Hydrogenation effects on the lithium ion battery performance of TiOF2

被引:24
作者
He, Min [1 ,2 ]
Wang, Zhihui [3 ]
Yan, Xiaodong [1 ]
Tian, Lihong [1 ,4 ]
Liu, Gao [3 ]
Chen, Xiaobo [1 ]
机构
[1] Univ Missouri, Dept Chem, Kansas City, MO 64110 USA
[2] Wuhan Univ Sci & Technol, Coll Sci, Dept Appl Phys, Wuhan 430065, Hubei, Peoples R China
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Adv Energy Technol Dept, Berkeley, CA 94720 USA
[4] Hubei Univ, Hubei Collaborat Innovat Ctr Adv Organochem Mat, Wuhan 430062, Peoples R China
关键词
Titanium oxyfluorides; Hydrogenation; Rate performance; Lithium ion battery; INSERTED METAL-OXIDES; ANATASE TIO2; CORE/SHELL NANOSHEETS; TITANIUM OXYFLUORIDE; ENERGY-CONVERSION; GENERATION; EVOLUTION; STORAGE; ELECTROCATALYSTS; NANOPARTICLES;
D O I
10.1016/j.jpowsour.2015.12.032
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hydrogenated titanium oxyfluorides (TiOF2) nanoparticles were synthesized via one-pot hydrothermal method and subsequent hydrogenation treatment. As anode materials for lithium ion batteries, the hydrogenated TiOF2 showed a superior rate performance compared to the pristine TiOF2. A charge capacity of 118.4 mA h g(-1) was achieved at the current density of 1053 mA g(-1) upon 150 cycles, which was 4 times higher than that of the pristine TiOF2. The rate performance of the hydrogenated TiOF2 at different current densities of 42, 210,1053, 2106, 5265, 10530, 21060 and 52650 mA g(-1) was 2.8, 6.0,13.2, 14.7, 21.5, 30.6, 67.9 and 483.3 times higher than those of the pristine TiOF2 electrode at the corresponding rates, respectively. The remarkable improvement of the electrochemical performance was likely related to the size breakdown in the (001) direction after hydrogenation, instead of oxygen vacancies induced better charge transfer properties. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:309 / 316
页数:8
相关论文
共 36 条
[1]   Nanostructured materials for advanced energy conversion and storage devices [J].
Aricò, AS ;
Bruce, P ;
Scrosati, B ;
Tarascon, JM ;
Van Schalkwijk, W .
NATURE MATERIALS, 2005, 4 (05) :366-377
[2]   THE STRUCTURES OF LITHIUM-INSERTED METAL-OXIDES - LIREO3 AND LI2REO3 [J].
CAVA, RJ ;
SANTORO, A ;
MURPHY, DW ;
ZAHURAK, S ;
ROTH, RS .
JOURNAL OF SOLID STATE CHEMISTRY, 1982, 42 (03) :251-262
[3]   THE CRYSTAL-STRUCTURES OF THE LITHIUM-INSERTED METAL-OXIDES LI0.5TIO2 ANATASE, LITI2O4 SPINEL, AND LI2TI2O4 [J].
CAVA, RJ ;
MURPHY, DW ;
ZAHURAK, S ;
SANTORO, A ;
ROTH, RS .
JOURNAL OF SOLID STATE CHEMISTRY, 1984, 53 (01) :64-75
[4]   Facile hydrothermal synthesis of single crystalline TiOF2 nanocubes and their phase transitions to TiO2 hollow nanocages as anode materials for lithium-ion battery [J].
Chen, Lin ;
Shen, Laifa ;
Nie, Ping ;
Zhang, Xiaogang ;
Li, Hongsen .
ELECTROCHIMICA ACTA, 2012, 62 :408-415
[5]   Nanomaterials for renewable energy production and storage [J].
Chen, Xiaobo ;
Li, Can ;
Graetzel, Michael ;
Kostecki, Robert ;
Mao, Samuel S. .
CHEMICAL SOCIETY REVIEWS, 2012, 41 (23) :7909-7937
[6]   Increasing Solar Absorption for Photocatalysis with Black Hydrogenated Titanium Dioxide Nanocrystals [J].
Chen, Xiaobo ;
Liu, Lei ;
Yu, Peter Y. ;
Mao, Samuel S. .
SCIENCE, 2011, 331 (6018) :746-750
[7]   Dual Lithium Insertion and Conversion Mechanisms in a Titanium-Based Mixed-Anion Nanocomposite [J].
Dambournet, Damien ;
Chapman, Karena W. ;
Chupas, Peter J. ;
Gerald, Rex E., II ;
Penin, Nicolas ;
Labrugere, Christine ;
Demourgues, Alain ;
Tressaud, Alain ;
Amine, Khalil .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2011, 133 (34) :13240-13243
[8]  
Jenkins R, 1996, INTRO XRAY POWDER DI, DOI DOI 10.1016/S0341-8162(03)00040-7
[9]   Lithium storage in nanostructured TiO2 made by hydrothermal growth [J].
Kavan, L ;
Kalbác, M ;
Zukalová, M ;
Exnar, I ;
Lorenzen, V ;
Nesper, R ;
Graetzel, M .
CHEMISTRY OF MATERIALS, 2004, 16 (03) :477-485
[10]   Li+ ion insertion in TiO2 (anatase) .2. Voltammetry on nanoporous films [J].
Lindstrom, H ;
Sodergren, S ;
Solbrand, A ;
Rensmo, H ;
Hjelm, J ;
Hagfeldt, A ;
Lindquist, SE .
JOURNAL OF PHYSICAL CHEMISTRY B, 1997, 101 (39) :7717-7722