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Engineering of Oxygen Vacancy and Electric‐Field Effect by Encapsulating Lithium Titanate in Reduced Graphene Oxide for Superior Lithium Ion Storage
Author(s) -
Meng Tao,
Li Bo,
Hu Lei,
Yang Hao,
Fan Wenjie,
Zhang Shanqing,
Liu Peng,
Li Mingyang,
Gu Feng Long,
Tong Yexiang
Publication year - 2019
Publication title -
small methods
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.66
H-Index - 46
ISSN - 2366-9608
DOI - 10.1002/smtd.201900185
Subject(s) - materials science , graphene , electrode , electrochemistry , oxide , lithium (medication) , raman spectroscopy , nanotechnology , chemical engineering , cathode , composite number , energy storage , titanate , lithium titanate , ion , lithium ion battery , composite material , battery (electricity) , chemistry , ceramic , metallurgy , medicine , power (physics) , physics , quantum mechanics , endocrinology , organic chemistry , engineering , optics
Rational design of nanostructured electrode materials is highly desired for developing high‐performance lithium‐ion batteries (LIBs). Encapsulating electrode materials in reduced graphene oxide (rGO) shows great potential for manipulation of physicochemical properties at the atomic level, promoting remarkable electrochemical properties. Here, a controllable strategy is proposed to synthesize a “pomegranate‐like” 3D rGO encapsulated lithium titanate composite (CT‐rGO@LTO). The experimental results demonstrate the enriched oxygen vacancies in LTO and the electronic interactions at the interface between LTO and rGO. Density functional theory (DFT) calculations confirm the charge redistribution in the CT‐rGO@LTO composite, establishing a strong electric field with oxygen vacancies. Furthermore, the extra active sites in rGO for Li‐ion storage are investigated via in situ Raman tests. Benefiting from the oxygen vacancies and the electric‐field effect, the CT‐rGO@LTO electrode delivers excellent cycling stability with a capacity retention of 87.1% after 1500 cycles at 5 C. Moreover, the CT‐rGO@LTO electrode is adopted to assemble a full cell with a LiCoO 2 cathode, which also displays superior rate capability with capacities of 139.4 and 109.7 mA h g −1 at 0.5 and 10 C, respectively. This work provides profound insights of fabricating high‐performance electrode materials for advanced energy storage.