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The efforts toward the experimental realization of spin-polarized transports in ideal materials or platforms, such as the magnetized graphene or various quantum Hall states, is a research hotspot in spintronics. Magnetic van der Waals materials open the door for exploring various physical phenomena, technologies, and integrating novel spintronic devices seamlessly within the 2D limit. Here, we demonstrate magnetic proximity effect in chromium trichloride (CrCl3)/bilayer graphene (BLG) heterostructures by low-temperature transport measurements. An effective exchange field induced in BLG has been demonstrated by the Zeeman spin Hall effect via nonlocal measurements. Furthermore, the exchange field modulates the quantum Hall ground state of BLG and thus favors the formation of a canted antiferromagnetic (CAF) phase in an external perpendicular magnetic field (B⊥). Asymmetric nonlocal magneto-transport behaviors are also observed at opposite B⊥ directions, due to the asymmetric modulation on the exchange field by external B⊥ directions. Our work suggests that the 2D magnetic van der Waals materials and graphene hybrid systems offer a unique platform for quantum Hall ferromagnetism physics.Nanodiamonds (NDs) are a type of biocompatible nanomaterial with easily modified surfaces and are considered as promising candidates in biomedicine. In this work, the inhibition of tumor cell migration by carboxylated nanodiamonds (cNDs) was investigated. AFM-based single cell adhesion and F-actin staining experiments demonstrated that cNDs treatment could enhance cell adhesion and impair assembly of the cytoskeleton. The mechanism analysis of the regulatory protein expression level also proved that cNDs could inhibit the migration of Hela cells by preventing the epithelial-mesenchymal transition (EMT) process through the transforming growth factor β (TGF-β) signaling pathway. The in vivo pulmonary metastasis model also showed that cNDs effectively reduced the metastasis of murine B16 melanoma cells. In summary, cNDs have been demonstrated to inhibit cancer cell migration in vitro and decrease tumor metastasis in vivo. Therefore, cNDs might have potential utility for specific cancer treatment.Dietary exposure to aflatoxins is a significant risk factor in the development of hepatocellular carcinomas. Following bioactivation by microsomal P450s, the reaction of aflatoxin B1 (AFB1) with guanine (Gua) in DNA leads to the formation of stable, imidazole ring-opened 8,9-dihydro-8-(2,6-diamino-4-oxo-3,4-dihydropyrimid-5-yl-formamido)-9-hydroxyaflatoxin B1 (AFB1-FapyGua) adducts. In contrast to most base modifications that result in destabilization of the DNA duplex, the AFB1-FapyGua adduct increases the thermal stability of DNA via 5'-interface intercalation and base-stacking interactions. Although it was anticipated that this stabilization might make these lesions difficult to repair relative to helix distorting modifications, prior studies have shown that both the nucleotide and base excision repair pathways participate in the removal of the AFB1-FapyGua adduct. see more Specifically for base excision repair, we previously showed that the DNA glycosylase NEIL1 excises AFB1-FapyGua and catalyzes strand scission ihe repair of this adduct, such that there was an inverse correlation between the stabilization of the duplex and the efficiency of NEIL1-mediated catalysis.Superconductors with exotic physical properties are critical to current and future technology. In this review, we highlight several important superconducting families and focus on their crystal structure, chemical bonding, and superconductivity correlations. We connect superconducting materials with chemical bonding interactions based on their structure-property relationships, elucidating our empirically chemical approaches and other methods used in the discovery of new superconductors. Furthermore, we provide some technical strategies to synthesize superconductors and basic but important characterization for chemists needed when reporting new superconductors. In the end, we share our thoughts on how to make new superconductors and where chemists can work on in the superconductivity field. This review is written using chemical terms, with a focus on providing some chemically intuitive thoughts on superconducting materials design.The high reactivity between lithium metal and traditional carbonate electrolytes is a great obstacle to realize the long-term cycling ability of lithium metal batteries. Ether-based electrolytes have good stability toward lithium metal anodes. However, the oxidation stability of ether-based electrolytes is generally lower than 4 V, which limits the application of high-voltage (>4 V) cathodes and restricts the energy density. The high flammability of ether is another key issue that hinders the commercialization of ether-based electrolytes. To address these issues, herein, we report a high-voltage, nonflammable ether-based electrolyte with F-, N-, and P-rich hexafluorocyclotriphosphazene (HFPN) as a cosolvent. HFPN can not only act as a highly efficient flame-retarding agent but also form a dense and homogeneous solid electrolyte interphase (SEI) layer rich in LiF and Li3N on the lithium metal anode, which stabilizes the lithium/electrolyte interface and inhibits the formation of lithium dendrites. Moreover, the HFPN-based electrolyte has a wider potential window than 4 V. As a result, with this electrolyte, high-voltage lithium metal batteries exhibit a capacity retention of ∼95% after 100 cycles. This study may provide a new pathway for developing safe, high-energy, and dendrite-free lithium metal batteries.The present study reports on the systematic characterization of the effectiveness of dielectric coating to tailor capture-to-translocation dynamics of single particles in solid-state pores. We covered the surface of SiNx membranes with SiO2, HfO2, Al2O3, TiO2, or ZnO, which allowed us to change the ζ-potential at the pore wall, reflecting the isoelectric points of these coating materials. Resistive pulse measurements of negatively charged polystyrene beads elucidated more facile electrophoretic capture of the particles and slower translocation motions in the channel under more negative electric potential at the oxide surface. These findings provide a guide to engineer pore wall surface for optimizing the translocation dynamics for efficient sensing of particles and molecules.