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Macrophage accumulation is central to the pathogenesis of atherosclerotic plaques. Reducing macrophages in plaques is an appealing approach to attenuate the development of atherosclerosis. Chemodynamic therapy, specifically inhibiting hydrogen peroxide (H2O2)-rich cells in slightly acidic microenvironment, has emerged as a new method in tumor treatment. Herein, we manufactured ultrasmall dopamine-modified hyaluronic acid (HD)-stabilized Fe(III)-tannic acid nanoparticles (HFTNPs). HFTNPs can specifically accumulate in inflammatory macrophages in atherosclerotic plaques, provide brighter magnetic resonance images, promote reactive oxygen species (ROS) generation, and induce the death of inflammatory macrophages without damaging normal cells and tissues. In conclusion, HFTNPs have a tremendous potential as safe and effective diagnostic and therapeutic reagents for atherosclerosis.

LAGP (Li1.5Al0.5Ge0.5P3O12) is a promising solid-state electrolyte (SSE) for all solid-state lithium-ion batteries (ASS-LIBs) with its favorable lithium ionic conductivity and good performance on inhibiting lithium dendrite. However, the ultrahigh interfacial resistance between lithium metal anode and LAGP SSEs greatly hinders its application. In this work, a thin film of metallic Bi was sputtered on LAGP to improve the chemical/physical properties of the Li/SSE interface. It is found that the Bi buffer not only inhibits the unfavorable reaction between LAGP SSEs and Li metal, but also improved their compatibility. As a result, the Li/LAGP interfacial resistance was effectively reduced from 2255.6 to 92.8 Ω cm2 at 30 °C. Furthermore, a good performance solid state full cell with a LiFePO4 cathode had been demonstrated. This work provides an effective avenue to address the interfacial challenges between Li metal and LAGP SSE.

We are presenting a sol–gel method for building novel nanostructures made of nanosized F-doped Na1–2xTi2(PO4)3–xFx (NTP-Fx, x = 0, 0.02, 0.05, and 0.10) particles embedded in three-dimensional (3D)...

A novel solid sodium-ion conductor, Na2Mg2TeO6 (NMTO) with a P2-type honeycomb-layered structure, has been synthesized for the first time by a simple solid-state synthetic route. The conductor of NMTO exhibits high conductivity of 2.3 × 10-4 S cm-1 at room temperature (RT) and a large electrochemical window of ∼4.2 V (versus Na+/Na). The conductor is remarkably stable, both in the ambient environment and within its metallic Na anode. This facile sodium-ion conductor displays potential for use in all-solid-state sodium-ion batteries (SS-SIBs).

Sodium iron hexacyanoferrate (Fe-HCF) has been proposed as a promising cathode material for sodium-ion batteries (SIBs) because of its desirable advantages, including high theoretical capacity (∼170 mAh g–1), eco-friendliness, and low cost of worldwide rich sodium and iron resources. Nonetheless, its application faces a number of obstacles due to poor electronic conductivity and structural instability. In this work, Fe-HCF nanospheres (NSs) were first synthesized and fabricated by an in situ graphene rolls (GRs) wrapping method, forming a 1D tubular hierarchical structure of Fe-HCF NSs@GRs. GRs not only provide fast electronic conduction path for Fe-HCF NSs but also effectively prevent organic electrolyte from reaching active materials and inhibit the occurrence of side reactions. The Fe-HCF NSs@GRs composite has been used as a binder-free cathode with a capacity of ∼110 mAh g–1 at a current density of 150 mA g–1 (∼1C), the capacity retention of ∼90% after 500 cycles. Moreover, the Fe-HCF NSs@GRs cathode ...