硫黄
材料科学
多硫化物
催化作用
化学工程
电解质
氧化物
磷化物
阴极
溶解
锂(药物)
电化学
金属
无机化学
电极
化学
有机化学
冶金
医学
物理化学
工程类
内分泌学
作者
Rui Gao,Liyuan Tian,Tao Wang,Hongjin Li,Peng Chen,Tianying Yan,Xueping Gao
标识
DOI:10.1021/acsami.4c02109
摘要
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–1. 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, in situ surface-phosphided Ni0.96Co0.03Mn0.01O (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 gs–1 at 0.1C), long cycling stability (491 mAh gs–1 after 1000 cycles at 1C), and excellent rate performance (565 mAh gs–1 at 5C). Importantly, the newly prepared sulfur cathode shows a high areal capacity of 4.0 mAh cm–2 and long cycle stability under harsh conditions (high sulfur loading of 5.3 mg cm–2 and lean electrolyte/sulfur ratio of 5.8 μL mg–1). This work proposes an effective strategy to develop the catalytic hosts of sulfur for achieving high-performance Li–S batteries via surface phosphidation.
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