Luo Dan, Li Chaojie, Zhang Yongguang, Ma Qianyi, Ma Chuyin, Nie Yihang, Li Matthew, Weng Xuefei, Huang Rong, Zhao Yan, Shui Lingling, Wang Xin, Chen Zhongwei
Guangdong Provincial Key Laboratory of Nanophotonic Functional Materials and Devices, School of Information and Optoelectronic Science and Engineering & International Academy of Optoelectronics at Zhaoqing, South China Normal University, Guangdong, 510006, China.
Department of Chemical Engineering, Waterloo Institute for Nanotechnology, University of Waterloo, Waterloo, ON, N2L 3G1, Canada.
Adv Mater. 2022 Jan;34(2):e2105541. doi: 10.1002/adma.202105541. Epub 2021 Nov 7.
Lithium-sulfur (Li-S) batteries are considered as one of the most promising next-generation rechargeable batteries owing to their high energy density and cost-effectiveness. However, the sluggish kinetics of the sulfur reduction reaction process, which is so far insufficiently explored, still impedes its practical application. Metal-organic frameworks (MOFs) are widely investigated as a sulfur immobilizer, but the interactions and catalytic activity of lithium polysulfides (LiPs) on metal nodes are weak due to the presence of organic ligands. Herein, a strategy to design quasi-MOF nanospheres, which contain a transition-state structure between the MOF and the metal oxide via controlled ligand exchange strategy, to serve as sulfur electrocatalyst, is presented. The quasi-MOF not only inherits the porous structure of the MOF, but also exposes abundant metal nodes to act as active sites, rendering strong LiPs absorbability. The reversible deligandation/ligandation of the quasi-MOF and its impact on the durability of the catalyst over the course of the electrochemical process is acknowledged, which confers a remarkable catalytic activity. Attributed to these structural advantages, the quasi-MOF delivers a decent discharge capacity and low capacity-fading rate over long-term cycling. This work not only offers insight into the rational design of quasi-MOF-based composites but also provides guidance for application in Li-S batteries.
锂硫(Li-S)电池因其高能量密度和成本效益被认为是最有前景的下一代可充电电池之一。然而,硫还原反应过程动力学缓慢,至今尚未得到充分研究,这仍然阻碍了其实际应用。金属有机框架(MOF)作为一种硫固定剂受到广泛研究,但由于有机配体的存在,多硫化锂(LiP)在金属节点上的相互作用和催化活性较弱。在此,我们提出了一种设计准MOF纳米球的策略,通过可控配体交换策略,使其具有介于MOF和金属氧化物之间的过渡态结构,用作硫电催化剂。这种准MOF不仅继承了MOF的多孔结构,还暴露出大量金属节点作为活性位点,具有很强的LiP吸附能力。准MOF的可逆去配体/配体过程及其在电化学过程中对催化剂耐久性的影响得到了认可,这赋予了其显著的催化活性。由于这些结构优势,准MOF在长期循环中具有良好的放电容量和低容量衰减率。这项工作不仅为基于准MOF的复合材料的合理设计提供了思路,也为其在锂硫电池中的应用提供了指导。