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Calcination Temperature Effect on Citrate-Capped Iron Oxide Nanoparticles as Lithium-Storage Anode Materials

机译:煅烧温度对柠檬酸包覆的氧化铁纳米颗粒作为储锂阳极材料的影响

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摘要

In this work, citrate-capped magnetites (cit-Fe_3O_4) are facilely synthesizedaccording to a modified co-precipitation method, and the resulting cit-Fe_3O_4underwent thermal calcination under N2 flow for 2 h. The calcined cit-Fe_3O_4at 500 ℃, so-called C-Fe_3O_4 (500 ℃), exhibits the XRD patterns attributedmainly to the fcc crystalline phases of magnetite (Fe_3O_4). On the other hand,the calcined cit-Fe_3O_4 at 700 ℃, so-called C-Fe2O3 (700 ℃), exhibits the X-raydiffraction (XRD) patterns attributed mostly to hexagonal crystalline phasesof hematite (α-Fe_2O_3). The iron oxides calcined at different temperatures(500, 600, 700 ℃) are employed as active anode materials for Li-ion batteries.After 80 cycles at the current rate of 0.1 C, the C-Fe_2O_3 (700 ℃) exhibits thehigher reversible capacity by ≈200% than that of the C-Fe_3O_4 (500 ℃). Theimproved reversible capacity of the C-Fe_2O_3 (700 ℃) is attributed to thetransformation of magnetite phases into hematite phases with highercrystallinity, which is more beneficial for faster transfer of charge carriers andstructural stability.
机译:在这项工作中,根据一种改进的共沉淀方法,可以轻松地合成柠檬酸盐封端的磁铁矿(cit-Fe_3O_4),然后在氮气流下将得到的cit-Fe_3O_4 r进行热煅烧2 h。煅烧后的cit-Fe_3O_4 r nat 500℃,即所谓的C-Fe_3O_4(500℃),表现出的XRD图谱主要归因于磁铁矿(Fe_3O_4)的fcc晶相。另一方面, r n在700℃下煅烧的cit-Fe_3O_4,即所谓的C-Fe2O3(700℃),表现出主要归因于六方晶相的X射线 r n衍射(XRD)模式 r 赤铁矿(α-Fe_2O_3)。在不同温度 r n(500、600、700℃)下煅烧的氧化铁被用作锂离子电池的活性阳极材料。 r n在0.1 C的电流速率下经过80次循环后,C-Fe_2O_3( 700℃)的可逆容量比C-Fe_3O_4(500℃)高约200%。 C-Fe_2O_3(700℃)的可逆容量提高归因于磁铁矿相转变为具有更高结晶度的赤铁矿相,这对于更快地转移载流子和更有利 n结构稳定。

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  • 来源
    《Physica status solidi》 |2018年第20期|1701004.1-1701004.7|共7页
  • 作者单位

    Department of Chemical and Biological Engineering Gachon University 1342 Seongnamdaero, Seongnam-si 461-701, Republic of Korea;

    Department of Chemical and Biological Engineering Gachon University 1342 Seongnamdaero, Seongnam-si 461-701, Republic of Korea;

    Department of Chemical and Biological Engineering Gachon University 1342 Seongnamdaero, Seongnam-si 461-701, Republic of Korea;

    Department of Chemical and Biological Engineering Gachon University 1342 Seongnamdaero, Seongnam-si 461-701, Republic of Korea;

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