Cheng Ma

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.

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.

Cross-linked Nanohybrid Polymer Electrolytes with POSS Cross-linker for Solid-state Lithium Ion Batteries

A new class of freestanding cross-linked hybrid polymer electrolytes (HPEs) with POSS as the cross-linker was prepared by a one-step free radical polymerization reaction. Octavinyl octasilsesquioxane (OV-POSS) with eight functional corner groups was used to provide cross-linking sites for the connection of polymer segments and the required mechanical strength to separate the cathode and anode. The unique cross-linked structure offers additional free volume for the motion of EO chains and provides fast and continuously interconnected ion-conducting channels along the nanoparticles/polymer matrix interface. The HPE exhibits the highest ionic conductivity of 1.39 × 10−3 S cm−1, as well as excellent interfacial compatibility with the Li electrode at 80°C. In particular, LiFePO4/Li cells based on the HPE deliver good rate capability and long-term cycling performance with an initial discharge capacity of 152.1 mAh g−1 and a capacity retention ratio of 88% after 150 cycles with a current density of 0.5 C at 80°C, demonstrating great potential application in high-performance LIBs at elevated temperatures.

High Ion‐Conducting Solid‐State Composite Electrolytes with Carbon Quantum Dot Nanofillers

Abstract Solid‐state polymer electrolytes (SPEs) with high ionic conductivity are desirable for next generation lithium‐ and sodium‐ion batteries with enhanced safety and energy density. Nanoscale fillers such as alumina, silica, and titania nanoparticles are known to improve the ionic conduction of SPEs and the conductivity enhancement is more favorable for nanofillers with a smaller size. However, aggregation of nanoscale fillers in SPEs limits particle size reduction and, in turn, hinders ionic conductivity improvement. Here, a novel poly(ethylene oxide) (PEO)‐based nanocomposite polymer electrolyte (NPE) is exploited with carbon quantum dots (CQDs) that are enriched with oxygen‐containing functional groups. Well‐dispersed, 2.0–3.0 nm diameter CQDs offer numerous Lewis acid sites that effectively increase the dissociation degree of lithium and sodium salts, adsorption of anions, and the amorphicity of the PEO matrix. Thus, the PEO/CQDs‐Li electrolyte exhibits an exceptionally high ionic conductivity of 1.39 × 10−4 S cm−1 and a high lithium transference number of 0.48. In addition, the PEO/CQDs‐Na electrolyte has ionic conductivity and sodium ion transference number values of 7.17 × 10−5 S cm−1 and 0.42, respectively. It is further showed that all solid‐state lithium/sodium rechargeable batteries assembled with PEO/CQDs NPEs display excellent rate performance and cycling stability.