成核
材料科学
纳米颗粒
热解
碳纤维
金属有机骨架
化学工程
纳米棒
透射电子显微镜
金属
纳米技术
多孔性
化学
复合数
吸附
冶金
有机化学
复合材料
工程类
作者
Zhe Cui,Qian Liu,Jinqi Zhu,Hao Wang,Mengluan Gao,Wenqing Wang,Muk Fung Yuen,Junqing Hu,Huifang Chen,Rujia Zou
出处
期刊:Nano Letters
[American Chemical Society]
日期:2023-01-10
卷期号:23 (4): 1600-1607
被引量:7
标识
DOI:10.1021/acs.nanolett.2c04244
摘要
Metal-Organic frameworks (MOFs) are increasingly being investigated for the synthesis of carbon-supported metal-based ultrafine nanoparticles (UNPs). However, the collapse of the carbon framework and aggregation of metal particles in the pyrolysis process have severely hindered their stability and applications. Here, we report the synchronous nucleation pseudopyrolysis of MOFs to confine Fe/FeOx UNPs in intact porous carbon nanorods (IPCNs), revealed by in situ transmission electron microscopy experiments and ex situ structure analysis. The pseudopyrolysis mechanism enables strong physical and chemical confinement effects between UNPs and carbon by moderate thermal kinetics and abundant oxygen defects. Further, this strong confinement is greatly beneficial for subsequent chemical transformations to obtain different Fe-based UNPs and excellent electrochemical performance. As a proof of concept, the as-prepared FeSe UNPs in IPCNs show superior lithium storage performance with an ultrahigh and stable capacity of 815.1 mAh g-1 at 0.1 A g -1 and 379.7 mAh g-1 at 5 A g-1 for 1000 cycles.
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