碳化
阳极
碳纤维
插层(化学)
材料科学
化学工程
硫黄
钾
无机化学
吸附
复合数
化学
有机化学
电极
复合材料
物理化学
工程类
冶金
作者
Yu Jiang,Nan Xiao,Xuedan Song,Kai Yu,Jieshan Qiu
出处
期刊:Small
[Wiley]
日期:2025-06-17
卷期号:21 (32): e2504946-e2504946
被引量:3
标识
DOI:10.1002/smll.202504946
摘要
The nitrogen/sulfur (N/S) co-doping strategy has gained significant attention in the development of carbon-based anodes for potassium-ion batteries (PIBs) due to its capapcity to enhance specific capacity and accelerate reaction kinetics. Yet, the C─S bond-driven conversion reaction would inevitably induce critical challenges, including poor stability and high charging voltage, thereby severely impeding the commercialization of N/S co-doped carbon anodes. Herein, a novel sulfonic group dominated N/S co-doped carbon (NSAC-600) is synthesized via a facile low-temperature carbonization strategy with coal tar pitch as a precursor. The sulfonic groups in NSAC-600 have strong sulfur-locking ability, that can suppress the formation of potassium polysulfides during K storage. Moreover, the N and sulfonic groups synergistically create abundant active sites for K+ adsorption, expand the carbon interlayer spacing, and help to create rapid charge diffusion pathways. Thereby, the NSAC-600 can deliver high-rate performance (217.0 mAh g-1 at 5 A g-1), good cycling stability (without any capacity decay after 1400 cycles at 2 A g-1 and stable operation for 5600 cycles at a high current density of 5 A g-1) and low depotassium voltage. An "adsorption/intercalation/limited-conversion" mechanism is proposed to elucidate the potassium storage behavior in this novel carbon material. This work may provide a new horizon for advanced N/S co-doped carbon anodes.
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