4.6 Article

Structure and Electrochemical Performance of Niobium-Substituted Spinel Lithium Titanium Oxide Synthesized by Solid-State Method

Journal

JOURNAL OF THE ELECTROCHEMICAL SOCIETY
Volume 158, Issue 3, Pages A266-A274

Publisher

ELECTROCHEMICAL SOC INC
DOI: 10.1149/1.3533391

Keywords

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Funding

  1. National Natural Science Foundation of China [50902001]
  2. Education Department of Anhui Province, China [KJ2010A045]
  3. Foundation for Young Talents in College of Anhui Province, China [2010SQRL033ZD]

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Niobium-substituted Li(4)Ti(5-x)Nb(x)O(12) electrodes (0 <= x <= 0.25) have been synthesized by a solid-state method. The structure and electrochemical performance of these as prepared powders have been characterized by differential thermal analysis (DTA) and thermogravimetery (TG), X-ray diffraction (XRD), Raman spectroscopy (RS), scanning electron microscopy (SEM), cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and the galvanostatic charge-discharge test. The XRD and RS results show that the Nb(5+) can partially replace Ti(4+) and Li(+) in the spinel and there are very few oxygen vacancies in the Li(4)Ti(4.95)Nb(0.05)O(12) with a higher electronic conductivity. The Nb-doped lithium titanium oxide samples show smaller particle size and more regular morphology structure, and Li(4)Ti(4.95)Nb(0.05)O(12) has the highest initial discharge capacity and cycling performance among all the samples cycled between 0.0 and 2.0 V. CV implies that the niobium doping is beneficial to the reversible intercalation and deintercalation of Li(+). EIS indicates that Li(4)Ti(4.95)Nb(0.05)O(12) has a smaller charge transfer resistance corresponding to a much higher conductivity than that of Li(4)Ti(5)O(12) corresponding to the extraction of Li(+) ions. The superior cycling performance and wide discharge voltage range, as well as simple synthesis route and low synthesis cost of the Li(4)Ti(4.95)Nb(0.05)O(12) are expected to show a potential commercial application. (C) 2011 The Electrochemical Society. [DOI:10.1149/1.3533391] All rights reserved.

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