介孔材料
热解炭
硫黄
热解
碳纤维
材料科学
碳化
化学工程
催化作用
锂(药物)
氧化还原
动力学
纳米技术
无机化学
化学
有机化学
扫描电子显微镜
复合数
工程类
内分泌学
物理
复合材料
医学
冶金
量子力学
作者
Yunxiang Li,Yinxiang Zeng,Ye Chen,Deyan Luan,Shuyan Gao,Xiong-Wen Lou
标识
DOI:10.1002/ange.202212680
摘要
Abstract Physicochemical confinement and catalytic conversion of lithium polysulfides (LiPSs) are crucial to suppress the shuttle effect and enhance the redox kinetics of lithium‐sulfur (Li‐S) batteries. In this study, a NH 4 Cl‐assisted pyrolysis strategy is developed to fabricate highly mesoporous N‐rich carbon (designed as NC(p)) featuring thin outer shells and porous inner networks, on which single‐Ni atoms are anchored to form an excellent sulfur host (designed as Ni‐NC(p)) for Li‐S batteries. During pyrolysis, the pyrolytic HCl from confined NH 4 Cl within ZIF‐8 will in situ etch ZIF‐8 to produce rich mesoporous in the carbonized product NC(p). The mesoporous Ni‐NC(p) enables favorable electron/ion transfer, high sulfur loading, and effective confinement of LiPSs, while the catalytic effect of single‐Ni species enhances the redox kinetics of LiPSs. As a result, the sulfur cathode based on the Ni‐NC(p) host delivers obviously improved Li‐S battery performance with high specific capacity, good rate capability, and cycling stability.
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