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Efficient and stable bifunctional oxygen evolution reaction (OER) and oxygen reduction reaction (ORR) catalysts are urgently needed to unlock the full potential of zinc‐air batteries (ZABs). High‐valence oxides (HVOs) and high entropy oxides (HEOs) are suitable candidates for their optimal electronic structures and stability but suffer from demanding synthesis. Here, a low‐cost fluorine‐lodged high‐valent high‐entropy layered double hydroxide (HV‐HE‐LDH) (FeCoNi2F4(OH)4) is conveniently prepared through multi‐ions co‐precipitation, where F− are firmly embedded into the individual hydroxide layers. Spectroscopic detections and theoretical simulations reveal high valent metal cations are obtained in FeCoNi2F4(OH)4, which enlarge the energy band overlap between metal 3d and O 2p, enhancing the electronic conductivity and charge transfer, thus affording high intrinsic OER catalytic activity. More importantly, the strengthened metal‐oxygen (M−O) bonds and stable octahedral geometry (M−O(F)6) in FeCoNi2F4(OH)4 prevent structural reorganization, rendering long‐term catalytic stability. Furthermore, an efficient three‐phase reaction interface with fast oxygen transportation was constructed, significantly improving the ORR activity. ZABs assembled with FeCoNi2F4(OH)4@HCC (hydrophobic carbon cloth) cathodes deliver a top performance with high round‐trip energy efficiency (61.3 % at 10 mA cm−2) and long‐term stability (efficiency remains at 58.8 % after 1050 charge–discharge cycles). [ABSTRACT FROM AUTHOR]

African swine fever (ASF) is a contagious viral disease affecting pigs and wild boars. It typically presents as a hemorrhagic fever but can also manifest in various forms, ranging from acute to asymptomatic. ASF has spread extensively globally, significantly impacting the swine industry. The complex and highly variable character of the ASFV genome makes vaccine development and disease surveillance extremely difficult. The overall trend in ASFV evolution is towards decreased virulence and increased transmissibility. Factors such as gene mutation, viral recombination, and the strain-specificity of virulence-associated genes facilitate viral variations. This review deeply discusses the influence of these factors on viral immune evasion, pathogenicity, and the ensuing complexities encountered in vaccine development, disease detection, and surveillance. The ultimate goal of this review is to thoroughly explore the genetic evolution patterns and variation mechanisms of ASFV, providing a theoretical foundation for advancement in vaccine and diagnostic technologies. [ABSTRACT FROM AUTHOR]

Qaidam cattle are a typical Chinese native breed inhabiting northwest China. They bear the characteristics of high cold and roughage tolerance, low‐oxygen adaptability and good meat quality. To analyze the genetic diversity of Qaidam cattle, 60 samples were sequenced using whole‐genome resequencing technology, along with 192 published sets of whole‐genome sequencing data of Indian indicine cattle, Chinese indicine cattle, North Chinese cattle breeds, East Asian taurine cattle, Eurasian taurine cattle and European taurine cattle as controls. It was found that Qaidam cattle have rich genetic diversity in Bos taurus, but the degree of inbreeding is also high, which needs further protection. The phylogenetic analysis, principal component analysis and ancestral component analysis showed that Qaidam cattle mainly originated from East Asian taurine cattle. Qaidam cattle had a closer genetic relationship with the North Chinese cattle breeds and the least differentiation from Mongolian cattle. Annotating the selection signals obtained by composite likelihood ratio, nucleotide diversity analysis, integrated haplotype score, genetic differentiation index, genetic diversity ratio and cross‐population extended haplotype homozygosity methods, several genes associated with immunity, reproduction, meat, milk, growth and adaptation showed strong selection signals. In general, this study provides genetic evidence for understanding the germplasm characteristics of Qaidam cattle. At the same time, it lays a foundation for the scientific and reasonable protection and utilization of genetic resources of Chinese local cattle breeds, which has great theoretical and practical significance. [ABSTRACT FROM AUTHOR]

