Explaining key properties of lithiation in TiO2-anatase Li-ion battery electrodes using phase-field modeling

被引:44
作者
de Klerk, Niek J. J. [1 ]
Vasileiadis, Alexandros [1 ]
Smith, Raymond B. [2 ]
Bazant, Martin Z. [2 ,3 ]
Wagemaker, Marnix [1 ]
机构
[1] Delft Univ Technol, Dept Radiat Sci & Technol, Mekelweg 15, NL-2629 JB Delft, Netherlands
[2] MIT, Dept Chem Engn, Cambridge, MA 02139 USA
[3] MIT, Dept Math, Cambridge, MA 02139 USA
基金
欧洲研究理事会;
关键词
ENHANCED ELECTROCHEMICAL PERFORMANCE; ANATASE TIO2; LITHIUM INSERTION; PARTICLE-SIZE; LIFEPO4; NANOPARTICLES; ANODE MATERIALS; SURFACE-AREA; HIGH-RATES; INTERCALATION; DYNAMICS;
D O I
10.1103/PhysRevMaterials.1.025404
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The improvement of Li-ion battery performance requires development of models that capture the essential physics and chemistry in Li-ion battery electrode materials. Phase-field modeling has recently been shown to have this ability, providing new opportunities to gain understanding of these complex systems. In this paper, a novel electrochemical phase-field model is presented that captures the thermodynamic and kinetic properties of lithium insertion in TiO2-anatase, a well-known and intensively studied Li-ion battery electrode material. Using a linear combination of two regular solution models, the two phase transitions during lithiation are described as lithiation of two separate lattices with different physical properties. Previous elaborate experimental work on lithiated anatase TiO2 provides all parameters necessary for the phase-field simulations, giving the opportunity to gain fundamental insight in the lithiation of anatase and validate this phase-field model. The phase-field model captures the essential experimentally observed phenomena, rationalizing the impact of C rate, particle size, surface area, and the memory effect on the performance of anatase as a Li-ion battery electrode. Thereby a comprehensive physical picture of the lithiation of anatase TiO2 is provided. The results of the simulations demonstrate that the performance of anatase is limited by the formation of the poor Li-ion diffusion in the Li 1 TiO2 phase at the surface of the particles. Unlike other electrode materials, the kinetic limitations of individual anatase particles limit the performance of full electrodes. Hence, rather than improving the ionic and electronic network in electrodes, improving the performance of anatase TiO2 electrodes requires preventing the formation of a blocking Li 1 TiO2 phase at the surface of particles. Additionally, the qualitative agreement of the phase-field model, containing only parameters from literature, with a broad spectrum of experiments demonstrates the capabilities of phase-field models for understanding Li-ion electrode materials, and its promise for guiding the design of electrodes through a thorough understanding of material properties and their interactions.
引用
收藏
页数:13
相关论文
共 77 条
[51]   Multiphase Porous Electrode Theory [J].
Smith, Raymond B. ;
Bazant, Martin Z. .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2017, 164 (11) :E3291-E3310
[52]   Intercalation Kinetics in Multiphase-Layered Materials [J].
Smith, Raymond B. ;
Khoo, Edwin ;
Bazant, Martin Z. .
JOURNAL OF PHYSICAL CHEMISTRY C, 2017, 121 (23) :12505-12523
[53]   TiO2 Nanoparticles for Li-Ion Battery Anodes: Mitigation of Growth and Irreversible Capacity Using LiOH and NaOH [J].
Sondergaard, Martin ;
Shen, Yanbin ;
Mamakhel, Aref ;
Marinaro, Mario ;
Wohlfahrt-Mehrens, Margret ;
Wonsyld, Karen ;
Dahl, Soren ;
Iversen, Bo B. .
CHEMISTRY OF MATERIALS, 2015, 27 (01) :119-126
[54]   Mapping the Inhomogeneous Electrochemical Reaction Through Porous LiFePO4-Electrodes in a Standard Coin Cell Battery [J].
Strobridge, Fiona C. ;
Orvananos, Bernardo ;
Croft, Mark ;
Yu, Hui-Chia ;
Robert, Rosa ;
Liu, Hao ;
Zhong, Zhong ;
Connolley, Thomas ;
Drakopoulos, Michael ;
Thornton, Katsuyo ;
Grey, Clare P. .
CHEMISTRY OF MATERIALS, 2015, 27 (07) :2374-2386
[55]   Electrochemical lithium reactivity with nanotextured anatase-type TiO2 [J].
Sudant, G ;
Baudrin, E ;
Larcher, D ;
Tarascon, JM .
JOURNAL OF MATERIALS CHEMISTRY, 2005, 15 (12) :1263-1269
[56]   Higher charge/discharge rates of lithium-ions across engineered TiO2 surfaces leads to enhanced battery performance [J].
Sun, Cheng Hua ;
Yang, Xiao Hua ;
Chen, Jun Song ;
Li, Zhen ;
Lou, Xiong Wen ;
Li, Chunzhong ;
Smith, Sean C. ;
Lu, Gao Qing ;
Yang, Hua Gui .
CHEMICAL COMMUNICATIONS, 2010, 46 (33) :6129-6131
[57]   On the complex interplay of crystallinity and surface area effects on Li-ion intercalation and pseudocapacitive storage properties of nanocrystalline anatase [J].
Sussman, Micah J. ;
Yasin, Amrita ;
Demopoulos, George P. .
JOURNAL OF POWER SOURCES, 2014, 272 :58-67
[58]   New charging strategy for lithium-ion batteries based on the integration of Taguchi method and state of charge estimation [J].
Thanh Tu Vo ;
Chen, Xiaopeng ;
Shen, Weixiang ;
Kapoor, Ajay .
JOURNAL OF POWER SOURCES, 2015, 273 :413-422
[59]   Lithium insertion and mobility in the TiO2-anatase/titanate structure:: A periodic DFT study [J].
Tielens, F ;
Calatayud, M ;
Beltrán, A ;
Minot, C ;
Andrés, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2005, 581 (02) :216-223
[60]   Atomic and electronic bulk versus surface structure:: Lithium intercalation in anatase TiO2 [J].
Wagemaker, M ;
Lützenkirchen-Hecht, D ;
van Well, AA ;
Frahm, R .
JOURNAL OF PHYSICAL CHEMISTRY B, 2004, 108 (33) :12456-12464