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https://www.selleckchem.com/products/Sunitinib-Malate-(Sutent).html Our findings demonstrated that toxic solvents such as n-heptane and benzene can be replaced by nontoxic ones (isopropyl myristate or methyl laurate) in AOT RMs without affecting the performance of micellar systems as nanoreactors, making them a green and promising alternative toward efficient and sustainable chemistry.Transition metal selenides (TMSs) are suitable for SIBs and PIBs owing to their satisfactory theoretical capacity and superior electrical conductivity. However, the large radius of Na+/K+ easily leads to sluggish kinetics and poor conductivity, which hinder the development of SIBs and PIBs. Structure design is an effective method to solve these obstacles. In this study, Co2+ ions combined with glycerol molecules to form self-assembled nanospheres at first, and then they were in situ converted into CoSe2 nanoparticles embedded in a carbon matrix during the selenization process. This structure has three-dimensional ion diffusion channels that can effectively hamper the aggregation of metal compound nanoparticles. Meanwhile, the CoSe2/C of the yolk-shell structure and a large number of pores help alleviate volume expansion and facilitate electrolyte wettability. These structural advantages of CoSe2/C endow it with remarkable electrochemical performances for full/half SIBs and full/half PIBs. The obtained CoSe2/C exhibits superior stability and excellent performance (312.1 mA h g-1 at 4 A g-1 after 1600 cycles) for SIBs. When it is used as an anode material for PIBs, 369.2 mA h g-1 can be retained after 200 cycles at 50 mA g-1 and 248.1 mA h g-1 can be retained after 200 cycles at 500 mA g-1; in addition, CoSe2/C also shows superior rate capacity (186.4 mA h g-1 at 1000 mA g-1). A series of ex situ XRD measurements were adapted to explore the possible conversion mechanism of CoSe2/C as the anode for PIBs. It is worth noting that the full-cell of CoSe2/C//Na3V2(PO4)3@rGO for SIBs and the fu

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