African swine fever (ASF) is an acute, hemorrhagic, highly contagious disease in pigs caused by African swine fever virus (ASFV). Our previous study identified that the ASFV MGF300-2R protein functions as a virulence factor and found that MGF300-2R degrades IKKβ via selective autophagy. However, the E3 ubiquitin ligase responsible for IKKβ ubiquitination during autophagic degradation still remains unknown. In order to solve this problem, we first pulled down 328 proteins interacting with MGF300-2R through immunoprecipitation-mass spectrometry. Next, we analyzed and confirmed the interaction between the E3 ubiquitin ligase TRIM21 and MGF300-2R and demonstrated the catalytic role of TRIM21 in IKKβ ubiquitination. Finally, we indicated that the degradation of IKKβ by MGF300-2R was dependent on TRIM21. In summary, our results indicate TRIM21 is the E3 ubiquitin ligase involved in the degradation of IKKβ by MGF300-2R, thereby augmenting our understanding of the functions of MGF300-2R and offering insights into the rational design of live attenuated vaccines and antiviral strategies against ASF. [ABSTRACT FROM AUTHOR]

Organic additives with high‐reduction potentials are generally applied in aqueous electrolytes to stabilize the Zn anode, while compromise safety and environmental compatibility. Highly concentrated water‐in‐salt electrolytes have been proposed to realize the high reversibility of Zn plating/stripping; however, their high cost and viscosity hinder their practical applications. Therefore, exploring low‐concentration Zn salts, that can be used directly to stabilize Zn anodes, is of primary importance. Herein, we developed an asymmetric anion group, bi(difluoromethanesulfonyl)(trifluoromethanesulfonyl)imide (DFTFSI‐)‐based novel zinc salt, Zn(DFTFSI)2, to obtain a high ionic conductivity and a highly stable dendrite‐free Zn anode. Experimental tests and theoretical calculations verified that DFTFSI− in the Zn2+ solvation sheath and inner Helmholtz plane would be preferentially reduced to construct layer‐structured SEI films, inhibiting hydrogen evolution and side reactions. Consequently, the Zn|| ${||}$ Zn symmetric cell with 1M Zn(DFTFSI)2 aqueous electrolyte delivers an ultralong cycle life for >2500 h outperforming many other conventional Zn salt electrolytes. The Zn|| ${||}$ Br2 battery also exhibits a long lifespan over 1200 cycles at ~99.8 % Coulombic efficiency with a high capacity retention of 92.5 %. Furthermore, this outstanding performance translates well to a high‐areal‐capacity Zn|| ${||}$ Br2 battery (~5.6 mAh ⋅ cm‐2), cycling over 320 cycles with 95.3 % initial capacity retained. [ABSTRACT FROM AUTHOR]

Although rechargeable aqueous zinc batteries are cost effectiveness, intrinsicly safe, and high activity, they are also known for bringing rampant hydrogen evolution reaction and corrosion. While eutectic electrolytes can effectively eliminate these issues, its high viscosity severely reduces the mobility of Zn2+ ions and exhibits poor temperature adaptability. Here, we infuse acetamide molecules with Lewis base and hydrogen bond donors into a solvated shell of Zn[(H2O)6]2+ to create Zn(H2O)3(ace)(BF4)2. The viscosity of 1ace‐1H2O is 0.032 Pa s, significantly lower than that of 1ace‐0H2O (995.6 Pa s), which improves ionic conductivity (9.56 mS cm−1) and shows lower freezing point of −45 °C, as opposed to 1ace‐0H2O of 4.04 mS cm−1 and 12 °C, respectively. The acidity of 1ace‐1H2O is ≈2.8, higher than 0ace‐1H2O at ≈0.76, making side reactions less likely. Furthermore, benefiting from the ZnCO3/ZnF2‐rich organic/inorganic solid electrolyte interface, the Zn || Zn cells cycle more than 1300 hours at 1 mA cm−2, and the Zn || Cu operated over 1800 cycles with an average Coulomb efficiency of ≈99.8 %. The Zn || PANI cell cycled over 8500 cycles, with a specific capacity of 99.8 mAh g−1 at 5 A g−1 at room temperature, and operated at −40 °C with a capacity of 66.8 mAh g−1. [ABSTRACT FROM AUTHOR]

