As a result, the Mn3O4/graphene composite displays superior lithium storage performance with high reversible capacity (741 mAh g-1 at 100 mA g-1), excellent rate capability (403 mAh g-1 at 1000 mA g-1) and long cycle life (527 mAg g-1 after 300 cycles at 500 mA g-1). The electrochemical performance highlights the importance of rational design nanocrystals anchoring on graphene nanosheets for high-performance LIBs application.Aqueous rechargeable batteries (ARBs) have the advantages of low cost, high safety and sustainable environmental friendliness. However, the key challenge for ARBs is the narrow electrochemical stability window of the water, undoubtedly leading to the low output voltage, the underachieved capacity and a low energy density. Prussian blues and their analogues have attracted great research interest for energy storage due to the advantages of facile synthesis, versatile categories and tunable three dimensional frameworks. Herein a flexible integrated potassium cobalt hexacyano ferrates (Co-HCF) on carbon fiber clothes (CFCs) were designed through a feasible route combining the controllable electrochemical deposition and the efficient co-precipitation process.  https://www.selleckchem.com/products/sitagliptin.html  The Co-HCF@CFCs demonstrate an excellent sodium ion storage with a high reversible capacity of 91 mAh g-1 at 1 A g-1 and 55 mAh g-1 at 10 A g-1 in aqueous electrolytes. The long cycling stability at the high current demonstrate the excellent structure stability of the Co-HCF@CFCs. Analysis on the rate Cyclic voltammograms (CV) profiles reveal the fast electrochemical kinetics with the capacitive controlled process, while galvanostatic intermittent titration technique (GITT) tests fast diffusion coefficient related with the sodium ions intercalation/deintercalation in the Co-HCF@CFCs. In addition, the flexible Co-CHF@CFCs also demonstrate excellent performance for quasi-solid-state ARBs even at the high bending angles. The high quality Co-HCF@CFCs with advantage of high rate capability and excellent reversible capacity make them a promising candidate for high performance ARBs.
  One of the main challenges in cancer therapy is the poor water solubility of many anticancer drugs which results in low bioavailability at the tumour sites and reduced efficacy. The currently available polymer-based anticancer drug delivery systems often suffer from low encapsulation efficiency, uncontrolled release, and lack of long-term stability. Herein, we report the development of novel stiffness-tuneable core-shell nanocarriers composed of naturally derived polymers silk fibroin (SF) and sodium alginate (SA) inside a liposomal shell for enhanced cellular uptake and controlled release of hydrophobic anticancer agent ASC-J9 (Dimethylcurcumin). It is anticipated that the stiffness of the nanocarriers has a significant effect on their cellular uptake and anticancer efficacy.
 
  The nanocarriers were prepared by thin film hydration method followed by extrusion and cross-linking of SA to obtain a uniform size and shape, avoiding harsh processing conditions. The structural transformation of SF in the nanocarrindings suggest that the designed core-shell nanocarriers can be used as a highly efficient drug delivery system for cancer therapy.
 The synthesized nanocarriers had high encapsulation efficiency (62-78%) and were physically stable for up to 5 months at 4 ˚C. The release profile of the drug from the nanocarriers was directed by their stiffness and was easily tuneable by changing the ratio of SF to SA in the core. Furthermore, the designed nanocarriers improved the cellular uptake and anticancer activity of ASC-J9, and enhanced its tumour penetration in HCT 116 3D colorectal cancer spheroids. These findings suggest that the designed core-shell nanocarriers can be used as a highly efficient drug delivery system for cancer therapy.A novel magnetic core-shell Fe3O4@CuS have been successfully synthesized by chemical etching and cation exchange method using Zeolitic imidazolate frameworks (ZIF) as the template. The morphology and microstructural properties characterization indicated that Fe3O4@CuS nanoparticles were rhombic dodecahedral shape, highly stable, and magnetic with a large specific surface area (772.20 m2/g). The catalytic activity of Fe3O4@CuS was assessed on sulfadiazine (SDZ) degradation by H2O2 activation. Multi-factors affecting the SDZ removal was adequately investigated. Approximately 93.2% SDZ (50 μM) was removed with 0.2 g/L Fe3O4@CuS and 5 mM H2O2 in 90 min. In particular, Fe3O4@CuS exhibited a quality catalytic performance within a wide pH range of 3.0-11.0. Radical scavenger tests and electron paramagnetic resonance (EPR) analysis confirmed that •O2-, •OH, and 1O2 all contributed to the SDZ degradation, and •OH played the dominant role. Meanwhile, mechanism investigation suggested that the effective catalytic activity of Fe3O4@CuS could be ascribed to the sulphur-enhanced copper-based Fenton reaction on the CuS shell, sulphur-enhanced iron-based Fenton reaction on the Fe3O4 core, and the effective electron transfer between the shell and core. Finally, the possible SDZ degradation pathways were further proposed on the basis of the intermediates identification. This work put forward a new strategy to synthesize magnetic core-shell Fe3O4@CuS using ZIF-8 as the template with outstanding performance for H2O2 activation to degrade SDZ.Theranostic nanoplatforms integrating simultaneously photodynamic therapy (PDT) and photothermal therapy (PTT) exhibit intrinsic advantages in tumor therapy due to distinct mechanisms of action. However, it is challenging to achieve PDT and PTT under single near-infrared (NIR) laser irradiation with a nanoplatform utilizing conventional organic photodynamic agent and inorganic photothermal agent owing to the difference in inherent excitation wavelengths. Particularly, the single NIR light (660 nm)-triggered PTT and PDT nanoplatform, constructed from chlorin e6 (Ce6) and copper sulfide (CuS) nanoparticles (NPs), has never been reported. Herein, we, for the first time, designed and established a dual-modal phototherapeutic nanoplatform that achieved both PTT and PDT under single NIR laser (660 nm) irradiation for Ce6 and CuS NPs with the strategy of core-shell structured CuS@Carbon integrated with Ce6. Introducing of carbon shell not only endows small CuS NPs with excellent tumor accumulation, but also significantly strengthens the photothermal performance of CuS NPs, realizing efficient photothermal performance under 660 nm laser irradiation.