Bingsheng Qin

Sustainable, heat-resistant and flame-retardant cellulose-based composite separator for high-performance lithium ion battery

A sustainable, heat-resistant and flame-retardant cellulose-based composite nonwoven has been successfully fabricated and explored its potential application for promising separator of high-performance lithium ion battery. It was demonstrated that this flame-retardant cellulose-based composite separator possessed good flame retardancy, superior heat tolerance and proper mechanical strength. As compared to the commercialized polypropylene (PP) separator, such composite separator presented improved electrolyte uptake, better interface stability and enhanced ionic conductivity. In addition, the lithium cobalt oxide (LiCoO2)/graphite cell using this composite separator exhibited better rate capability and cycling retention than that for PP separator owing to its facile ion transport and excellent interfacial compatibility. Furthermore, the lithium iron phosphate (LiFePO4)/lithium cell with such composite separator delivered stable cycling performance and thermal dimensional stability even at an elevated temperature of 120°C. All these fascinating characteristics would boost the application of this composite separator for high-performance lithium ion battery.

Taichi-inspired rigid-flexible coupling cellulose-supported solid polymer electrolyte for high-performance lithium batteries

Inspired by Taichi, we proposed rigid-flexible coupling concept and herein developed a highly promising solid polymer electrolyte comprised of poly (ethylene oxide), poly (cyano acrylate), lithium bis(oxalate)borate and robust cellulose nonwoven. Our investigation revealed that this new class solid polymer electrolyte possessed comprehensive properties in high mechanical integrity strength, sufficient ionic conductivity (3 × 10−4 S cm−1) at 60°C and improved dimensional thermostability (up to 160°C). In addition, the lithium iron phosphate (LiFePO4)/lithium (Li) cell using such solid polymer electrolyte displayed superior rate capacity (up to 6 C) and stable cycle performance at 80°C. Furthermore, the LiFePO4/Li battery could also operate very well even at an elevated temperature of 160°C, thus improving enhanced safety performance of lithium batteries. The use of this solid polymer electrolyte mitigates the safety risk and widens the operation temperature range of lithium batteries. Thus, this fascinating study demonstrates a proof of concept of the use of rigid-flexible coupling solid polymer electrolyte toward practical lithium battery applications with improved reliability and safety.

Rigid-Flexible Coupling High Ionic Conductivity Polymer Electrolyte for an Enhanced Performance of LiMn2O4/Graphite Battery at Elevated Temperature

LiMn2O4-based batteries exhibit severe capacity fading during cycling or storage in LiPF6-based liquid electrolytes, especially at elevated temperatures. Herein, a novel rigid-flexible gel polymer electrolyte is introduced to enhance the cyclability of LiMn2O4/graphite battery at elevated temperature. The polymer electrolyte consists of a robust natural cellulose skeletal incorporated with soft segment poly(ethyl α-cyanoacrylate). The introduction of the cellulose effectively overcomes the drawback of poor mechanical integrity of the gel polymer electrolyte. Density functional theory (DFT) calculation demonstrates that the poly(ethyl α-cyanoacrylate) matrices effectively dissociate the lithium salt to facilitate ionic transport and thus has a higher ionic conductivity at room temperature. Ionic conductivity of the gel polymer electrolyte is 3.3 × 10(-3) S cm(-1) at room temperature. The gel polymer electrolyte remarkably improves the cycling performance of LiMn2O4-based batteries, especially at elevated temperatures. The capacity retention after the 100th cycle is 82% at 55 °C, which is much higher than that of liquid electrolyte (1 M LiPF6 in carbonate solvents). The polymer electrolyte can significantly suppress the dissolution of Mn(2+) from surface of LiMn2O4 because of strong interaction energy of Mn(2+) with PECA, which was investigated by DFT calculation.

Single-ion dominantly conducting polyborates towards high performance electrolytes in lithium batteries

A couple of thermally stable polyborate salts, polymeric lithium pentaerythrite borate (PLPB) and polymeric lithium di(trimethylolpropane) borate (PLDB), for applications in lithium ion batteries were synthesized via a facile one-step reaction in aqueous solution. Both the lithium polyborate salts exhibited a high thermal decomposition temperature at about 240 degrees C. Besides, their corresponding single-ion dominantly conducting gel polymer electrolytes of ethylene carbonate (EC) and dimethyl carbonate (DMC) (1 : 1, v/v) swollen PLPB@PVDF-HFP (poly(vinylidenefluoride-co-hexafluoropropene)) and PLDB@PVDF-HFP exhibited favorable ionic conductivity over a wide temperature range, superior electrochemical stability, high lithium ion transference number and Al passivating ability. The Li/LiFePO4 batteries using these single-ion dominantly conducting electrolytes exhibited stable charge-discharge behavior and excellent cycling performance both at room temperature and at elevated temperatures. These superior performances could make this class of gel polymer electrolytes very promising candidates for lithium batteries especially at elevated temperatures.