Remote sensing images are very vulnerable to cloud interference during the imaging process. Cloud occlusion, especially thick cloud occlusion, significantly reduces the imaging quality of remote sensing images, which in turn affects a variety of subsequent tasks using the remote sensing images. The remote sensing images miss ground information due to thick cloud occlusion. The thick cloud removal method based on a temporality global–local structure is initially suggested as a solution to this problem. This method includes two stages: the global multi-temporal feature fusion (GMFF) stage and the local single-temporal information restoration (LSIR) stage. It adopts the fusion feature of global multi-temporal to restore the thick cloud occlusion information of local single temporal images. Then, the featured global–local structure is created in both two stages, fusing the global feature capture ability of Transformer with the local feature extraction ability of CNN, with the goal of effectively retaining the detailed information of the remote sensing images. Finally, the local feature extraction (LFE) module and global–local feature extraction (GLFE) module is designed according to the global–local characteristics, and the different module details are designed in this two stages. Experimental results indicate that the proposed method performs significantly better than the compared methods in the established data set for the task of multi-temporal thick cloud removal. In the four scenes, when compared to the best method CMSN, the peak signal-to-noise ratio (PSNR) index improved by 2.675, 5.2255, and 4.9823 dB in the first, second, and third temporal images, respectively. The average improvement of these three temporal images is 9.65%. In the first, second, and third temporal images, the correlation coefficient (CC) index improved by 0.016, 0.0658, and 0.0145, respectively, and the average improvement for the three temporal images is 3.35%. Structural similarity (SSIM) and root mean square (RMSE) are improved 0.33% and 34.29%, respectively. Consequently, in the field of multi-temporal cloud removal, the proposed method enhances the utilization of multi-temporal information and achieves better effectiveness of thick cloud restoration. [ABSTRACT FROM AUTHOR]

White yak is a unique economic livestock animal on the Qilian Mountains of Qinghai-Tibet Plateau (QTP). Here, 369 mitochondrial D-loop sequences from three Chinese white yak breeds/populations (Tianzhu, Menyuan and Huzhu) were comprehensively analyzed to indicate their maternal genetic diversity, differentiation and phylogenetic relationship. Our results showed that the haplotype diversity (Hd) was found to be highest in Tianzhu white yak (Hd ± SD = 0.9501 ± 0.0058), while the lowest was recorded in Huzhu white yak (Hd ± SD = 0.7178 ± 0.0474). Totally, the haplotype and nucleotide diversities of white yak were 0.9407 ± 0.0069 and 0.0187 ± 0.0094, respectively, indicating an abundant maternal genetic diversity in white yak. Estimates of FST (Fixation Index) values showed a high genetic differentiation between Tianzhu and Menyuan populations (FST = 0.2928, p < 0.05) as well as that between Tianzhu and Huzhu populations (FST = 0.2721, p < 0.05), but a moderate genetic differentiation between Menyuan and Huzhu populations (FST = 0.1352, p > 0.05) was observed. Cluster analysis based on FST values among populations indicated that the genetic relationship between Menyuan and Huzhu white yak was closer, but they had a far genetic relationship with Tianzhu white yak. Maternal phylogenetic analysis revealed that white yak represented two maternal lineages (I and II), suggesting two maternal origins. In addition, it is notable that taurine mtDNA haplotypes were detected in Tianzhu and Huzhu white yak populations, indicating taurine genetic introgression to some extent. Our study would provide useful information for the conservation and utilization of white yak. [ABSTRACT FROM AUTHOR]

Though massive efforts have been devoted to exploring Br‐based batteries, the highly soluble Br2/Br3− species causing rigorous "shuttle effect", leads to severe self‐discharge and low Coulombic efficiency. Conventionally, quaternary ammonium salts such as methyl ethyl morpholinium bromide (MEMBr) and tetrapropylammonium bromide (TPABr) are used to fix Br2 and Br3−, but they occupy the mass and volume of battery without capacity contribution. Here, we report an all‐active solid interhalogen compound, IBr, as a cathode to address the above challenges, in which the oxidized Br0 is fixed by iodine (I), thoroughly eliminating cross‐diffusing Br2/Br3− species during the whole charging and discharging process. The Zn||IBr battery delivers remarkably high energy density of 385.8 Wh kg−1, which is higher than those of I2, MEMBr3, and TPABr3 cathodes. Our work provides new approaches to achieve active solid interhalogen chemistry for high‐energy electrochemical energy storage devices. [ABSTRACT FROM AUTHOR]

