Low‐Temperature Carbonization Synthesis of Sulfonic Group Dominated N/S Co‐Doped Carbon for High‐Performance Potassium‐Ion Batteries

碳化 阳极 碳纤维 插层(化学) 材料科学 化学工程 硫黄 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]
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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