Search

The development of green, controllable, and simplified pathways for rapid dopamine polymerization holds significant importance in the field of polydopamine (PDA) surface chemistry. In this study, a green strategy is successfully devised to accelerate and control the polymerization of dopamine through the introduction of ozone (O3). The findings reveal that ozone serves as an eco‐friendly trigger, significantly accelerating the dopamine polymerization process across a broad pH range, spanning from 4.0 to 10.0. Notably, the deposition rate of PDA coatings on a silicon wafer reaches an impressive value of ≈64.8 nm h−1 (pH 8.5), which is 30 times higher than that of traditional air‐assisted PDA and comparable to the fastest reported method. Furthermore, ozone exhibits the ability to accelerate dopamine polymerization even under low temperatures. It also enables control over the inhibition–initiation of the polymerization process by regulating the "ON/OFF" mode of the ozone gas. Moreover, the ozone‐induced PDA coatings demonstrate exceptional characteristics, including high homogeneity, good hydrophilicity, and remarkable chemical and mechanical stability. Additionally, the ozone‐induced PDA coatings can be rapidly and effectively deposited onto a wide range of substrates, particularly those that are adhesion‐resistant, such as polytetrafluoroethylene (PTFE). [ABSTRACT FROM AUTHOR]

As one of the most promising sodium-ion battery (SIB) anodes, transition metal sulfides (TMSs) have been extensively studied for their high capacity and abundant resources. However, the performance of TMS electrodes has been plagued by the poor rate capability and short cycle life, resulting from the huge volume change and the shuttling of polysulfides during cycling. Here, rationally-designed nitrogen-doped carbon-coated Co9S8–Co1−xS yolk–shell hollow spheres (Co9S8–Co1−xS@NC) are synthesized as the SIB anode. The hollow nanostructure shortens the diffusion length of sodium ions/electrons and affords abundant space to accommodate the volume expansion during sodiation. The Co9S8–Co1−xS@NC anode delivers a large sodium-ion storage capacity of 578 mA h g−1 even after 500 cycles at 0.5 A g−1 and superior rate capability and cycling stability (323 mA h g−1 at 5 A g−1 over 1200 cycles) in a half cell. In addition, when combined with the advanced Na3V2(PO4)2O2F electrode, the full SIB shows a highly stable specific capacity and reversibility. The reaction mechanism of Co9S8–Co1−xS@NC was studied using operando X-ray diffraction (operando XRD), revealing the reversible conversion between cobalt sulfides and Co/Na2S. [ABSTRACT FROM AUTHOR]