Quantifying Sodiation Kinetics in Alloying Tin Electrodes for Sodium-Ion Batteries
Quantifying Sodiation Kinetics in Alloying Tin Electrodes for Sodium-Ion Batteries
复制标题
DOI:
10.1149/1945-7111/ac2708
复制
发表时间:
2021-09
影响因子:
3.9
通讯作者:
S. Sarkar;A. Verma;P. Mukherjee
中科院分区:
文献类型:
--
作者:
S. Sarkar;A. Verma;P. Mukherjee
Sodium-ion batteries (SIBs) are promising next-generation energy storage devices because of the elemental abundance and low sodium cost. However, the lower storage capacity and short lifespan of SIBs necessitate the need for a fundamental understanding of the sodiation/de-sodiation kinetics complexation due to the inherent electrode materials and electrolyte interactions. This study comprehensively studied the kinetics of the sodium alloying and de-alloying mechanism in tin (Sn) electrodes, a promising anode, relying on GITT-based (galvanostatic intermittent titration technique) analytics. This study includes a limited combinatorial analysis of sodium salts, namely, NaPF 6 and NaClO 4, in conjunction with different carbonate solvents. This comprehensive analysis elicits a comparative paradigm of diffusivity, charge transfer resistance, intercalation rate constant, and exchange current density for the salt/solvent combinations. Overall, NaClO 4 exhibits better kinetic and transport properties as compared to NaPF 6. This study further elucidates the variation of ionic mobility and reaction rate with interfacial passivation due to excess fluorine donation from additives. The effect of active particle size reveals that nanoparticles exhibit reduced electrochemical (charge/discharge) hysteresis than microparticles. Overall, this study demonstrates a more considerable sensitivity of the charge transfer resistance, exchange current density, and reaction rate constants compared to the diffusivity.