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Hollow-sphere ZnSe is successfully obtained through Ostwald ripening. Carbon nanoparticles are designed and utilized to form a wrapped carbon network as a conductive buffering matrix by subsequent annealing. The ZnSe/C composites, as anode materials for lithium-ion batteries (LIBs), exhibit excellent Li+ storage properties, delivering a high reversible capacity of 573.7 mA h g−1 at 1.0 A g−1 after 800 cycles. Even upon increasing the high current density to 20.0 A g−1, the reversible capacity can achieve 318.8 mA h g−1 after 5000 cycles. The superior rate capability is confirmed through the current density return from 20.0 to 1.0 A g−1, and ZnSe/C composites still recover up to 469 mA h g−1, with a retention of 92%. The enhanced electrochemical performances of ZnSe/C composites are attributed to the unique structure and the introduction of conductive carbon networks, which can improve the Li+ diffusion coefficient in the insertion and extraction process. Furthermore, the interconnected network also alleviates the volume variation during cycling and further enhances the structural stability. [ABSTRACT FROM AUTHOR]

The recycling of spent lithium-ion batteries (LIBs) is an effectual strategy for mitigating environmental and resource crises. Lithium iron phosphate batteries, renowned for their unique safety and stability, are widely utilized in energy storage systems and electric vehicles, consequently resulting in a growing number of spent LIBs. Herein, a one-pot mechanochemical process that integrates the recycling and preparation of LiFePO4 is proposed to drive the rapid regeneration of spent LiFePO4. Benefiting from the inherent characteristics of the input material, more than 98% of Li is selectively released, while less than 1.5% of Fe is leached without any impurity output. To this end, these reclaimed precursors in a ball mill can be directly re-used for the regeneration of LiFePO4 with an appropriate lithium source addition, eliminating the need to recover LiFePO4 with various degrees of lithium deficiency. As expected, the regenerated LiFePO4 delivers a discharge specific capacity of 143 mA h g−1 without negligible capacity fading after 250 cycles at 1 C, featuring significantly improved rate capability and long-term cycling stability. Designed with sustainable, integrated, and close-loop operation routes, this process pioneers a novel strategy to scale up the direct recycling for the LiFePO4 cathode. [ABSTRACT FROM AUTHOR]

A new flexible aromatic polymer sulfonated polybenzothiazole (sPBT-SE) with sulphone and ether units is reported as an advanced cathode material for storing Na+, which delivers a high discharge capacity of 103 mA h g−1 after 350 cycles at 30 mA g−1. [ABSTRACT FROM AUTHOR]

The recycling of spent lithium-ion batteries (LIBs) is a crucial issue that has engaged extensive attention worldwide, along with the rapidly increasing usage of lithium-ion batteries. State-of-art recycling approaches, in terms of chemical leaching, have imperfections such as excessive chemical consumption, tedious recycling procedure and aggravated secondary pollution. In this research, a green and closed-loop route for the recycling of spent LiFePO4 involving oxidation leaching is demonstrated. By properly adjusting or controlling the leaching parameters, the leaching efficiency of lithium is up to 97.6% with the introduction of hydrogen peroxide, which is facilitated to achieve the transformed high-purity lithium carbonate and iron phosphate. The oxidation reaction mechanisms are clarified through thermodynamic and kinetic analyses, which identified that the oxidation leaching reaction is co-controlled by the internal diffusion and chemical reaction. Consequently, LiFePO4 cathode materials are regenerated by utilizing the obtained raw materials, as expected, which deliver superior cycling stability with less than 1% of capacity loss after 300 cycles and excellent rate performances. This research embodies the possibility of efficient recycling of LiFePO4 from spent lithium-ion batteries based on the principles of green chemistry that is possibly committed to the sustainability of the lithium-ion battery industry. [ABSTRACT FROM AUTHOR]

Cycloaddition reactions of carbynes in metallacycles with π-bond substrates have been rarely reported. We report the first [2+2] cycloaddition of metallapentalynes with nitrosoarenes to obtain the first metallapentalenoxazetes, and their photophysical and electrochemical properties were studied by UV-Vis spectroscopy and cyclic voltammetry with the help of theoretical calculations. [ABSTRACT FROM AUTHOR]

We constructed a series of novel chiral molecular face-rotating polyhedra (FRP) from two 10,15-dihydro-5H-diindolo[3,2-a:3′,2′-c]carbazole (triazatruxene) derivatives and trans-1,2-cyclohexane diamine, and investigated how facial interactions and the positions of substituents determine the diastereoselectivity and geometry of the final assemblies. [ABSTRACT FROM AUTHOR]

We report the post-synthesis interconversion of two enantiomeric organic cages through turning inside out. By scrutinizing the thermodynamics and kinetics, we are able to control the racemization rate by various reaction conditions and reveal that the turning-inside-out interconversion is realized through a partial disassembly pathway. The kinetics investigation also provides insight into the dynamic essence of imine chemistry using different solvents and catalysts. [ABSTRACT FROM AUTHOR]