Shi Tianyu, Zhao Chenyuan, Zhou Yuxiang, Yin Haihong, Song Changqing, Qin Lin, Wang Zhiliang, Shao Haibao, Yu Ke
School of Information Science and Technology, Nantong University, Nantong 226019, China.
School of Information Science and Technology, Nantong University, Nantong 226019, China.
J Colloid Interface Sci. 2021 Oct;599:416-426. doi: 10.1016/j.jcis.2021.04.063. Epub 2021 Apr 17.
Lithium-sulfur batteries (LSBs) are regarded as promising candidates for next-generation electrochemical energy storage systems due to their low cost and high energy density. However, the insulative sulfur, the volume expansion and high soluble polysulfides are three roots impeding their practical applications, and consequently bring challenges of low sulfur utilization, poor cyclic stability and sluggish redox kinetics. Herein, a special core-shell ZnS-CNTs/S@Ni(OH) (labeled as ZnS-CNTs/S@NH) cathode has been designed to overcome above obstacles and elevate the electrochemical performance. The ZnS-CNTs/S@NH cathode is synthesized via a facile step-by-step strategy, in which ZnS-decorated CNTs was used as a framework to load sulfur and followed with a ultrathin Ni(OH) (NH) layer encapsulation. The ZnS-CNT core combines merits of CNT network and polar ZnS quantum dots (QDs), accommodating the volume change, offering efficient pathways for fast electron/ion transport, and anchoring polysulfides through polar interactions. The outer Ni(OH) shell physically confines the active material and meanwhile provides plenty of catalytic sites for effective polysulfide chemisorption. Benefiting from these merits, the ZnS-CNTs/S@NH cathode exhibits excellent cell performances in comparison with ZnS-CNTs/S and CNTs/S. Its discharge capacity at different C-rates is optimal in the three cathodes, which decreases from 1037.0 mAh g at 0.1 C to 646.1 mAh g at 2.0 C. Its cyclic capacity also manifests the slowest reduction from 861.1 to 760.1 mAh g after 150 cycles at 0.5 C, showing a high retention (88.3%) and a tiny average fading rate (0.078%). The strategy in this work provides a feasible approach to design and construct core-shell cathode materials for realizing practically usable Li-S batteries.
锂硫电池(LSBs)因其低成本和高能量密度,被视为下一代电化学储能系统的有前景的候选者。然而,绝缘的硫、体积膨胀和高可溶性多硫化物是阻碍其实际应用的三个根源,因此带来了低硫利用率、差的循环稳定性和缓慢的氧化还原动力学等挑战。在此,设计了一种特殊的核壳结构ZnS-CNTs/S@Ni(OH)(标记为ZnS-CNTs/S@NH)阴极,以克服上述障碍并提升电化学性能。ZnS-CNTs/S@NH阴极通过一种简便的逐步策略合成,其中用ZnS修饰的碳纳米管(CNTs)作为负载硫的框架,随后进行超薄Ni(OH)(NH)层封装。ZnS-CNT核结合了CNT网络和极性ZnS量子点(QDs)的优点,适应体积变化,为快速电子/离子传输提供有效途径,并通过极性相互作用锚定多硫化物。外部的Ni(OH)壳在物理上限制了活性材料,同时提供大量催化位点用于有效的多硫化物化学吸附。受益于这些优点,与ZnS-CNTs/S和CNTs/S相比,ZnS-CNTs/S@NH阴极表现出优异的电池性能。其在不同C倍率下的放电容量在三种阴极中是最优的,从0.1C时的1037.0 mAh g降至2.0C时的646.1 mAh g。其循环容量在0.5C下150次循环后也表现出最慢的下降,从861.1降至760.1 mAh g,显示出高保留率(88.3%)和微小的平均衰减率(0.078%)。这项工作中的策略为设计和构建核壳阴极材料以实现实际可用的锂硫电池提供了一种可行的方法。