Si/C composite is one of the most promising candidate materials for next-generation lithium-ion battery anodes. Herein, we demonstrate the novel structure of carbon cages encapsulating porous Si synthesized by the reaction between magnesium silicide (MgSi) and carbon dioxide (CO) and subsequent acid washing. Benefitting from the in situ deposition through magnesiothermic reduction of CO, the carbon cage seals the inner Si completely and shows higher graphitization than that obtained from the decomposition of acetylene. After removing MgO, pores are created, which can accommodate the volume change of the Si anode during the charge/discharge process. As the anode material for lithium-ion batteries, the porous Si/C electrode shows a charge capacity of ∼1124 mA h g after 100 cycles with 86.4% capacity retention at the current density of 0.4 A g. When the current density increases to 1.6 and 3.2 A g, the capacity can still be maintained at ∼860 and ∼460 mA h g, respectively. The prominent cycling and rate performance is contributed by the built-in space for Si expansion, static carbon cages that prevent penetration of electrolyte and stabilize the solid electrolyte interface (SEI) outside, and fast charge transport by the novel structure.
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http://dx.doi.org/10.1039/c7nr09599f | DOI Listing |
Inorg Chem
January 2025
Departament de Química Física i Inorgànica, Universitat Rovira i Virgili, c/Marcel·lí Domingo 1, 43007 Tarragona, Spain.
Gas-phase synthesis and detection of boron-doped nitride clusterfullerenes and a large variety of monometallofullerenes have been achieved using a pulsed laser vaporization cluster source. Density functional theory (DFT) calculations show that the electronic structures of boron-doped endohedral metallofullerenes differ from those of the pristine all-carbon cages due to the lack of one electron upon boron substitution. For monometallofullerenes, this is likely the main reason for the somewhat different abundance distribution observed for boron-doped with respect to all-carbon cages.
View Article and Find Full Text PDFJ Chem Eng Data
December 2024
Institute for Materials and Processes, School of Engineering, The University of Edinburgh, Edinburgh EH9 3FB, Scotland, U.K.
A comprehensive quantitative grasp of methane (CH), nitrogen (N), and their mixture's adsorption and diffusion in MIL-101(Cr) is crucial for wide and important applications, e.g., natural gas upgrading and coal-mine methane capturing.
View Article and Find Full Text PDFFitoterapia
January 2025
Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education and Yunnan Province, School of Chemical Science and Technology, Yunnan University, Kunming 650091, PR China; State Key Laboratory of Phytochemistry and Plant Resources in West China, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming 650201, PR China. Electronic address:
Alstoscholarisine L is an architecturally complex monoterpenoid indole alkaloid with a unique ring fusion pattern, isolated from the leaves of Alstonia scholaris. The 6/5/5/6/6/6-membered rings contain two lactonic rings and one aminal carbon and possess seven contiguous aligned stereocenters, three of which are quaternary. Its structure was elucidated by extensive spectroscopic data analyses, quantum chemical computations, and single-crystal X-ray diffraction.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
November 2024
Institute for Chemical Research, Kyoto University, Uji, Kyoto, 611-0011, Japan.
Opening up [60]fullerene makes itself inherently chiral without loss of congenital π-conjugation. An immoderately large aperture on [60]fullerene, however, renders the molecule less rigid and therefore it would reduce dissymmetry factors. Herein, we examined supramolecular technique in geometrical reinforcement of chiral open-[60]fullerenes by encasing achiral guests such as Ar, CO, and CHCN.
View Article and Find Full Text PDFChem Commun (Camb)
December 2024
School of Chemistry, Xi'an Jiaotong University, Xi'an 710049, China.
Since the discovery of La@C, a wide array of endohedral metallofullerenes (EMFs) have been synthesized and documented. Various metals, including lanthanides, transition metals, alkali metals, alkaline earth metals and actinides, have been successfully incorporated into the inert fullerene cavities. The interaction between these encapsulated metal species and the fullerene cage isomers plays a crucial role in determining distinct molecular structures and imparting versatile chemical behaviors to these compounds.
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