Jiatu Liu

A Li-rich Layered@Spinel@Carbon heterostructured cathode material for high capacity and high rate lithium-ion batteries fabricated via an in situ synchronous carbonization-reduction method

A novel Layered@Spinel@Carbon heterostructure is successfully fabricated via an in situ synchronous carbonization-reduction process based on a bio-inspired coating method, which comprises a core of Li-rich layered (Rm) oxide, a spinel phase (Fdm) interlayer and a carbon nano-coating. This unique structure, which combines the advantages of the high capacity Li-rich layered structure, 3D fast Li+ diffusion channels of the spinel structure and the high conductivity of the carbon coating, shows extremely high discharge capacity (as high as 334.5 mA h g−1) and superior rate capability. This strategy may provide some new insights into the design and synthesis of various electrode materials for high performance energy storage devices.

Hierarchical Nanocomposite of Hollow N-Doped Carbon Spheres Decorated with Ultrathin WS2 Nanosheets for High-Performance Lithium-Ion Battery Anode

Hierarchical nanocomposite of ultrathin WS2 nanosheets uniformly attached on the surface of hollow nitrogen-doped carbon spheres (WS2@HNCSs) were successfully fabricated via a facile synthesis strategy. When evaluated as an anode material for LIBs, the hierarchical WS2@HNCSs exhibit a high specific capacity of 801.4 mA h g(-1) at 0.1 A g(-1), excellent rate capability (545.6 mA h g(-1) at a high current density of 2 A g(-1)), and great cycling stability with a capacity retention of 95.8% after 150 cycles at 0.5 A g(-1). The Li-ion storage properties of our WS2@HNCSs nanocomposite are much better than those of the previously most reported WS2-based anode materials. The impressive electrochemical performance is attributed to the robust nanostructure and the favorable synergistic effect between the ultrathin (3-5 layers) WS2 nanosheets and the highly conductive hollow N-doped carbon spheres. The hierarchical hybrid can simultaneously facilitate fast electron/ion transfer, effectively accommodate mechanical stress from cycling, restrain agglomeration, and enable full utilization of the active materials. These characteristics make WS2@HNCSs a promising anode material for high-performance LIBs.

The Effect of Boron Doping on Structure and Electrochemical Performance of Lithium-Rich Layered Oxide Materials

Polyanion doping shows great potential to improve electrochemical performance of Li-rich layered oxide (LLO) materials. Here, by optimizing the doping content and annealing temperature, we obtained boron-doped LLO materials Li1.2Mn0.54Ni0.13Co0.13BxO2 (x = 0.04 and 0.06) with comprehensively improved performance (94% capacity retention after 100 cycles at 60 mA/g current density and a rate capability much higher compared to that of the pristine sample) at annealing temperatures of 750 and 650 °C, respectively, which are much lower than the traditional annealing temperature of similar material systems without boron. The scenario of the complex crystallization process was captured using Cs-corrected high-angle annular dark field scanning transmission electron microscopic (HAADF-STEM) imaging techniques. The existence of layered, NiO-type, and spinel-like structures in a single particle induced by boron doping and optimization of annealing temperature is believed to contribute to the remarkable improvement of cycling stability and rate capability.

Understanding the Enhanced Kinetics of Gradient-Chemical-Doped Lithium-Rich Cathode Material

Although chemical doping has been extensively employed to improve the electrochemical performance of Li-rich layered oxide (LLO) cathodes for Li ion batteries, the correlation between the electrochemical kinetics and local structure and chemistry of these materials after chemical doping is still not fully understood. Herein, gradient surface Si/Sn-doped LLOs with improved kinetics are demonstrated. The atomic local structure and surface chemistry are determined using electron microscopy and spectroscopy techniques, and remarkably, the correlation of local structure-enhanced kinetics is clearly described in this work. The experimental results suggest that Si/Sn substitution decreases the TMO2 slab thickness and enlarges the interslab spacing, and the concentration gradient of Si/Sn affects the magnitude of these structural changes. The expanded interslab spacing accounts for the enhanced Li+ diffusivity and rate performance observed in Si/Sn-doped materials. The improved understanding of the local structure-enhanced kinetic relationship for doped LLOs demonstrates the potential for the design and development of other high-rate intercalated electrode materials.

Novel solid metal–organic self-propagation combustion for controllable synthesis of hierarchically porous metal monoliths

We demonstrate a solid glycine–nitrate self-propagation combustion route to fabricate hierarchically porous metallic monoliths. The solidifying temperature (Ts) and environmental gas pressure (P) were effective controlling factors over chemistry, topography and microstructures. This may offer easy scale-up and controllable synthesis of porous metal monoliths for wide applications like electrode current collectors, catalysts, catalyst substrates and sensors.