Improved electro-grafting of nitropyrene onto onion-like carbon via in situ electrochemical reduction and polymerization: Tailoring redox energy density of the supercapacitor positive electrode
Bihag Anothumakkool, Yuman Sayed-Ahmad-Baraza, Chris Ewels,, Pierre-Louis Taberna, Barbara Daffos, Patruce Simon, Thierry Brousse, Joel, Gaubicher

TL;DR
This study introduces an improved in situ electrochemical method for grafting nitropyrene onto carbon onions, significantly enhancing supercapacitor electrode capacity and stability through tailored redox properties.
Contribution
The paper presents a novel in situ electrochemical grafting technique that increases redox activity and capacity of supercapacitor electrodes using nitropyrene on carbon onions.
Findings
Electrode capacity increased from 20 to 38 mAh g-1 with 20 wt % Pyr-NO2 grafting.
The average potential increased by 200 mV due to grafting.
The electrode maintained over 4000 cycles with high retention.
Abstract
Herein, we report a improved method for the physical grafting of 1-nitropyrene (Pyr-NO2) onto highly graphitized carbon onion. This is achieved through a lowering of the onset potential of the pyrene polymerization via in situ reduction of the NO2 group. The additional redox activity pertaining to the reduced NO2 enables exceeding the faradaic capacity which is associated with the p-doping of the grafted pyrene backbone, as observed for pyrene, 1-aminopyrene, and unreduced Pyr- NO2. Theoretical calculations demonstrate the charge transfer and binding enthalpy capabilities of Pyr-NO2, which are significantly higher than those of the other two species, and which allow for improved p-stacking on the carbon surface. Upon 20 wt % grafting of Pyr-NO2, the capacity of the electrode jumps from 20 mAh g-1 electrode to 38 mAh g- electrode, which corresponds to 110 mAh g-1 per mass of Pyr-NO2 and…
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