Highlights: The strong interaction between Ti3C2Sx and FeN4 species induces the central metal Fe(II) in FeN4 species with intermediate spin state transferred to high spin state, in which the latter is favorable to initiate the reduction of oxygen. This strong interaction induces a remarkable Fe 3d electron delocalization with d band center upshift, boosting oxygen-containing groups adsorption on FeN4 species and oxygen reduction reaction kinetics. The resulting FeN4–Ti3C2Sx with FeN4 moieties in high spin state exhibits high half-wave potential of 0.89 V vs. RHE and high limiting current density of 6.5 mA cm−2, enabling wearable zinc–air battery showing a good discharge performance with a maximum power density of 133.6 mW cm−2. Transition metal–nitrogen–carbon materials (M–N–Cs), particularly Fe–N–Cs, have been found to be electroactive for accelerating oxygen reduction reaction (ORR) kinetics. Although substantial efforts have been devoted to design Fe–N–Cs with increased active species content, surface area, and electronic conductivity, their performance is still far from satisfactory. Hitherto, there is limited research about regulation on the electronic spin states of Fe centers for Fe–N–Cs electrocatalysts to improve their catalytic performance. Here, we introduce Ti3C2 MXene with sulfur terminals to regulate the electronic configuration of FeN4 species and dramatically enhance catalytic activity toward ORR. The MXene with sulfur terminals induce the spin-state transition of FeN4 species and Fe 3d electron delocalization with d band center upshift, enabling the Fe(II) ions to bind oxygen in the end-on adsorption mode favorable to initiate the reduction of oxygen and boosting oxygen-containing groups adsorption on FeN4 species and ORR kinetics. The resulting FeN4–Ti3C2Sx exhibits comparable catalytic performance to those of commercial Pt-C. The developed wearable ZABs using FeN4–Ti3C2Sx also exhibit fast kinetics and excellent stability. This study confirms that regulation of the electronic structure of active species via coupling with their support can be a major contributor to enhance their catalytic activity. [ABSTRACT FROM AUTHOR]

Introduction: Immunosuppressive therapy (IST) for acquired hemophilia A (AHA) results in remission within days to months in 60% to 80% of patients. However, little is known regarding the predictors of response. Aim: This study aimed to identify the factors that influence response to treatment. Methods: The data of 42 patients with AHA from three hospitals were retrospectively analyzed. Results: All 42 AHA patients received IST; complete treatment data were available for 34 patients. The response rate was 60% among the 5/34 (14.7%) patients who received steroids alone, 70.8% among the 24/34 (70.6%) patients who received steroids plus cyclophosphamide, and 80% among the 5/34 (14.7%) patients who received steroids plus cyclophosphamide and rituximab. Overall, 29/34 (85.3%) patients achieved CR; 4/34 (13.8%) of them relapsed after a median time of 410 (21-1279) days. Adverse events occurred in 14/34 (41.2%) patients: 13/34 (38.2%) had infections and 1/34 (2.9%) developed pancytopenia. In univariate and multivariate Cox regression analyses, FVIII inhibitor titer ≥20 BU/mL was the only significant prognostic factor affecting time to CR. No variable had significant effect on OS. Conclusion: FVIII inhibitory antibody titer ≥20 BU/mL appears to be an important predictor of time to complete response in patients with acquired hemophilia A treated with immunosuppressive therapy. [ABSTRACT FROM AUTHOR]

