期刊
CARBON
卷 214, 期 -, 页码 -出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.carbon.2023.118318
关键词
Porous carbon; High mass loading; Potassium -ion storage; Areal capacity; High rate
Nitrogen-doped hollow carbon nanoparticles (NHCP) with optimized multiscale nanostructures are synthesized using a natural template-assisted chemical vapor deposition process. The NHCP anode shows superior K+ storage properties, including high reversible capacity, favorable rate capability, and long cyclic stability. The assembled full-carbon potassium-ion capacitor based on NHCP anode exhibits high energy and power densities and a long cycling lifespan, showing potential for practical application.
Carbon-based materials are considered as promising anode candidates for potassium-ion storage with the key bottlenecks lying in the slow kinetics and huge volume expansion caused by the large size of K+. Herein, nitrogen-doped hollow carbon nanoparticles (NHCP) with optimized multiscale nanostructures are synthesized by a natural template-assisted chemical vapor deposition process. Benefiting from the stacking nanoparticles structure with hierarchical pores, high level of pyridinic-/pyrrolic-N, and enlarged interlayer spacing, the constructed NHCP anode delivers superior K+ storage properties in terms of high reversible capacity (412.7 mAh g-1 at 0.03 A g-1), favorable rate capability, and long cyclic stability. The detailed experimental and computational studies reveal the combined storage mechanism of K+ adsorption and insertion in the multiscale nanostructure of NHCP. To achieve high areal capacities, self-supported NHCP electrodes with high mass loadings (3.41 and 6.23 mg cm-2) were constructed by a vacuum-assisted infiltration process which exhibits greatly improved areal capacities as compared with the traditional slurry coating electrode. The assembled full-carbon potassium-ion capacitor based on NHCP anode exhibits high energy and power densities (168 Wh kg-1 and 9.4 kW kg-1) and a long cycling lifespan (83.9% capacity retention after 10000 cycles at 1.0 A g-1). This work provides a facile fabrication method for porous carbon electrodes with high mass loadings and capacities, which holds the potential for practical application.
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