NiS1.23Se0.77 nanosheets closely attached to the internal surface of hollow mesoporous carbon sphere (HMCS) to form a NiS1.23Se0.77 nanosheets embedded in HMCS (NSSNs@HMCS) composite as the anode of sodium ion batteries (SIBs) is reported by a facile synthesis route. The anode exhibits a superior reversible capacity (520 mAh g−1 at 0.1 A g−1), impressive coulombic efficiency (CE) of up to 95.3%, a high rate capacity (353 mAh g−1 at 5.0 A g−1), excellent capacity retention at high current density (95.6%), and high initial coulombic efficiency (ICE) (95.1%). Firstly, the highest ICE for NiS2/NiSe2‐based anode can be ascribed to ultrathin layered structure of NiS1.23Se0.77 nanosheet and highly efficient electron transfer between the active material and HMCS. Secondly, the optimized NiS2/NiSe2 heterostructure at the nanoscale of the inside HMCS is formed after the first discharge/charge cycles, which can provide rich heterojunction interfaces/boundaries of sulfide/selenides to offer faster Na+ pathways, decrease the Na+ diffusion barriers, increase electronic conductivity, and limit the dissolution of polysulfides or polyselenides in the electrolyte. Finally, the hollow structure of the HMCS accommodates the volume expansion, prevents the pulverization and aggregation issues of composite materials, which can also promote outstanding electrochemical performance.
To retain the agents in tumors for cancer diagnosis and therapy, and then to remove them from the body, are key for the clinical applications of ideal inorganic theranostic agents. To meet these needs, we have developed a transformed theranostic platform, employing PVP coated Fe3S4 tetragonal nanosheets (TNSs), which could effectively accumulate in the tumor under magnetic targeting, whilst gradually transforming to small particles (∼5 nm) over three weeks. These were then effectively excreted from the body in normal physiological conditions after exerting their therapeutic effect. The aqueous dispersion of PVP coated Fe3S4 TNSs had an intense near-infrared absorption, excellent photothermal conversion efficiency (64.3%) and great T2 weighted magnetic resonance imaging properties (71.3 mM-1 S-1). In addition, Fe3S4 TNSs could realize a synergistic photothermal therapy (PTT)/chemodynamic therapy (CDT), because the localized heat produced by PTT from the defect-rich structure could enhance the Fenton process by utilizing the overproduced H2O2 in the tumor microenvironment, and in return, the produced ˙OH could inhibit tumor growth and recurrence after PPT. We thus developed a high-efficiency inorganic theranostic platform which was effectively cleared from the body. This will open up a new avenue for the design of inorganic agents for clinical applications in the future.
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