Explore the vast range of titles available.

A practical high-specific-energy Li metal battery requires thin (≤20 μm) and free-standing Li metal anodes, but the low melting point and strong diffusion creep of lithium metal impede their scalable processing towards thin-thickness and free-standing architecture. In this paper, thin (5 to 50 μm) and free-standing lithium strips were achieved by mechanical rolling, which is determined by the in situ tribochemical reaction between lithium and zinc dialkyldithiophosphate (ZDDP). A friction-induced organic/inorganic hybrid interface (~450 nm) was formed on Li with an ultra-high hardness (0.84 GPa) and Young’s modulus (25.90 GPa), which not only enables the scalable process mechanics of thin lithium strips but also facilitates dendrite-free lithium metal anodes by inhibiting dendrite growth. The rolled lithium anode exhibits a prolonged cycle lifespan and high-rate cycle stability (in excess of more than 1700 cycles even at 18.0 mA cm −2 and 1.5 mA cm −2 at 25 °C). Meanwhile, the LiFePO 4 (with single-sided load 10 mg/cm 2 ) ||Li@ZDDP full cell can last over 350 cycles with a high-capacity retention of 82% after the formation cycles at 5 C (1 C = 170 mA/g) and 25 °C. This work provides a scalable approach concerning tribology design for producing practical thin free-standing lithium metal anodes. Thin, freestanding Li metal foils are key to improving the energy density of Li batteries but are difficult to manufacture. Here, authors achieve thin Li foils by mechanical rolling, exploiting tribochemistry to form a protective surface film that improves mechanical and electrochemical properties.

HighlightsThe robust organic/inorganic hybrid interlayer derived from in situ formed tribofilms were fabricated by using a scalable rolling method.The interlayer facilitates dendrite-free lithium metal anodes by building local de-solvation environments near the interface and inhibiting both dendrite growth and electrolytes corrosion.The symmetrical cell exhibits a remarkable lifespan of 5,600 h (1.0 mA cm-2 and 1.0 mAh cm-2) and 1,350 cycles even at a harsh condition (18.0 mA cm-2 and 3.0 mAh cm-2). The practical application of Li metal anodes (LMAs) is limited by uncontrolled dendrite growth and side reactions. Herein, we propose a new friction-induced strategy to produce high-performance thin Li anode (Li@CFO). By virtue of the in situ friction reaction between fluoropolymer grease and Li strips during rolling, a robust organic/inorganic hybrid interlayer (lithiophilic LiF/LiC6 framework hybridized -CF2-O-CF2- chains) was formed atop Li metal. The derived interface contributes to reversible Li plating/stripping behaviors by mitigating side reactions and decreasing the solvation degree at the interface. The Li@CFO||Li@CFO symmetrical cell exhibits a remarkable lifespan for 5,600 h (1.0 mA cm−2 and 1.0 mAh cm−2) and 1,350 cycles even at a harsh condition (18.0 mA cm−2 and 3.0 mAh cm−2). When paired with high-loading LiFePO4 cathodes, the full cell lasts over 450 cycles at 1C with a high-capacity retention of 99.9%. This work provides a new friction-induced strategy for producing high-performance thin LMAs.

High energy density lithium metal batteries (LMBs) are promising next‐generation energy storage devices. However, the uncontrollable dendrite growth and huge volume change limit their practical applications. Here, a new Mg doped Li–LiB alloy with in situ formed lithiophilic 3D LiB skeleton (hereinafter called Li–B–Mg composite) is presented to suppress Li dendrite and mitigate volume change. The LiB skeleton exhibits superior lithiophilic and conductive characteristics, which contributes to the reduction of the local current density and homogenization of incoming Li+ flux. With the introduction of Mg, the composite achieves an ultralong lithium deposition/dissolution lifespan (500 h, at 0.5 mA cm−2) without short circuit in the symmetrical battery. In addition, the electrochemical performance is superior in full batteries assembled with LiCoO2 cathode and the manufactured composite. The currently proposed 3D Li–B–Mg composite anode may significantly propel the advancement of LMB technology from laboratory research to industrial commercialization. A Li–B–Mg composite with in situ formed 3D LiB fiber network shows a dendrite‐free morphology and less volume change during cycling. The symmetrical battery achieves a long and stable cycle lifespan of more than 500 h at 0.5 mA cm−2 due to the effect of skeleton and the addition of Mg. The full battery also displays improved electrochemical performance.

Interfacial modification strategies for lithium metal anodes have emerged as a promising method to improve cycling stability, suppress lithium dendrite growth, and increase Coulombic efficiency. However, the reported chemical synthesis methods lead to side reactions and side products, which hinder their electrochemical performance. In this study, we propose a novel and facile red phosphorus-assisted solid-state friction method to in situ fabricate a uniform Li3P interphase directly on the surface of lithium metal. Interestingly, the as-formed artificial Li3P interphase with high ionic conductivity and lithium affinity features significantly enhanced interfacial stability and electrochemical kinetics. The symmetric cells based on Li@P with the Li3P interphase achieved a prolonged lifespan, over 1000 h, at 1 mA/cm2 with low polarization. When paired with a high-loading LiFePO4 cathode (10.5 mg/cm2), the Li@P||LiFePO4 full cell retained 88.9% of its capacity after stable cycling for 550 cycles at 2 C and further demonstrated the excellent performance and stability of the Li@P‖LiCoO2 full pouch cell. This study provides an efficient and scalable strategy for stabilizing lithium metal anodes, expanding new ideas for the development of next-generation high-energy-density batteries.

