Equatorial auroral records reveal dynamics of the paleo-West Pacific geomagnetic anomaly.

Localized regions of low geomagnetic intensity such as the South Atlantic Anomaly allow energetic particles from the Van Allen radiation belt to precipitate into the atmosphere and have been linked to a signature in the form of red aurora-like airglow visible to the naked eye. Smoothed global geomagnetic models predict a low-intensity West Pacific Anomaly (WPA) during the sixteenth to nineteenth centuries characterized by a simple time dependence. Here, we link the WPA to an independent database of equatorial aurorae recorded in Seoul, South Korea. These records show a complex fluctuating behavior in auroral frequency, whose overall trend from 1500 to 1800 AD is consistent with the locally weak geomagnetic field of the WPA, with a minimum at 1650 AD. We propose that the fluctuations in auroral frequency are caused by corresponding and hitherto unknown fluctuations in the regional magnetic intensity with peaks at 1590 and 1720 AD, a time dependence that has been masked by the smoothing inherent in regularized global geomagnetic models. A physical core flow model demonstrates that such behavior requires localized time-dependent upwelling flows in the Earth's core, possibly driven by regional lower-mantle anomalies.

High concentration from resources to market heightens risk for power lithium-ion battery supply chains globally.

Global low-carbon contracts, along with the energy and environmental crises, have encouraged the rapid development of the power battery industry. As the current first choice for power batteries, lithium-ion batteries have overwhelming advantages. However, the explosive growth of the demand for power lithium-ion batteries will likely cause crises such as resource shortages and supply-demand imbalances. This study adopts qualitative and quantitative research methods to comprehensively evaluate the power lithium-ion battery supply and demand risks by analyzing the global material flow of these batteries. The results show that the processes from resources to market of the power lithium-ion battery industry are highly concentrated with growing trends. The proportion of the top three power lithium-ion battery-producing countries grew from 71.79% in 2016 to 92.22% in 2020, increasing by 28%. The top three power lithium-ion battery-demand countries accounted for 83.07% of the demand in 2016 and 88.16% in 2020. The increasing concentration increases the severity of the supply risk. The results also imply that different processes are concentrated within different countries or regions, and the segmentation puts the development of the power lithium-ion battery industry at significant risk. It is urgent to address this situation so that this severe risk can be ameliorated.

Correlation analysis between the occurrence of epidemic in ancient China and solar activity.

As the globe has witnessed the pandemic, epidemic diseases exert a strong impact on human beings and ecosystems. Since the Sun is the primary energy source of the Earth, some scientific pioneers attempted to search for the discernible relation between solar activity and the incidence of epidemics. In this study, the periodic changes and trends of ancient Chinese epidemic data were analyzed in comparison with those of sunspot numbers, a solar activity proxy. The results show that the epidemic and solar activity changes are in good agreement to a certain extent, especially during the Gleissberg and the de Vries cycles. The wavelet coherence shows that the frequency of the epidemic data and sunspot numbers are highly associated. In addition, results from the ensemble empirical mode decomposition illustrate consistent variations in low-frequency decompositions. This study has important implications for further understanding of the potential impact of solar activity on Earth's biosphere, the underlying mechanism of which needs further exploration.

Graphitized Carbon-Coated Iron Fluoride Nanocavities for Enhanced Kinetics of Multielectron Cathode Conversion Reactions.

As for the conversion-type iron fluoride (FeF3) cathode material with multielectron reactions for lithium-ion batteries (LIBs), sluggish reaction kinetics and low electrical conductivity pose certain limitations for the long-lasting reversible conversion processes. Herein, the three-dimensional porous nitrogen-doped carbon matrix in situ anchoring FeF3 nanocavities coated by graphitized carbon (FeF3/GC) are rationally prepared. Through the Kirkendall effect, the low-temperature fluorination of NF3 enables the resultant hollow FeF3 nanoparticles to possess a large number of lithium storage cavities and outer graphitized carbon structure, further effectively buffering the expansion of volume. The FeF3/GC cathode delivers a superior discharge capacity of 504.2 mAh g-1 after 1200 cycles at 1000 mA g-1, with a capacity decay rate of only 0.01% per cycle. Even at a rate of 5000 mA g-1, the composite cathode still delivers a discharge capacity of 309.6 mAh g-1. Impressively, the existence of graphitized carbon and the short Li+ diffusion length ensure fast electron/ion transfer, which significantly enhances the conversion reaction kinetics. This study aims to provide a promising strategy for the efficiency enhancement of multielectron cathode conversion reactions for LIBs.

Oxygen vacancies in MnOx regulating reaction kinetics for aqueous zinc-ion batteries.

MnO2 cathode materials have presented challenges due to their poor conductivity, unstable structure, and sluggish diffusion kinetics for aqueous zinc-ion batteries (AZIBs). In this study, a nanostructured MnOx cathode material was synthesized using an acid etching method, Which introduced abundant Mn(III) sites, resulting in the formation of numerous oxygen vacancies. Comprehensive characterizations revealed that these oxygen vacancies facilitated the reversible adsorption/desorption of Zn2+ ions and promoted efficient electron transfer. In addition, the designed mesoporous structure offered ample active sites and shortened the diffusion path for Zn2+ and H+ ions. Consequently, the nanosized MnOx cathode exhibited enhanced reaction kinetics, achieving a considerable reversible specific capacity of 388.7 mAh/g at 0.1 A/g and superior durability with 72.0% capacity retention over 2000 cycles at 3.0 A/g. The material delivered a maximum energy density of 639.7 Wh kg-1 at 159.94 W kg-1. Furthermore, a systematic analysis of the zinc storage mechanism was performed. This work demonstrates that engineering oxygen vacancies with nanostructure regulation provides valuable insights into optimizing MnO2 cathode materials for AZIBs.

Preparation of Small-Particle and High-Density Cobalt Carbonate Using a Continuous Carbonate Precipitation Method and Evaluation of Its Growth Mechanism.

Spherical CoCO3 powder with a small particle size and high density was successfully prepared using a continuous carbonate liquid precipitation method with a raw material of cobalt chloride solution, a precipitant of NH4HCO3, and without a template. The effects of the concentration of ammonium carbonate, process pH, and feeding rate on the tap density and apparent density of cobalt carbonate were investigated. It was found that the apparent and tap density values of 4.4 µm of cobalt carbonate were 1.27 g/cm3 and 1.86 g/cm3, respectively, when the initial concentration of NH4HCO3 solution was 60 g/L, the pH was 7.15-7.20, and the feeding rate of cobalt chloride was 2 L/h. The anisotropic growth process of the crystal lattice plane of CoCO3 under the aforementioned optimal conditions were studied. The results demonstrated that the crystal grew fastest along the (110) facet orientation, which was the dominant growth surface, determining the final morphology of the primary particles. The scanning electron microscopy (SEM) and high-resolution transmission electron microscopy (HR-TEM) results demonstrated that the primary particle morphology of the cobalt carbonate was a nanosheet. The unit cell of cobalt carbonate, of a hexagonal structure in the horizontal direction, grew horizontally along the (110) facet orientation, while 20-35 unit cells of the carbon carbonate were stacked along the c-axis in the thickness direction. Finally, the sheet-shaped particles were agglomerated into dense spherical secondary particles, as presented through the crystal re-crystallization model.