SLS 3D Printing To Fabricate Poly(vinyl alcohol)/Hydroxyapatite Bioactive Composite Porous Scaffolds and Their Bone Defect Repair Property.

Poly(vinyl alcohol) (PVA) exhibits a wide range of potential applications in the biomedical field due to its favorable mechanical properties and biocompatibility. However, few studies have been carried out on selective laser sintering (SLS) of PVA due to its poor thermal processability. In this study, in order to impart PVA powder the excellent thermal processability, the molecular complexation technology was performed to destroy the strong hydrogen bonds in PVA and thus significantly reduced the PVA melting point and crystallinity to 190.9 °C and 27.9%, respectively. The modified PVA (MPVA) was then compounded with hydroxyapatite (HA) to prepare PVA/HA composite powders suitable for SLS 3D printing. The final SLS 3D-printed MPVA/HA composite porous scaffolds show high precision and interconnected pores with a porosity as high as 68.3%. The in vitro cell culture experiments revealed that the sintered composite scaffolds could significantly promote the adhesion and proliferation of osteoblasts and facilitate bone regeneration, and the quantitative real-time polymerase chain reaction results further demonstrate that the printed MPVA/20HA scaffold could significantly enhance the expression levels of both early osteogenic-specific marker of alkaline phosphatase stain and runt-related transcription factor 2. Meanwhile, in in vivo experiments, it is encouragingly found that the resultant MPVA/20HA SLS 3D-printed part has an obvious effect on promoting the growth of new bone tissue as well as a better bone regeneration capability. This work could provide a promising strategy for fabrication of PVA scaffolds through SLS 3D printing, exhibiting a great potential for clinical applications in bone tissue engineering.

Nanocavity-enriched Co3O4@ZnCo2O4@NC porous nanowires derived from 1D metal coordination polymers for fast Li+ diffusion kinetics and super Li+ storage.

Nanocavity-enriched Co3O4@ZnCo2O4@NC porous nanowires have been successfully prepared by a two-step annealing process of one-dimensional (1D) coordination polymer precursors. Such unique nanowires with nanocavity-based porous channels can provide a large specific surface area, which allows fast electron/ion transfer and alleviates the volume expansion caused by strain during the charge/discharge processes. While used as the anode material of lithium-ion batteries (LIBs), Co3O4@ZnCo2O4@NC electrodes exhibit outstanding rate capacity and cycling stability, such as a high reversible capacity of 931 mA h g-1 after 50 cycles at a current density of 0.1 A g-1 and a long-term cycling efficiency of 649 mA h g-1 after 600 cycles at 1 A g-1. This coordination polymer template method lays a solid foundation for the design and preparation of bimetal oxide materials with outstanding electrochemical performance for LIBs.

Ultrafast Li+ diffusion kinetics enhanced by cross-stacked nanosheets loaded with Co3O4@NiO nanoparticles: Constructing superstructure to enhance Li-ion half/full batteries.

Novel CoNi binary metal oxide superstructures assembled with cross-stacked nanosheets (Co3O4/NiO/NC) have been successfully prepared by two-step thermal annealing process with CoNi-based and cyano-bridged coordination polymer (CoNiCP). Ascribing to the super decussate structure and as-obtained three-dimensional carbon conductive network, the obtained material exhibited excellent lithium-ion storage capacity including superior cycling stability and rate performance through facilitating the easy electron/ion transport. For example, CoNi binary metal oxide superstructures exhibit an excellent rate capacity of 493 mA h g-1 at 5.0 A g-1 and a long-lifetime cycling performance of 1390 mA h g-1 after 100 cycles at 0.2 A g-1. This strategy may pave a way for designing and preparing binary metal oxide superstructures materials with excellent electrochemical performance for lithium-ion battery by using coordination polymers as the sacrificial template.