With the development of energy storage technology, the new energy storage materials are more diverse. The sodium metal has the advantages of high energy density, rich resource reserves, and low costs for raw materials, becoming promising advanced energy storage materials for application. However, the low tensile strength of sodium metal makes it difficult to process deformation while its severe viscosity and low melting point affect the subsequent manufactory and application of batteries. These characteristics hinder the processing and preparation of thin‐sodium metal. The designs of composite‐supporting structure, alloying, and the interface strengthening for sodium metal can effectively overcome the difficulties in preparation of the thin sodium. In this review, the design principles of thin sodium in terms of processing and preparation, according to the physical and chemical properties of sodium metal, are discussed. Meanwhile, the key challenges and new development opportunities are addressed for the processing and preparation of the thin‐sodium metal, which is beneficial for deeply understanding the reliable fabrication and realizing the practical application of thin‐sodium metals. This review provides three design strategies systematically (Support structure composite, interface design and alloying) for the preparation of thin sodium metal based on the characteristics of sodium metal. The electrochemical application characteristics of each design are also explained. In addition, it provides an overview of the challenges on large‐scale processing thin sodium metal.

Enteric viruses, as a potential pathogen, have been found to be vital causes of economic losses in poultry industry worldwide. The enteric viruses widely studied to date mainly include avian nephritis virus (ANV), avian reovirus (ARe), chicken astrovirus (CAstV), chicken parvovirus (ChPV), fowl adenovirus group I (FAdV-1), infectious bronchitis virus (IBV), and avian rotavirus (ARoV). This paper aimed to identify single and multiple infections of the seven enteric viruses using the data obtained from positive 145 enteric virus samples in poultry flocks from different areas in Hebei Province, throughout the period from 2019 to 2021. Next, the correlation between bird age and clinical signs was investigated using PCR and RT-PCR techniques. Furthermore, the whole genomes of seven parvovirus strains and open reading frame 2 (ORF2) of six CAstV strains and eight ANV strains were sequenced for phylogenetic analysis and recombination analysis, to characterize the viruses and evaluate species correlation and geographic patterns. A total of 11 profiles of virus combinations were detected; 191 viruses were detected in 145 samples; 106 single infections were reported in 73.1% of the samples; and multiple infections were detected in the remaining 26.9%. For viruses, 69% of ChPV was correlated with single infection, while ANV (61.4%) and CAstV (56.1%) were correlated with multiple infections. However, IBV and ARe were not detected in any of the samples. Recombination events were reported in parvovirus, and all CAstV sequences investigated in this paper were included within genotype Bii. The eight ANV strains pertained to different subtypes with significant differences. The above results revealed for the first time the complexity of enteric viruses over the past several years, thus contributing to disease prevention and control in the future.

Background The molecular genetic diagnosis of congenital adrenal hyperplasia (CAH) is very challenging due to the high homology between the CYP21A2 gene and its pseudogene CYP21A1P . Methodology This study aims to assess the clinical efficacy of targeted long-read sequencing (T-LRS) by comparing it with a control method based on the combined assay (NGS, Multiplex ligation-dependent probe amplification and Sanger sequencing) and to introduce T-LRS as a first-tier diagnostic test for suspected CAH patients to improve the precise diagnosis of CAH. Results A large cohort of 562 participants including 322 probands and 240 family members was enrolled for the perspective (96 probands) and prospective study (226 probands). The comparison analysis of T-LRS and control method have been performed. In the perspective study, 96 probands were identified using both the control method and T-LRS. Concordant results were detected in 85.42% (82/96) of probands. T-LRS performed more precise diagnosis in 14.58% (14/96) of probands. Among these, a novel 4141 kb deletion involving CYP21A2 and TNXB was established. A new diagnosis was improved by T-LRS. The duplications were also precisely identified to clarify the misdiagnosis by MLPA. In the prospective study, Variants were identified not only in CYP21A2 but also in HSD3B2 and CYP11B1 in 226 probands . Expand to 322 probands, the actual frequency of duplication haplotype (1.55%) could be calculated due to the accurate genotyping. Moreover, 75.47% of alleles with SNVs/indels, 22.20% of alleles with deletion chimeras. Conclusion T-LRS has higher resolution and reduced cost than control method with accurate diagnosis. The clinical utility of L-LRS could help to provide precision therapy to CAH patients, advance the life-long management of this complex disease and promote our understanding of CAH.

Cathode materials have impeded the development of aqueous Zn batteries (AZBs) for a long time due to their low capacity and poor cycling stability. Here, a “two birds with one stone” strategy is devised to optimize the Ni–Co hydroxide cathode material (NCH) for AZBs, which plays an essential role in both composition adjustment and morphology majorization. The F-doped Ni–Co hydroxide (FNCH) exhibits a unique nanoarray structure consisting of the 2D flake-like unit, furnishing abundant active sites for the redox reaction. A series of analyses prove that FNCH delivers improved electrical conductivity and enhanced electrochemical activity. Contributing to the unique morphology and adjusted characteristics, FNCH presents a higher discharge-specific capacity, more advantageous rate capability and competitive cycling stability than NCH. As a result, an aqueous Zn battery assembled with a FNCH cathode and Zn anode exhibits a high capacity of 0.23 mAh cm−2 at 1 mA cm−2, and retains 0.10 mAh cm−2 at 10 mA cm−2. More importantly, the FNCH–Zn battery demonstrates no capacity decay after 3000 cycles with a conspicuous capacity of 0.15 mAh cm−2 at 8 mA cm−2, indicating a superior cycling performance. This work provides a facile approach to develop high-performance cathodes for aqueous Zn batteries.

Owing to the superior mechanical, thermal, and electrical properties, graphene was a perfect candidate to improve the performance of lithium ion batteries. Herein, we review the recent advances in graphene-based composites and their application as cathode materials for lithium ion batteries. We focus on the synthesis methods of graphene-based composites and the superior electrochemical performance of graphene-based composites as cathode materials for lithium ion batteries.