Xuan Lu

Honeycomb-like carbon nanoflakes as a host for SnO2 nanoparticles allowing enhanced lithium storage performance

While possessing potential advantages as electrodes for lithium-ion batteries, SnO2@carbon composites have been suffering from one common drawback – aggregation of Sn particles during the repeated alloying–dealloying cycles and the resulting pulverization issue. We combat this issue through the fabrication of honeycomb-like SnO2@carbon nanoflakes (SnO2@CNFs) that are able to confine SnO2 nanoparticles within well-separated carbon cavities, so that the Li–Sn alloying–dealloying reaction occurs in the independent microreactors thus avoiding aggregation of Sn metal particles formed. The SnO2 particle size, loading amount and the coverage density are controlled by adjusting the weight ratio between the tin precursor and the CNF. Transmission electron microscopy confirms that the highly graphitic honeycomb-like CNF matrix efficiently buffers and accommodates volume changes of the Li–Sn alloy. Used as anode materials for lithium-ion batteries, the SnO2@CNFs with 66.0 wt% SnO2 display the highest lithium storage capacity, delivering a discharge capacity of 940 mA h g−1 after 150 cycles at 200 mA g−1. For the long-term and high-rate applications, the SnO2@CNFs with 41.5 wt% SnO2 show the best electrochemical performance, delivering a discharge capacity of 400 mA h g−1 at 1 A g−1 after 500 cycles.

Synthesis of Hierarchical Sb2MoO6 Architectures and Their Electrochemical Behaviors as Anode Materials for Li-Ion Batteries.

We report a facile microwave-hydrothermal synthesis of hierarchical Sb2MoO6 architectures assembled from single-crystalline nanobelts, which are first demonstrated as anode materials for lithium-ion batteries (LIBs) with superior electrochemical properties. Sb2MoO6 delivers a high initial reversible capacity of ∼1140 mA h/g at 200 mA/g with large initial Coulombic efficiency of ∼89%, and a reversible capacity of ∼878 mA h/g after 100 cycles at 200 mA/g. As a new anode, the electrochemical behaviors are investigated through ex situ TEM and XPS measurements, revealing that the superior electrochemical performance is attributed to the novel hierarchical structures and the synergistic interaction between both the active Sb- and Mo-species, in which the in situ generated Li2O-MoOx serves as matrix and efficiently buffers the volume changes of the Li-Sb alloying-dealloying upon cycling.