Pore-intrusion of Polymeric Binder in Supercapacitor Electrodes Decreases Capacitance
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A combined study of electrochemical characterization, scanning electron microscopy, gas sorption, and solid-state nuclear magnetic resonance spectroscopy was conducted to understand the effect of polymeric binder in the performance of... A combined study of electrochemical characterization, scanning electron microscopy, gas sorption, and solid-state nuclear magnetic resonance spectroscopy was conducted to understand the effect of polymeric binder in the performance of supercapacitor electrodes. We show that increasing the quantity of PTFE binder in the carbon electrode decreases the gravimetric capacitance. The decrease in capacitance is caused by the decrease in porosity of the carbon electrode, as determined by gas sorption and NMR spectroscopy. Importantly, 19 F NMR reveals the significant intrusion of the PTFE binder into the carbon micropores, evidenced through the observation of a nucleus-independent chemical shift. 23 Na NMR of aqueous electrolyte adsorption further shows that increasing the quantity of the PTFE binder hinders the amount of Na + ions adsorbed within the pores, affecting the charge storage mechanism. To mitigate this effect, an alternative dry electrode processing method was investigated which revealed a substantial reduction in PTFE pore intrusion. Summarizing, our study reveals the significant intrusion of polymeric binder into the pores of carbon electrodes, which decreases porosity and the corresponding charge storage performance. These findings may guide the design of new electrode formulations, such as dry process, with improved energy storage capacities.
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Acknowledgements: The authors thank Dr Heather Greer for help with performing SEM and TEM measurements. We also thank Drs Hasan Celik, Raynald Giovine, and Pines Magnetic Resonance Center's Core NMR Facility (PMRC Core) for spectroscopic assistance. The instrument used in this work is supported by the National Science Foundation under Grant No. 2018784. This work was also supported by a UKRI Future Leaders Fellowship to A.C.F. (MR/T043024/1), and an ERC Starting Grant to A.C.F., funded through the UKRI guarantee scheme (EP/X042693/1).
Publication status: Published
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2040-3372
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Horizon Europe UKRI Underwrite ERC (EP/X042693/1)

