From Sodium Storage Mechanism to Design of High-Capacity Carbon-Based Anode: A Review

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Abstract

Sodium-ion batteries (SIBs) have emerged as a viable alternative to lithium-ion technologies, with carbon-based anodes playing a pivotal role in addressing key challenges of sodium storage. This review systematically examines hard carbon as the premier anode material, elucidating its dual sodium storage mechanisms: 1) sloping capacity (2.0-0.1 V vs Na+/Na) from surface/defect adsorption and 2) plateau capacity (<0.1 V) via closed-pore filling and pseudo-graphitic intercalation. Through critical analysis of recent advancements, we establish that optimized hard carbon architectures delivering 300-400 mAh/g capacity require precise coordination of pseudo-graphitic domains (d002 = 0.36-0.40 nm) and sub-1 nm closed pores. This review ultimately provides a design blueprint for next-generation carbon anodes, proposing three research frontiers: 1) machine learning-guided microstructure optimization, 2) dynamic sodiation/desodiation control in sub-nm pores, and 3) scalable manufacturing of heteroatom-doped architectures with engineered pseudo-graphitic domains. These advancements position hard carbon anodes as critical enablers for high-performance, cost-effective SIBs in grid-scale energy storage applications.

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