W-doped In_(2)O_(3) nanofiber optoelectronic neuromorphic transistors with synergistic synaptic plasticity

Neuromorphic devices that mimic the information processing function of biological synapses and neurons have attracted considerable attention due to their potential applications in brain-like perception and computing. In this paper,neuromorphic transistors with W-doped In_(2)O_(3)nanofibers as the channel layers are fabricated and optoelectronic synergistic synaptic plasticity is also investigated. Such nanofiber transistors can be used to emulate some biological synaptic functions, including excitatory postsynaptic current(EPSC), long-term potentiation(LTP), and depression(LTD). Moreover, the synaptic plasticity of the nanofiber transistor can be synergistically modulated by light pulse and electrical pulse.At last, pulsed light learning and pulsed electrical forgetting behaviors were emulated in 5×5 nanofiber device array.Our results provide new insights into the development of nanofiber optoelectronic neuromorphic devices with synergistic synaptic plasticity.

Cobalt tungsten phosphide with tunable W-doping as highly efficient electrocatalysts for hydrogen evolution reaction

It has been of interest in seeking electrocatalysts that could exercise equally high-efficient and durable hydrogen evolution upon nonselective electrolytes in both acidic and alkaline environments. Herein, we report a facile strategy to fabricate cobalt tungsten phosphides (CoxW2−xP2/C) hollow polyhedrons with tunable composition based on metal-organic frameworks (MOFs) template method. By the deliberate control of W doping, the synthesized catalyst with the composition of Co0.9W1.1P2/C is found to be able to achieve a current density of 10 mA·cm^(−2) at overpotentials of 35 and 54 mV in acidic and alkaline media, respectively. This combined electrochemical property stands atop the state-of-the-art electrocatalyst counterparts. To unveil the peculiar behavior of the structure, density functional theory (DFT) calculation was implemented and reveals that the surface W-doping facilitates the optimization of hydrogen absorption free energy (ΔGH*) as well as the thermodynamic and kinetics barriers for water dissociation, which is coupled with the hollow structure of Co-W phosphides, leading to the prominent HER catalytic performance.

Crystallization and inter-diffusional behaviors in the formation of VO2(B) thin film with layered W-doping

To achieve a better material for uncooled infrared (IR) detector, polycrystalline VO2(B) thin films with layered W-doping were fabricated on Si substrates by magnetron sputtering, and the best temperature coefficient of resistance (TCR) value reached -4.1%/K. The film synthesis was in a two-step route, first deposition at room temperature and then post-deposition annealing at 450 ℃, to better control the crystallization behavior. Various transmission electron microscopy (TEM) methods were employed to investigate three sets of multi-layered films with different deposition time, 10, 20, and 30 min, with especial emphasis on the effect of layered W-doping scheme on the formation of multiple VO2(B) layers. Spatial-resolved energy dispersive X-ray spectroscopy (EDS) revealed the alternative patterns of W-rich layers and W-poor layers, while the thinner films exhibited better crystallinity and texturing. By comparison with an as-deposited film, it was found that the inter-diffusion between the two types of layers was completed in the deposition step while both remained in amorphous structure. A stable W solution of about 8 cat% in VO2(B) layers measured from all these films indicated that the layered doping can tailor the multi-layered microstructure to optimize the performance of VO2(B) films.

Synthesis and Characterization of W-doped TiO_2 Supported by Hybrid Carbon Nanomaterials of Multi-walled Carbon Nanotubes and C_(60) Fullerene by a Hydrothermal Method

W-doped TiO2 supported by hybrid carbon nanomaterials of multi-walled carbon nanotubes and C60 fullerene was synthesized by a simple hydrothermal method. The material displayed high visible light photocatalytic activity. X-ray diffraction, field emission transmission electron microscopy, ultra violet/visible light absorption and photoluminescence spectroscopy were used to characterize the material as photoeatalyst. Photocatalytic activity on the degradation of Rhodamine B dye in an aqueous solution under ultraviolet light and visible light irradiation was also studied. The experimental results indicated that the photocatalytic activity of the material was much higher than that of pure TiO2 or Degussa P25 TiO2.

High-quality CdS quantum dots sensitized ZnO nanotube array films for superior photoelectrochemical performance

The surface characteristics of ZnO were synthetically optimized by a self-designed simultaneous etching and W-doping hydrothermal method utilizing as-prepared ZnO nanorod(NR)array films as the template.Benefiting from the etching and regrowth process and the different structural stabilities of the various faces of ZnO NRs,the uniquely etched and W-doped ZnO(EWZ)nanotube(NT)array films with larger surface area,more active sites and better energy band structure were used to improve the photoelectrochemical(PEC)performance and the loading quality of CdS quantum dots(QDs).On the basis of their better surface characteristics,the CdS QDs were uniformly loaded on EWZ NT array film with a good coverage ratio and interface connection;this effectively improved the light-harvesting ability,charge transportation and separation as well as charge injection efficiency during the PEC reaction.Therefore,all the CdS QD-sensitized EWZ NT array films exhibited significantly enhanced PEC performance.The CdS/EWZ-7 composite films exhibited the optimal photocurrent density with a value of 12 mA·cm^(-2),2.5 times higher than that of conventional CdS/ZnO-7 composite films under the same sensitization times with CdS QDs.The corresponding etching and optimizing mechanisms were also discussed.