Rate Dependent Performance Related to Crystal Structure Evolution of Na0.67Mn0.8Mg0.2O2 in a Sodium-Ion Battery

被引:100
作者
Sharma, Neeraj [1 ]
Tapia-Ruiz, Nuria [2 ]
Singh, Gurpreet [3 ]
Armstrong, A. Robert [4 ]
Pramudita, James C. [1 ]
Brand, Helen E. A. [5 ]
Billaud, Juliette [4 ]
Bruce, Peter G. [2 ]
Rojo, Teofilo [3 ,6 ]
机构
[1] UNSW Australia, Sch Chem, Sydney, NSW 2052, Australia
[2] Univ Oxford, Dept Mat, Oxford OX1 3PH, England
[3] CIC Energigune, ED CIC, Minano 01510, Spain
[4] Univ St Andrews, Sch Chem, St Andrews KY16 9ST, Fife, Scotland
[5] Australian Synchrotron, Melbourne, Vic 3168, Australia
[6] Univ Basque Country, EHU, Dept Quim Inorgan, E-48080 Bilbao, Spain
基金
英国工程与自然科学研究理事会;
关键词
X LESS-THAN; ELECTROCHEMICAL-CELL; POWDER DIFFRACTION; HIGH-ENERGY; ELECTRODE; P2-TYPE; CATHODE; PHASE; NI;
D O I
10.1021/acs.chemmater.5b02142
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
Sodium-ion batteries are considered as a favorable alternative to the widely used lithium-ion batteries for applications such as grid-scale energy storage. However, to meet the energy density and reliability that is necessary, electrodes that are structurally stable and well characterized during electrochemical cycling need to be developed. Here, we report on how the applied discharge current rate influences the structural evolution of Na0.67Mn0.8Mg0.2O2 electrode materials. A combination of ex situ and in situ X-ray diffraction (XRD) data were used to probe the structural transitions at the discharged state and during charge/discharge. Ex situ data shows a two-phase electrode at the discharged state comprised of phases that adopt Cmcm and P6(3)/mmc symmetries at the 100 mA/g rate but a predominantly P6(3)/mmc electrode at 200 and 400 mA/g rates. In situ synchrotron XRD data at 100 mA/g shows a solely P6(3)/mmc electrode when 12 mA/g charge and 100 mA/g discharge is used even though ex situ XRD data shows the presence of both Cmcm and P6(3)/mmc phases. The in situ data allows the Na site occupancy evolution to be determined as well as the rate of lattice expansion and contraction. Electrochemically, lower applied discharge currents, e.g., 100 mA/g, produce better capacity than higher applied currents, e.g., 400 mA/g, and this is related in part to the quantity of the Cmcm phase that is formed near the discharged state during a two-phase reaction (via ex situ measurements), with lower rates producing more of this Cmcm phase. Thus, producing more Cmcm phase allows access to higher capacities while higher rates show a lower utilization of the cathode during discharge as less (if any) Cmcm phase is formed. Therefore, this work shows how structural transitions can depend on the electrochemically applied current which has significant ramifications on how sodium-ion batteries, and batteries in general, are analyzed for performance during operation.
引用
收藏
页码:6976 / 6986
页数:11
相关论文
共 36 条
[21]   Structural evolution of high energy density V3+/V4+ mixed valent Na3V2O2x(PO4)2F3-2x (x=0.8) sodium vanadium fluorophosphate using in situ synchrotron X-ray powder diffraction [J].
Serras, Paula ;
Palomares, Veronica ;
Rojo, Teofilo ;
Brand, Helen E. A. ;
Sharma, Neeraj .
JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (21) :7766-7779
[22]   In Situ Powder Diffraction Studies of Electrode Materials in Rechargeable Batteries [J].
Sharma, Neeraj ;
Pang, Wei Kong ;
Guo, Zaiping ;
Peterson, Vanessa K. .
CHEMSUSCHEM, 2015, 8 (17) :2826-2853
[23]   The Unique Structural Evolution of the O3-Phase Na2/3Fe2/3Mn1/3O2 during High Rate Charge/Discharge: A Sodium-Centred Perspective [J].
Sharma, Neeraj ;
Gonzalo, Elena ;
Pramudita, James C. ;
Han, Man Huon ;
Brand, Helen E. A. ;
Hart, Judy N. ;
Pang, Wei Kong ;
Guo, Zaiping ;
Rojo, Teofilo .
ADVANCED FUNCTIONAL MATERIALS, 2015, 25 (31) :4994-5005
[24]   Sodium Distribution and Reaction Mechanisms of a Na3V2O2(PO4)2F Electrode during Use in a Sodium-Ion Battery [J].
Sharma, Neeraj ;
Serras, Paula ;
Palomares, Veronica ;
Brand, Helen E. A. ;
Alonso, Javier ;
Kubiak, Pierre ;
Luisa Fdez-Gubieda, M. ;
Rojo, Teofilo .
CHEMISTRY OF MATERIALS, 2014, 26 (11) :3391-3402
[25]   Current-dependent electrode lattice fluctuations and anode phase evolution in a lithium-ion battery investigated by in situ neutron diffraction [J].
Sharma, Neeraj ;
Peterson, Vanessa K. .
ELECTROCHIMICA ACTA, 2013, 101 :79-85
[26]   Direct Evidence of Concurrent Solid-Solution and Two-Phase Reactions and the Nonequilibrium Structural Evolution of LiFePO4 [J].
Sharma, Neeraj ;
Guo, Xianwei ;
Du, Guodong ;
Guo, Zaiping ;
Wang, Jiazhou ;
Wang, Zhaoxiang ;
Peterson, Vanessa K. .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2012, 134 (18) :7867-7873
[27]   Structural changes in a commercial lithium-ion battery during electrochemical cycling: An in situ neutron diffraction study [J].
Sharma, Neeraj ;
Peterson, Vanessa K. ;
Elcombe, Margaret M. ;
Avdeev, Maxim ;
Studer, Andrew J. ;
Blagojevic, Ned ;
Yusoff, Rozila ;
Kamarulzaman, Norlida .
JOURNAL OF POWER SOURCES, 2010, 195 (24) :8258-8266
[28]   Single-crystal synthesis, structure refinement and electrical properties of Li0.5CoO2 [J].
Takahashi, Y. ;
Kijima, N. ;
Tokiwa, K. ;
Watanabe, T. ;
Akimoto, J. .
JOURNAL OF PHYSICS-CONDENSED MATTER, 2007, 19 (43)
[29]   Structure of the high voltage phase of layered P2-Na2/3-z[Mn1/2Fe1/2]O2 and the positive effect of Ni substitution on its stability [J].
Talaie, Elahe ;
Duffort, Victor ;
Smith, Hillary L. ;
Fultz, Brent ;
Nazar, Linda F. .
ENERGY & ENVIRONMENTAL SCIENCE, 2015, 8 (08) :2512-2523
[30]   EXPGUI, a graphical user interface for GSAS [J].
Toby, BH .
JOURNAL OF APPLIED CRYSTALLOGRAPHY, 2001, 34 :210-213