Feng Wang

Transition metal fluorides are an appealing alternative to conventional intercalation compounds for use as cathodes in next-generation lithium batteries due to their extremely high capacity (3-4 times greater than the current state-of-the-art). However, issues related to reversibility, energy efficiency and kinetics prevent their practical application. Here we report on the synthesis, structural and electrochemical properties of ternary metal fluorides (M(1)yM(2)(1-y)F(x): M(1), M(2) = Fe, Cu), which may overcome these issues. By substituting Cu into the Fe lattice, forming the solid-solution Cu(y)Fe(1-y)F(2), reversible Cu and Fe redox reactions are achieved with surprisingly small hysteresis (<150 mV). This finding indicates that cation substitution may provide a new avenue for tailoring key electrochemical properties of conversion electrodes. Although the reversible capacity of Cu conversion fades rapidly, likely due to Cu(+) dissolution, the low hysteresis and high energy suggest that a Cu-based fluoride cathode remains an intriguing candidate for rechargeable lithium batteries.

A comprehensive understanding of the evolution of the immune landscape in humans across the entire lifespan at single-cell transcriptional and protein levels, during development, maturation and senescence is currently lacking. We recruited a total of 220 healthy volunteers from the Shanghai Pudong Cohort (NCT05206643), spanning 13 age groups from 0 to over 90 years, and profiled their peripheral immune cells through single-cell RNA-sequencing coupled with single T cell and B cell receptor sequencing, high-throughput mass cytometry, bulk RNA-sequencing and flow cytometry validation experiments. We revealed that T cells were the most strongly affected by age and experienced the most intensive rewiring in cell–cell interactions during specific age. Different T cell subsets displayed different aging patterns in both transcriptomes and immune repertoires; examples included GNLY+CD8+ effector memory T cells, which exhibited the highest clonal expansion among all T cell subsets and displayed distinct functional signatures in children and the elderly; and CD8+ MAIT cells, which reached their peaks of relative abundance, clonal diversity and antibacterial capability in adolescents and then gradually tapered off. Interestingly, we identified and experimentally verified a previously unrecognized ‘cytotoxic’ B cell subset that was enriched in children. Finally, an immune age prediction model was developed based on lifecycle-wide single-cell data that can evaluate the immune status of healthy individuals and identify those with disturbed immune functions. Our work provides both valuable insights and resources for further understanding the aging of the immune system across the whole human lifespan. In this Resource, authors profile peripheral immune cells from a total of 220 healthy volunteers from birth to over 90 years. This revealed that T cells were most affected by aging with divergent aging patterns in different subsets and identified a population of cytotoxic B cells that were enriched in children.

BACKGROUND: There is a need for studying bone characteristics systematically for a better understanding of planning (i.e., timing of placement and loading) and outcomes of implant therapy. Therefore, the aim of the present review is to evaluate alveolar bone microarchitecture and its modifiers. METHODS: Two independent reviewers conducted electronic and manual literature searches in several databases, including MEDLINE, EMBASE, Cochrane Central Register of Controlled Trials, and Cochrane Oral Health Group Trials Register, for articles published up to February 2015 reporting alveolar bone microstructure. The random-effect model was applied to calculate the weighted mean (WM) of total bone volume (TBV), which has a range from 0 to 1. TBV was stratified by anatomic locations, atrophic status, and types of specimens. Correlations between TBV and other bone-related parameters were also analyzed. RESULTS: A total of 800 articles were initially identified. After abstract/full-text review, 24 articles were included in the systematic review, of which 23 were also included in the quantitative analysis. The WM TBV was 0.365 (95% confidence interval = 0.278 to 0.452), higher in the maxillary/mandibular anterior sites than the maxillary/mandibular posterior sites. However, great variations existed within each anatomic location. Additionally, WM TBV was lower in atrophic sites than non-atrophic sites. TBV was correlated negatively with trabecular spacing (R(2) = 0.11). CONCLUSIONS: The present systematic review suggests that the TBV might not be different between the defined anatomic locations. However, the atrophy status might influence TBV.