A zeolitic-imidazolate frameworks (ZIF-8)/copolymer-derived carbon composite is synthesized via in situ growth of porous ZIF-8 on conducting carbon, combining high surface area with efficient charge transport. The electrode achieves 25.7 Wh kg
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Magnesiated Si‐Rich SiOx Materials for High‐Performance Lithium‐Ion Batteries
Von Wiley-VCH zur Verfügung gestellt
Premagnesiated Si-rich SiO x composite delivers high ICE and reversible capacity. Si/Mg2SiO4 composite is synthesized via high-energy mechanical milling followed by MgH2 treatment. Cycle performance is improved without compromising ICE by forming a Mg2SiO4 phase that suppresses irreversible a-SiO2 reactions and buffers volume changes in the Si-rich structure.
Silicon monoxide (SiO)-based materials have significant potential as high-capacity anode materials for lithium-ion batteries (LIBs). However, the low initial Coulombic efficiency (ICE) associated with the irreversible electrochemical reaction of the amorphous SiO2 phase (a-SiO2) in SiO hinders its application in commercial LIBs. The preemptive phase transition of a-SiO2 to an inactive silicate phase using a metal hydride is a promising strategy for improving the ICE. However, this process inevitably leads to reversible capacity loss. In this study, a high-capacity Si-rich SiO x composite prepared by high-energy mechanical milling is premagnesiated using MgH2, resulting in a significantly improved capacity and ICE compared to those of pristine SiO and Si-rich SiO x composites. The resulting Si/Mg2SiO4 composite electrode exhibited a high initial discharge capacity of 1961 mAh g−1 with a high ICE of 87.0% and maintained highly stable capacity retention after 200 cycles compared to the Si-rich SiO x . These improved electrochemical properties are attributed to the preemptively synthesized Mg2SiO4, which not only prevents irreversible reactions between lithium and a-SiO2 during the initial lithiation but also acts as a buffer phase that effectively reduces volume expansion during cycling.
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