Potassium ion storage technology as a promising substitute for the well‐developed lithium ion storage technology is still at the infancy stage of development, and exploring suitable electrode materials is critical for its practical application. Here, the great feasibility of disordered, large interlayer spacing, and oxygen‐rich carbon nanosheets (CNSs) prepared by chemical vapor deposition for potassium ion storage applications is demonstrated. As an anode material, the CNSs exhibit outstanding rate capability as well as excellent cyclic stability. Taking advantage of this, a potassium ion hybrid capacitor (PIHC) is constructed by employing such CNSs as the battery‐type anode and activated carbon as the capacitor‐type cathode. The resulting device displays a high energy density of 149 Wh kg?1, an ultrahigh power output of 21 kW kg?1, as well as a long cycling life (80% capacity retention after 5000 cycles), which are all close to the state‐of‐the‐art values for PIHCs. This work promotes the development of high‐performance anode material for potassium ion storage devices, and the designed PIHC pushes the energy density and power density to a higher level. 相似文献
High‐Ni layered oxide cathodes are considered to be one of the most promising cathodes for high‐energy‐density lithium‐ion batteries due to their high capacity and low cost. However, surfice residues, such as NiO‐type rock‐salt phase and Li2CO3, are often formed at the particle surface due to the high reactivity of Ni3+, and inevitably result in an inferior electrochemical performance, hindering the practical application. Herein, unprecedentedly clean surfaces without any surfice residues are obtained in a representative LiNi0.8Co0.2O2 cathode by Ti‐gradient doping. High‐resolution transmission electron microscopy (TEM) reveals that the particle surface is composed of a disordered layered phase (≈6 nm in thickness) with the same rhombohedra structure as its interior. The formation of this disordered layered phase at the particle surface is electrochemically favored. It leads to the highest rate capacity ever reported and a superior cycling stability. First‐principles calculations further confirm that the excellent electrochemical performance has roots in the excellent chemical/structural stability of such a disordered layered structure, mainly arising from the improved robustness of the oxygen framework by Ti doping. This strategy of constructing the disordered layered phase at the particle surface could be extended to other high‐Ni layered transition metal oxides, which will contribute to the enhancement of their electrochemical performance. 相似文献
Fulminant myocarditis is primarily caused by infection with any number of a variety of viruses. It arises quickly, progresses rapidly, and may lead to severe heart failure or circulatory failure presenting as rapid-onset hypotension and cardiogenic shock, with mortality rates as high as 50%–70%. Most importantly, there are no treatment options, guidelines or an expert consensus statement. Here, we provide the first expert consensus, the Chinese Society of Cardiology Expert Consensus Statement on the Diagnosis and Treatment of Fulminant Myocarditis, based on data from our recent clinical trial (NCT03268642). In this statement, we describe the clinical features and diagnostic criteria of fulminant myocarditis, and importantly, for the first time, we describe a new treatment regimen termed life support-based comprehensive treatment regimen. The core content of this treatment regimen includes (i) mechanical life support (applications of mechanical respirators and circulatory support systems, including intraaortic balloon pump and extracorporeal membrane oxygenation, (ii) immunological modulation by using sufficient doses of glucocorticoid, immunoglobulin and (iii) antiviral reagents using neuraminidase inhibitor. The proper application of this treatment regimen may and has helped to save the lives of many patients with fulminant myocarditis.
