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Intercalation-type layered vanadium oxides have been widely explored as cathode materials for aqueous zinc-ion batteries (AZIBs). However, attaining both high power density and superior stability remains a formidable challenge. Herein, layered vanadium oxides are pre-intercalated with Zn to form ZnVO·7.4HO (ZVO), which is then combined with RuO nanoparticles to construct a ZVO/RuO heterostructure featuring interphase V─O─Ru bonds. ZVO/RuO heterostructure exhibits a dynamic stable coupling at the interphase via V─O─Ru chemical bonds reconstruction during discharging/charging processes. The dynamically reversible reconstruction of interphase V─O─Ru bonds provides a fast electron transfer channel between RuO and ZVO cathode, as demonstrated by ex situ X-ray photoelectron spectroscopy (XPS) and density functional theory (DFT) calculations, making RuO an additional electron acceptor and donor, and accelerating the migration of H/Zn in layered ZVO cathode. Therefore, an ultra-high capacity (411 mAh g at 0.5 A g, 225 mAh g at 20 A g) and long cycling stability (a retention of 92.2% at 20 A g over 20000 cycles) performances are achieved. This interphase reversible reconstruction route provides a promising approach to achieving excellent cycling stability in cathode materials.
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http://dx.doi.org/10.1002/adma.202501624 | DOI Listing |
Cell Stem Cell
September 2025
Life Sciences Institute, Department of Cellular & Physiological Sciences, University of British Columbia, Vancouver, BC, Canada; Department of Surgery, University of British Columbia, Vancouver, BC, Canada; School of Biomedical Engineering, University of British Columbia, Vancouver, BC, Canada. Elec
While current stem cell differentiation protocols generate β cell-enriched islets that reverse hyperglycemia post-implantation, they can cause hypoglycemia. Meng et al. reconstruct endocrine subtype-complete islets, which restore counterregulatory responses and protect against hypoglycemia in diabetic mice, highlighting the importance of endocrine diversity in designing physiologically regulated cell therapies for diabetes.
View Article and Find Full Text PDFIEEE Trans Med Imaging
September 2025
The T1rho mapping technique necessitates acquiring multiple T1rho-weighted images at various spin-lock times (TSL), which results in a lengthy scan time and significantly limits its widespread clinical use. Undersampling is a significant strategy to accelerate T1rho imaging, where it is crucial to model and utilize the joint spatiotemporal correlations priors among different TSL multi-contrast images for high-quality reconstruction. However, current methods that use simplified physical relaxation correlations or black-box deep neural networks to define joint correlations often yield inaccurate results.
View Article and Find Full Text PDFGlob Chang Biol
September 2025
Elkhorn Slough National Estuarine Research Reserve, Watsonville, California, USA.
To halt and reverse the trends of ecosystem loss and degradation under global change, nations globally are promoting ecosystem restoration. Restoration is particularly crucial to coastal wetlands (including tidal marshes, mangrove forests, and tidal flats), which are among the most important ecosystems on Earth but have been severely depleted and degraded. In this review, we explore the question of how to make restoration more effective for coastal wetlands in light of the often-overlooked dynamic nature of these transitional ecosystems between land and ocean.
View Article and Find Full Text PDFDirect myelin imaging with inversion-recovery ultrashort-echo-time (IR-UTE) is highly motion-sensitive, yet extra hardware or longer scans are impractical. We evaluated whether a superior-inferior (SI) self-navigator with bit-reversed spoke-angles mitigates motion artifacts without extending acquisition. Dual-echo IR-UTE was implemented at 3T.
View Article and Find Full Text PDFUnlabelled: Neutrophils and neutrophil extracellular traps (NETs) contribute to early neuromyelitis optica (NMO) histopathology initiated by IgG targeting astrocytic aquaporin-4 water (AQP4) channels. Yet, the mechanisms recruiting neutrophils and their pathogenic roles in disease progression remain unclear. To investigate molecular-cellular events preceding classical complement cascade activation in a mouse NMO model, we continuously infused, via spinal subarachnoid route, a non-complement-activating monoclonal AQP4-IgG.
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