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Three-dimensional ordered macroporous ZIF-8 nanoparticle-derived nitrogen-doped hierarchical porous carbons for high-performance lithium–sulfur batteries

Lithium–sulfur (Li–S) batteries have attracted considerable attention due to their ultra-high specific capacity and energy density. However, there are still problems to be resolved such as poor conductivity of sulfur cathodes and dissolution of polysulfides in organic electrolytes. Herein, a novel Z...

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Detalles Bibliográficos
Autores principales: Ji, Xinxin, Li, Qian, Yu, Haoquan, Hu, Xiaolin, Luo, Yuanzheng, Li, Buyin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9057854/
https://www.ncbi.nlm.nih.gov/pubmed/35516741
http://dx.doi.org/10.1039/d0ra07114e
Descripción
Sumario:Lithium–sulfur (Li–S) batteries have attracted considerable attention due to their ultra-high specific capacity and energy density. However, there are still problems to be resolved such as poor conductivity of sulfur cathodes and dissolution of polysulfides in organic electrolytes. Herein, a novel ZIF-8-derived nitrogen-doped connected ordered macro–microporous carbon (COM-MPC) was developed by a dual solvent-assisted in situ crystallization method within a face-centered cubic stacking sphere template, which acts as an advanced sulfur host for enhanced Li–S battery performance. Compared with the conventional predominant microporous C-ZIF-8, the unique hierarchical macro–microporous structure with nitrogen doping not only renders polysulfide intermediates enhanced entrapment by confining the effect of micropores and chemisorption of doping N atoms, but also facilitates electrolyte accessibility and efficient ion transport owing to the ordered macroporous structure. Benefitting from this, the COM-MPC@S cathode delivers a high initial specific capacity of 1498.5 mA h g(−1) and a reversible specific capacity of 1118.9 mA h g(−1). Moreover, the COM-MPC@S cathode exhibits 82.3% of capacity retention within 10th to 50th cycle at 0.5C and a large capacity of 608.5 mA h g(−1) after 50 cycles at a higher rate of 1C, and this enhanced cycling stability and rate capability demonstrate great practical application potential in Li–S battery systems.