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一种用于稳定硅阳极的具有高能量耗散的梯度分布粘结剂。

A gradient-distributed binder with high energy dissipation for stable silicon anode.

作者信息

Zhang Dongyang, Ouyang Yuxin, Wang Yong, Liu Limin, Wang Haijie, Cui Jia, Wang Mingyue, Li Na, Zhao Hongyang, Ding Shujiang

机构信息

School of Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an Jiaotong University, Xi'an 710049, People's Republic of China.

School of Chemistry, Engineering Research Center of Energy Storage Materials and Devices, Ministry of Education, Xi'an Jiaotong University, Xi'an 710049, People's Republic of China.

出版信息

J Colloid Interface Sci. 2024 Nov;673:312-320. doi: 10.1016/j.jcis.2024.06.086. Epub 2024 Jun 10.

Abstract

Silicon is considered as a promising alternative to traditional graphite anode for lithium-ion batteries. Due to the dramatic volume expansion of silicon anode generated from the insertion of Li ions, the binder which can suppress the severe volume change and repeated massive stress impact during cycling is required greatly. Herein, we design a gradient-distributed two-component binder (GE-PAA) to achieve excellent cyclic stability, and reveal the mechanism of high energy dissipative binder stabilized silicon electrodes. The inner layer of the electrode is the polyacrylic acid polymer (PAA) with high Young's modulus, which is used as the skeleton binder to stabilize the silicon particle interface and the electrode structure. The outer layer is the gel electrolyte polymer (GE) with lower Young's modulus, which releases the stress generated during the lithiation and de-lithiation process effectively, achieving the high structural stability at the molecular level and silicon particles. Due to the synergistic effect of the gradient binder design, the silicon electrode retains a reversible capacity of 1557.4 mAh g after 200 cycles at the current density of 0.5 C and 1539.2 mAh g at a high rate of 1.8 C. This work provides a novel binder design strategy for Si anode with long cycle stability.

摘要

硅被认为是锂离子电池传统石墨负极的一种有前途的替代材料。由于锂离子嵌入导致硅负极发生剧烈的体积膨胀,因此迫切需要一种能够抑制循环过程中严重体积变化和反复巨大应力冲击的粘结剂。在此,我们设计了一种梯度分布的双组分粘结剂(GE-PAA)以实现优异的循环稳定性,并揭示了高能耗散粘结剂稳定硅电极的机制。电极的内层是具有高杨氏模量的聚丙烯酸聚合物(PAA),用作骨架粘结剂以稳定硅颗粒界面和电极结构。外层是具有较低杨氏模量的凝胶电解质聚合物(GE),它有效地释放了锂化和脱锂过程中产生的应力,在分子水平和硅颗粒上实现了高结构稳定性。由于梯度粘结剂设计的协同效应,硅电极在0.5 C的电流密度下循环200次后保持1557.4 mAh g的可逆容量,在1.8 C的高倍率下保持1539.2 mAh g。这项工作为具有长循环稳定性的硅负极提供了一种新颖的粘结剂设计策略。

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