Self-Protecting Aqueous Lithium-Ion Batteries.

Capacity degradation and destructive hazards are two major challenges for the operation of lithium-ion batteries at high temperatures. Although adding flame retardants or fire extinguishing agents can provide one-off self-protection in case of emergency overheating, it is desirable to directly regulate battery operation according to the temperature. Herein, smart self-protecting aqueous lithium-ion batteries are developed using thermos-responsive separators prepared through in situ polymerization on the hydrophilic separator. The thermos-responsive separator blocks the lithium ion transport channels at high temperature and reopens when the battery cools down; more importantly, this transition is reversible. The influence of lithium salts on the thermos-responsive behaviors of the hydrogels is investigated. Then suitable lithium salt (LiNO3 ) and concentration (1 m) are selected in the electrolyte to achieve self-protection without sacrificing battery performance. The shut-off temperature can be tuned from 30 to 80 °C by adjusting the hydrophilic and hydrophobic moiety ratio in the hydrogel for targeted applications. This self-protecting LiMn2 O4 /carbon coated LiTi2 (PO4 )3 (LMO/C-LTP) battery shows promise for smart energy storage devices with high safety and extended lifespan in case of high operating temperatures.

Improved lithium-ion battery performance by introducing oxygen-containing functional groups by plasma treatment.

Metal sulfides are often used as cathode materials for lithium-ion batteries (LIBs) owing to their high theoretical specific capacity; however, excessively fast capacity decay during charging/discharging and rapid shedding during cycling limits their practical application in batteries. In this study, we proposed a strategy using plasma treatment combined with the solvothermal method to prepare cobalt sulfide (Co1-xS)-carbon nanofibers (CNFs) composite. The plasma treatment could introduce oxygen-containing polar groups and defects, which could improve the hydrophilicity of the CNFs for the growth of the Co1-xS, thereby increasing the specific capacity of the composite electrode. The results show that the composite electrode present a high discharge specific capacity (839 mAh g-1at a current density of 100 mA g-1) and good cycle stability (the capacity retention rate almost 100% at 2000 mA g-1after 500 cycles), attributing to the high conductivity of the CNFs. This study proves the application of plasma treatment and simple vulcanization method in high-performance LIBs.

In situ grown α-Cos/Co heterostructures on nitrogen doped carbon polyhedra enabling the trapping and reaction-intensification of polysulfides towards high performance lithium sulfur batteries.

Lithium sulfur (Li-S) batteries are considered as one of the most promising next generation energy storage systems, whereas their intrinsic drawbacks impeded their practical implementation. Herein, a nitrogen doped porous carbon polyhedron coupled with a well distributed α-CoS/Co heterostructure mediator was designed and prepared as the sulfur cathode host for lithium sulfur batteries. The α-CoS/Co heterostructure on a nitrogen doped carbon polyhedron (NCP) not only provides a strong adsorption interaction towards soluble polysulfides, but more importantly, also promotes the fast conversion of polysulfides to insoluble products, chemically suppressing the shuttling of polysulfides through the simultaneous advantages of α-CoS and Co. As a result, the α-CoS/Co-NCP-S cathode exhibits high sulfur utilization with a 1611.4 mA h g-1 first discharge capacity and a well satisfactory redox cycling stability with a low capacity fade rate of 0.042% per cycle at 0.5 C for over 800 cycles. Moreover, the hybrid cathode delivers 860.2 mA h g-1 specific capacity for a high sulfur loading of 4.8 mg cm-2 with remarkable cycling performance.