Direct epitaxial growth of III-Vs on silicon for optical emitters and detectors is an elusive goal. Nanowires enable the local integration of high-quality III-V material, but advanced devices are hampered by their high-aspect ratio vertical geometry. Here, we demonstrate the in-plane monolithic integration of an InGaAs nanostructure p-i-n photodetector on Si. Using free space coupling, photodetectors demonstrate a spectral response from 1200-1700 nm. The 60 nm thin devices, with footprints as low as ~0.06 μm2, provide an ultra-low capacitance which is key for high-speed operation. We demonstrate high-speed optical data reception with a nanostructure photodetector at 32 Gb s−1, enabled by a 3 dB bandwidth exceeding ~25 GHz. When operated as light emitting diode, the p-i-n devices emit around 1600 nm, paving the way for future fully integrated optical links.
Shewanella oneidensis MR-1 is a platform microorganism for understanding extracellular electron transfer (EET) with a fully sequenced and annotated genome. In comparison to other model microorganisms such as Escherichia coli, the available plasmid parts (such as promoters and replicons) are not sufficient to conveniently and quickly fine-tune the expression of multiple genes in S. oneidensis MR-1. Here, we constructed and characterized a plasmid toolkit that contains a set of expression vectors with a combination of promoters, replicons, antibiotic resistance genes, and an RK2 origin of transfer (oriT) cassette, in which each element can be easily changed by fixed restriction enzyme sites. The expression cassette is also compatible with BioBrick synthetic biology standards. Using green fluorescent protein (GFP) as a reporter, we tested and quantified the strength of promoters. The copy number of different replicons was also measured by real-time quantitative PCR. We further transformed two compatible plasmids with different antibiotic resistance genes into the recombinant S. oneidensis MR-1, enabling control over the expression of two different fluorescent proteins. This plasmid toolkit was further used for overexpression of the MtrCAB porin-c-type cytochrome complex in the S. oneidensis ΔmtrA strain. Tungsten trioxide (WO3) reduction and microbial fuel cell (MFC) assays revealed that the EET efficiency was improved most significantly when MtrCAB was expressed at a moderate level, thus demonstrating the utility of the plasmid toolkit in the EET regulation in S. oneidensis. The plasmid toolkit developed in this study is useful for rapid and convenient fine-tuning of gene expression and enhances the ability to genetically manipulate S. oneidensis MR-1.
Piezoelectric materials have been widely explored, due to their potential applications related to wearable sensors, energy harvesting, and electronics. However, the majority of previously reported flexible sensors cannot simultaneously possess the properties of conductivity, washability, and air permeability, which limits their further development in textile applications. Herein, we have processed a nanofibrous mat to successfully develop a textile, which acquired effective conductivity, while maintaining a soft and porous nature for comfortable wearing. Two steps were implemented in this strategy. First, the surface of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) nanofibers was coated with multiwalled carbon nanotubes (MWCNTs) through electrospinning; second, for preventing the damage by washing, the MWCNTs were welded into the nanofibers to generate a strong connection with the nanofibers by a thermal welding process. With the incorporation of MWCNTs, the electrospun PVDF-HFP nanofibrous mat manifests good conductivity with a sheet resistance of 7.1 ± 2.8 kΩ and excellent mechanical properties (up to 35.4 ± 7.3 MPa). The as-prepared nanofibrous mat exhibits high stability, good bending stability over 10 000 bending cycles, and superior wearability in terms of washability and breathability. Besides, such a nanofibrous mat can be used in contact with the human skin or attached to textiles for body motion monitoring, displaying great potential for wearable devices.
In the synthesis of Au/Pd bimetallic nanocrystals, a layer-by-layer growth is favored, owing to the low bonding energy between Pd atoms (E Pd–Pd) in comparison with E Au–Pd, resulting in homogeneous core/shell nanostructures. Herein, we demonstrate designed synthetic tactics to unconventional Au/Pd heterostructures through a deposition-dominant growth pathway of the newly reduced Pd atoms, which break the intrinsically favored layer-by-layer growth. Pd thus grows on Au seeds in a heterogeneous nucleation manner. The resulting anisotropic Pd nanorods array on the two basal facets and three side facets of the Au triangular seeds in a high density to form 2D/1D Au/Pd heterostructures. It is noticed that Pd nanorods align in an extremely high order. They grow almost in a row with the base of the rod located overlapped on the Au surface. This versatile approach has been also applied to other Au nanocrystal seeds, involving hexagonal nanoplates, circular nanodisks, nanorods, and nanobipyramids. Furthermore, the 2D/1D Au/Pd heterostructures exhibit an enhanced electrocatalytic performance toward ethanol oxidation in alkaline condition, owing to their unique structure and the exposure of Au. We believe that our synthetic strategy is highly valuable for the construction of multimetallic nanostructures with desired architectures and thus intriguing properties.
