多硫化物
材料科学
尖晶石
合理设计
电化学
储能
硫黄
化学工程
电池(电)
硫系化合物
镍
电极
纳米技术
锂(药物)
化学
冶金
医学
功率(物理)
物理
物理化学
量子力学
内分泌学
工程类
电解质
作者
Dan Luo,Gaoran Li,Ya‐Ping Deng,Zhen Zhang,Jingde Li,Ruilin Liang,Matthew Li,Yi Jiang,Weiwei Zhang,Yangshuai Liu,Wen Lei,Aiping Yu,Zhongwei Chen
标识
DOI:10.1002/aenm.201900228
摘要
Abstract Lithium–sulfur (Li–S) batteries have great promise to support the next‐generation energy storage if their sluggish redox kinetics and polysulfide shuttling can be addressed. The rational design of sulfur electrodes plays key roles in tacking these problems and achieving high‐efficiency sulfur electrochemistry. Herein, a synergetic defect and architecture engineering strategy to design highly disordered spinel Ni–Co oxide double‐shelled microspheres (NCO‐HS), which consist of defective spinel NiCo 2 O 4– x ( x = 0.9 if all nickel is Ni 2+ and cobalt is Co 2.13+ ), as the multifunctional sulfur host material is reported. The in situ constructed cation and anion defects endow the NCO‐HS with significantly enhanced electronic conductivity and superior polysulfide adsorbability. Meanwhile, the delicate nanoconstruction offers abundant active interfaces and reduced ion diffusion pathways for efficient Li–S chemistry. Attributed to these synergistic features, the sulfur composite electrode achieves excellent rate performance up to 5 C, remarkable cycling stability over 800 cycles and good areal capacity of 6.3 mAh cm −2 under high sulfur loading. This proposed strategy based on synergy engineering could also inform material engineering in related energy storage and conversion fields.
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