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
[31]  
Wallwork KS, 2007, AIP CONF PROC, V879, P879
[32]   P2-Na0.6[Cr0.6Ti0.4]O2 cation-disordered electrode for high-rate symmetric rechargeable sodium-ion batteries [J].
Wang, Yuesheng ;
Xiao, Ruijuan ;
Hu, Yong-Sheng ;
Avdeev, Maxim ;
Chen, Liquan .
NATURE COMMUNICATIONS, 2015, 6
[33]   CHEMISTRY OF INTERCALATION COMPOUNDS - METAL GUESTS IN CHALCOGENIDE HOSTS [J].
WHITTINGHAM, MS .
PROGRESS IN SOLID STATE CHEMISTRY, 1978, 12 (01) :41-99
[34]   A new electrode material for rechargeable sodium batteries: P2-type Na2/3[Mg0.28Mn0.72]O2 with anomalously high reversible capacity [J].
Yabuuchi, Naoaki ;
Hara, Ryo ;
Kubota, Kei ;
Paulsen, Jens ;
Kumakura, Shinichi ;
Komaba, Shinichi .
JOURNAL OF MATERIALS CHEMISTRY A, 2014, 2 (40) :16851-16855
[35]  
Yabuuchi N, 2012, NAT MATER, V11, P512, DOI [10.1038/nmat3309, 10.1038/NMAT3309]
[36]   NaFe0.5Co0.5O2 as high energy and power positive electrode for Na-ion batteries [J].
Yoshida, Hiroaki ;
Yabuuchi, Naoaki ;
Komaba, Shinichi .
ELECTROCHEMISTRY COMMUNICATIONS, 2013, 34 :60-63