A novel type of flexible fiber/wearable supercapacitor that is composed of two fiber electrodes - a helical spacer wire and an electrolyte - is demonstrated. In the carbon-based fiber supercapacitor (FSC), which has high capacitance performance, commercial pen ink is directly utilized as the electrochemical material. FSCs have potential benefits in the pursuit of low-cost, large-scale, and efficient flexible/wearable energy storage systems.
Designing efficient electrocatalysts for hydrogen evolution reaction is significant for renewable and sustainable energy conversion. Here, we report single-atom platinum decorated nanoporous Co 0 . 85 Se (Pt/np-Co 0 . 85 Se) as efficient electrocatalysts for hydrogen evolution. The achieved Pt/np-Co 0 . 85 Se shows high catalytic performance with a near-zero onset overpotential, a low Tafel slope of 35 mV dec −1 , and a high turnover frequency of 3.93 s −1 at −100 mV in neutral media, outperforming commercial Pt/C catalyst and other reported transition-metal-based compounds. Operando X-ray absorption spectroscopy studies combined with density functional theory calculations indicate that single-atom platinum in Pt/np-Co 0 . 85 Se not only can optimize surface states of Co 0 . 85 Se active centers under realistic working conditions, but also can significantly reduce energy barriers of water dissociation and improve adsorption/desorption behavior of hydrogen, which synergistically promote thermodynamics and kinetics. This work opens up further opportunities for local electronic structures tuning of electrocatalysts to effectively manipulate its catalytic properties by an atomic-level engineering strategy.
Cassava is a major tropical food crop in the Euphorbiaceae family that has high carbohydrate production potential and adaptability to diverse environments. Here we present the draft genome sequences of a wild ancestor and a domesticated variety of cassava and comparative analyses with a partial inbred line. We identify 1,584 and 1,678 gene models specific to the wild and domesticated varieties, respectively, and discover high heterozygosity and millions of single-nucleotide variations. Our analyses reveal that genes involved in photosynthesis, starch accumulation and abiotic stresses have been positively selected, whereas those involved in cell wall biosynthesis and secondary metabolism, including cyanogenic glucoside formation, have been negatively selected in the cultivated varieties, reflecting the result of natural selection and domestication. Differences in microRNA genes and retrotransposon regulation could partly explain an increased carbon flux towards starch accumulation and reduced cyanogenic glucoside accumulation in domesticated cassava. These results may contribute to genetic improvement of cassava through better understanding of its biology.
Dimethylsulfoniopropionate (DMSP) and its catabolite dimethyl sulfide (DMS) are key marine nutrients 1,2 , with roles in global sulfur cycling 2 , atmospheric chemistry 3 , signalling 4,5 and, potentially, climate regulation 6,7. DMSP production was previously thought to be an oxic and photic process, mainly confined to the surface oceans. 2 However, here we show that DMSP concentrations and DMSP/DMS synthesis rates were higher in surface marine sediment from e.g., saltmarsh ponds, estuaries and the deep ocean than in the overlying seawater. A quarter of bacterial strains isolated from saltmarsh sediment produced DMSP (up to 73 mM), and previously unknown DMSPproducers were identified. Most DMSP-producing isolates contained dsyB 8 , but some alphaproteobacteria, gammaproteobacteria and actinobacteria utilised a methionine methylation pathway independent of DsyB, previously only associated with higher plants. These bacteria contained a methionine methyltransferase 'mmtN' gene-a marker for bacterial DMSP synthesis via this pathway. DMSP-producing bacteria and their dsyB and/or mmtN transcripts were present in all tested seawater samples and Tara Oceans bacterioplankton datasets, but were far more abundant in marine surface sediment. Approximately 10 8 bacteria per gram of surface marine sediment are predicted to produce DMSP, and their contribution to this process should be included in future models of global DMSP production. We propose that coastal and marine sediments, which cover a large part of the Earth's surface, are environments with high DMSP and DMS productivity, and that bacteria are important producers within them. Approximately eight billion tonnes of DMSP is produced by phytoplankton in the Earth's surface oceans annually 9. However, surface sediment from saltmarsh ponds, an estuary and the deep ocean (with high pressures and no light) contained DMSP levels (5-128 nmol DMSP g-1) that were up to ~three orders of magnitude higher than the overlying seawater (0.01-0.70 nmol DMSP ml-1) (Fig. 1a-b, Supplementary Tables 1a and 2), a phenomenon also observed in 10,11. DMSP concentration decreased with depth, being much lower in anoxic sediment, but even in deeper sediments the concentration was approximately an order of magnitude higher than in the overlying seawater (Supplementary Table 1a). This study focused on DMSP synthesis in coastal surface sediments, where DMSP concentrations were highest. The
With its extraordinary properties as the strongest and stiffest material ever measured and the best-known electrical conductor, graphene could have promising applications in many fields, especially in the area of nanocomposites. However, processing graphene-based nanocomposites is very difficult. So far, graphene-based nanocomposites exhibit rather poor properties. Nacre, the gold standard for biomimicry, provides an excellent example and guidelines for assembling two-dimensional nanosheets into high performance nanocomposites. The inspiration from nacre overcomes the bottleneck of traditional approaches for constructing nanocomposites, such as poor dispersion, low loading, and weak interface interactions. This tutorial review summarizes recent research on graphene-based artificial nacre nanocomposites and focuses on the design of interface interactions and synergistic effects for constructing high performance nanocomposites. This tutorial review also focuses on a perspective of the dynamic area of graphene-based nanocomposites, commenting on whether the concept is viable and practical, on what has been achieved to date, and most importantly, what is likely to be achieved in the future.