Alkaline aqueous batteries such as the Zn||Ni batteries have attracted substantial interests due to their merits of high energy density, high safety and low cost. However, the freeze of aqueous electrolyte and the poor cycling stability in alkaline condition have hindered their operation in subzero conditions. Herein, we construct a stable aqueous electrolyte with lowest freezing point down to −90 °C by adding dimethyl sulfoxide (DMSO) as alkaline tolerant antifreezing additive into 1 M KOH solution. Meanwhile, we find the DMSO can also retard Zn anode corrosion and prevent Zn dendrite formation in alkaline condition, which enables the Zn plating/stripping over 700 h cycle at 1 mA cm−2 and 0.5 mAh cm−2. The fabricated Zn||Ni battery can endure low working temperature even down to −60 °C and its dischage capacity retains 84.1 % at −40 °C, 60.6 % at −60 °C at 0.5 C. Meanwhile, it can maintain 600 cycles with a specific capacity retention of 86.5 % at −40 °C at 2 C. [ABSTRACT FROM AUTHOR]

Batteries usually deliver mass loading‐dependent electrochemical performance. Taking the selenium cathode as an example, the Se reaction kinetics, utilization, and cycling lifespan seriously deteriorate with increased Se mass loading. Here, an electrocatalytic Se reduction/oxidation reaction strategy to realize high‐Se‐loading Zn||Se batteries with fast kinetics and high Se utilization is proposed. Specifically, the synergetic effects of Cu and Co transition‐metal species inside the channel structure of the host can effectively immobilize and catalytically convert Sen during cycling, which thus facilitates Se utilization and 6‐electron (Se4+ ↔ Se2–) conversion kinetics. In particular, the Cu[Co(CN)6] host exhibits a remarkably low energy barrier (1.63 kJ mol–1) and low Tafel slope (95.23 mV dec–1) for the Se reduction, and the highest current response for Se oxidation. Accordingly, the Zn battery employing a Se‐in‐Cu[Co(CN)6] cathode delivers a capacity of 664.7 mAh g–1 at 0.2 A g–1, an excellent rate capability with 430.6 mAh g–1 achieved even at 10 A g–1, and long‐cyclic life over 6000 cycles with 90.6% capacity retention. Furthermore, an A‐h‐level (≈1350 mAh) Zn||Se pouch‐type battery with high Se loading (≈12.3 mg(Se) cm–2) shows a high Se utilization of 83.3% and outstanding cyclic stability with 89.4% initial capacity retained after 400 cycles at exceeding 98% Coulombic efficiency. [ABSTRACT FROM AUTHOR]

In this paper, we have investigated the nonlinear optical response and theoretical efficiency of CH3NH3PbI3−xClx thin films from the optical transmission and reflection measurements. The dispersion of the complex refractive index is evaluated using the Wemple–DiDomenico single oscillator model. The oscillator energy (E0) of CH3NH3PbI3−xClx follows by an empirical relationship with optical bandgap (Eg) as E0 ≈ 2.41 Eg for chemical dip coating, spray, and E0 ≈ 1.63 Eg for dipping deposited samples, respectively. The long wavelength refractive index, average oscillator wavelength, and oscillator strength are also determined using the Sellmeier oscillator equation. The estimated third-order nonlinear optical susceptibility is found to be the order of 10−12 esu. The incident photon and charge carrier interaction in CH3NH3PbI3−xClx is studied from the dielectric response of the samples. The charge carrier excitation is found higher at lower wavelength and experienced bulk excitation in volume while surface excitation on the surface region. The optical conductivity of CH3NH3PbI3−xClx is notably high, which leads to an increase in carrier transfer through the extrinsic halide perovskite material expedient for higher conversion efficiency. The highest theoretical efficiency of CH3NH3PbI3−xClx is estimated to be 17.4%, which is in excellent agreement with the experimental report. From photosensitivity study, it is confirmed that CH3NH3PbI3−xClx films are highly photosensitive. All these results comprehend that CH3NH3PbI3−xClx is a potential candidate for photonic applications. [ABSTRACT FROM AUTHOR]