Fibers are raw materials used for manufacturing yarns and fabrics, and their properties are closely related to the performances of their derivatives. It is indispensable to implement fiber identification in analyzing textile raw materials. In this paper, seven common fibers, including cotton, tencel, wool, cashmere, polyethylene terephthalate (PET), polylactic acid (PLA), and polypropylene (PP), were prepared. After analyzing the merits and demerits of the current methods used to identify fibers, near-infrared (NIR) spectroscopy was used owing to its significant superiorities, the foremost of which is it can capture the tiny information differences in chemical compositions and morphological features to display the characteristic spectral curve of each fiber. First, the fibers’ spectra were collected, and then, the relationships between the vibrations of characteristic chemical groups and the corresponding wavelengths were researched to organize a spectral information library that would be beneficial to achieve quick identification and classification. Finally, to achieve intelligent detection, pattern recognition approaches, including principal component analysis (PCA) (used to extract information of interest), soft independent modeling of class analogy (SIMCA), and linear discrimination analysis (LDA) (defined using two classifiers), assisted in accomplishing fiber identification. The experimental results – obtained by combining PCA and SIMCA – displayed that five of seven target fibers, namely, cotton, tencel, PP, PLA, and PET, were distributed with 100% recognition rate and 100% rejection rate, but wool and cashmere fibers yielded confusing results and led to relatively low recognition rate because of the high proportion of similarities between these two fibers. Therefore, the six spectral bands of interest unique to wool and cashmere fibers were selected, and the absorbance intensities were imported into the classifier LDA, where wool and cashmere were group-distributed in two different regions with 100% recognition rate. Consequently, the seven target fibers were accurately and quickly distinguished by the NIR method to guide the fiber identification of textile materials.
Multifunctional metal nanostructures with a hollow feature, especially for nanoframes, are highly attractive owing to their high surface‐to‐volume ratios. However, pre‐grown metal nanocrystals are always involved during the preparation procedure, and a synthetic strategy without the use of a pre‐grown template is still a challenge. In this article, a template‐free strategy is reported for the preparation of novel AuPt alloy nanoframes through simply mixing HAuCl4 and H2PtCl6 under mild conditions. The alloy nanostructures show a bipyramid‐frame hollow architecture with the existence of only the ten ridges and absence of their side faces. This is the first report of bipyramid‐like nanoframes and a template‐free method under mild conditions. This configuration merges the plasmonic features of Au and highly active catalytic sites of Pt in a single nanostructure, making it an ideal multifunctional platform for catalyzing and monitoring the catalytic reaction in real time. The superior catalytic activity is demonstrated by using the reduction of nitrobenzene to the corresponding aminobenzene as a model reaction. More importantly, the AuPt nanoframes can track the reduction process on the basis of the SERS signals of the reactants, intermediates, and products, which helps to reveal the reaction mechanism. In addition, the AuPt nanoframes show much higher electrocatalytic properties toward the methanol oxidation reaction than commercial Pt/C electrocatalysts.
Dielectric shielded nanoscale patch laser resonators are introduced. Low-index dielectric shield layers surrounding a high-index core are shown to significantly reduce both metal and radiation losses. Structures suitable for both optical and electrical pumping and smaller than the vacuum wavelength in all three dimensions are shown to have a low enough threshold gain to lase at room temperature. Shifting the gain medium core provides control over the radiation pattern of the resonator and enables coupling of the laser light into a waveguide, opening opportunities for chipscale integration.
High performance aluminum-ion (Al-ion) batteries are widely concerned owning to high theoretical capacity, abundance of Al metal and good safety. Here, we develop a hierarchical VS2@VS4 composing of VS4 nanorod...
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.