Unveiling the role of intrinsic defects in N/S Co-Doped hard carbon for superior sodium-ion batteries
Yunlei Yang, Chang Liu, Junjun Yao, Zhenqi Tang, Ying Sun, Kun Zhang, Hui Li, Tianyi Ma, Jieshan Qiu
Abstract
This article introduces the catalytic polymerization of phenothiazines through the crosslinking of aromatic rings with methylene (–CH2-) groups. By sacrificing methylene at a low carbonization temperature of 700°C, a large number of intrinsic defects are generated in situ within the carbon layers. The coupling effect between N/S co-doping and the intrinsic defect structure not only enhances the sodium storage capacity at low voltages (< 1 V), but also improves the sodium ions transfer capability. • Intrinsic defects were obtained via bridge-linked polymerization and in-situ elimination. • The role of intrinsic defects in N/S doped hard carbon for sodium storage was investigated. • Synergistic effect of co-doping and intrinsic defects enhances low-voltage sodium storage capacity. Hard carbon materials have emerged as a crucial anode choice for commercial sodium-ion batteries (SIBs), owing to their inherent abundance in porosity and the adaptability in adjusting interlayer spacing. However, the low capacity below 1 V and sluggish transportation kinetics respectively hinders the output voltage and rate performance. In this work, a one-step polymerization technique has been proposed to synthesize interconnected three-dimensional N/S-rich molecules via a methylene (–CH 2 -) bridge. During the subsequent carbonization process, the in-situ elimination of –CH 2 - bridge and partial heteroatoms facilitated the formation of intrinsic defects within the carbon layers, yielding an N/S co-doping hard carbon with intrinsic defect structures. This innovative approach provides a remarkable reversible capacity of 238mAh g −1 at voltages below 1 V, a high-rate capability of 150mAh g −1 at 5 A/g, along with exceptional cyclic stability of nearly 100 % capacity extension after 2000 cycles. This obviously enhancement in low-voltage sodium storage capacity and rate performance is attributed to the enhanced effect through N/S co-doping with intrinsic defect structures. This work highlights the critical role of defect engineering in carbon materials for efficient low-voltage sodium ions storage, offering a promising anode material with superior rate and cyclic stability.