Bus service is of great significance to urban residents. With the convergence of bus lines and the formation of bus hubs, a multi-line operation mode which can realize the centralized management of vehicles is applied to the daily bus service planning. To solve the bus service planning problem systematically in the multi-line operation mode, we propose an integrated framework for bus timetabling (TT) and vehicle scheduling (VS), which are the two fundamental processes of bus service planning. Firstly, the determination processes of TT and VS are correlated by constructing the multiple vehicles' trip-link chains with departure time information to facilitate simultaneous optimization. Secondly, a multi-objective optimization model is constructed, which considers higher service quality and lower operating costs as objectives. Logic and operational rules are also considered as constraints to ensure the implementation of the solutions. Thirdly, we propose and implement a heuristic solution algorithm based on neighborhood search to achieve high-performance solutions. Finally, we validate the efficiency and effectiveness of our framework under the actual bus operation scenario in Chongqing, China. The Pareto frontier solutions are provided to bus operators as alternative operation schemes. [ABSTRACT FROM AUTHOR]

Inv22-1 present in 45% of inhibitor-positive HA patients, but also present in 33% of inhibitor-negative HA patients (see Figure 1A), so Inv22-1 is not a good genetic marker for inhibitor production. Low FVIII activity is also found in other diseases, such as von Willebrand disease (vWD) and acquired haemophilia A (AHA), so diagnosis of HA should be more cautious. Dear Editor, Haemophilia A (HA) is a coagulation disorder with deficiency/dysfunction of coagulation factor VIII (FVIII) and is one of the most common recessive X-linked hereditary diseases. [Extracted from the article]

Proposed are Prussian blue analogue hosts with ordered and continuous channels, and electrocatalytic functionality with open Co and Fe species, which facilitate maximum I2 utilization efficiency and direct I2 to I− conversion kinetics of the I2 reduction reaction, and free up 1/3 I− from I3−. Co[Co1/4Fe3/4(CN)6] exhibits a low energy barrier (0.47 kJ mol−1) and low Tafel slope (76.74 mV dec−1). Accordingly, the Co[Co1/4Fe3/4(CN)6]/I2//Zn battery delivers a capacity of 236.8 mAh g−1 at 0.1 A g−1 and a rate performance with 151.4 mAh g−1 achieved even at 20 A g−1. The battery delivers both high energy density and high‐power density of 305.5 Wh kg−1 and 109.1 kW kg−1, higher than I2//Zn batteries reported to date. Furthermore, solid‐state flexible batteries were constructed. A 100 mAh high capacity solid‐state I2//Zn battery is demonstrated with excellent cycling performance of 81.2 % capacity retained after 400 cycles. [ABSTRACT FROM AUTHOR]

Zn batteries are usually considered as safe aqueous systems that are promising for flexible batteries. On the other hand, any liquids, including water, being encapsulated in a deformable battery may result in problems. Developing completely liquid‐free all‐solid‐state Zn batteries needs high‐quality solid‐state electrolytes (SSEs). Herein, we demonstrate in situ polymerized amorphous solid poly(1,3‐dioxolane) electrolytes, which show high Zn ion conductivity of 19.6 mS cm−1 at room temperature, low interfacial impedance, highly reversible Zn plating/stripping over 1800 h cycles, uniform and dendrite‐free Zn deposition, and non‐dry properties. The in‐plane interdigital‐structure device with the electrolyte completely exposed to the open atmosphere can be operated stably for over 30 days almost without weight loss or electrochemical performance decay. Furthermore, the sandwich‐structure device can normally operate over 40 min under exposure to fire. Meanwhile, the interfacial impedance and the capacity using in situ‐formed solid polymer electrolytes (SPEs) remain almost unchanged after various bending tests, a key criterion for flexible/wearable devices. Our study demonstrates an approach for SSEs that fulfill the requirement of no liquid and mechanical robustness for practical solid‐state Zn batteries. [ABSTRACT FROM AUTHOR]

