Zinc-regulated hard carbon as a sodium-ion battery anode material

被引:0
作者
Song, Zhenqi [1 ,2 ]
Ma, Yanjiao [3 ]
Wang, Ke [1 ,2 ]
Liu, Chengyu [1 ,2 ]
Wu, Aojie [1 ,2 ]
Cheng, Xinbing [1 ,2 ]
Wang, Tao [1 ,2 ]
Wang, Faxing [1 ,2 ]
Ma, Yuan [1 ,2 ]
Wu, Yuping [1 ,2 ]
机构
[1] Southeast Univ, Key Lab Energy Thermal Convers, Sch Energy & Environm, Minist Educ,Confucius Energy Storage Lab, Nanjing 211189, Peoples R China
[2] Southeast Univ, Z Energy Storage Ctr, Nanjing 211189, Peoples R China
[3] Nanjing Normal Univ, Sch Energy & Mech Engn, Nanjing 210023, Peoples R China
关键词
Sodium-ion batteries; Hard carbon; Microporous; Zinc-regulated; Initial coulomb efficiency; ENERGY-STORAGE;
D O I
10.1016/j.jpowsour.2025.236798
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Due to their excellent stability and low cost, hard carbon (HC) materials have gained significant attention as anode materials in sodium-ion batteries (SIBs). However, the low initial Coulomb efficiency (ICE) and reversible capacity of HC limit its practical application. To address this issue, this study successfully prepared zincregulated HC (Zn-HC) with a rich microporous structure, significantly enhancing its sodium-ion storage performance. Electrochemical tests showed that Zn-HC exhibited high reversible capacity (386 mAh g-1 at 1.0 A g-1) and ICE (73.1 %). In-situ Raman spectroscopy, electrochemical impedance spectroscopy, and galvanostatic intermittent titration technique revealed that sodium-ion storage in Zn-HC occurs primarily through surface adsorption and intercalation/pore filling processes. Density functional theory (DFT) calculations further confirmed that the increased interlayer spacing and the introduction of C=O functional groups enhance sodiumion storage capacity. This study provides important insights for the design of high-performance anode materials for SIBs with superior electrochemical properties.
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页数:6
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