插层(化学)
锂(药物)
臼齿
摩尔比
化学工程
化学
无机化学
体积热力学
材料科学
有机化学
热力学
催化作用
地质学
物理
工程类
内分泌学
古生物学
医学
作者
Wenzao Li,Jeffrey D. Cain,Nicholas P. W. Pieczonka,Zhongyi Liu,Sayed Youssef Sayed,Yue Qi
标识
DOI:10.1021/acsenergylett.4c03063
摘要
Conversion-type anode materials generally suffer from significant volume change upon lithiation despite a high energy storage capacity. Here we report a new intercalation and conversion hybrid-type lithiation mechanism that enables a layered silicane (L-SiH) material to balance high capacity with low volume change. Using first-principles simulations of lithiation and delithiation processes, we predict L-SiH only shows a 3.8 cm3/mol volume expansion upon lithiation, significantly lower than that of crystalline Si (∼9.2 cm3/mol). During lithium intercalation, hydrogen in L-SiH is redox active, and LiH bonds are formed in the interlayer, without destruction of Si planes. The predicted lithiation proceeds via a two-phase coexisting process at an open-circuit voltage (OCV) plateau of ∼0.43 V, which coincides with experimental observation of a 0.4 V plateau upon the lithiation of synthesized L-SiH. This study introduces a promising anode material with a low volume change fulfilled by an intriguing mechanism.
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