Summary: Oxygen concentration influences oocyte quality and subsequent embryo development, but it remains unclear whether oxygen concentrations affect the developmental competence and transcriptomic profile of yak oocytes. In this study, we investigated the effects of different oxygen concentrations (5% versus 20%) on the developmental competence, reactive oxygen species (ROS) levels, glutathione (GSH) content, and transcriptomic profile of yak oocytes. The results showed that a low oxygen concentration significantly increased the maturation rate of yak oocytes (81.2 ± 2.2% vs 75.9 ± 1.3%) and the blastocyst quality of yak in vitro fertilized embryos. Analysis of ROS and GSH showed that a low oxygen concentration reduced ROS levels and increased the content of GSH (75.05 ± 7.1 ng/oocyte vs 50.63 ± 5.6 ng/oocyte). Furthermore, transcriptomic analysis identified 120 differentially expressed genes (DEGs) between the two groups of oocytes. Gene enrichment analysis of the DEGs indicated multiple cellular processes, including oxidative phosphorylation, transcription regulation, mitochondrial regulation, oestrogen signalling pathway, HIF-1 signalling pathway, TNF signalling pathway, were involved in the response to oxygen concentration alterations. Taken together, these results indicated that a low oxygen concentration improved the developmental competence of yak oocytes. [ABSTRACT FROM AUTHOR]

Zn‐air batteries (ZABs) offer promising commercialization perspectives for stretchable and wearable electronic devices as they are environment‐friendly and have high theoretical energy density. However, current devices suffer from limited energy efficiency and durability because of the sluggish oxygen reduction and evolution reactions kinetics in the air cathode as well as degenerative stretchability of solid‐state electrolytes under highly alkaline conditions. Herein, excellent bifunctional catalytic activity and cycling stability is achieved by using a newly developed Co–N–C nanomaterial with a uniform virus‐like structure, prepared via a facile carbonization of a prussian blue analogue (PBA). Furthermore, a solid‐state dual‐network sodium polyacrylate and cellulose (PANa‐cellulose) based hydrogel electrolyte is synthesized with good alkaline‐tolerant stretchability. A solid‐state fiber‐shaped ZAB fabricated using this hydrogel electrolyte, the virus‐like Co–N–Cs air cathode, and a zinc spring anode display excellent stretchability of up to 500% strain without damage, and outstanding electrochemical performance with 128 mW cm−2 peak power density and good cycling stability for >600 cycles at 2 mA. The facile synthesis strategy demonstrated here opens up a new avenue for developing highly active PBA‐derived catalyst and shows, for the first time, that virus‐like structure can be favorable for electrochemical performance. [ABSTRACT FROM AUTHOR]

Tongde County is located in the southeast of Qinghai Province, China, harboring rich yak genetic resources. In the present study, the complete mitochondrial genome (mitogenome) of the Tongde yak (Bos grunniens) was firstly sequenced using Illumina sequencing technique and the corresponding sequence characterization was identified. Our results showed that the mitogenome of Tongde yak is a circular molecule with 16,323 bp length consisting of 37 genes (13 protein-coding genes, 2 rRNA genes, 22 tRNA genes) and a non-coding control region (D-loop), which is consistent with most bovine species. The overall nucleotide composition was found as: A (33.72%), T (27.27%), C (25.80%), and G (13.21%), respectively, yielding a higher AT content (60.99%). The complete mitogenome sequence of Tongde yak would provide useful information for further studies on its genetic resource conservation and molecular breeding programmes in the future. [ABSTRACT FROM AUTHOR]

High electrochemical performance energy storage devices coupled with low cost and high safety operation are in urgent need due to the increasing demand for flexible and wearable electronics. For these applications lithium-ion and sodium-ion batteries are vastly limited due to their relatively low power density and security risks. On the other hand, conventional supercapacitors are suitable for flexible and wearable electronics due to their high power density while their low energy density has hindered their wide applications. Lithium or sodium ion hybrid supercapacitors are promising energy storage devices that benefit from the combined high energy density of batteries and high power density of supercapacitors. However, the use of organic electrolytes and shortage of lithium resources are expected to limit their widespread commercialization for flexible and wearable electronics. Here, for the first time, we introduce a safe and flexible solid-state zinc ion hybrid supercapacitor (ZHS) based on co-polymer derived hollow carbon spheres (HCSs) as the cathode, polyacrylamide (PAM) hydrogel as the electrolyte and Zn deposited on carbon cloth as the anode. Owing to the high surface area of the HCSs and the hollow structure which improves the ion adsorption and desorption kinetics of the cathode, the flexible solid-state ZHS delivers a highest capacity of 86.8 mA h g−1 and a maximum energy density of 59.7 W h kg−1 with a power density of 447.8 W kg−1. Besides, it displays excellent cycling stability with 98% capacity retention over 15 000 cycles at a current density of 1.0 A g−1. Moreover, the solid-state ZHS is flexible enough to sustain various deformations including squeezing, twisting and folding due to the use of flexible electrodes and electrolytes. Our study unveils a pioneering flexible solid-state ZHS with high safety, which is a promising candidate for flexible and wearable energy storage devices. [ABSTRACT FROM AUTHOR]

