Wang Zilong, Lu Jianhao, Li Songze, Guo Yang, Lian Fang, Wang Anbang, Jin Zhaoqing, Wang Weikun
Beijing Key Laboratory of Advanced Chemical Energy Storage Technology and Materials, Research Institute of Chemical Defense, Beijing 100191, P. R. China.
School of Science, Beijing Jiaotong University, Beijing 100044, P. R. China.
ACS Appl Mater Interfaces. 2021 Dec 15;13(49):58789-58798. doi: 10.1021/acsami.1c19915. Epub 2021 Dec 4.
The shuttle effects of polysulfide intermediates (LiPSs) and sluggish kinetics during sulfur reduction reaction (SRR) process severely exacerbate the electrochemical performances of Li-S batteries. Herein, a unique nanocatalyst comprising β-NiOOH nanosheets uniformly implanted on the surface of carbon nanotubes (CNT@NiOOH) was designed and synthesized for sulfur cathodes. The β-NiOOH nanosheets have great capability of adsorbing LiPSs as well as superior catalytic activity for accelerating LiPS conversion, providing a more efficient method to restrain shuttle effects and improve the kinetics of SRR. Moreover, the nanometer-scale epitaxial growth and uniform distribution of β-NiOOH on CNTs provide a multidimensional catalytic skeleton with sufficient accessible active surfaces, unimpeded LiPS diffusion pathways, and resultant high utilization of active sites. Simultaneously, stable electron transportation pathways are also obtained by being synthesized on CNTs to avoid the faultiness of poor electron conductivity of β-NiOOH. These conspicuous advantages contribute to fully exert the catalytic and LiPS anchoring potential of CNT@NiOOH, bringing about the ultralong cycle performance and excellent capacity reversibility at a high discharge rate. Reticular CNT@NiOOH frameworks are assembled with the sulfur composite materials (SCMs) by a self-assembly method, and a super-high capacity of 813.3 mA h g after 400 cycles at 0.5 C with a small capacity degradation of 0.07% per cycle is achieved. Furthermore, the 3 A h pouch-type cell with the SCM/CNT@NiOOH cathode attains a super-high energy density of about 320 W h kg and shows a superior capacity retention as high as 75.9% after 50 cycles at 0.2 C. This work provides a promising method to accelerate the SRR process and restrain the shuttle effects for practical long-life and high-capacity Li-sulfur batteries.
多硫化物中间体(LiPSs)的穿梭效应以及硫还原反应(SRR)过程中的缓慢动力学严重加剧了锂硫电池的电化学性能。在此,设计并合成了一种独特的纳米催化剂,其由均匀植入碳纳米管(CNT@NiOOH)表面的β-NiOOH纳米片组成,用于硫正极。β-NiOOH纳米片具有很强的吸附LiPSs的能力以及加速LiPS转化的优异催化活性,为抑制穿梭效应和改善SRR动力学提供了一种更有效的方法。此外,β-NiOOH在碳纳米管上的纳米级外延生长和均匀分布提供了一个具有足够可及活性表面、畅通的LiPS扩散途径以及由此产生的高活性位点利用率的多维催化骨架。同时,通过在碳纳米管上合成还获得了稳定的电子传输途径,以避免β-NiOOH电子导电性差的缺陷。这些显著优势有助于充分发挥CNT@NiOOH的催化和LiPS锚定潜力,从而在高放电率下实现超长循环性能和优异的容量可逆性。通过自组装方法将网状CNT@NiOOH框架与硫复合材料(SCMs)组装在一起,在0.5 C下循环400次后实现了813.3 mA h g的超高容量,每循环容量衰减仅0.07%。此外,采用SCM/CNT@NiOOH正极的3 A h软包电池实现了约320 W h kg的超高能量密度,在0.2 C下循环50次后显示出高达75.9%的优异容量保持率。这项工作为加速SRR过程和抑制穿梭效应提供了一种有前景的方法,可用于实际的长寿命和高容量锂硫电池。