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Boosting fast and stable symmetric sodium-ion storage by synergistic engineering and amorphous structure
Nano Energy ( IF 16.8 ) Pub Date : 2022-06-09 , DOI: 10.1016/j.nanoen.2022.107481
Sahar Osman , Chao Peng , Jiadong Shen , Fangkun Li , Wenjie Huang , Jun Liu , Jiangwen Liu , Dongfeng Xue , Min Zhu

Tuning the microstructure and crystallinity of electrode materials is a great challenge and crucial for the development of high-performance sodium-ion batteries (SIBs). Herein, we develop a series of rationally designed carbon-coated V2O5 core-shell nanostructures (S-V2O5-HS, S-V2O5-HCS, P-V2O5/C-SCS, A-V2O5/C-SCS, and A-V2O5/C-WCS) in which the phase (single/polycrystalline, amorphous), microstructure (hollow, solid, porous) for the V2O5 core, and the thickness of the carbon shell are controlled via a one-pot solvothermal method followed by a single calcination process, and the performance differences between them are systematically studied. In this composite of amorphous carbon-coated V2O5 well-defined porous core-shell heterostructure (A-V2O5/C-WCS), synergistically the amorphous V2O5 core accelerates ions diffusion, carbon shell boosts the electronic conductivity, and the defect-rich porous structure lowers the binding energy compared to its counterparts as confirmed by DFT calculations and electrochemical results. Out of the ordinary, the A-V2O5/C-WCS used as a symmetric electrode for SIBs exhibits an excellent rate capability of 148 mAh g−1 at 5.0 A g−1 and outstanding ultralong cyclic stability (95% capacity retentions over 3000 cycles at 2.0 A g−1), when applied as a cathode (1.5–4.0 V) and anode (0.01–3.0 V) for SIBs. The A-V2O5/C-WCS displays a fully pseudocapacitive manner over the whole voltage thus the electrochemical performance of cathode and anode are well-matched. Impressively, the symmetric full-cell possesses a superior energy density of 219 Wh kg−1 at a high specific density of 6.0 KW kg−1 and superior cycling stability (95% capacity retained over 1200 cycles at 1.0 A g−1), demonstrating the great potential for practical application.



中文翻译:

通过协同工程和无定形结构促进快速稳定的对称钠离子存储

调整电极材料的微观结构和结晶度是开发高性能钠离子电池(SIB)的一个巨大挑战和关键。在此,我们开发了一系列设计合理的碳包覆V 2 O 5核壳纳米结构(SV 2 O5-HS、SV 2 O 5 -HCS、PV 2 O 5 /C-SCS、AV 2 O 5 /C- SCS, 和 AV 2 O 5 /C-WCS) 其中相(单晶/多晶、无定形)、微观结构(空心、实心、多孔)为 V 2 O 5通过一锅溶剂热法和单次煅烧工艺控制核心和碳壳的厚度,并系统地研究了它们之间的性能差异。在这种由无定形碳包覆的 V 2 O 5明确的多孔核壳异质结构 (AV 2 O 5 /C-WCS) 组成的复合材料中,无定形 V 2 O 5核协同地加速了离子扩散,碳壳提高了电子电导率, DFT计算和电化学结果证实,与对应物相比,富含缺陷的多孔结构降低了结合能。与众不同的是,AV 2 O 5/C-WCS 用作 SIB 的对称电极,在 5.0 A g -1下表现出 148 mAh g -1的优异倍率性能和出色的超长循环稳定性(在 2.0 A g -1下 3000 次循环后的容量保持率为 95% ),当用作SIB的阴极(1.5-4.0 V)和阳极(0.01-3.0 V)。AV 2 O 5 /C-WCS 在整个电压范围内显示出完全赝电容方式,因此正极和负极的电化学性能非常匹配。令人印象深刻的是,对称全电池在 6.0 KW kg -1的高比密度下具有 219 Wh kg -1的出色能量密度和出色的循环稳定性(在 1.0 A g 下 1200 次循环后仍保持 95% 的容量)-1 ),展示了实际应用的巨大潜力。

更新日期:2022-06-14
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