4.8 Article

Designing and Understanding the Superior Potassium Storage Performance of Nitrogen/Phosphorus Co-Doped Hollow Porous Bowl-Like Carbon Anodes

Journal

ADVANCED FUNCTIONAL MATERIALS
Volume 31, Issue 1, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adfm.202007158

Keywords

anode materials; heteroatom dual doped; hollow and porous carbon; in situ transmission electron microscopy; potassium‐ ion batteries

Funding

  1. National Natural Science Foundation of China [52072323, 21703185, 51872098]
  2. Leading Project Foundation of Science Department of Fujian Province [2018H0034]
  3. Double-First Class Foundation of Materials and Intelligent Manufacturing Discipline of Xiamen University
  4. Opening Project of National Joint Engineering Research Center for Abrasion Control and Molding of Metal Materials, & Henan Key Laboratory of High-temperature Structural and Functional Materials, Henan University of Science and Technology [HKDNM2019013]

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A novel carbon-based anode material N/P-HPCB was developed for high-performance potassium-ion batteries (PIBs), demonstrating high reversible capacity, superior rate performance, and long-term cycling stability. Density-functional theory calculations and experimental validation reveal that N/P dual doping advantages facilitate adsorption/diffusion of K+ and enhance electronic conductivity in the electrode.
Potassium-ion batteries (PIBs) are promising alternatives to lithium-ion batteries because of the advantage of abundant, low-cost potassium resources. However, PIBs are facing a pivotal challenge to develop suitable electrode materials for efficient insertion/extraction of large-radius potassium ions (K+). Here, a viable anode material composed of uniform, hollow porous bowl-like hard carbon dual doped with nitrogen (N) and phosphorus (P) (denoted as N/P-HPCB) is developed for high-performance PIBs. With prominent merits in structure, the as-fabricated N/P-HPCB electrode manifests extraordinary potassium storage performance in terms of high reversible capacity (458.3 mAh g(-1) after 100 cycles at 0.1 A g(-1)), superior rate performance (213.6 mAh g(-1) at 4 A g(-1)), and long-term cyclability (205.2 mAh g(-1) after 1000 cycles at 2 A g(-1)). Density-functional theory calculations reveal the merits of N/P dual doping in favor of facilitating the adsorption/diffusion of K+ and enhancing the electronic conductivity, guaranteeing improved capacity, and rate capability. Moreover, in situ transmission electron microscopy in conjunction with ex situ microscopy and Raman spectroscopy confirms the exceptional cycling stability originating from the excellent phase reversibility and robust structure integrity of N/P-HPCB electrode during cycling. Overall, the findings shed light on the development of high-performance, durable carbon anodes for advanced PIBs.

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