In-Situ Construction of V2 O5 Nanosheet/Nitrogen-Doped Carbon Nanosheet Heterostructures with Interfacial C─O Bridging Bonds as the Cathode Material for Zn Ion Batteries.

Layered oxides are widely used as the electrode materials for metal ion batteries. However, for large radius size ions, such as Zn2+ and Al3+ , the tightly stacked layers and poor electrical conductivity of layered oxides result in restricted number of active sites and sluggish reaction kinetics. In this work, a facile in-situ construction strategy is provided to synthesize layered oxide nanosheets/nitrogen-doped carbon nanosheet (NC) heterostructure, which shows larger interlayer spacing and better electrical conductivity than the layered oxides. As a result, the Zn2+ ion diffusion inside the interlayer gallery is greatly enhanced and the storage sites inside the gallery can be better used. Meanwhile, the NC layers and oxide nanosheets are bridged by the C─O bonds to form a stable structure, which contributes to a better cycling stability than the pure layered oxides. The optimal V2 O5 @NC-400 cathode shows a capacity of 467 mA h g-1 at 0.1 A g-1 for 300 cycles, and long-term cyclic stability of 4000 cycles at 5 A g-1 with a capacity retention of 92%. All these performance parameters are among the best for vanadium oxide-based cathode materials.

Lithium in breast milk transiently affects the renal electrolytic balance of infants.

BACKGROUND: The use of lithium during breast-feeding has not been comprehensively investigated in humans due to concerns about lithium toxicity. PROCEDURE: We analyzed lithium in the kidneys of nursed pups of lithium medicated mothers, using analytical spectroscopy in a novel rat model. The mothers were healthy rats administered lithium via gavage (1000 mg/day Li2 CO3 per 50 kg body weight). RESULTS: Lithium was detected in the breast milk, and in the blood of pups (0.08 mM), of lithium-exposed dams at post-natal day 18 (P18), during breast-feeding. No lithium was detected after breast-feeding, at P25 (4 days after cessation of nursing). The lithium pups blood had elevated urea nitrogen at P18 and reduced total T4 at P18 and P25, indicating a longer-term effect on the kidneys and the thyroid gland. Multivariate machine-learning analysis of spectroscopy data collected from the excised kidneys of pups showed elevated potassium in lithium-exposed animals both during- and after breast-feeding. The elevated renal potassium was associated with low nephrin expression in the kidneys measured immunohistochemically during breast-feeding. After lithium exposure is stopped, the filtration of lithium from the kidneys reverses these effects. Our study showed that breastfeeding during lithium use has an effect on the kidneys of the offspring in rats.

A Metal Coordination Number Determined Catalytic Performance in Manganese Borides for Ambient Electrolysis of Nitrogen to Ammonia.

A new strategy that can effectively increase the nitrogen reduction reaction performance of catalysts is proposed and verified by tuning the coordination number of metal atoms. It is found that the intrinsic activity of Mn atoms in the manganese borides (MnBx) increases in tandem with their coordination number with B atoms. Electron-deficient boron atoms are capable of accepting electrons from Mn atoms, which enhances the adsorption of N2 on the Mn catalytic sites (*) and the hydrogenation of N2 to form *NNH intermediates. Furthermore, the increase in coordination number reduces the charge density of Mn atoms at the Fermi level, which facilitates the desorption of ammonia from the catalyst surface. Notably, the MnB4 compound with a Mn coordination number of up to 12 exhibits a high ammonia yield rate (74.9 ± 2.1 µg h-1 mgcat -1) and Faradaic efficiency (38.5 ± 2.7%) at -0.3 V versus reversible hydrogen electrode (RHE) in a 0.1 m Li2SO4 electrolyte, exceeding those reported for other boron-related catalysts.

Correction: Enhanced charge transport properties of an LFP/C/graphite composite as a cathode material for aqueous rechargeable lithium batteries.

[This corrects the article DOI: 10.1039/D3RA04143C.].

Enhanced charge transport properties of an LFP/C/graphite composite as a cathode material for aqueous rechargeable lithium batteries.

