Atom-Level Understanding of the Sodiation Process in Silicon Anode Material

被引:125
作者
Jung, Sung Chul [1 ,2 ]
Jung, Dae Soo [3 ]
Choi, Jang Wook [3 ]
Han, Young-Kyu [1 ,2 ]
机构
[1] Dongguk Univ Seoul, Dept Energy & Mat Engn, Seoul 100715, South Korea
[2] Dongguk Univ Seoul, Adv Energy & Elect Mat Res Ctr, Seoul 100715, South Korea
[3] Korea Adv Inst Sci & Technol, Grad Sch EEWS WCU, Taejon 305701, South Korea
基金
新加坡国家研究基金会;
关键词
SODIUM-ION BATTERIES; IN-SITU XRD; NEGATIVE ELECTRODES; STRUCTURAL-CHANGES; HIGH-CAPACITY; LITHIUM; LI; STORAGE; CHALLENGES; DIFFUSION;
D O I
10.1021/jz5002743
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Despite the exceptionally large capacities in Li ion batteries, Si has been considered inappropriate for applications in Na ion batteries. We report an atomic-level study on the applicability of a Si anode in Na ion batteries using ab initio molecular dynamics simulations. While crystalline Si is not suitable for alloying with Na atoms, amorphous Si can accommodate 0.76 Na atoms per Si atom, corresponding to a specific capacity of 725 mA h g(-1). Bader charge analyses reveal that the sodiation of an amorphous Si electrode continues until before the local Na-rich clusters containing neutral Na atoms are formed. The amorphous Na0.76Si phase undergoes a volume expansion of 114% and shows a Na diffusivity of 7 x 10(-10) cm(2) s(-1) at room temperature. Overall, the amorphous Si phase turns out quite attractive in performance compared to other alloy-type anode materials. This work suggests that amorphous Si might be a competitive candidate for Na ion battery anodes.
引用
收藏
页码:1283 / 1288
页数:6
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