In this study, we sought to identify influent carbon-to-nitrogen (C/N) ratios that yield relatively high nutrient removal efficiency with relatively low greenhouse gas (GHG) emissions. The earthworm eco-filter (EE) system, which is composed of earthworms and plants (EP group), was found to be optimal for maximizing nutrient removal while reducing GHG emissions. In this EE system, the optimal influent C/N ratio for nutrient removal and GHG emission under C2N treatment conditions. Nutrient removal efficiency under this condition was 85.19 ± 6.40 % chemical oxygen demand, 71.99 ± 11.28 % total nitrogen, and 77.91 ± 8.51 % total phosphorus, while the CO2 emission rate was 678.89 ± 201.87 mg m?2 h?1. Moreover, the highest nutrient removal and GHG emission rates were both achieved in late summer (August). Thus, carbon variation, season, system variation, as well as synergistic interaction between system variations and seasons, significantly affect nutrient removal efficiencies and GHG emissions. 相似文献
It has been recently reported that the solution diffusion, efficiency porosity, and electrode thickness can dominate the high rate performance in the 3D‐printed and traditional LiMn0.21Fe0.79PO4 electrodes for Li‐ions batteries. Here, the intrinsic properties and performances of the single‐particle (SP) of LiFePO4 are investigated by developing the SP electrode and creating the SP‐model, which will share deep insight on how to further improve the performance of the electrode and related materials. The SP electrode is generated by fully scattering and distributing LiFePO4 nanoparticles to contact with the conductive network of carbon nanotube or conductive carbon to demonstrate the sharpest cyclic voltammetry peak and related SP‐model is developed, by which it is found that the interfacial rate constant in aqueous electrolyte is one order of magnitude higher, accounting for the excellent rate performance in aqueous electrolyte for LiFePO4. For the first time it has been proposed that the insight of pre‐exponential factor of interface kinetic Arrhenius equation is related to desolvation/solvation process. Thus, this much higher interfacial rate constant in aqueous electrolyte shall be attributed to the much larger pre‐exponential factor of interface kinetic Arrhenius equation, because the desolvation process is much easier for Li‐ions jumping from aqueous electrolyte to the Janus solid–liquid interface of LiFePO4. 相似文献
Programmed ‘-1’ ribosomal frameshifting is necessary for expressing the pol gene overlapped from a gag of human immunodeficiency virus. A viral RNA structure that requires base pairing across the overlapping sequence region suggests a mechanism of regulating ribosome and helicase traffic during expression. To get precise roles of an element around the frameshift site, a review on architecture of the frameshifting RNA is performed in combination of reported information with augments of a representative set of 19 viral samples. In spite of a different length for the viral RNAs, a canonical comparison on the element sequence allocation is performed for viewing variability associations between virus genotypes. Additionally, recent and historical insights recognized in frameshifting regulation are looked back as for indel and single nucleotide polymorphism of RNA. As specially noted, structural changes at a frameshift site, the spacer sequence, and a three-helix junction element, as well as two Watson–Crick base pairs near a bulge and a C–G pair close a loop, are the most vital strategies for the virus frameshifting regulations. All of structural changes, which are dependent upon specific sequence variations, facilitate an elucidation about the RNA element conformation-dependent mechanism for frameshifting. These facts on disrupting base pair interactions also allow solving the problem of competition between ribosome and helicase on a same RNA template, common to single-stranded RNA viruses. In a broad perspective, each new insight of frameshifting regulation in the competition systems introduced by the RNA element construct changes will offer a compelling target for antiviral therapy. 相似文献
With the progressive focus on renewable energy via biofuels production from lignocellulosic biomass, cellulases are the key enzymes that play a fundamental role in this regard. This study aims to unravel the characteristics of Thermotoga maritima MSB8 (Tma) (a hyperthermophile from hot springs) thermostable glycoside hydrolase enzyme. Here, a glycoside hydrolase gene of Thermotoga maritima (Tma) was heterologously expressed and characterized. The gene was placed in the pQE-30 expression vector under the T5 promotor, and the construct pQE-30-Gh was then successfully integrated into Escherichia coli BL21 (DH5α) genome by transformation. Sequence of the glycoside hydrolase contained an open reading frame of 2.124 kbp, encoded a polypeptide of 721 amino acid residues. The molecular weight of the recombinant protein estimated was 79 kDa. The glycoside hydrolase was purified by Ni+2-NTA affinity chromatography and its enzymatic activity was investigated. The recombinant enzyme is highly stable within an extreme pH range (2.0–7.0) and highly thermostable at 80 °C for 72 h indicating its viability in hyperthermic environment and acidic nature. Moreover, the Ca2+ and Mn2+ introduction stimulated the residual activity of recombinant enzyme. Conclusively, the thermostable glycoside hydrolase possesses potential to be exploited for industrial applications at hyperthermic environment. 相似文献