Electrodes that offer quick ion transport, a large surface area, and excellent electrical conductivity support high performance aqueous rechargeable lithium batteries. LiFePO4 (LFP) nanoparticles have been successfully coated with carbon by a chemical sol-gel route, and assembled on graphite by an ultrasonication method to acquire LFP/C/graphite. This LFP/C/graphite composite exhibits exceptional electrochemical performance at various current densities (1C to 20C). LFP/C/graphite delivers better capacity that is higher than that of LFP/C particles and high stability after 60 cycles at a current density of 1C for aqueous rechargeable lithium batteries as a cathode material. The graphite serves as a good volume buffer in improving the lithium performance of LFP/C/graphite during the charge/discharge process. The LFP/C/graphite composite shows high rate capability at 20C that returned to the initial capacity at 1C after 25 cycles with coulombic efficiency of 97%. Therefore, this effort presents a super low-cost route to fabricate high performance cathode materials in aqueous rechargeable lithium batteries and other energy storage appliances.

A hybrid composite of H2V3O8 and graphene for aqueous lithium-ion batteries with enhanced electrochemical performance.

Aqueous rechargeable lithium-ion batteries (ARLBs) are regarded as a competitive challenger for large-scale energy storage systems because of their high safety, modest cost, and green nature. A kind of modified composite material composed of H2V3O8 nanorods and graphene sheets (HVO/G) has been effectively made by a one-step hydrothermal method and following calcination at 523 K. XRD, SEM, TEM, and TG are used to determine the phase structures and morphologies of the composite materials. Owing to the advantage of the layered structure of H2V3O8 nanorods, the excellent conductivity of the graphene sheets, and the 3D network structure of the modified composite, the ARLBs with HVO/G can deliver an adequate specific capacity of 271 mA h g-1 at 200 mA g-1 and have a retention rate of 73.4% after 50 cycles. The average discharge capacity of ARLB with HVO/G as anode has a considerable improvement over that of HVO/CNTs and HVO, whatever the current rate used. Moreover, we find that the diffusion coefficient of lithium-ion increases by an order of magnitude through the theoretical calculation for HVO/G ARLB. The new ARLB with HVO/G electrode is a potential energy storage system with great advantages, such as simple preparation, easy assembly process, excellent safety and low-cost environmental protection.

Superior cycling performance of a novel NKVO@polypyrrole composite anode for aqueous rechargeable lithium-ion batteries.

An aqueous rechargeable lithium-ion battery (ARLB) system has been assembled using as-prepared polypyrrole (PPy) to coat Na0.8K0.2K6O15 (NKVO) anode coupled with LiMn2O4 cathode, both immersed in an aqueous LiNO3 solution. The chemical polymerization techniques have been employed to uniformly coat the surface of NKVO with PPy. The phase of NKVO@PPy composite has been characterized by X-ray diffraction; for quantifying PPy content, the thermal gravimetric analysis was performed. Spectroscopy techniques have been used to visualize the microscale morphological changes on the particle surface of NKVO caused by PPy coating. The staircase cyclic voltammetry and galvanic charge-discharge tests have been conducted at various current rates in the voltage range of -1 to 1 V vs. saturated calomel electrode (SCE). The PPy coated NKVO material showed a similar intercalation/deintercalation mechanism to that of pristine NKVO. When subjected to cyclic performance evaluation at a higher rate of 4 A g-1, PPy-coated NKVO@PPy exhibited a preliminary discharge capacity of 115 mA h g-1 and 64.5 mA h g-1 following 400 cycles of charge-discharge with a retention rate of 55.6%, whereas the uncoated NKVO showed only 18.8% capacity retention rate. The significantly improved cyclic capacity retention has been attributed to the PPy coating, which acted as a protective layer preventing the unwanted side reactions, buffering the volume change and simultaneously increasing the electrical conductivity of pristine NKVO electrode during charge-discharge cycles. The decent performance demonstrated that NKVO@PPy is a promising electrode material for ARLB.