Temperature-Induced Activation of Graphite Co-intercalation Reactions for Glymes and Crown Ethers in Sodium-Ion Batteries

2018-11-29
Goktas, Mustafa
Akduman, Baris
Huang, Peihua
Balducci, Andrea
Adelhelm, Philipp
The intercalation of solvated ions into graphite leads to ternary graphite intercalation compounds (t-GICs). Here, we study the impact of temperature on the electro-chemical activity of graphite electrodes for co-intercalation reactions between 20 and 80 degrees C in sodium cells. For this, a range of linear ethers (mono-, di-, tri-, and tetraglyme) are studied. For the first time, pentaglyme and several crown ethers are also investigated. We find that several solvents that appear as unsuitable for the co-intercalation reaction at room provide higher capacities at elevated temperatures. The most evident example is pentaglyme. While poor performance is found at room temperature for this solvent (20 mAhg(-1) and large polarization), almost complete utilization (similar to 110 mAh g(-1)) and excellent rate capability are obtained at 45 degrees C. We find that the reactions involving mono-, di-, tetra-, and (at elevated temperatures also) pentaglyme are thermodynamically controlled, whereas the reaction with triglyme is kinetically limited. We also find that the crown ether 18c6 can be used as an electrolyte solvent above its melting point, which, for the first time, demonstrates the synthesis of t-GICs with crown ethers by electrochemical methods. Additionally, parasitic reactions are found to appear at elevated temperatures. Overall, we demonstrate that new co-intercalation reactions can be activated by temperature. The chemistry of these compounds might therefore be much richer than previously thought.
JOURNAL OF PHYSICAL CHEMISTRY C

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Citation Formats
M. Goktas, B. Akduman, P. Huang, A. Balducci, and P. Adelhelm, “Temperature-Induced Activation of Graphite Co-intercalation Reactions for Glymes and Crown Ethers in Sodium-Ion Batteries,” JOURNAL OF PHYSICAL CHEMISTRY C, pp. 26816–26824, 2018, Accessed: 00, 2020. [Online]. Available: https://hdl.handle.net/11511/67930.