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Anode-free lithium batteries represent a promising avenue for high-energy-density storage, yet their practical application is hindered by lithium inventory loss from parasitic interfacial reactions, cathode degradation, and limited Li reversibility. Herein, we propose a polyolefin separator integrated with a LiS@C sacrificial layer, achieving multiscale interfacial stabilization in Ah-class anode-free pouch cells. This approach simultaneously replenishes the customized Li inventory during the formation cycle and establishes the lithium polysulfide-containing cathode interface with high-voltage tolerance (till 4.5 V). Real-time tracking via in-situ electrochemical impedance spectroscopy and transmission-mode operando X-ray diffraction reveals accelerated Li diffusion kinetics and stabilized phase evolution in LiNiCoMnO cathode interfaced with LiS@C|PE prelithiation separator. Consequently, a 1.22 Ah pouch cell with an Ag-modified Cu foil and LiNiCoMnO cathode is assembled with LiS@C|PE separator and exhibits gravimetric and volumetric energy densities of 450 Wh kg and 1355 Wh L, respectively. This prelithiation protocol demonstrates upscaling potential and generic applicability to secure the interfacial chemistries for anode free/less lithium metal batteries.
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http://dx.doi.org/10.1038/s41467-025-59521-8 | DOI Listing |
Nanoscale
September 2025
School of Mechanical Engineering, Shandong University of Technology, Zibo 255000, China.
Metal matrix composites are widely employed in aerospace and marine engineering due to their excellent mechanical properties and chemical stability. However, their surfaces remain vulnerable to corrosion, icing, and mechanical wear, severely compromising long-term reliability in harsh environments. Inspired by natural superhydrophobic surfaces such as lotus leaves, functional interfaces with high water repellency and interfacial stability can be engineered through the synergistic design of hierarchical micro/nanostructures and low-surface-energy chemical modifications.
View Article and Find Full Text PDFWater Res
September 2025
Key Lab of Groundwater Resources and Environment Ministry of Education, Jilin University, Changchun 130021, China; Jilin Provincial Key Laboratory of Water Resources and Water Environment, Jilin University, Changchun 130021, China; National and Local Joint Engineering Laboratory for Petrochemical Co
As an abundant natural mineral, pyrite presents a highly promising solution for sustainable groundwater remediation, owing to its distinct electron transfer properties. However, research on pyrite's remediation capabilities has often focused on isolated mechanisms, neglecting the complex interplay between the mineral's properties, the environmental matrix, and interfacial processes, thereby limiting comprehensive understanding of its efficacy and constraints. Herein, an integrated "mechanism-application-sustainability" framework is proposed to bridge this knowledge gap.
View Article and Find Full Text PDFSmall
September 2025
Collaborative Innovation Center for Eco-Friendly and Fire-Safety Polymeric Materials (MoE), National Engineering Laboratory of Eco-Friendly Polymeric Materials (Sichuan), State Key Laboratory of Advanced Polymeric Materials, College of Chemistry, Sichuan University, Chengdu, 610064, China.
The LiAlTi(PO) (LATP)-polymer composite solid electrolyte offers environmental stability and safety for high-energy lithium metal batteries (LMBs), yet suffers from interfacial instability and high interfacial resistance. Herein, a Janus self-supporting skeleton (J-SSK) is engineered via multi-scale coupling of poly(vinylidene fluoride-trifluorethylene) (PVDF-TrFE), LATP, 2-(3-(6-methyl-4-oxo-1,4-dihydropyrimidin-2-yl) ureido) ethyl methacrylate (UPyMA) monomer, where intermolecular multiple hydrogen bonds reinforce mechanical robustness while the Janus structure isolates LATP from direct Li contact. In situ copolymerizing vinylene carbonate (VC) and UPyMA monomer in J-SSK to construct Janus composite quasi-solid electrolyte (J-CQSE) achieves seamless integration of electrode/electrolyte interfaces and establishes hierarchical coupling across J-SSK, polymer matrix, and lithium salts.
View Article and Find Full Text PDFJ Phys Chem A
September 2025
School of Environmental Engineering, Henan University of Technology, Zhengzhou, Henan 450001, China.
Hydroxymethyl-methyl-α-lactone (HMML) is a key epoxide precursor in forming tracer compounds 2-methylglyceric acid (2-MG) or 2-methylglyceric acid sulfate (2-MGOS) from isoprene under high-NOx conditions. Despite its importance, the formation and transformation of HMML─particularly under acidic aerosol conditions─are still poorly understood, limiting comprehensive knowledge of secondary organic aerosol (SOA) formation. In this study, quantum chemical calculations, Born-Oppenheimer molecular dynamics (BOMD), and metadynamics (MTD) simulations are employed to investigate both the formation of HMML from methacryloyl peroxynitrate (MPAN) and its interfacial transformation mechanisms on sulfuric acid aerosols.
View Article and Find Full Text PDFACS Omega
August 2025
Grupo de Diseño de Procesos y Productos (GDPP), Departamento de Ingeniería Química y de Alimentos, Universidad de los Andes, Cra 1 N. 18A - 12, Bogota 111711, Colombia.
Industry 4.0 is driving innovation in cosmetics, with artificial intelligence (AI) playing a transformative role in modeling, prediction, and product design. This review explores the integration and current advances in emulsified cosmetic product design from a multiscale approach at molecular, microscopic, and macroscopic stages.
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