Issue 23, 2024

Balancing interlayer spacing, pore structures and conductivity endows hard carbon with high capacity for rechargeable aluminum batteries

Abstract

As a key configuration, hard carbon (HC) is widely regarded as a promising cathode for rechargeable aluminum batteries (RABs), because of its enlarged interlayer spacing and well-developed pore structures. However, the trade-off between the pore structure, interlayer spacing and conductivity easily leads to an unsatisfactory electrochemical performance in terms of capacity and cycling stability. Hence, N-doped hard carbon (P-M) is synthesized at a relatively low temperature (700 °C) and anion intercalation associated with the energy storage process is investigated. The results demonstrate that the introduction of a N-doping agent not only expands the layer spacing and creates rich pore structures, but also boosts the conductivity. Compared with HC without N-doping, the expanded interlayer spacing in P-M can increase ion storage ability, and the rich pore channels contribute to electron transfer. Besides, compared with HC annealed at a higher temperature (900 °C), the enhanced conductivity in P-M is conducive to accelerating ion diffusion. Benefiting from these structure merits, the optimized P-M cathode delivers a high capacity (323 mA h g−1 at 500 mA g−1) and a prolonged cycle lifespan over 1000 cycles at 1 A g−1 retaining 109 mA h g−1. This work can provide a guidance for developing other high-performance hard carbon cathodes.

Graphical abstract: Balancing interlayer spacing, pore structures and conductivity endows hard carbon with high capacity for rechargeable aluminum batteries

Supplementary files

Article information

Article type
Paper
Submitted
06 Apr 2024
Accepted
19 May 2024
First published
20 May 2024

Phys. Chem. Chem. Phys., 2024,26, 16838-16846

Balancing interlayer spacing, pore structures and conductivity endows hard carbon with high capacity for rechargeable aluminum batteries

S. Li, Z. Zhang, F. Yuan, Z. Wang and B. Wang, Phys. Chem. Chem. Phys., 2024, 26, 16838 DOI: 10.1039/D4CP01415D

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