Terahertz technology promises broad applications, which calls for terahertz electromagnetic interference (EMI) shielding materials to alleviate radiation pollution. 2D transition metal carbides and/or nitrides (MXenes) with metallic conductivity are promising for EMI shielding, but simultaneously realizing light weight, high stability, and foldability in a MXene shielding material to meet the requirements of increasingly popular portable and wearable equipment has remained a great challenge. Herein, an ion-diffusion-induced gelation method is demonstrated to synthesize free-standing, light-weight, foldable, and highly stable MXene foams, in which MXene sheets are cross-linked by multivalent metal ions and graphene oxide to form an oriented porous structure. The method is highly efficient, controllable, and versatile for scalable generation of functional 3D MXene structures with arbitrary shapes and synergistic properties. The distinctive cross-linked porous structure endows the light-weight MXene foam with good foldability, outstanding durability and stability in wet environments, and an excellent terahertz shielding effectiveness of 51 dB at a small thickness of 85 μm. This work not only provides an insight for the on-target design of high-performance terahertz shielding materials but also expands the applications of MXenes in 3D macroscopic form.
Nitrogen-doped graphene was demonstrated as an efficient and alternative metal-free electrocatalyst for dye-sensitized solar cells. Electrochemical measurements showed that the nitrogen-doping process can remarkably improve the catalytic activity of graphene toward triiodide reduction, lower the charge transfer resistance, and thus enhance the corresponding photovoltaic performance. Furthermore, the nitrogen doping levels ranging from 3.5 at% to 18 at%, as well as the nitrogen states (including pyrrolic, pyridinic and quaternary configurations) in graphene, were controlled to interpret the roles of graphene structure in catalytic activity and device performance. The results suggested that the nitrogen states, rather than the total N content, have a significant effect on the catalytic activity. Both pyridinic and quaternary nitrogen states can provide active sites for promoting triiodide reduction reaction, probably due to the shift in redox potential and the lowered adsorption energy.
Exposure of neonatal rat cardiac myocytes to ouabain concentrations that caused partial inhibition of Na+/K+-ATPase but no loss of viability, increased c-fos and c-jun mRNAs and the transcription factor AP-1. The increased mRNAs were proportional to the extent of inhibition of Na+/K+-ATPase and the resulting rise in steady state intracellular Ca2+ concentration. The rapid and sustained increase of c-fos mRNA was shown to be due to increased transcriptional rate. Induction of c-fos by ouabain was prevented when either extracellular or intracellular Ca2+ was lowered and was attenuated by pretreatment of myocytes with a phorbol ester under conditions known to down-regulate protein kinase C. Exposure to ouabain for 24-48 h also increased total transcriptional activity and protein content of myocytes. The findings suggest that the same signal responsible for the positive inotropic action of ouabain, i.e. net influx of Ca2+ caused by partial inhibition of Na+/K+-ATPase, also initiates the rapid protein kinase C-dependent inductions of the early-response genes, the subsequent regulations of other cardiac genes by the resulting transcription factors, and stimulation of myocyte growth. Whether these hitherto unrecognized effects of cardiac glycosides are obtained in the intact heart and their relevance to the therapeutic uses of these drugs remain to be determined.
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