Gao Rui, Tian Li-Yuan, Wang Tao, Li Hong-Jin, Chen Peng, Yan Tian-Ying, Gao Xue-Ping
Institute of New Energy Material Chemistry, School of Materials Science and Engineering, Nankai University, Tianjin 300350, China.
ACS Appl Mater Interfaces. 2024 May 1;16(17):21943-21952. doi: 10.1021/acsami.4c02109. Epub 2024 Apr 18.
Lithium-sulfur (Li-S) batteries are one of the most promising high-energy density secondary batteries due to their high theoretical energy density of 2600 Wh kg. However, the sluggish kinetics and severe "shuttle effect" of polysulfides are the well-known barriers that hinder their practical applications. A carefully designed catalytic host of sulfur may be an effective strategy that not only accelerates the conversion of polysulfides but also limit their dissolution to mitigate the "shuttle effect." Herein, surface-phosphided NiCoMnO (p-NCMO) oxide microspheres are prepared via gas-phase phosphidation as a catalytic host of sulfur. The as-prepared unique heterostructured microspheres, with enriched surface-coated metal phosphide, exhibit superior synergistic effect of catalytic conversion and absorption of the otherwise soluble intermediate polysulfides. Correspondingly, the sulfur cathode exhibits excellent electrochemical performance, including a high initial discharge capacity (1162 mAh g at 0.1C), long cycling stability (491 mAh g after 1000 cycles at 1C), and excellent rate performance (565 mAh g at 5C). Importantly, the newly prepared sulfur cathode shows a high areal capacity of 4.0 mAh cm and long cycle stability under harsh conditions (high sulfur loading of 5.3 mg cm and lean electrolyte/sulfur ratio of 5.8 μL mg). This work proposes an effective strategy to develop the catalytic hosts of sulfur for achieving high-performance Li-S batteries via surface phosphidation.
锂硫(Li-S)电池因其2600 Wh/kg的高理论能量密度,成为最具前景的高能量密度二次电池之一。然而,多硫化物缓慢的动力学和严重的“穿梭效应”是阻碍其实际应用的众所周知的障碍。精心设计的硫催化主体可能是一种有效的策略,不仅可以加速多硫化物的转化,还可以限制它们的溶解,从而减轻“穿梭效应”。在此,通过气相磷化制备了表面磷化的NiCoMnO(p-NCMO)氧化物微球作为硫的催化主体。所制备的具有独特异质结构的微球,其表面包覆有丰富的金属磷化物,对原本可溶的中间多硫化物表现出优异的催化转化和吸附协同效应。相应地,硫正极表现出优异的电化学性能,包括高初始放电容量(0.1C时为1162 mAh/g)、长循环稳定性(1C下1000次循环后为491 mAh/g)和优异的倍率性能(5C时为565 mAh/g)。重要的是,新制备的硫正极在苛刻条件下(高硫负载量为5.3 mg/cm²和贫电解质/硫比为5.8 μL/mg)显示出4.0 mAh/cm²的高面积容量和长循环稳定性。这项工作提出了一种通过表面磷化开发硫催化主体以实现高性能锂硫电池的有效策略。