like ZnO-MWCNT hybrid paper demonstrates excellent photocatalytic performance under UV irradiation, enabling photo-degradation of organic dyes such as Rhodamine B (RhB) within 90 minutes, with good recyclability.
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Organic phase change materials (PCMs) have been utilized as latent heat energy storage and release media for effective thermal management. A major challenge exists for organic PCMs in which their low thermal conductivity leads to a slow transient temperature response and reduced heat transfer efficiency. In this work, 2D thermally annealed defect-free graphene sheets (GSs) can be obtained upon high temperature annealing in removing defects and oxygen functional groups. As a result of greatly reduced phonon scattering centers for thermal transport, the incorporation of ultralight weight and defect free graphene applied as nanoscale additives into a phase change composite (PCC) drastically improve thermal conductivity and meanwhile minimize the reduction of heat of fusion. A high thermal conductivity of the defect-free graphene-PCC can be achieved up to 3.55 W/(m K) at a 10 wt % graphene loading. This represents an enhancement of over 600% as compared to pristine graphene-PCC without annealing at a comparable loading, and a 16-fold enhancement than the pure PCM (1-octadecanol). The defect-free graphene-PCC displays rapid temperature response and superior heat transfer capability as compared to the pristine graphene-PCC or pure PCM, enabling transformational thermal energy storage and management.
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We report a simple, efficient and versatile method for assembling metal oxide nanomaterial-graphene core-shell structures. An ultraviolet photodetector fabricated from the ZnO nanoparticle-graphene core-shell structures showed high responsivity and fast transient response, which are attributed to the improved carrier transport efficiency arising from graphene encapsulation.
Asunto(s)
Grafito/química , Nanopartículas del Metal/química , Óxido de Zinc/química , Nanopartículas del Metal/ultraestructura , Nanocables/química , Porosidad , Espectrofotometría UltravioletaRESUMEN
A heterojunction photodiode was fabricated from ZnO nanowires (NWs) grown on a p-type Si (100) substrate using a hydrothermal method. Post growth hydrogen treatment was used to improve the conductivity of the ZnO NWs. The heterojunction photodiode showed diode characteristics with low reverse saturation current (5.58 × 10(-7) A), relatively fast transient response, and high responsivity (22 A/W at 363 nm). Experiments show that the photoresponsivity of the photodiode is dependent on the polarity of the voltages. The photoresponsivity of the device was discussed in terms of the band diagrams of the heterojunction and the carrier diffusion process.