Although some progress has been made in flexible supercapacitors (SCs), their high energy density, mechanical robustness, and device-level editability and programmability are still highly desirable for the development of advanced portable and miniaturized electronics, especially considering the fact that these flexible devices are likely to experience some mechanical impact and potential damage. Herein, we demonstrate the fabrication of hybrid electrodes containing self-assembled 2D metal–organic framework (MOF)/reduced graphene oxide (rGO) papers, which not only efficiently alleviate the self-restacking of rGO and the MOF but also maintain high electrical conductivity (0.32 Ω cm), excellent flexibility and mechanical properties with a Young's modulus of 34.4 GPa and a tensile strength of 89.9 MPa. In addition, a one-for-two strategy is introduced to construct two types of porous electrodes for flexible asymmetric SCs via a one MOF-derived synthesis route with simply changing metal ion precursors. As a consequence, the flexible asymmetric SCs possess a high volumetric energy density of 1.87 mW h cm−3 and an outstanding volumetric power density of 250 mW cm−3. More importantly, the all-solid-state asymmetric SCs exhibit high editability and bending-tolerance properties and perform very well under various severe service conditions, such as being seriously cut, bent, and heavily loaded. Particularly, the operations of micro-SCs with artistically designed patterns are demonstrated. Being high-strength, easily programmable and connectable in series and in parallel, the editable supercapacitor is promising for developing stylish energy storage devices to power various portable, miniaturized, and wearable devices. [ABSTRACT FROM AUTHOR]

Flexible supercapacitors with high areal capacitance are a promising approach for wearable energy-storage technology due to the limitation of the surface area of the human body (about 2 m2). Meanwhile, a tolerance to deformation and mechanic damage is critical for wearable applications. However, it is still a challenge to achieve supercapacitors with outstanding electrochemical performance and wearability, simultaneously. To solve this problem, we report high-performance, flexible, and tailorable solid-state supercapacitors enabled by Co3O4@PPy nanorod bundle arrays immobilized on carbon fiber cloth (CFC). Furthermore, a solid-state asymmetric supercapacitor was assembled using a freestanding Co3O4@PPy electrode, a freestanding porous carbon electrode, and PVA gel electrolyte. Benefiting from a 3D structure and the synergetic contribution of the Co3O4 nanorods and electrically conductive PPy layer, the Co3O4@PPy electrode and our developed supercapacitor exhibit a high areal capacitance of 6.67 F cm−2 at a current density of 2 mA cm−2, and 2.47 F cm−2 at 4 mA cm−2, respectively, as well as excellent rate capability. More importantly, the solid-state supercapacitor can be tailored into several units and various shapes. Each unit retains its original electrochemical performance. This work provides a new route to wearable energy-storage technology. [ABSTRACT FROM AUTHOR]

Contrasting Y-chromosomal lineage distributions in Chinese domestic yak Yak ( I Bos grunniens i ) is a valuable bovine species that lives in the central Asian highlands with more than 15 million animals living in China.[1] Previous Y-SNP markers analyses revealed two yak paternal lineages, Y1 and Y2, in the Gaoyuan, Datong, Huanhu and Tianzhu breeds.[[2]] Here, we present a comprehensive survey of the lineage distributions in the 12 recognized Chinese domestic yak breeds. The differential distributions of the yak lineages Y1 and Y2 reveal a clear phylogeographical structure among Chinese domestic yak breeds, in clear contrast to nuclear microsatellite and mitochondrial analyses on domestic yak.[[4]]. [Extracted from the article]