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通过锡的层间限制增强零下温度下的钠离子存储

Enhancing Na-Ion Storage at Subzero Temperature via Interlayer Confinement of Sn.

作者信息

Que Lan-Fang, Yu Fu-Da, Xia Yang, Deng Liang, Goh Kokswee, Liu Chang, Jiang Yun-Shan, Sui Xu-Lei, Wang Zhen-Bo

机构信息

MIIT Key Laboratory of Critical Materials Technology for New Energy Conversion and Storage, School of Chemistry and Chemical Engineering, State Key Lab of Urban Water Resource and Environment, Harbin Institute of Technology, No.92 West-Da Zhi Street, Harbin 150001, China.

出版信息

ACS Nano. 2020 Oct 27;14(10):13765-13774. doi: 10.1021/acsnano.0c05925. Epub 2020 Oct 7.

Abstract

Sluggish kinetics and limited reversible capacity present two major challenges for layered titanates to achieve satisfactory sodium-ion storage performance at subzero-temperatures (subzero-T). To facilitate sodiation dynamics and improve reversible capacity, we proposed an additive-free anode with Sn(II) located between layers. Sn-5s in interlayer-confining Sn(II), which has a larger negative charge, will hybridize with O-2p to trigger charge redistribution, thereby enhancing electronic conductivity. H-titanates with an open framework are designed to stabilize Sn(II) and restrain subsequent volume expansion, which could potentially surpass the capacity limitation of titanate-based materials via a joint alloying-intercalation reaction with high reversibility. Moreover, the generation of conductive NaSn and the expansion of interlayer spacing resulting from the interlayered alloying reaction are beneficial for charge transfer. These effects synergistically endow the modified sample with a considerably lower activation energy and a 3-fold increase in diffusion. Consequently, the designed anode delivers excellent subzero-T adaptability when compared to the unmodified sample, maintaining capacity retention of 91% after 1200 cycles at -20 °C and 90% after 850 cycles at -30 °C.

摘要

动力学迟缓以及可逆容量有限,是层状钛酸盐在低温(零下温度,subzero-T)下实现令人满意的钠离子存储性能面临的两大主要挑战。为了促进钠化动力学并提高可逆容量,我们提出了一种层间含有Sn(II)的无添加剂负极。层间受限的Sn(II)中的Sn-5s具有更大的负电荷,它将与O-2p杂化以触发电荷重新分布,从而提高电子导电性。具有开放框架的氢氧化物钛酸盐被设计用于稳定Sn(II)并抑制随后的体积膨胀,这有可能通过具有高可逆性的联合合金化-嵌入反应超越钛酸盐基材料的容量限制。此外,层间合金化反应产生的导电NaSn以及层间距的扩大有利于电荷转移。这些效应协同作用,使改性样品具有显著更低的活化能和3倍的扩散增加。因此,与未改性样品相比,所设计的负极具有出色的低温适应性,在-20°C下1200次循环后容量保持率为91%,在-30°C下850次循环后容量保持率为90%。

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