调控木材基硬炭的开孔结构以提高钠离子电池负极性能OA
Modulating the open pore structure of hard carbons derived from wood for sodium-ion battery anodes
可再生生物质硬炭(HC)是一种极具应用前景的钠离子电池负极材料.然而,硬炭负极的多孔结构调控以同时实现高能量密度、优异倍率性能和循环稳定性仍面临挑战.本文提出一种通过高温炭化过程中添加碳酸钠来调控木材基硬炭开孔结构的策略来优化其钠离子存储性能,得到的硬炭材料呈现出增大的层间距和优化的开孔分布(2~3 nm),具有高斜坡容量特征,从而实现了高效的钠离子传输与存储.优化后的硬炭负极在 30 mA g-1 电流密度下可逆容量达 326 mAh g-1,在倍率性能测试中,1 A g-1 电流密度下仍保持 270 mAh g-1 的可逆容量,甚至在 10 A g-1 高倍率下仍有 68 mAh g-1 的容量保持.经 300次循环后,在 1.0 A g-1 电流密度下容量保持率为 76.7%(207 mAh g-1).原位拉曼光谱和恒电流间歇滴定技术测试(GITT)结果表明,其储钠机制符合"吸附-插层-填充"的协同作用机制.该研究为优化木材硬炭的开孔结构以实现高性能钠离子存储提供了有效策略.
Hard carbon(HC)derived from renewable biomass is a promising anode material for sodium-ion batteries(SIBs).However,controlling the structure of hard carbon so that it has a high energy density,favorable rate performance,and cycling sta-bility is still a challenge.We propose a strategy to control the open pore structure of hard carbon derived from wood for sodium-ion storage by the addition of sodium carbonate under carbonization at 1100 ℃.The resulting HC has an increased interlayer spacing,and a more uniform open pore distribution(2-3 nm)with a high slope capacity,thereby enabling efficient sodium-ion transport and storage.The HC anode has a reversible capacity of 326 mAh g-1 at a current density of 30 mA g-1,and maintains a reversible capacity of 270 mAh g-1 at 1 A g-1 and a capacity of 68 mAh g-1 even at 10 A g-1 during rate performance tests.After 300 cycles,it retains 76.7%(207 mAh g-1)of its capacity at 1.0 A g-1.In situ Raman spectroscopy and the galvanostatic inter-mittent titration testing results reveal an adsorption-intercalation-filling sodium storage mechanism.This work provides a strategy to optimize the open pore structure of biomass derived hard carbon for high performance sodium ion storage.
李梦龙;龚俊;李金铭;谢海鹏;李业军
湖南科技大学 机电工程学院,湖南 湘潭,411201湖南科技大学 机电工程学院,湖南 湘潭,411201中南大学 物理学院,湖南省纳米光子学与器件重点实验室,湖南 长沙,410083中南大学 物理学院,湖南省纳米光子学与器件重点实验室,湖南 长沙,410083中南大学 材料科学与工程学院,湖南 长沙,410083
化学化工
钠离子电池硬炭生物质孔隙结构
Sodium-ion batteriesHard carbonBiomassPore structure
《新型炭材料(中英文)》 2026 (3)
652-663,12
This work was supported by National Natural Science Foundation of China(11904411).国家自然科学基金(11904411).
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