| Literature DB >> 33475665 |
Xuechun Li1, Huanlei Wang1, Wenzhe Zhang1, Wenrui Wei1, Ranxia Liao1, Jing Shi1, Minghua Huang1, Shuai Liu1, Zhicheng Shi1.
Abstract
The development of carbon materials for potassium storage is limited by their low specific capacity and poor cycling stability due to the sluggish kinetics of K ions. Herein, fucoidan-derived oxygen-rich carbon nanosheets are reported as a fantastic anode for potassium ion batteries. Attributed to its 2D porous sheet-like structure (morphology engineering), rich oxygen doping (defect engineering), and dilated graphitic layer in an amorphous structure (structure engineering), a competitive capacity of 392 mA h g-1 at 0.05 A g-1 and a long cycling span over 2500 cycles at 2 A g-1 was achieved for the carbon anode, outperforming most of the reported carbons. The kinetic analyses reveal that rich active sites and a porous nanosheet structure account for the superb rate performance and cycling stability of the material. Ex situ X-ray photoelectron spectroscopy measurements demonstrate that the introduction of C[double bond, length as m-dash]O greatly promotes K+ adsorption, and that the improvement of the C[double bond, length as m-dash]O bonds during cycling contributes to enhancement in the capacity. The fabricated potassium ion hybrid capacitor displays an exceptional energy/power density of 193 W h kg-1/22 324 W kg-1, and a promising cycling stability with 99.3% capacity retention over 2000 cycles. This work provides a large-scale synthesis strategy for preparing oxygen-rich carbon nanosheets for advanced potassium ion storage.Entities:
Year: 2021 PMID: 33475665 DOI: 10.1039/d0nr08628b
Source DB: PubMed Journal: Nanoscale ISSN: 2040-3364 Impact factor: 7.790