成核
纳米颗粒
碳纳米管
材料科学
锂(药物)
化学工程
薄膜
纳米技术
无机化学
化学
有机化学
医学
工程类
内分泌学
作者
Chunzhen Yang,Raymond Albert Wong,Misun Hong,Keisuke Yamanaka,Toshiaki Ohta,Hye Ryung Byon
出处
期刊:Nano Letters
[American Chemical Society]
日期:2016-04-22
卷期号:16 (5): 2969-2974
被引量:160
标识
DOI:10.1021/acs.nanolett.5b05006
摘要
In lithium-oxygen (Li-O2) batteries, it is believed that lithium peroxide (Li2O2) electrochemically forms thin films with thicknesses less than 10 nm resulting in capacity restrictions due to limitations in charge transport. Here we show unexpected Li2O2 film growth with thicknesses of ∼60 nm on a three-dimensional carbon nanotube (CNT) electrode incorporated with cerium dioxide (ceria) nanoparticles (CeO2 NPs). The CeO2 NPs favor Li2O2 surface nucleation owing to their strong binding toward reactive oxygen species (e.g., O2 and LiO2). The subsequent film growth results in thicknesses of ∼40 nm (at cutoff potential of 2.2 V vs Li/Li(+)), which further increases up to ∼60 nm with the addition of trace amounts of H2O that enhances the solution free energy. This suggests the involvement of solvated superoxide species (LiO2(sol)) that precipitates on the existing Li2O2 films to form thicker films via disproportionation. By comparing toroidal Li2O2 formed solely from LiO2(sol), the thick Li2O2 films formed from surface-mediated nucleation/thin-film growth following by LiO2(sol) deposition provides the benefits of higher reversibility and rapid surface decomposition during recharge.
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