材料科学
化学吸附
电化学
碳纤维
电极
氧化还原
化学工程
吸附
X射线光电子能谱
储能
流动电池
制作
纳米技术
电化学动力学
电池(电)
密度泛函理论
多孔性
吸收(声学)
表面改性
工作(物理)
兴奋剂
作者
Jinfeng Yi,Senwei Zeng,Runfa Zhao,Guangfu Wu,Zhi Liu,Tianhang Zhou,Chunming Xu,Jia Guo,Quan Xu,Yingchun Niu
标识
DOI:10.1002/adfm.202530893
摘要
ABSTRACT The iron‐chromium flow battery (ICRFB) is a promising large‐scale energy storage technology; however, its performance is largely limited by the sluggish Cr(II)/Cr(III) redox kinetics arising from poor carbon electrode‐electrolyte interfacial compatibility. Herein, we propose a targeted doping strategy that utilizes an eco‐friendly urea precursor to construct a pyridinic nitrogen‐rich carbon cloth electrode via a facile impregnation–calcination process. Density functional theory (DFT) calculations reveal that the pyridinic‐N configuration strengthens the adsorption of Cr(H 2 O) 5 Cl 2 + , reduces charge transfer resistance, thereby improving the reaction kinetics. Soft X‐ray absorption near‐edge structure (XANES) and X‐ray photoelectron spectroscopy (XPS) analyses further confirm the successful incorporation of pyridinic nitrogen into the carbon lattice, forming electron‐rich active centers that optimize the surface charge distribution and chemisorption behavior. The optimized electrode delivers a high discharge capacity of 689.3 mAh and maintains an energy efficiency of 72.83% at 200 mA cm −2 , together with exceptional cycling stability over 500 cycles at 140 mA cm −2 . This work offers a new pathway for precursor‐enabled interfacial engineering, bridging molecular design with electrochemical performance optimization in ICRFBs.
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