Li Yong, Wang Xuzhen, Sun Minghui, Xiao Jian, Zhang Bolun, Ai Lishen, Zhao Zongbin, Qiu Jieshan
State Key Lab of Fine Chemicals, School of Chemical Engineering, Liaoning Key Lab for Energy Materials and Chemical Engineering, Dalian University of Technology, Dalian116024, Liaoning, People's Republic of China.
College of Chemical Engineering, State Key Laboratory of Chemical Resource Engineering, Beijing University of Chemical Technology, Beijing100029, People's Republic of China.
ACS Nano. 2022 Oct 25;16(10):17008-17020. doi: 10.1021/acsnano.2c07137. Epub 2022 Oct 10.
The lithium polysulfide (LiPSs) shuttling and slow chemical reactions at the sulfur cathode and the formation of dendritic lithium in metal anodes severely hinder the popularization of lithium-sulfur batteries. Here, a B,N-codoped carbon nanotube (BNCNTs) array decorated with sulfilic and lithiophilic CoSe nanoparticles grown on a carbon cloth (CoSe@BNCNTs/CC) as both a sulfur and a lithium host is reported. Density functional theory (DFT) calculations, simulations, and electrochemical performance determinations demonstrate that CoSe@BNCNTs/CC can simultaneously exert catalytic effects for accelerating LiPSs conversion and realize smooth and uniform lithium deposition to regulate the S and Li electrochemistry. Moreover, the unique structure of the BNCNTs array provides sufficient storage space for sulfur and homogenizes the distribution of Li ions and the electric field of the electrode. The assembled Li-S full battery with a CoSe@BNCNTs/CC dual-functional host exhibits a long-term cycling stability (800 cycles at 0.5 C with a decay rate of 0.066% per cycle) and a high rate capacity (684 mAh g at 2 C). Even at a high sulfur loading of 7.9 mg cm, the Li-S full battery has a high areal capacity of 9.76 mAh cm at 0.2 C. This study proposes a viable strategy to solve the challenges of both S and Li electrodes for practical Li-S full batteries.
多硫化锂(LiPSs)穿梭以及硫正极处缓慢的化学反应和金属负极中枝晶锂的形成严重阻碍了锂硫电池的推广。在此,报道了一种在碳布(CoSe@BNCNTs/CC)上生长有亲硫和亲锂的CoSe纳米颗粒修饰的B、N共掺杂碳纳米管(BNCNTs)阵列,其作为硫宿主和锂宿主。密度泛函理论(DFT)计算、模拟和电化学性能测定表明,CoSe@BNCNTs/CC可以同时发挥催化作用以加速LiPSs转化,并实现平滑且均匀的锂沉积,从而调节硫和锂的电化学。此外,BNCNTs阵列的独特结构为硫提供了足够的存储空间,并使锂离子分布和电极电场均匀化。采用CoSe@BNCNTs/CC双功能宿主组装的锂硫全电池表现出长期循环稳定性(在0.5 C下循环800次,每次循环衰减率为0.066%)和高倍率容量(在2 C下为684 mAh g)。即使在硫负载量高达7.9 mg cm时,锂硫全电池在0.2 C下仍具有9.76 mAh cm的高面积容量。本研究提出了一种可行的策略,以解决实际锂硫全电池中硫电极和锂电极面临的挑战。