锐钛矿
锂(药物)
介电谱
比表面积
过电位
纳米颗粒
化学
材料科学
动能
电极
化学工程
微尺度化学
电化学
热力学
纳米技术
物理化学
光催化
有机化学
工程类
内分泌学
物理
数学教育
医学
催化作用
量子力学
数学
作者
Edyta Madej,Stefan Klink,Wolfgang Schuhmann,Edgar Ventosa,Fabio La Mantia
标识
DOI:10.1016/j.jpowsour.2015.07.079
摘要
Anatase TiO2 nanoparticles with a specific surface area of 100 m2 g−1 and 300 m2 g−1 have been investigated as negative insertion electrode material for lithium-ion batteries. Galvanostatic intermittent titration (GITT) and electrochemical impedance spectroscopy (EIS) were used to investigate the effect of the specific surface area on the performance of the material. GITT was performed at C/10 rate, followed by an EIS measurement after each relaxation step. Separation of kinetic and thermodynamic contributions to the overpotential of the phase transformation on Li+ (de-)insertion allowed revealing a dependency of both terms on the specific surface area. The material with higher surface area undergoes intrinsic transformation during the initial cycles affecting the thermodynamics of (de-)insertion while the sample with lower surface area shows large and asymmetric kinetic hindrances. For the material with 15 nm particles, Li+ de-insertion appears to have a higher resistance than lithium insertion.
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