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羧甲基纤维素粘合剂极大地稳定了用于电容性钾离子存储的多孔空心碳亚微球。

Carboxymethyl Cellulose Binder Greatly Stabilizes Porous Hollow Carbon Submicrospheres in Capacitive K-Ion Storage.

作者信息

Li Jinliang, Zhuang Ning, Xie Junpeng, Zhu Yongqian, Lai Haojie, Qin Wei, Javed Muhammad Sufyan, Xie Weiguang, Mai Wenjie

机构信息

Siyuan Laboratory, Guangdong Provincial Engineering Technology Research Center of Vacuum Coating Technologies and New Energy Materials, Department of Physics , Jinan University , Guangzhou , 510632 People's Republic of China .

Department of Materials Science and Engineering , Jinan University , Guangzhou 510632 , People's Republic of China .

出版信息

ACS Appl Mater Interfaces. 2019 May 1;11(17):15581-15590. doi: 10.1021/acsami.9b02060. Epub 2019 Apr 19.

Abstract

On account of the large radius of K-ions, the electrodes can suffer huge deformation during K-ion insertion and extraction processes. In our work, we unveil the impact of using carboxymethyl cellulose (CMC) instead of poly(vinylidene fluoride) (PVDF) as binders for K-ion storage. Our porous hollow carbon submicrosphere anodes using the CMC binder exhibit a reversible capacity of 208 mA h g after 50 cycles at 50 mA g, and even at a high current density of 1 A g, they achieve a reversible capacity of 111 mA h g over 3000 cycles with almost no decay, demonstrating remarkably improved reversibility and cycling stability than those using PVDF (18 mA h g after 3000 cycles at 1 A g). It is showed that the CMC binder can result in higher adhesion force and better mechanical performance than the PVDF binder, which can restrain the crack during a potassiation/depotassiation process. According to the test of adhesion force, the hollow carbon submicrospheres using the CMC binder show above three times of average adhesion force than that using the PVDF binder. Furthermore, based on the rational design, our hollow carbon submicrospheres also exhibit 62.3% specific capacity contribution below 0.5 V vs K/K region, which is helpful to design the full cell with high energy density. We believe that our work will highlight the binder effect to improve the K-ion storage performance.

摘要

由于钾离子半径较大,在钾离子嵌入和脱出过程中,电极会发生巨大变形。在我们的工作中,我们揭示了使用羧甲基纤维素(CMC)代替聚偏氟乙烯(PVDF)作为钾离子存储的粘结剂的影响。我们使用CMC粘结剂的多孔空心碳亚微球阳极在50 mA g下循环50次后,可逆容量为208 mA h g,即使在1 A g的高电流密度下,在3000次循环中也能实现111 mA h g的可逆容量,且几乎没有衰减,与使用PVDF的阳极相比(在1 A g下3000次循环后为18 mA h g),其可逆性和循环稳定性得到了显著改善。结果表明,CMC粘结剂比PVDF粘结剂具有更高的粘附力和更好的机械性能,这可以抑制钾化/去钾化过程中的裂纹。根据粘附力测试,使用CMC粘结剂的空心碳亚微球的平均粘附力比使用PVDF粘结剂的高出三倍以上。此外,基于合理的设计,我们的空心碳亚微球在相对于K/K区域0.5 V以下还表现出62.3%的比容量贡献,这有助于设计具有高能量密度的全电池。我们相信我们的工作将突出粘结剂对改善钾离子存储性能的作用。

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